Cmah knockout effect on mdx model of Duchenne Muscular Dystrophy (DMD): skeletal muscle - - GEO DataSets - NCBI

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Full record GDS4200

Cmah knockout effect on mdx model of Duchenne Muscular Dystrophy (DMD): skeletal muscle

Analysis of muscle from mdx males with a human-specific deletion in the Cmah (cytidine monophosphate-sialic acid hydroxylase) gene. Cmah-/-mdx mice show increased disease severity that better approximates DMD in humans. Results provide insight into the contributions of glycosylation defects to DMD.

Organism:: Mus musculus

Type:: Expression profiling by array, count, 4 genotype/variation, 2 strain sets

Platform:: GPL1261
Series:: GSE16438
12 Samples

Download data: CEL

DataSet

Accession:: GDS4200

ID:: 4200

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Cmah knockout effect on mdx model of Duchenne Muscular Dystrophy (DMD): skeletal...
Cmah knockout effect on mdx model of Duchenne Muscular Dystrophy (DMD): skeletal muscle
Accession: GDS4200

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