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Items: 5

1.

mTORC1-mediated growth of kidney cysts is rapidly bypassed by other signaling pathways

(Submitter supplied) Cystic kidney disease (CyKD) is the leading monogenetic cause of endstage renal disease. In both mice and humans CyKD has been consistently linked to the activation of the mTORC1 pathway. Yet, the utility of mTORC1 inhibitors in CyKD patients remains controversial despite promising preclinical data. To conclusively define the cell intrinsic role of mTORC1 for cyst development, mTORC1 was selectively inactivated in renal tubular cells of an aciliary mouse model of CyKD by deleting the decisive scaffolding protein RAPTOR. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL19559
142 Samples
Download data: CEL
Series
Accession:
GSE58044
ID:
200058044
2.

Expression Data for Cisplatin Treated Dorsal Root Ganglia from A/J and C57BL/6J Mice

(Submitter supplied) Peripheral sensory neuropathy is a common complication to cisplatin treatment in cancer patients. Multiple signaling pathways are likely to be implicated in the pathophysiology, there are no explicit treatments and little is known about predictive factors associated with the onset or progression of cisplatin induced peripheral neuropathy. The transcriptional profiles of differentially senesitive strains of dorsal root ganglion across two inbreed strain of mice will promote better understanding of progression and risk factors assocciated with cisplatin induced peripheral neuropathy. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL19559
47 Samples
Download data: CEL
Series
Accession:
GSE64174
ID:
200064174
3.

Significant obesity associated gene expression changes are in the stomach but not intestines in obese mice

(Submitter supplied) The gastrointestinal (GI) tract can have significant impact on the regulation of the whole body metabolism and may contribute to the development of obesity and diabetes. To systemically elucidate the role of the GI tract in obesity, we performed a transcriptomic analyses in different parts of the GI tract of two obese mouse models: ob/ob and high-fat diet (HFD) fed mice. Compared to their lean controls, both obese mouse groups had significant amount of gene expression changes in the stomach (ob/ob: 959; HFD: 542), much more than the number of changes in the intestine. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL19559
129 Samples
Download data: CEL
Series
Accession:
GSE69306
ID:
200069306
4.

Snf5F/Fp53L/LGFAP-Cre tumors and human AT/RT show similar gene expression signatures

(Submitter supplied) Human medulloblastoma (MB) can be segregated into four major categories based on gene expression patterns: Hedgehog (HH) subtype, Wnt subtype, Group 3, and Group 4. However, they all exhibit strikingly different gene expression profiles from Atypical Teratoid/Rhabdoid Tumor (AT/RT). We re-analyzed published gene expression microarray dataset of pediatric brain tumors to identify a gene expression profile that clearly distinguished human AT/RT from human MB. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL19559
10 Samples
Download data: CEL
Series
Accession:
GSE68627
ID:
200068627
5.

Genetic ablation of CD38 protects against Western diet-induced exercise intolerance and metabolic inflexibility

(Submitter supplied) CD38, a multi-functional membrane receptor and enzyme, consumes NAD+ to generate products such as cyclic-ADP-ribose. CD38 knockout mice show elevated tissue and blood NAD+ level. Chronic feeding of high-fat, high-sucrose diet to wild type mice leads to exercise intolerance and reduced metabolic flexibility. Loss of CD38 by genetic mutation protects mice from diet-induced metabolic deficit. These animal model results suggest that elevation of tissue NAD+ through genetic ablation of CD38 can profoundly alter energy homeostasis in animals that are maintained on a calorically-excessive Western diet.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL19559
16 Samples
Download data: CEL
Series
Accession:
GSE69062
ID:
200069062
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