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Links from GEO DataSets

Items: 8

1.
Full record GDS4546

Metabolic stress effect on MCAD-deficient mutants: liver

Analysis of liver from medium-chain acyl-coenzyme A dehydrogenase-deficient (MCAD-/-) adult males during fasting and during an LPS-induced acute phase response. Results provide insight into the molecular basis of disturbed hepatic carbohydrate management during metabolic stress in MCAD-/- mutants.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation, 2 stress sets
Platform:
GPL1261
Series:
GSE37546
20 Samples
Download data: CEL
DataSet
Accession:
GDS4546
ID:
4546
2.

Disturbed Hepatic Carbohydrate Management During High Metabolic Demand in Medium-Chain Acyl-CoA Dehydrogenase (MCAD)-deficient Mice

(Submitter supplied) Medium-chain acyl-coenzyme A (CoA) dehydrogenase (MCAD) catalyzes crucial steps in mitochondrial fatty acid oxidation, a process that is of key relevance for maintenance of energy homeostasis, especially during high metabolic demand. To gain insight into the metabolic consequences of MCAD deficiency under these conditions, we compared hepatic carbohydrate metabolism in vivo in wild-type and MCAD-/- mice during fasting and during a lipopolysaccharide (LPS)-induced acute phase response (APR). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4546
Platform:
GPL1261
20 Samples
Download data: CEL
Series
Accession:
GSE37546
ID:
200037546
3.

Transcriptome analysis suggests a compensatory role of the cofactors coenzyme A and NAD+ in medium-chain acyl-CoA dehydrogenase knockout mice

(Submitter supplied) During fasting, mitochondrial fatty-acid β-oxidation (mFAO) is essential for the generation of glucose by the liver. Children with a loss-of-function deficiency in the mFAO enzyme medium-chain acyl-Coenzyme A dehydrogenase (MCAD) are at serious risk of life-threatening low blood glucose levels during fasting in combination with intercurrent disease. However, a subset of these children remains asymptomatic throughout life. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
32 Samples
Download data: TXT
Series
Accession:
GSE136309
ID:
200136309
4.

The transcriptomic signature of hungry murine liver

(Submitter supplied) Background In the postabsorptive state, the portal-drained viscera are a major energy consumer, but a comprehensive overview of the adaptive fasting response in the liver is lacking. Hence, gene-expression profiling, pathway, network and gene-set enrichment analysis and immunohistochemistry were carried out on mouse liver after 0, 12, 24, and 72 hours of fasting. Results Liver weight has fallen to 50% of control after three days of fasting, hepatocyte size was reduced with no apparent increase in apoptosis, while the basic liver structure and metabolic zonnation were preserved. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3642
Platform:
GPL922
12 Samples
Download data: TIFF, TXT
Series
Accession:
GSE10653
ID:
200010653
5.
Full record GDS3642

Fasting effect on the liver

Analysis of livers from male FVB animals fasting for up to 72 hours. Results provide insight into the adaptive response of the liver to fasting.
Organism:
Mus musculus
Type:
Expression profiling by array, log ratio, 4 time sets
Platform:
GPL922
Series:
GSE10653
12 Samples
Download data: TIFF, TXT
6.

Capase-1 cleaves PPARg for potentitating the pro-tumor action of TAMs

(Submitter supplied) Tumor-associated macrophages (TAMs) are increasingly viewed as a target of great relevance in the tumor microenvironment, because of their important role in cancer progression and metastasis. However, the endogenous regulatory mechanisms underlying TAM differentiation remain largely unknown. Here, we report that caspase-1 promotes TAM differentiation by cleaving peroxisome proliferator-activated receptor gamma (PPARγ) at Asp64, thus generating a 41 kDa fragment. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL15207
9 Samples
Download data: CEL
Series
Accession:
GSE99960
ID:
200099960
7.

Effects of diet and Acads genotype on transcriptional response in brain and liver

(Submitter supplied) How signals from fatty acid metabolism are translated into changes in food intake remains unclear. Previously we reported that mice with a genetic inactivation of Acads (short-chain acyl-CoA dehydrogenase), encoding the enzyme responsible for mitochondrial beta-oxidation of C4-C6 short-chain fatty acids (SCFAs), shift consumption away from fat and toward carbohydrate when offered a choice. This finding demonstrated that the loss of a specific enzyme in fatty acid oxidation alters the choice of diet intake. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL2995
24 Samples
Download data: TXT
Series
Accession:
GSE35180
ID:
200035180
8.

Fasting induces a biphasic adaptive metabolic response in murine small intestine

(Submitter supplied) Background The gut is a major energy consumer, but a comprehensive overview of the adaptive response to fasting is lacking. Gene-expression profiling, pathway analysis, and immunohistochemistry were therefore carried out on mouse small intestine after 0, 12, 24, and 72 hours of fasting. Results Intestinal weight declined to 50% of control, but this loss of tissue mass was distributed proportionally among the gut’s structural components, so that the microarrays’ tissue base remained unaffected. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL922
12 Samples
Download data: TIFF, TXT
Series
Accession:
GSE8019
ID:
200008019
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