Mus musculus (ID 343729) - BioProject

Format

Choose Destination

Accession: PRJNA343729 ID: 343729

Mus musculus (house mouse)

See Genome Information for Mus musculus

Navigate Across

We found that lipid-derived acetyl-CoA is a major source of carbon for histone acetylation. More...

Accession	PRJNA343729; GEO: GSE87156
Data Type	Transcriptome or Gene expression
Scope	Multiisolate
Organism	Mus musculus[Taxonomy ID: 10090] Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus; Mus musculus
Publications	McDonnell E et al., "Lipids Reprogram Metabolism to Become a Major Carbon Source for Histone Acetylation.", Cell Rep, 2016 Nov 1;17(6):1463-1472
Grants	"Ethanol-induced Protein Acylation Regulates Metabolism" (Grant ID R01 AA022146, National Institute on Alcohol Abuse and Alcoholism) "Novel SIRT5 Enzymatic Activity Regulates Cellular Mechanisms of Aging and Disease" (Grant ID R01 AG045351, National Institute on Aging)
Submission	Registration date: 21-Sep-2016 Duke Molecular Physiology Institute, Department of Medicine, Duke University Medical Center
Relevance	Model Organism

Project Data:

Parameter	Value
Data volume, Spots	815058
Data volume, Processed Mbytes	26
Data volume, Supplementary Mbytes	34

Supplemental Content

Effects of acute and chronic stress on the transcriptome and epigenome of Atlant...
Effects of acute and chronic stress on the transcriptome and epigenome of Atlantic salmon
Contrasting effects of acute and chronic stress on the transcriptome, epigenome, and on immune response to a pathogen challenge in Atlantic salmon

BioProject
Homo sapiens
Homo sapiens
Homo sapiens Raw sequence reads

BioProject
Arabica-evolution
Arabica-evolution
Allopolyploid coffee genome evolution

BioProject
Mus musculus
Mus musculus
Lipids reprogram metabolism to become a major carbon source for histone acetylation

BioProject

Your browsing activity is empty.

Activity recording is turned off.