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Accession: PRJNA116387 ID: 116387

Array profiling of dystrophin-deficient mice with a secondary glycosylation defect (house mouse)

See Genome Information for Mus musculus
A deletion in the CMAH gene in humans occurred approximately 3.5 million years ago. More...
AccessionPRJNA116387; GEO: GSE16438
Data TypeTranscriptome or Gene expression
ScopeMultiisolate
OrganismMus musculus[Taxonomy ID: 10090]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Sciurognathi; Muroidea; Muridae; Murinae; Mus; Mus; Mus musculus
PublicationsChandrasekharan K et al., "A human-specific deletion in mouse Cmah increases disease severity in the mdx model of Duchenne muscular dystrophy.", Sci Transl Med, 2010 Jul 28;2(42):42ra54
SubmissionRegistration date: 31-Jul-2010
Columbus Children's Research Institute
RelevanceModel Organism
Project Data:
Resource NameNumber
of Links
Publications
PubMed1
PMC1
Other datasets
GEO DataSets3
GEO Data Details
ParameterValue
Data volume, Spots1082424
Data volume, Processed Mbytes23
Data volume, Supplementary Mbytes84

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