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dp427 (11) 11
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Proteomes, ISSN 2227-7382, 09/2015, Volume 3, Issue 3, pp. 298 - 327
The full-length dystrophin protein isoform of 427 kDa (Dp427), the absence of which represents the principal abnormality in X-linked muscular dystrophy, is... 
Dp427 | Myofibrosis | Dystrophin | Collagen | Duchenne muscular dystrophy | collagen | myofibrosis | dystrophin
Journal Article
Biochemical journal, ISSN 0264-6021, 04/2004, Volume 379, Issue 2, pp. 479 - 488
Although the primary abnormality in dystrophin is the underlying cause for mdx (X-chromosome-linked muscular dystrophy), abnormal Call handling after... 
MDX MOUSE | calcium handling | BIOCHEMISTRY & MOLECULAR BIOLOGY | MEMBRANE CYTOSKELETON | dystrophin | SARCOPLASMIC-RETICULUM | SKELETAL-MUSCLE | DEPENDENT PROTEOLYSIS | muscular dystrophy | Dp427 (dystrophin of 427 kDa) | RYANODINE RECEPTOR | ELEVATED LEVELS | sarcalumenin | LEAK CHANNELS | EXTRACELLULAR-MATRIX | LOW-FREQUENCY STIMULATION
Journal Article
Wellcome open research, ISSN 2398-502X, 2020, Volume 5, p. 76
Background: The dystrophin gene has multiple isoforms: full-length dystrophin (dp427) is principally known for its expression in skeletal and cardiac muscle,... 
Journal Article
Neurochemistry international, ISSN 0197-0186, 2019, Volume 129, p. 104489
Journal Article
03/2019, ISBN 9783030030940
The development of molecular therapies enabling compensation of brain alterations in Duchenne muscular dystrophy is a major objective given the high level of... 
Life Sciences | Cognitive Sciences | Neurons and Cognition | Psychology and behavior | Neurobiology
Book Chapter
Biochimica et Biophysica Acta - Molecular Basis of Disease, ISSN 0925-4439, 08/2004, Volume 1689, Issue 3, pp. 252 - 258
Journal Article
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