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Links from GEO DataSets

Items: 10

1.

Genome-wide 10K SNP profiles in heterogeneous stock rats that differ in glucose tolerance

(Submitter supplied) Using heterogeneous stock (HS) rats, we have identified a region on rat chromosome 1 that maps multiple diabetic traits. We sought to use global expression analysis to determine if genes within this region are differentially expressed between HS rats with normal glucose tolerance and those with glucose intolerance
Organism:
Rattus norvegicus
Type:
SNP genotyping by SNP array
Platform:
GPL18612
54 Samples
Download data: CEL
Series
Accession:
GSE57117
ID:
200057117
2.

Heterogeneous stock rats that differ in glucose tolerance

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Rattus norvegicus
Type:
Expression profiling by array; SNP genotyping by SNP array
Platforms:
GPL1355 GPL18612
112 Samples
Download data: CEL
Series
Accession:
GSE57118
ID:
200057118
3.

Gene expression profiles in heterogeneous stock rats that differ in glucose tolerance

(Submitter supplied) Using heterogeneous stock (HS) rats, we have identified a region on rat chromosome 1 that maps multiple diabetic traits. We sought to use global expression analysis to determine if genes within this region are differentially expressed between HS rats with normal glucose tolerance and those with glucose intolerance
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL1355
58 Samples
Download data: CEL
Series
Accession:
GSE54935
ID:
200054935
4.

Identification of two novel candidate genes for insulin secretion by comparative genomics of multiple backcross populations

(Submitter supplied) To identify novel disease genes for type 2 diabetes (T2D) we generated two backcross populations of obese and diabetes-susceptible New Zealand Obese (NZO) with the two lean mouse strains 129P2 and C3H/FeJ. Subsequent whole-genome linkage scan revealed 36 novel quantitative trait loci (QTL) for T2D-associated traits. The strongest association with blood glucose (12 cM, LOD 13.3) and plasma insulin (17 cM, LOD 4.8) was detected on proximal chromosome 7 (designated Cdp7prox) exclusively in the NZOxC3H crossbreeding, suggesting that the causal gene is unique for the C3H genome. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
10 Samples
Download data: CEL, CHP
Series
Accession:
GSE117553
ID:
200117553
5.

Bglu3 congenic mice - gene expression in liver

(Submitter supplied) A congenic line was constructed by introgressing a C3H chromosome 1 region harboring Bglu3 into C57BL/6 apoE-/- background. RNA was extracted from liver using a QIAGEN kit . Total RNA was pooled in an equal amount from 3 mice for each group. Standard Affymetrix procedures were performed using 8ug of total RNA. Microarrays were used to detect gene expression in the liver of Bglu3 congenic mice and C57BL/6 apoE-deficient mouse strains fed a western diet.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
2 Samples
Download data: CEL
Series
Accession:
GSE29151
ID:
200029151
6.

Genetic dissection of nutrition-induced plasticity in insulin/insulin-like growth factor signaling in a Drosophila MPP

(Submitter supplied) The nutritional environments that organisms experience are inherently variable, requiring tight coordination of how resources are allocated to different functions relative to the total amount of resources available. A growing body of evidence supports the hypothesis that key endocrine pathways play a fundamental role in this coordination. In particular, the insulin/insulin-like growth factor signaling (IIS) and target of rapamycin (TOR) pathways have been implicated in nutrition-dependent changes in metabolism and nutrient allocation, however little is known about the genetic basis of standing variation in the pathways. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by RT-PCR
Platform:
GPL22881
918 Samples
Download data: TXT
Series
Accession:
GSE93117
ID:
200093117
7.

Comparitive genomics of multiple backcross mouse populations identifies Sgcg as a novel potential obesity-modifier gene

(Submitter supplied) To nominate novel disease genes for obesity and type 2 diabetes (T2D) we recently generated two mouse backcross populations of obese and T2D- susceptible New Zealand Obese (NZO/HI) mice with the two lean mouse strains 129P2/OlaHsd and C3HeB/FeJ. Comparative linkage analysis of our two female backcross populations identified seven novel body fat-associated quantitative trait loci (QTL). Only the locus Nbw14 (NZO body weight on chromosome 14) showed linkage to obesity-related traits in both backcross populations, indicating that the causal gene variant is likely specific for the NZO strain as NZO allele carriers in both crosses displayed elevated body weight and fat mass. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
15 Samples
Download data: CEL, CHP
Series
Accession:
GSE197101
ID:
200197101
8.

Genetic mapping of multiple metabolic traits identifies novel genes for adiposity, lipids and insulin secretory capacity in outbred rats II

(Submitter supplied) RNA-Seq was used in an attempt to identify candidate genes regulating metabolic and physiological traits
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18694
448 Samples
Download data: TXT
Series
Accession:
GSE200453
ID:
200200453
9.

Genetic mapping of multiple metabolic traits identifies novel genes for adiposity, lipids and insulin secretory capacity in outbred rats

(Submitter supplied) RNA-Seq was used in an attempt to identify candidate genes regulating metabolic and physiological traits
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18694
415 Samples
Download data: TXT
Series
Accession:
GSE196572
ID:
200196572
10.

Novel diabetes gene discovery through comprehensive characterization and integrative analysis of longitudinal gene expression changes

(Submitter supplied) Type 2 diabetes is a complex, systemic disease affected by both genetic and environmental factors. Previous research has identified genetic variants associated with type 2 diabetes risk, however gene regulatory changes underlying progression to disease are still largely unknown. We investigated RNA expression changes that occur during diabetes progression using a two-stage approach. In our discovery stage, we compared changes in gene expression using two longitudinally collected blood samples from subjects who transitioned to type 2 diabetes between the time points against those who did not with a novel analytical network approach. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
116 Samples
Download data: TXT
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