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Links from GEO DataSets

Items: 4

1.
Full record GDS4199

Wild-type embryonic stem cell rescue of mdx model of Duchenne muscular dystrophy: skeletal muscle

Analysis of pectoralis muscle from 4 month-old, wildtype/mdx chimeric males. Chimeras were created by injecting WT ESCs into mdx mutant blastocysts; injected blastocysts developed in the uterus of pseudopregnant females. Results provide insight into molecular basis of WT ESC rescue of mdx mice.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 5 genotype/variation sets
Platform:
GPL8321
Series:
GSE12580
5 Samples
Download data: CEL
2.

Blastocyst Injection of Wild Type Embryonic Stem Cells Induces Global Corrections in Mdx Mice.

(Submitter supplied) Duchenne muscular dystrophy (DMD) is an incurable neuromuscular degenerative disease, caused by a mutation in the dystrophin gene. Mdx mice recapitulate DMD features. Here we show that injection of wild-type (WT) embryonic stem cells (ESCs) into mdx blastocysts produces mice with improved pathology. A small fraction of WT ESCs incorporates into the mdx mouse nonuniformly to upregulate protein levels of dystrophin in the skeletal muscle. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4199
Platform:
GPL8321
5 Samples
Download data: CEL
Series
Accession:
GSE12580
ID:
200012580
3.

mRNA expression in regenerated mdx mouse skeletal muscle

(Submitter supplied) Despite over 3,000 articles published on dystrophin in the last 15 years, the reasons underlying the progression of the human disease, differential muscle involvement, and disparate phenotypes in different species are not understood. The present experiment employed a screen of 12,488 mRNAs in 16-wk-old mouse mdx muscle at a time when the skeletal muscle is avoiding severe dystrophic pathophysiology, despite the absence of a functional dystrophin protein. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS236
Platform:
GPL81
10 Samples
Download data: CEL
Series
Accession:
GSE466
ID:
200000466
4.
Full record GDS236

Dystrophin-deficient mdx muscle regeneration

Examination of mdx mouse, Duchenne muscular dystrophy model. 16 week regenerating mdx muscle analyzed in search for salvage pathways that maintain skeletal muscle integrity in the absence of functional dystrophin protein.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 strain sets
Platform:
GPL81
Series:
GSE466
10 Samples
Download data: CEL
DataSet
Accession:
GDS236
ID:
236
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