Identification of altered gene expression in skeletal muscles from Duchenne muscular dystrophy patients
- 1 April 2001
- journal article
- Published by Elsevier BV in Neuromuscular Disorders
- Vol. 11 (3), 269-277
- https://doi.org/10.1016/s0960-8966(00)00198-x
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Genomic Organization of M Line Titin and its Tissue-specific Expression in Two Distinct IsoformsJournal of Molecular Biology, 1996
- Purine and carnitine metabolism in muscle of patients with Duchenne muscular dystrophyClinica Chimica Acta; International Journal of Clinical Chemistry, 1995
- Down‐regulation of mitochondrial mRNAs in the mdx mouse model for Duchenne muscular dystrophyFEBS Letters, 1995
- Characterization of the Gene for dbpA, a Family Member of the Nucleic-Acid-Binding Proteins Containing a Cold-Shock DomainEuropean Journal of Biochemistry, 1995
- Dystrophin deficiency, altered cell signalling and fibre hypertrophyNeuromuscular Disorders, 1994
- Dystrophin–glycoprotein complex: Its role in the molecular pathogenesis of muscular dystrophiesMuscle & Nerve, 1994
- Dystrophin and dystrophin-related protein (utrophin) distribution in normal and dystrophin-deficient skeletal musclesNeuromuscular Disorders, 1993
- Increased Activity of Calcium Leak Channels in Myotubes of Duchenne Human and mdx Mouse OriginScience, 1990
- Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individualsCell, 1987
- Sequence and organization of the human mitochondrial genomeNature, 1981