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Accession: PRJNA167030 ID: 167030

Mus musculus (house mouse)

Genome-wide analysis of E157D PPARγ transcriptional activity in NIH-3T3 fibroblasts

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47588 additional projects are related by organism.
The E157D PPARγ mutation presents as an atypical case of familial partial lipodystrophy and diabetes in a human cohort and has a novel molecular mechanism. More...
AccessionPRJNA167030; GEO: GSE37990
Data TypeTranscriptome or Gene expression
ScopeMultiisolate
OrganismMus musculus[Taxonomy ID: 10090]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus; Mus musculus
PublicationsCampeau PM et al., "Clinical and molecular characterization of a severe form of partial lipodystrophy expanding the phenotype of PPARγ deficiency.", J Lipid Res, 2012 Sep;53(9):1968-78
SubmissionRegistration date: 15-May-2012
Brendan Lee Lab, Molecular and Human Genetics, Baylor College of Medicine
RelevanceModel Organism
Project Data:
Resource NameNumber
of Links
Publications
PubMed1
PMC1
Other datasets
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Spots543372
Data volume, Processed Mbytes16
Data volume, Supplementary Mbytes4

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