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MetabolomicsNMR analysis of DMD mouse serum
Not available
ORGANISM(S): Mus musculus 
ST000099 | MetabolomicsWorkbench
TranscriptomicsDeletion of DMD exon 52 in the pig results in fulminant muscular dystrophy
Duchenne muscular dystrophy (DMD) is caused by mutations in the X-linked dystrophin (DMD) gene. The absence of dystrophin protein leads to progressive muscle weakness and wasting, disability and death. To establish a tailored large animal model of DMD, we deleted DMD exon 52 in male pig cells by gen...
ORGANISM(S): Sus scrofa 
2013-08-06 | E-GEOD-44096 | biostudies-arrayexpress
TranscriptomicsRNA-seq data from healthy and DMD human cells, along skeletal muscle differentiation from induced pluripotent stem cells
3 healthy cells - 3 DMD cells - 7 time points (tissue-derived myoblasts, tissue-derived myotubes, hiPSCs, Day 3 of differentiation, Day 10 of differentiation, Day 17 of differentiation, Day 25 of differentiation) - 1 replicate per cell line for the tissue-derived samples and 3 biological replicates ...
ORGANISM(S): Homo sapiens 
2020-10-05 | E-MTAB-8321 | biostudies-arrayexpress
TranscriptomicsmiRNA-seq data from healthy and DMD human cells, along skeletal muscle differentiation from induced pluripotent stem cells
3 or 4 healthy cells - 3 DMD cells - 7 time points (tissue-derived myoblasts, tissue-derived myotubes, hiPSCs, Day 3 of differentiation, Day 10 of differentiation, Day 17 of differentiation, Day 25 of differentiation).
ORGANISM(S): Homo sapiens 
2020-10-05 | E-MTAB-8293 | biostudies-arrayexpress
TranscriptomicsTime course Healthy DMD myogenesis
Primairy human myoblast cell cultures Healthy DMD
ORGANISM(S): Homo sapiens 
2010-06-09 | E-GEOD-2693 | biostudies-arrayexpress
TranscriptomicsDMD vs. AGING
Comparative effects of Duchenne Muscular Dystrophy (DMD) and Aging in skeletal muscle Expression profiling established by microarray technology provides a powerful tool by which complex pathways can be assembled. The pathophysiology of Duchenne Muscular Dystrophy (DMD) is a complex process involving...
ORGANISM(S): Homo sapiens 
2011-11-01 | E-GEOD-32720 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of human quadriceps muscle of young Duchenne muscular dystrophy patients and age matched controls
Albeit increased serum CK level and abnormal muscle histology are always present, boys with DMD are phenotipically indistinguishable from the normal ones at birth and, in their first years of life, acquire early motor milestones at normal times. A clear defect in muscle function becomes generally ap...
ORGANISM(S): Homo sapiens 
2008-06-14 | E-GEOD-6011 | biostudies-arrayexpress
TranscriptomicsRNA-seq from myogenic satellite cells from a translational porcine model for Duchenne muscular dystrophy, heterozygous female carriers, and their healthy wild-type counterpart
Satellite cells (SCs), the stem cell population of skeletal muscle, are crucial for growth and regeneration, and their dysfunction is increasingly recognized as a contributing factor to Duchenne muscular dystrophy (DMD). DMD is a severe, X-linked disorder caused by DMD gene mutations, leading to lo...
ORGANISM(S): Sus scrofa 
2025-12-11 | E-MTAB-16179 | biostudies-arrayexpress
GenomicsDMD-TGFb-SETDB1
DMD-TGFb-SETDB1
PRJEB63300 | ENA
TranscriptomicsTranscription profiling of mouse mdx animals expressing high levels of utrophin therapeutic implications for DMD
Duchenne Muscular Dystrophy (DMD) is a fatal muscle wasting disorder caused by dystrophin deficiency. Previous work suggested that increased expression of the dystrophin-related protein utrophin in the mdx mouse model of DMD can prevent dystrophic pathophysiology. Physiological tests showed that t...
ORGANISM(S): Mus musculus 
2008-06-15 | E-GEOD-7187 | biostudies-arrayexpress
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