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X-linked muscular dystrophy with abnormal dystrophin
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
MYH3
MYH8
DMD
SPP1
COL1A2
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
MODULE_1
MODULE_5
SCHUETZ_BREAST_CANCER_DUCTAL_INVASIVE_UP
MODULE_2
WONG_ADULT_TISSUE_STEM_MODULE
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Curated Studies
Most Correlated Studies
Gastrocnemius muscles of mdx mice treated with activin receptor B and exercise
Quadriceps from DMD[mdx/mdx] mice treated with Tadalafil
Soleus muscles from Duchenne muscular dystrophy model mice with conditional RUNX1 knockout
Muscle satellite cells of STAT3 knockout and DMD mutant mice
Skeletal muscle biopsies from Duchenne muscular dystrophy patients
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Literature
Most Relevant Literature
Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy.
Prevalence of cardiomyopathy in Duchenne and Becker's muscular dystrophy.
Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immuno…
Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immuno…
Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immuno…
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Clinical Trials
Most Relevant Clinical Trials
Biomarker for Duchenne Muscular Dystrophy
Pentoxifylline in Duchenne Muscular Dystrophy
Efficacy Study of AVI-4658 to Induce Dystrophin Expression in Selected Duchenne Muscular Dystrophy P…
Safety Study of Transvenous Limb Perfusion in Human Muscular Dystrophy
Longitudinal Study of the Natural History of Duchenne Muscular Dystrophy (DMD)
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