title: Organ culture 20E-treated replicate 1

description: 20E treated organ cultures


title: Organ culture non-treated control replicate 1

status: Public on Oct 04 2005

type: RNA

city: Athens

first: Robert

middle: B

last: Beckstead

state: GA

address: 119 Poultry Science Building

department: Poultry Science

country: USA

institute: The University of Georgia

description: Non-treated control for 20E, 20E+cycloheximide, and cycloheximide treated organ cultures.

hyb_protocol: standard Affymetrix procedures

scan_protocol: standard Affymetrix procedures

data_processing: dChip 1.2

label: biotin

molecule: total RNA

organism: Drosophila melanogaster

source_name: whole animal

label_protocol: Approximately 12 ug of total RNA was processed to produce biotinylated cRNA targest

growth_protocol: Larvae were staged by addition of 0.05% bromophenol blue to food and collected as actively wandering third instar larvae with partial blue guts (~8 hour prior to pupariation).

extract_protocol: RNA was isolated using TriPure (Roche) followed by further purification with RNAeasy (Qiagen)

treatment_protocol: Eight animals were dissected in a 9 well glass dish (Corning) and cultured in ~100 µl oxygenated Schneiders Drosophila Medium (Gibco) at 25°C. Cultures were incubated in an a styrofoam box under a constant flow of oxygen. Following an initial incubation of 1 hour, the medium was removed and replaced with fresh Schneiders Drosophila Medium (no hormone) and incubated for 6 hours at 25°C.


title: Organ culture 20E+cycloheximide-treated replicate 2

description: 20E+cycloheximide treated organ cultures

treatment_protocol: Eight animals were dissected in a 9 well glass dish (Corning) and cultured in ~100 µl oxygenated Schneiders Drosophila Medium (Gibco) at 25°C. Cultures were incubated in an a styrofoam box under a constant flow of oxygen. Following an initial incubation of 1 hour, the medium was removed and replaced with fresh Schneiders Drosophila Medium plus 5x10-6 M 20-hydroxyecdysone and 8.5x10-5 M cycloheximide and incubated for 6 hours at 25°C.


title: Organ culture non-treated control replicate 2


title: 12 hour pupae replicate 2

description: w1118 pupae

label_protocol: Approximately 12 µg of total RNA was processed to produce biotinylated cRNA targets

growth_protocol: Pupae were staged relative to pupariation

extract_protocol: RNA was isolated from 10 animals using TriPure (Roche) followed by further purification with RNAeasy columns (Qiagen)


title: Organ culture non-treated control replicate 3


title: 10 hour prepupae replicate 3

description: w1118 prepupae

growth_protocol: Prepupae were staged relative to pupariation


title: third instar larvae -4 hours relative to pupariation EcRi mutant replicate 2

description: EcR mutants die during early stages of development, complicating their use for studying receptor function during metamorphosis. To circumvent this problem, we employed a transgenic system that allows heat-induced expression of double-stranded RNA corresponding to the EcR common region to disrupt EcR function at puparium formation (EcRi)

label_protocol: Approxiamately 12 ug of total RNA was processed to produce biotinylated cRNA targets

growth_protocol: Larvae were staged by addition of 0.05% bromophenol blue and collected as actively wandering larvae with clear guts

treatment_protocol: hs-EcRi-11 third instar larvae were heat-treated twice at 37°C, each time for 1 hour, at 24 hours and 18 hours prior to pupariation

tag: Transgenic animal containing a heat-inducible transgene that expresses a double-stranded RNA corresponding to the EcR common region (hs-EcRi-11)


title: 4 hour prepupae EcRi control replicate 1

description: Control data set for EcRi data set from the 4 hour prepupae


title: 10 hour prepupae replicate 1

description: w1118 prepupae


title: 0 hour prepupae EcRi control replicate 1

description: Control data set for EcRi data set from the 0 hour prepupae


title: 0 hour prepupae EcRi control replicate 2


title: 8 hour prepupae replicate 2

description: w1118 prepupae


title: 8 hour prepupae replicate 3

description: w1118 prepupae


title: Organ culture cycloheximide-treated replicate 3

description: Cycloheximide treated organ cultures

treatment_protocol: Eight animals were dissected in a 9 well glass dish (Corning) and cultured in ~100 µl oxygenated Schneiders Drosophila Medium (Gibco) at 25°C. Cultures were incubated in an a styrofoam box under a constant flow of oxygen. Following an initial incubation of 1 hour, the medium was removed and replaced with fresh Schneiders Drosophila Medium plus 8.5x10-5 M cycloheximide and incubated for 6 hours at 25°C.


title: Organ culture 20E+cycloheximide-treated replicate 1


title: 4 hour prepupae EcRi control replicate 3


title: 4 hour prepupae replicate 1

description: w1118 prepupae


title: Organ culture cycloheximide-treated replicate 1

description: Cycloheximide treated organ cultures


title: 2 hour prepupae replicate 2

description: w1118 prepupae


title: 2 hour prepupae replicate 1

description: w1118 prepupae


title: 0 hour prepupae replicate 1

description: w1118 prepupae


title: Organ culture 20E+cycloheximide-treated replicate 3


title: 4 hour prepupae replicate 2

description: w1118 prepupae


title: 12 hour pupae replicate 3

description: w1118 pupae


title: third instar larvae -4 hours relative to pupariation replicate 1

description: w1118 third instar animal

growth_protocol: Larvae were staged by addition of 0.05% bromophenol blue to food and collected as actively wandering larvae with clear guts


title: third instar larvae -18 hours relative to pupariation replicate 2

description: w1118 third instar animal

growth_protocol: Larvae were staged by addition of 0.05% bromophenol blue to food and collected as actively wandering larvae with dark blue guts


title: third instar larvae -18 hours relative to pupariation replicate 3

description: w1118 third instar animal


title: 10 hour prepupae replicate 2

description: w1118 prepupae


title: 6 hour prepupae replicate 3

description: w1118 prepupae


title: 8 hour prepupae replicate 1

description: w1118 prepupae


title: 6 hour prepupae replicate 2

description: w1118 prepupae


title: Cerebral cortical contusion in rat, 1 dpi, #2

status: Public on Oct 01 2005

city: Stockholm

first: A G Christina

last: von Gertten

address: Nkklab R2:02, Karolinska hospital

department: Clinical Neuroscience

country: Sweden

institute: Karolinska Institutet

description: Cortex from rats with cerebral cortical contusion 1 day post injury, injured cortex (ipsilateral side) -uninjured cortex (contralateral side) were hybridised onto a 6240 cDNA probe microarray. Expression ratios were calculated using injured/ un-injured cortex

data_processing: log 2 ratio (injured/uninjured)

organism: Rattus norvegicus

source_name: rat brain cortex, 470, ipsi Cy5 total RNA

extract_protocol: Qiagen RNeasy

treatment_protocol: cerebral cortical contusion by weight drop, 2.5 mm posterior and 2.5 mm lateral to bregma, decapitation 1 dpi

tag: male Sprague Dawley, 250g, cerebral cortex

source_name: rat brain cortex, 470, contra Cy3 total RNA

tag: male Sprague Dawley, 250 g, cerebral cortex


title: 6 hour prepupae replicate 1

description: w1118 prepupae


title: 4 hour prepupae replicate 3

description: w1118 prepupae


title: 0 hour prepupae replicate 3

description: w1118 prepupae


title: third instar larvae -4 hours relative to pupariation replicate 3

description: w1118 third instar animal


title: stem_mutant35S31-5_rep2

city: Davis

first: Andrew

last: Groover

state: CA

address: 1100 West Chiles Rd

department: Institute of Forest Genetics

institute: USDA Forest Service

description: While clones 35S31-5 and 35S31-1-7 carry the same T-DNA construct, they represent independent transformation events. Each clone was assayed by two independent RNA preps which were seperately labeled as probes, and which are represented within the experiment as replications.

hyb_protocol: Hybridization by NimbleGen company

scan_protocol: Scanning by NimbleGen company

data_processing: Expression values reflect across-array quantile normalization and gene calls generated using the Robust Multichip Average (RMA) expressed as log2. For information on RMA see Biostatistics 2003 Apr; 4(2): 249-264

organism: Populus tremula x Populus alba

source_name: Apical 10cm of stems of greenhouse grown plants.

label_protocol: Labeling by NimbleGen company

growth_protocol: Plants grown in standard tissue culture conditions for Populus alba X P. tremula clone INRA 717 described by Han et al 2000.

extract_protocol: Ground in liquid N, bead beat in Qiagen buffer RLT, then isolated by Qiagen RNAeasy.

tag: Populus alba X P. tremula clone INRA 717, tranformed with T-DNA carrying cauliflower mosaic virus promoter 35S driving expression of the Populus ARK2 KNOX class homeodomain protein, ortholog of KNAT1/BP from Arabidopsis. Entire, defoliated stems sampled.


title: 0 hour prepupae replicate 2

description: w1118 prepupae


title: stem_mutant35S31-1-7_rep1

growth_protocol: Plants grown in standard tissue culture conditions for Populus alba X P. tremula clone INRA 717 described by Han et al 2000


title: 2 hour prepupae replicate 3

description: w1118 prepupae


title: 12 hour pupae replicate 1

description: w1118 pupae


title: stem_WildType_rep1

description: Wild type control plant was assayed by two independent RNA preps which were seperately labeled as probes, and which are represented within the experiment as replications.


title: iUB_PTN_replicate3

status: Public on Sep 30 2005

city: La Jolla

first: Hiroyuki

last: Sakurai

address: 9500 Gilman Drive 0693

institute: University of California, San Diego

description: Isolated ureteric buds in three-dimensional culture exhibited non-branching growth

data_processing: Affymetrix GCOS (GeneChip Operating Software) version 1.2

source_name: cultured isolated ureteric bud

extract_protocol: Three ureteric buds were isolated from E13 Sprague-Dawley rats. Isolated UBs were suspended in a mixture of  50% growth factor reduced-Matrigel and 50% type 1 collagen matrix in a inner well of Transwell filter (Corning). Medium containing pleiotrophin (PTN) purified from BSN-CM (approximately 3 microgram/ml), FGF1 (250 ng/ml), and GDNF (125 ng/ml) was applied to an outer well and the culture was placed in 5% CO2 incubator at 37 C. At 4 days of culture, isolated UBs were removed from the gel. Total RNA was extracted using PicoPure RNA isolation kit (Arcturus). Double IVT was performed using MessageAmp kit (Ambion).

tag: Wild type, Sprague-Dawley rat, E13 ureteric bud, culture for 4 days


title: third instar larvae -4 hours relative to pupariation replicate 2

description: w1118 third instar animal


title: stem_mutant35S31-5_rep1


title: stem_mutant35S31-1-7_rep2


title: third instar larvae -18 hours relative to pupariation replicate 1

description: w1118 third instar animal

growth_protocol: Larvae were staged by addition of 0.05%bromophenol blue to food and collected as actively wandering larvae with dark blue guts


title: Organ culture 20E-treated replicate 2

description: 20E treated organ cultures

treatment_protocol: Eight animals were dissected in a 9 well glass dish (Corning) and cultured in ~100 µl oxygenated Schneiders Drosophila Medium (Gibco) at 25°C. Cultures were incubated in an a styrofoam box under a constant flow of oxygen. Following an initial incubation of 1 hour, the medium was removed and replaced with fresh Schneiders Drosophila Medium plus 5x10-6 M 20-hydroxyecdysone and incubated for 6 hours at 25°C.


title: Cerebral cortical contusion in rat, 1 dpi #3

data_processing: reversed log 2 ratio (uninjured/injured)

source_name: rat brain cortex, 467, contra Cy5 total RNA

tag: Male Sprague Dawley, 250 g, brain

source_name: rat brain cortex, 467, ipsi Cy3 total RNA


title: Cerebral cortical contusion in rat, 4 dpi #4

description: Cortex from rats with cerebral cortical contusion 4 days post injury, injured cortex (ipsilateral side) -uninjured cortex (contralateral side) were hybridised onto a 6240 cDNA probe microarray. Expression ratios were calculated using injured/ un-injured cortex

data_processing: reversed log2 ratio (uninjured/injured)

source_name: cerebral cortex, 483, contra Cy5 total RNA

extract_protocol: Qiagen RNeasy kit

source_name: contused cerebral cortex, 483, ipsi Cy3 total RNA

treatment_protocol: Cerebral cortical contusion was made using weight drop, 2.5 mm posterior and 2.5 lateral to bregma, decapitation at 4 dpi


title: Cerebral cortical contusion in rat, 4 dpi #1

description: Cortex from rats with cerebral cortical contusion 4 day post injury, injured cortex (ipsilateral side) -uninjured cortex (contralateral side) were hybridised onto a 6240 cDNA probe microarray. Expression ratios were calculated using  injured/un-injured cortex

source_name: rat brain cortex, 471, contra Cy5 total RNA

tag: male Sprague Dawley, 250 g, brain

source_name: rat brain cortex, 471, ipsi Cy3 total RNA

treatment_protocol: cerebral cortical contusion using weight drop, 2.5 mm posterior and 2.5 mm lateral to bregma, decapitation 4 dpi


title: Cerebral cortical contusion in rat 4 dpi, #3

data_processing: log2 ratio (injured/uninjured)

source_name: rat brain cortex, 482, ipsi cy5 total RNA

treatment_protocol: Cerebral cortical contusion was made using weight drop, 2.5 mm posterior and 2.5 lateral to bregma

tag: Male Sprague Dawley, 250g, brain

source_name: rat brain cortex, 482, contra cy3 total RNA


title: Cerebral cortical contusion in rat, 1dpi, #1

source_name: rat brain cortex, 466, ipsi Cy5 total RNA

treatment_protocol: cerebral cortical contusion using weight drop, 2.5 mm posterior and 2.5 lateral to bregma, decapitation 1 dpi

tag: male Sprague Dawley rats, 250g, brain

source_name: brain cortex 466 contra Cy3 total RNA


title: Cerebral cortical contusion in rat 4 dpi, #2

data_processing: log 2 (injured/uninjured)

source_name: rat brain cortex ,465, ipsi Cy5 total RNA

treatment_protocol: cerebral cortical contusions by weight drop, 2.5 mm posterior and 2.5 lateral to bregma, decapitation 4 dpi

tag: Sprague Dawley rats, males, 250 g, cerebral cortex

source_name: rat brain cortex, 465, Cy3 total RNA


title: Lo I3C_rep2_Cy3

status: Public on Sep 28 2005

city: Corvallis

first: Susan

middle: C.

last: Tilton

state: OR

address: 1007 ALS Bldg

department: AG Envr & Molec Toxicology

institute: Oregon State University

description:
Lo I3C treated- rep2
Hybridized with reference sample.
Packard ScanArray Model 4000
QuantArray
Genisphere labeling and hybridization kit.
Invitrogen TRIzol extraction followed by cleanup with Qiagen RNeasy according to vendor protocol.

hyb_protocol: Hybridizations were performed with the Genisphere Array 350 kit and instructions (Hatfield, PA) using standard reference design with dye-swapping. Briefly, 10 ug total RNA were reverse-transcribed with Superscript II (Invitrogen) using the Genisphere oligo d(T) primer containing a capture sequence for the Cy3 or Cy5 labelling reagents. Each reaction was spiked with increasing concentrations of three of the Arabidopsis thaliana cDNA controls included on the array. Each cDNA sample containing the capture sequence for the Cy3 or Cy5 label was combined with equal amounts of reference cDNA (pooled from sham-initiated controls) containing the capture sequence for the opposite label. cDNA from two of the three biological replicates were dye-swapped and hybridized to two slides as technical replicates. cDNA from the reference sample was also hybridized to dye-swapped slides (against itself) following the same protocol as experimental samples for use as a negative control. Prior to hybridization, microarrays were processed post-printing by washing twice in 0.1% SDS for 5 min, twice in Milli-Q water for 5 min, immersion in boiling water for 3 min and then dried by centrifugation. Arrays were then washed in 2X SSC, 0.1% SDS at 49C for 20 min, 0.1X SSC for 5 min and Milli-Q water for 3 min prior to drying by centrifugation. The cDNAs (35 ul) were hybridized to arrays in formamide buffer [50% formamide, 8X SSC, 1% SDS, 4X Denhardt?s solution] for 16 h at 49C with 22x60 mm Lifterslips (Erie Scientific, Portsmouth, NH). Arrays were then washed once in 2X SSC, 0.1% SDS at 49C for 10 min, twice in 2X SSC, 0.1% SDS for 5 min, twice in 1X SSC for 5 min, twice in 0.1X SSC for 5 min and dried by centrifugation. Shaded from light, the Cy3 and Cy5 fluorescent molecules (3DNA capture reagent, Genisphere) were hybridized in formamide buffer for 3 h at 49C to corresponding capture sequences on cDNAs bound to the arrays. Arrays were washed in the dark with SSC containing 0.1 M DTT and dried as described earlier.

scan_protocol: Scanned images (5 um) were acquired with ScanArray Express (PerkinElmer, Boston, MA) at an excitation of 543 nm for Cy3 and 633 nm for Cy5 and at 90% power. The photomultiplier tube (PMT) settings for each fluor were set based on intensity of spiked internal alien controls to normalize among all slides in the experiment. Image files were quantified in QuantArray (PerkinElmer) and raw median signal and background values were exported to BioArray Software Environment (BASE; Saal et al. 2002) for analysis.

data_processing: Raw median signal and background values are included. For experiment, data were background subtracted and normalized by LOWESS. Stringent criteria were used to filter for genes that were regulated at least 2-fold compared to vehicle controls consistently in all features (n=8 per treatment) from biological replicates, dye-swapped technical replicates and duplicate spots printed on arrays.

organism: Oncorhynchus mykiss

source_name: 500 ppm I3C Liver

label_protocol: Labeled using Genisphere Array 350 kit adapted from manufacturer protocol.

treatment_protocol: Juvenile trout, 12-18 months old, were maintained in separate 375-L tanks (n=2 tanks) for each treatment with 6 fish per tank. Animals were fed a maintenance ration (2.8% w/w) of Oregon test diet, a semi-purified casein-based diet. Administration of 500 ppm I3C in the diet was carried out for 12 days. On day 13, fish were euthanized by deep anesthesia with 250 ppm MS-222 and sampled.

tag: Strain

value: Mt. Shasta

tag: Age

value: 12-18 months

tag: Tissue

value: liver

source_name: Reference

treatment_protocol: Juvenile trout, 12-18 months old, were maintained in separate 375-L tanks (n=2 tanks) for each treatment with 6 fish per tank. Animals were fed a maintenance ration (2.8% w/w) of Oregon test diet, a semi-purified casein-based diet. Administration of 0.15 % dimethyl sulfoxide vehicle control in the diet was carried out for 12 days. On day 13, fish were euthanized by deep anesthesia with 250 ppm MS-222 and sampled. Reference sample RNA was isolated from individual livers of 12 trout and aliquots were pooled in equal amounts (ug).


title: iUB_PTN_replicate 1


title: iUB_PTN_replicate 2


title: Lo I3C_rep2_Cy5

extract_protocol: Invitrogen TRIzol extraction followed by cleanup with Qiagen RNeasy according to vendor protocol.


title: Lo DIM_rep2_Cy3

description:
Lo DIM treated- rep2
Hybridized with reference sample.
Packard ScanArray Model 4000
QuantArray
Genisphere labeling and hybridization kit.
Invitrogen TRIzol extraction followed by cleanup with Qiagen RNeasy according to vendor protocol.

source_name: 500 ppm DIM Liver

treatment_protocol: Juvenile trout, 12-18 months old, were maintained in separate 375-L tanks (n=2 tanks) for each treatment with 6 fish per tank. Animals were fed a maintenance ration (2.8% w/w) of Oregon test diet, a semi-purified casein-based diet. Administration of 500 ppm DIM in the diet was carried out for 12 days. On day 13, fish were euthanized by deep anesthesia with 250 ppm MS-222 and sampled.


title: NST1 over-expression no.36 vs wild type

status: Public on Sep 29 2005

city: Tsukuba

first: Nobutaka

last: Mitsuda

state: Ibaraki

address: Central 6 Higashi 1-1-1

department: Bioproduction Research Institute

country: Japan

institute: National Institute of Advanced Industrial Science and Technology

description: NST1 over-expressed plant shows ectopic secondary wall thickenings in various above-ground organs.

data_processing: Agilent Feature-extraction software version A.6.1.1

organism: Arabidopsis thaliana

source_name: wild-type plant

growth_protocol: 16h light / 8h dark

treatment_protocol: No treatment

tag: Rosette leaf of 2-week-old plant

source_name: NST1 over-expressed plant


title: Hi I3C_rep2_Cy3

description:
Hi I3C treated- rep2
Hybridized with reference sample.
Packard ScanArray Model 4000
QuantArray
Genisphere labeling and hybridization kit.
Invitrogen TRIzol extraction followed by cleanup with Qiagen RNeasy according to vendor protocol.

source_name: 1500 ppm I3C Liver

treatment_protocol: Juvenile trout, 12-18 months old, were maintained in separate 375-L tanks (n=2 tanks) for each treatment with 6 fish per tank. Animals were fed a maintenance ration (2.8% w/w) of Oregon test diet, a semi-purified casein-based diet. Administration of 1500 ppm I3C in the diet was carried out for 12 days. On day 13, fish were euthanized by deep anesthesia with 250 ppm MS-222 and sampled.


title: iUB_HRG_replicate 3

source_name: cultured isolated ureteric bud

extract_protocol: Three ureteric buds were isolated from E13 Sprague-Dawley rats. Isolated UBs were suspended in a mixture of  50% growth factor reduced-Matrigel and 50% type 1 collagen matrix in a inner well of Transwell filter (Corning). Medium containing HRG (500 ng/ml), FGF1 (250 ng/ml), and GDNF (125 ng/ml) was applied to an outer well and the culture was placed in 5% CO2 incubator at 37 C. At 4 days of culture, isolated UBs were removed from the gel. Total RNA was extracted using PicoPure RNA isolation kit (Arcturus). Double IVT was performed using MessageAmp kit (Ambion).


title: iUB_HRG_replicate 2


title: stem_WildType_rep2

source_name: Apical 10cm of stems of greenhouse grown plants.


title: iUB_HRG_replicate 1

extract_protocol: Three ureteric buds were isolated from E13 Sprague-Dawley rats. Isolated UBs were suspended in a mixture of  50% growth factor reduced-Matrigel and 50% type 1 collagen matrix in a inner well of Transwell filter (Corning). Medium containing human recombinant heregulin alpha (HRG, 500 ng/ml), FGF1 (250 ng/ml), and GDNF (125 ng/ml) was applied to an outer well and the culture was placed in 5% CO2 incubator at 37 C. At 4 days of culture, isolated UBs were removed from the gel. Total RNA was extracted using PicoPure RNA isolation kit (Arcturus). Double IVT was performed using MessageAmp kit (Ambion).


title: iUB_BSN_replicate 3

description: Isolated ureteric buds in three-dimensional culture exhibited branching growth

extract_protocol: Three ureteric buds were isolated from E13 Sprague-Dawley rats. Isolated UBs were suspended in a mixture of  50% growth factor reduced-Matrigel and 50% type 1 collagen matrix in a inner well of Transwell filter (Corning). Medium containing BSN-CM (conditioned medium derived from metanephric mesenchymal cell line), FGF1 (250 ng/ml), and GDNF (125 ng/ml) was applied to an outer well and the culture was placed in 5% CO2 incubator at 37 C. At 4 days of culture, isolated UBs were removed from the gel. Total RNA was extracted using PicoPure RNA isolation kit (Arcturus). Double IVT was performed using MessageAmp kit (Ambion).


title: Hi I3C_rep1_Cy3

description:
Hi I3C treated- rep1
Hybridized with reference sample.
Packard ScanArray Model 4000
QuantArray
Genisphere labeling and hybridization kit.
Invitrogen TRIzol extraction followed by cleanup with Qiagen RNeasy according to vendor protocol.


title: iUB_BSN_replicate 2

extract_protocol: Three ureteric buds were isolated from E13 Sprague-Dawley rats. Isolated UBs were suspended in a mixture of  50% growth factor reduced-Matrigel and 50% type 1 collagen matrix in a inner well of Transwell filter (Corning). Medium containing BSN-CM (conditioned medium derived from metanephric mesenchymal cell line), fibroblast growth factor (FGF1 ,250 ng/ml), and glial cell line-derived neurotrophic growth factor (GDNF, 125 ng/ml) was applied to an outer well and the culture was placed in 5% CO2 incubator at 37 C. At 4 days of culture, isolated UBs were removed from the gel. Total RNA was extracted using PicoPure RNA isolation kit (Arcturus). Double IVT was performed using MessageAmp kit (Ambion).


title: Hi DIM_rep1_Cy5

description:
HI DIM treated- rep1
Hybridized with reference sample.
Packard ScanArray Model 4000
QuantArray
Genisphere labeling and hybridization kit.
Invitrogen TRIzol extraction followed by cleanup with Qiagen RNeasy according to vendor protocol.

source_name: 1500 ppm DIM Liver

treatment_protocol: Juvenile trout, 12-18 months old, were maintained in separate 375-L tanks (n=2 tanks) for each treatment with 6 fish per tank. Animals were fed a maintenance ration (2.8% w/w) of Oregon test diet, a semi-purified casein-based diet. Administration of 1500 ppm DIM in the diet was carried out for 12 days. On day 13, fish were euthanized by deep anesthesia with 250 ppm MS-222 and sampled.


title: iUB_BSN_replicate 1


title: Hi DIM_rep2_Cy5

description:
HI DIM treated- rep2
Hybridized with reference sample.
Packard ScanArray Model 4000
QuantArray
Genisphere labeling and hybridization kit.
Invitrogen TRIzol extraction followed by cleanup with Qiagen RNeasy according to vendor protocol.


title: Hi DIM_rep1_Cy3


title: BNF_rep2_Cy5

description:
BNF treated- rep2
Hybridized with reference sample.
Packard ScanArray Model 4000
QuantArray
Genisphere labeling and hybridization kit.
Invitrogen TRIzol extraction followed by cleanup with Qiagen RNeasy according to vendor protocol.

source_name: 500 ppm BNF Liver

treatment_protocol: Juvenile trout, 12-18 months old, were maintained in separate 375-L tanks (n=2 tanks) for each treatment with 6 fish per tank. Animals were fed a maintenance ration (2.8% w/w) of Oregon test diet, a semi-purified casein-based diet. Administration of 500 ppm BNF in the diet was carried out for 12 days. On day 13, fish were euthanized by deep anesthesia with 250 ppm MS-222 and sampled.


title: Lo DIM_rep2_Cy5


title: NST1 over-expression no.44 vs wild type


title: E2_rep1_Cy3

description:
E2 treated- rep1
Hybridized with reference sample.
Packard ScanArray Model 4000
QuantArray
Genisphere labeling and hybridization kit.
Invitrogen TRIzol extraction followed by cleanup with Qiagen RNeasy according to vendor protocol.

source_name: 5 ppm E2 Liver

treatment_protocol: Juvenile trout, 12-18 months old, were maintained in separate 375-L tanks (n=2 tanks) for each treatment with 6 fish per tank. Animals were fed a maintenance ration (2.8% w/w) of Oregon test diet, a semi-purified casein-based diet. Administration of 5 ppm E2in the diet was carried out for 12 days. On day 13, fish were euthanized by deep anesthesia with 250 ppm MS-222 and sampled.


title: Hi DIM_rep2_Cy3


title: hsf1-ba1 #2

status: Public on Sep 27 2005

city: Kanazawa

first: Hiroshi

state: Ishikawa

address: 5-11-80 Kodatsuno

department: School of Health Sciences

institute: Kanazawa University

description: Probe cDNA was primed by oligo(dT).

data_processing: The filters were scanned at a resolution of 25 microns on a BAS5000 Image Analyzer (FujiFilm, Tokyo, Japan). The intensity of signals was quantified by ArrayGauge, an image analyzing application (FujiFilm). The local background intensity was subtracted from each ORF and then each ORF value was normalized to adjust the total intensity 200000.

organism: Saccharomyces cerevisiae

source_name: Yeast cells grown at 39oC for 15 min

value: hsf1-ba1 mutant


title: hsf1-ba1 #1

description: Probe cDNA was primed by oligo(dT).


title: BNF_rep2_Cy3


title: E2_rep1_Cy5


title: HSF1 wt #3

description: Probe cDNA was primed by oligo(dT).

value: HSF1 wild type


title: Lo I3C_rep1_Cy3

description:
Lo I3C treated- rep1
Hybridized with reference sample.
Packard ScanArray Model 4000
QuantArray
Genisphere labeling and hybridization kit.
Invitrogen TRIzol extraction followed by cleanup with Qiagen RNeasy according to vendor protocol.


title: Hi I3C_rep2_Cy5


title: E2_rep2_Cy5

description:
E2 treated- rep2
Hybridized with reference sample.
Packard ScanArray Model 4000
QuantArray
Genisphere labeling and hybridization kit.
Invitrogen TRIzol extraction followed by cleanup with Qiagen RNeasy according to vendor protocol.

source_name: E5 ppm E2 Liver

treatment_protocol: Juvenile trout, 12-18 months old, were maintained in separate 375-L tanks (n=2 tanks) for each treatment with 6 fish per tank. Animals were fed a maintenance ration (2.8% w/w) of Oregon test diet, a semi-purified casein-based diet. Administration of 5 ppm E2 in the diet was carried out for 12 days. On day 13, fish were euthanized by deep anesthesia with 250 ppm MS-222 and sampled.


title: E2_rep2_Cy3


title: Lo I3C_rep1_Cy5


title: Lo DIM_rep1_Cy5

description:
Lo DIM treated- rep1
Hybridized with reference sample.
Packard ScanArray Model 4000
QuantArray
Genisphere labeling and hybridization kit.
Invitrogen TRIzol extraction followed by cleanup with Qiagen RNeasy according to vendor protocol.


title: Hi I3C_rep1_Cy5


title: Lo DIM_rep1_Cy3


title: GC077-04

city: Suita

first: Naoharu

last: Iwai

address: 5-7-1 Fujishiro-dai

department: Epidemiology

institute: National Cardiovascular Center

description: HUVECs sample 2 treated with fullerene for 24 h

data_processing: GeneChip Operating Software version1.1

organism: Homo sapiens

source_name: HUVECs

tag: Fullerene-treated HUVECs sample 2


title: 03 JOS 32_tumor_367-08

type: genomic

city: Amsterdam

first: Daoud

last: Sie

address: Plesmanlaan 161

country: Netherlands

institute: Dutch Cancer Institute

description: described in Jonkers et al, Nature Genetics, 2001, vol. 29, 418-425

hyb_protocol: described in Chung et al., Genome Research, 2004, vol.14, 188-196

scan_protocol: Agilent Scanner G2505B, Agilent Technologies

molecule: genomic DNA

organism: Mus musculus

source_name: mouse 03 JOS 32

value: Kcre; Br2F/F; p53F/F

tag: Gender

value: female

value: 23 days

value: spleen

source_name: mouse 03 Jos 32

value: Brca2 deficient p53 deficient mamma epithelial tumor

tag: Tumor stage


title: 03 JOS 32_tumor_367-25

data_processing: described in Chung et al., Genome Research, 2004, vol.14, 188-196

growth_protocol: described in Jonkers et al, Nature Genetics, 2001, vol. 29, 418-425


title: 99 JOS 32_tumor_367-16

source_name: mouse 99 JOS 32

label_protocol: described in Chung et al., Genome Research, 2004, vol.14, 188-196

treatment_protocol: described in Jonkers et al, Nature Genetics, 2001, vol. 29, 418-425

source_name: mouse 99 Jos 32


title: del337 with WY14643 replicate 1

status: Public on Sep 26 2005

city: Seattle

first: Norman

last: Buroker

state: WA

address: 4800 Sand Point Way N.E.

institute: Seattle Children's Hospital

description: del337 treated with WY14643

data_processing: Robust Multichip Analysis (RMA)

source_name: Mouse heart

label_protocol: Approximately 5 µg of total RNA was processed to produce biotinylated cRNA targets.

extract_protocol: Total mRNA was extracted from the frozen heart tissue using the RNeasy fibrous tissue Kit from QIAGEN (Chatsworth, CA).  Contaminating DNA was removed by deoxyribonuclease I digestion of the RNA preparation when still bound to the column. An average of 27ug of total RNA was obtained from 20mg of frozen mouse heart tissue.

tag: del337 treated with WY14643


title: del337 with WY14643 replicate 5

description: del337 treated with WY14643


title: 99 JOS 32_tumor_367-15

extract_protocol: described in Chung et al., Genome Research, 2004, vol.14, 188-196


title: del337 with WY14643 replicate 7

description: del337 treated with WY14643


title: del337 with WY14643 replicate 3

description: del337 treated with WY14643


title: Control with WY14643 replicate 4

description: Control treated with WY14643

tag: Control treated with WY14643


title: BNF_rep1_Cy3

description:
BNF treated- rep1
Hybridized with reference sample.
Packard ScanArray Model 4000
QuantArray
Genisphere labeling and hybridization kit.
Invitrogen TRIzol extraction followed by cleanup with Qiagen RNeasy according to vendor protocol.

hyb_protocol: Hybridizations were performed with the Genisphere Array 350 kit and instructions (Hatfield, PA) using standard reference design with dye-swapping. Briefly, 10 ug total RNA were reverse-transcribed with Superscript II (Invitrogen) using the Genisphere oligo d(T) primer containing a capture sequence for the Cy3 or Cy5 labelling reagents. Each reaction was spiked with increasing concentrations of three of the Arabidopsis thaliana cDNA controls included on the array. Each cDNA sample containing the capture sequence for the Cy3 or Cy5 label was combined with equal amounts of reference cDNA (pooled from sham-initiated controls) containing the capture sequence for the opposite label. cDNA from two of the three biological replicates were dye-swapped and hybridized to two slides as technical replicates. cDNA from the reference sample was also hybridized to dye-swapped slides (against itself) following the same protocol as experimental samples for use as a negative control. Prior to hybridization, microarrays were processed post-printing by washing twice in 0.1% SDS for 5 min, twice in Milli-Q water for 5 min, immersion in boiling water for 3 min and then dried by centrifugation.  Arrays were then washed in 2X SSC, 0.1% SDS at 49C for 20 min, 0.1X SSC for 5 min and Milli-Q water for 3 min prior to drying by centrifugation.  The cDNAs (35 ul) were hybridized to arrays in formamide buffer [50% formamide, 8X SSC, 1% SDS, 4X Denhardt?s solution] for 16 h at 49C with 22x60 mm Lifterslips (Erie Scientific, Portsmouth, NH).  Arrays were then washed once in 2X SSC, 0.1% SDS at 49C for 10 min, twice in 2X SSC, 0.1% SDS for 5 min, twice in 1X SSC for 5 min, twice in 0.1X SSC for 5 min and dried by centrifugation.  Shaded from light, the Cy3 and Cy5 fluorescent molecules (3DNA capture reagent, Genisphere) were hybridized in formamide buffer for 3 h at 49C to corresponding capture sequences on cDNAs bound to the arrays.  Arrays were washed in the dark with SSC containing 0.1 M DTT and dried as described earlier.

treatment_protocol: Juvenile trout, 12-18 months old, were maintained in separate 375-L tanks (n=2 tanks) for each treatment with 6 fish per tank.  Animals were fed a maintenance ration (2.8% w/w) of Oregon test diet, a semi-purified casein-based diet.  Administration of 500 ppm BNF in the diet was carried out for 12 days.  On day 13, fish were euthanized by deep anesthesia with 250 ppm MS-222 and sampled.

source_name: Reference

treatment_protocol: Juvenile trout, 12-18 months old, were maintained in separate 375-L tanks (n=2 tanks) for each treatment with 6 fish per tank.  Animals were fed a maintenance ration (2.8% w/w) of Oregon test diet, a semi-purified casein-based diet.  Administration of 0.15 % dimethyl sulfoxide vehicle control in the diet was carried out for 12 days.  On day 13, fish were euthanized by deep anesthesia with 250 ppm MS-222 and sampled.  Reference sample RNA was isolated from individual livers of 12 trout and aliquots were pooled in equal amounts (ug).


title: del337 with WY14643 replicate 6

description: del337 treated with WY14643


title: del337 with WY14643 replicate 2

description: del337 treated with WY14643


title: del337TR replicate 2

description: deletion in 337TR

tag: deletion in 337TR


title: Control with WY14643 replicate 7

description: Control treated with WY14643


title: del337 with WY14643 replicate 4

description: del337 treated with WY14643


title: Control with WY14643 replicate 5

description: Control treated with WY14643


title: del337TR replicate 5

description: deletion in 337TR


title: del337TR replicate 6

description: deletion in 337TR


title: Control replicate 7

description: Control, untreated

tag: Control, untreated


title: BNF_rep1_Cy5


title: GC077-02

description: HUVECs sample 1 treated with fullerene for 24 h

tag: Fullerene-treated HUVECs sample 1


title: Control with WY14643 replicate 6

description: Control treated with WY14643


title: del337TR replicate 7

description: deletion in 337TR


title: GC077-01

description: HUVEC sample 1 untreated with fullerene

tag: Untreated control HUVECs sample 1


title: Control with WY14643 replicate 2

description: Control treated with WY14643


title: del337TR replicate 1

description: deletion in 337TR


title: del337TR replicate 3

description: deletion in 337TR


title: del337TR replicate 4

description: deletion in 337TR


title: Control with WY14643 replicate 3

description: Control treated with WY14643


title: Control with WY14643 replicate 1

description: Control treated with WY14643


title: GC077-03

description: HUVEC sample 2 untreated with fullerene

tag: Untreated control HUVECs sample 2


title: Control replicate 6

description: Control, untreated


title: Control replicate 3

description: Control, untreated


title: Control replicate 2

description: Control, untreated


title: Control replicate 4

description: Control, untreated


title: oocyte from small antral follicle stage MOE430B rep3

city: Philadelphia

first: Hua

last: Pan

state: PA

address: 415 S University Avenue

department: Department of Biology

institute: University of Pennsylvania

description: oocyte from small antral follicle stage in vivo

data_processing: Affymetrix Microarray Suite version 5.0

source_name: oocyte

label_protocol: total RNA from 60 oocytes was processed to produce biotinylated cRNA targets using Affy Small Sample Target Labeling Assay Version II.

extract_protocol: 60 oocytes were collected from ovary of 12 day old SJLB6 female mouse.Total RNA was extracted and purified using an Picopure kit (Arcturus).

tag: in vivo,small antral follicle stage, oocyte


title: oocyte from large antral follicle stage MOE430B rep2

description: oocyte from large antral follicle stage in vivo

label_protocol: total RNA from 20 oocytes was processed to produce biotinylated cRNA targets using Affy Small Sample Target Labeling Assay Version II.

extract_protocol: 20 oocytes were collected from ovary of 24 day old SJLB6 female mouse.Total RNA was extracted and purified using an Picopure kit (Arcturus).

tag: in vivo,large antral follicle stage, oocyte


title: oocyte from small antral follicle stage MOE430B rep2


title: Control replicate 5

description: Control, untreated


title: oocyte from large antral follicle stage MOE430B rep1


title: oocyte from small antral follicle stage MOE430B rep1

label_protocol: total RNA from 30 oocytes was processed to produce biotinylated cRNA targets using Affy Small Sample Target Labeling Assay Version II.

extract_protocol: 30 oocytes were collected from ovary of 17 day old SJLB6 female mouse.Total RNA was extracted and purified using an Picopure kit (Arcturus).


title: oocyte from large antral follicle stage MOE430B rep3


title: oocyte from secondary follicle stage MOE430B rep3

description: oocyte from secondary follicle stage in vivo

tag: in vivo,secondary follicle stage, oocyte


title: Control replicate 1

description: Control, untreated


title: oocyte from secondary follicle stage MOE430B rep1


title: oocyte from secondary follicle stage MOE430B rep4


title: oocyte from large antral follicle stage MOE430B rep4


title: oocyte from primordial follicle stage MOE430B rep4

description: oocyte from primordial follicle stage in vivo

label_protocol: total RNA from 400 oocytes was processed to produce biotinylated cRNA targets using Affy Small Sample Target Labeling Assay Version II.

extract_protocol: 400 oocytes were collected from ovary of 2 day old SJLB6 female mouse.Total RNA was extracted and purified using an Picopure kit (Arcturus).

tag: in vivo,primordial follicle stage, oocyte


title: oocyte from primordial follicle stage MOE430B rep3


title: oocyte from small antral follicle stage MOE430A rep4


title: oocyte from secondary follicle stage MOE430B rep2


title: oocyte from large antral follicle stage MOE430A rep3


title: oocyte from primordial follicle stage MOE430B rep2


title: oocyte from large antral follicle stage MOE430A rep4


title: oocyte from large antral follicle stage MOE430A rep1


title: oocyte from small antral follicle stage MOE430A rep3


title: oocyte from large antral follicle stage MOE430A rep2


title: oocyte from primordial follicle stage MOE430B rep1


title: oocyte from secondary follicle stage rep4


title: oocyte from small antral follicle stage MOE430A rep1


title: oocyte from small antral follicle stage MOE430B rep4


title: oocyte from small antral follicle stage MOE430A rep2


title: oocyte from secondary follicle stage rep3


title: oocyte from secondary follicle stage rep1


title: F2-ob/ob(A) 553

status: Public on Sep 21 2005

city: Madison

first: Alan

middle: D

last: Attie

state: WI

address: 433 Babcock Drive

department: Biochemistry

institute: University of Wisconsin-Madison

description: (C57BL/6J X BTBR) F2-553. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

data_processing: The data were processed with MAS5.0 to generate cell intensity files. Quantitative expression levels of all the transcripts were estimated using the RMA algorithm for normalization (Irizarry et al. 2003).

label: biotin.

source_name: Liver

label_protocol: Approximately 10 µg of total RNA was processed to produce biotinylated cRNA targets according to Affymetrix Expression Analysis Technical Manual.

extract_protocol: Liver total RNA was extracted from frozen tissue samples with RNAzol reagent (Tel-Test, Inc.). Crude RNA samples were purified with RNeasy mini columns (Qiagen, Inc.) before being subjected to microarray studies. The RNA samples were processed according to the Affymetrix Expression Analysis Technical Manual. A total of 60 MOE430A and MOE430B arrays were used. Quantitative expression levels of all the transcripts were estimated using the RMA algorithm for normalization.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 553A100703, MOE430B ArrayID = 553B100803.


title: F2-ob/ob(A) 608

description: (C57BL/6J X BTBR) F2-608. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 608A100703, MOE430B ArrayID = 608B100803.


title: F2-ob/ob(A) 517

description: (C57BL/6J X BTBR) F2-517. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 517A100703, MOE430B ArrayID = 517B100803.


title: animal_cap_mixer_expressing_rep2

status: Public on Sep 22 2005

city: Stanford

first: Julie

last: Baker

address: 300 Pasteur Drive

department: Genetics

institute: Stanford University

data_processing: RMA

label: Biotin

organism: Xenopus laevis

source_name: Mixer Expressing Animal Cap Tissue

tag: Tissue

value: Animal Cap/ Ectodermal Explant

tag: Stage

value: Gastrula/ 10.5

value: Mixed


title: F2-ob/ob(A) 489

description: (C57BL/6J X BTBR) F2-489. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 489A100603, MOE430B ArrayID = 489B100803.


title: oocyte from primordial follicle stage MOE430A rep2


title: animal_cap_mixer_expressing_rep1

tag: Gender


title: animal_cap_uninjected_rep2

source_name: Uninjected Animal Cap Tissue


title: F2-ob/ob(A) 560

description: (C57BL/6J X BTBR) F2-560. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 560A100703, MOE430B ArrayID = 560B100803.


title: F2-ob/ob(A) 486

description: (C57BL/6J X BTBR) F2-486. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 486A100603, MOE430B ArrayID = 486B100803.


title: F2-ob/ob(A) 499

description: (C57BL/6J X BTBR) F2-499. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 499A100603, MOE430B ArrayID = 499B100803.


title: oocyte from secondary follicle stage rep2


title: F2-ob/ob(A) 549

description: (C57BL/6J X BTBR) F2-549. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 549A100703, MOE430B ArrayID = 549B100803.


title: F2-ob/ob(A) 617

description: (C57BL/6J X BTBR) F2-617. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 617A100703, MOE430B ArrayID = 617B100803.


title: F2-ob/ob(A) 615

description: (C57BL/6J X BTBR) F2-615. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 615A100703, MOE430B ArrayID = 615B100803.


title: F2-ob/ob(A) 523

description: (C57BL/6J X BTBR) F2-523. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 523A100703, MOE430B ArrayID = 523B100803.


title: F2-ob/ob(A) 566

description: (C57BL/6J X BTBR) F2-566. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 566A100703, MOE430B ArrayID = 566B100803.


title: oocyte from primordial follicle stage MOE430A rep1


title: F2-ob/ob(A) 513

description: (C57BL/6J X BTBR) F2-513. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 513A100603, MOE430B ArrayID = 513B100803.


title: F2-ob/ob(A) 559

description: (C57BL/6J X BTBR) F2-559. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 559A100703, MOE430B ArrayID = 559B100803.


title: F2-ob/ob(A) 484

description: (C57BL/6J X BTBR) F2-484. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 484A100603, MOE430B ArrayID = 484B100803.


title: F2-ob/ob(A) 479

description: (C57BL/6J X BTBR) F2-479. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 479A100603, MOE430B ArrayID = 479B100803.


title: F2-ob/ob(A) 493

description: (C57BL/6J X BTBR) F2-493. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 493A100603, MOE430B ArrayID = 493B100803.


title: animal_cap_uninjected_rep1

tag: Tissue


title: oocyte from primordial follicle stage MOE430A rep4

description: oocyte from primordial follicle stage in vivo

tag: in vivo,primordial follicle stage, oocyte


title: animal_cap_sox17_expressing_rep1

source_name: Sox17 Expressing Animal Cap Tissue

tag: Stage


title: animal_cap_sox17_expressing_rep2

tag: Gender


title: oocyte from primordial follicle stage MOE430A rep3


title: F2-ob/ob(A) 472

description: (C57BL/6J X BTBR) F2-472. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 472A100603, MOE430B ArrayID = 472B100803.


title: F2-ob/ob(A) 440

description: (C57BL/6J X BTBR) F2-440. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 440A100603, MOE430B ArrayID = 440B100803.


title: F2-ob/ob(A) 458

description: (C57BL/6J X BTBR) F2-458. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 458A100603, MOE430B ArrayID = 458B100803.


title: F2-ob/ob(A) 438

description: (C57BL/6J X BTBR) F2-438. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 438A100603, MOE430B ArrayID = 438B100703.


title: F2-ob/ob(A) 416

description: (C57BL/6J X BTBR) F2-416. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 416A100603, MOE430B ArrayID = 416B100703.


title: F2-ob/ob(A) 455

description: (C57BL/6J X BTBR) F2-455. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 455A100603, MOE430B ArrayID = 455B100803.


title: F2-ob/ob(A) 419

description: (C57BL/6J X BTBR) F2-419. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 419A100603, MOE430B ArrayID = 419B100703.


title: F2-ob/ob(A) 318

description: (C57BL/6J X BTBR) F2-318. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 318A100603, MOE430B ArrayID = 318B100703.


title: F2-ob/ob(A) 260

description: (C57BL/6J X BTBR) F2-260. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 260A100603, MOE430B ArrayID = 260B100703.


title: F2-ob/ob(A) 324

description: (C57BL/6J X BTBR) F2-324. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 324A100603, MOE430B ArrayID = 324B100703.


title: F2-ob/ob(A) 343

description: (C57BL/6J X BTBR) F2-343. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 343A100603, MOE430B ArrayID = 343B100703.


title: F2-ob/ob(A) 474

description: (C57BL/6J X BTBR) F2-474. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 474A100603, MOE430B ArrayID = 474B100803.


title: F2-ob/ob(A) 310

description: (C57BL/6J X BTBR) F2-310. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 310A100603, MOE430B ArrayID = 310B100703.


title: F2-ob/ob(A) 224

description: (C57BL/6J X BTBR) F2-224. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 224A100303, MOE430B ArrayID = 224B100503.


title: F2-ob/ob(A) 317

description: (C57BL/6J X BTBR) F2-317. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 317A100603, MOE430B ArrayID = 317B100703.


title: F2-ob/ob(A) 620

description: (C57BL/6J X BTBR) F2-620. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 620A100703, MOE430B ArrayID = 620B100803.


title: F2-ob/ob(A) 327

description: (C57BL/6J X BTBR) F2-327. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 327A100603, MOE430B ArrayID = 327B100703.


title: F2-ob/ob(A) 554

description: (C57BL/6J X BTBR) F2-554. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 554A100703, MOE430B ArrayID = 554B100803.


title: F2-ob/ob(A) 190

description: (C57BL/6J X BTBR) F2-190. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 190A100303, MOE430B ArrayID = 190B100503.


title: F2-ob/ob(A) 253

description: (C57BL/6J X BTBR) F2-253. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 253A100303, MOE430B ArrayID = 253B100503.


title: F2-ob/ob(A) 212

description: (C57BL/6J X BTBR) F2-212. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 212A100303, MOE430B ArrayID = 212B100503.


title: F2-ob/ob(A) 264

description: (C57BL/6J X BTBR) F2-264. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 264A100603, MOE430B ArrayID = 264B100703.


title: F2-ob/ob(A) 207

description: (C57BL/6J X BTBR) F2-207. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 207A100303, MOE430B ArrayID = 207B100503.


title: F2-ob/ob(A) 209

description: (C57BL/6J X BTBR) F2-209. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 209A100303, MOE430B ArrayID = 209B100503.


title: F2-ob/ob(A) 194

description: (C57BL/6J X BTBR) F2-194. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 194A100303, MOE430B ArrayID = 194B100503.


title: F2-ob/ob(A) 254

description: (C57BL/6J X BTBR) F2-254. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 254A100603, MOE430B ArrayID = 254B100703.


title: F2-ob/ob(A) 200

description: (C57BL/6J X BTBR) F2-200. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 200A100303, MOE430B ArrayID = 200B100503.


title: F2-ob/ob(A) 186

description: (C57BL/6J X BTBR) F2-186. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 186A100303, MOE430B ArrayID = 186B100503.


title: F2-ob/ob(A) 223

description: (C57BL/6J X BTBR) F2-223. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 223A100303, MOE430B ArrayID = 223B100503.


title: F2-ob/ob(A) 173

description: (C57BL/6J X BTBR) F2-173. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 173A100303, MOE430B ArrayID = 173B100503.


title: F2-ob/ob(A) 167

description: (C57BL/6J X BTBR) F2-167. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 167A100303, MOE430B ArrayID = 167B100503.


title: F2-ob/ob(A) 165

description: (C57BL/6J X BTBR) F2-165. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 165A100303, MOE430B ArrayID = 165B100503.


title: F2-ob/ob(A) 061

description: (C57BL/6J X BTBR) F2-061. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 061A100203, MOE430B ArrayID = 061B100503.


title: F2-ob/ob(A) 111

description: (C57BL/6J X BTBR) F2-111. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 111A100303, MOE430B ArrayID = 111B100503.


title: F2-ob/ob(B) 617

description: (C57BL/6J X BTBR) F2-617. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 617A100703, MOE430B ArrayID = 617B100803.


title: F2-ob/ob(B) 620

description: (C57BL/6J X BTBR) F2-620. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 620A100703, MOE430B ArrayID = 620B100803.


title: F2-ob/ob(B) 553

description: (C57BL/6J X BTBR) F2-553. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 553A100703, MOE430B ArrayID = 553B100803.


title: F2-ob/ob(B) 615

description: (C57BL/6J X BTBR) F2-615. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 615A100703, MOE430B ArrayID = 615B100803.


title: F2-ob/ob(A) 012

description: (C57BL/6J X BTBR) F2-012. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 012A100203, MOE430B ArrayID = 012B100503.


title: F2-ob/ob(A) 044

description: (C57BL/6J X BTBR) F2-044. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 044A100203, MOE430B ArrayID = 044B100503.


title: F2-ob/ob(A) 100

description: (C57BL/6J X BTBR) F2-100. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 100A100303, MOE430B ArrayID = 100B100503.


title: F2-ob/ob(A) 046

description: (C57BL/6J X BTBR) F2-046. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 046A100203, MOE430B ArrayID = 046B100503.


title: F2-ob/ob(A) 002

description: (C57BL/6J X BTBR) F2-002. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 002A100203, MOE430B ArrayID = 002B100503.


title: F2-ob/ob(B) 559

description: (C57BL/6J X BTBR) F2-559. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 559A100703, MOE430B ArrayID = 559B100803.


title: F2-ob/ob(A) 156

description: (C57BL/6J X BTBR) F2-156. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 156A100303, MOE430B ArrayID = 156B100503.


title: F2-ob/ob(A) 105

description: (C57BL/6J X BTBR) F2-105. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 105A100303, MOE430B ArrayID = 105B100503.


title: F2-ob/ob(B) 486

description: (C57BL/6J X BTBR) F2-486. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 486A100603, MOE430B ArrayID = 486B100803.


title: F2-ob/ob(B) 493

description: (C57BL/6J X BTBR) F2-493. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 493A100603, MOE430B ArrayID = 493B100803.


title: F2-ob/ob(B) 499

description: (C57BL/6J X BTBR) F2-499. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 499A100603, MOE430B ArrayID = 499B100803.


title: F2-ob/ob(B) 549

description: (C57BL/6J X BTBR) F2-549. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 549A100703, MOE430B ArrayID = 549B100803.


title: F2-ob/ob(B) 560

description: (C57BL/6J X BTBR) F2-560. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 560A100703, MOE430B ArrayID = 560B100803.


title: F2-ob/ob(B) 608

description: (C57BL/6J X BTBR) F2-608. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 608A100703, MOE430B ArrayID = 608B100803.


title: F2-ob/ob(B) 523

description: (C57BL/6J X BTBR) F2-523. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 523A100703, MOE430B ArrayID = 523B100803.


title: F2-ob/ob(B) 554

description: (C57BL/6J X BTBR) F2-554. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 554A100703, MOE430B ArrayID = 554B100803.


title: F2-ob/ob(B) 517

description: (C57BL/6J X BTBR) F2-517. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 517A100703, MOE430B ArrayID = 517B100803.


title: F2-ob/ob(B) 513

description: (C57BL/6J X BTBR) F2-513. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 513A100603, MOE430B ArrayID = 513B100803.


title: F2-ob/ob(A) 022

description: (C57BL/6J X BTBR) F2-022. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 022A100203, MOE430B ArrayID = 022B100503.


title: F2-ob/ob(A) 123

description: (C57BL/6J X BTBR) F2-123. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 123A100303, MOE430B ArrayID = 123B100503.


title: F2-ob/ob(B) 479

description: (C57BL/6J X BTBR) F2-479. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 479A100603, MOE430B ArrayID = 479B100803.


title: F2-ob/ob(B) 489

description: (C57BL/6J X BTBR) F2-489. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 489A100603, MOE430B ArrayID = 489B100803.


title: F2-ob/ob(B) 474

description: (C57BL/6J X BTBR) F2-474. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 474A100603, MOE430B ArrayID = 474B100803.


title: F2-ob/ob(B) 317

description: (C57BL/6J X BTBR) F2-317. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 317A100603, MOE430B ArrayID = 317B100703.


title: F2-ob/ob(B) 458

description: (C57BL/6J X BTBR) F2-458. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 458A100603, MOE430B ArrayID = 458B100803.


title: F2-ob/ob(B) 472

description: (C57BL/6J X BTBR) F2-472. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 472A100603, MOE430B ArrayID = 472B100803.


title: F2-ob/ob(B) 440

description: (C57BL/6J X BTBR) F2-440. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 440A100603, MOE430B ArrayID = 440B100803.


title: F2-ob/ob(B) 455

description: (C57BL/6J X BTBR) F2-455. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 455A100603, MOE430B ArrayID = 455B100803.


title: F2-ob/ob(B) 419

description: (C57BL/6J X BTBR) F2-419. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 419A100603, MOE430B ArrayID = 419B100703.


title: F2-ob/ob(B) 438

description: (C57BL/6J X BTBR) F2-438. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 438A100603, MOE430B ArrayID = 438B100703.


title: F2-ob/ob(B) 416

description: (C57BL/6J X BTBR) F2-416. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = M, 4-hr fasting, MOE430A ArrayID = 416A100603, MOE430B ArrayID = 416B100703.


title: F2-ob/ob(B) 264

description: (C57BL/6J X BTBR) F2-264. We selected 60 (C57BL/6J X BTBR) F2-ob/ob mice based on the selective phenotyping algorithm (Jin et al. 2004). The 60 mice used in this study were a subset of F2 mice segregating for phenotypes associated with obesity and diabetes (Stoehr et al. 2000). The framework map consists of 145 microsatellite markers spanning the 19 mouse autosomes, with average spacing of 20 cM, augmented by markers in identified regions.

tag: (C57BL/6J X BTBR) F2-ob/ob (leptin deficient) mice, Liver, 14 weeks, Gender = F, 4-hr fasting, MOE430A ArrayID = 264A100603, MOE430B ArrayID = 264B100703.