
NCBI . NLM . NIH . GOV {
}
Title[redir]:
Cellular and molecular mechanisms underlying muscular dystrophy - PMC
Description:
The muscular dystrophies are a group of heterogeneous genetic diseases characterized by progressive degeneration and weakness of skeletal muscle. Since the discovery of the first muscular dystrophy gene encoding dystrophin, a large number of genes ...
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Keywords {🔍}
doi, pubmed, google, scholar, muscular, dystrophy, muscle, mutations, pmc, protein, article, sarcolemma, free, genet, cell, proteins, gene, dystrophin, van, disease, dystrophies, nat, dapc, hum, genes, membrane, skeletal, myotonic, intracellular, domain, splicing, nnos, fshd, repair, biol, molecular, ecm, loss, dmd, repeat, complex, type, repeats, dux, mol, science, caused, expression, actin, limbgirdle,
Topics {✒️}
putative e3-ubiquitin-ligase gene n-octyl beta-d-glucoside limb-girdle muscular dystrophy beltrán-valero de bernab� proximal limb-girdle musculature muscular dystrophy-dystroglycanopathy type beltran-valero de bernab� ca2+-activated cl- channels emery-dreifuss muscular dystrophy beltrán-valero de bernabe plectin-1f isoform-encoding exon n-terminal actin-binding domain muscle-specific chloride channel phosphorylated o-mannosyl glycans ca2+-dependent repair pathway cytoskeletal filamentous actin serine/threonine residues catalyzed pmc beta search α-adrenergic receptor activation mediates sarcolemmal wound-healing pmc copyright notice dysferlin-deficient muscular dystrophy muscular dystrophy-dystroglycanopathy dystrophin-related protein α-dystrobrevin dysferlin-dependent repair pathway cross-links actin filaments reduce exercise-induced fatigue cysteine-rich domain binds pro-apoptosis protein bax reduced exercise-induced fatigue dystrophin-dependent muscular dystrophies double-stranded hairpin structure neuronal nos binding increased steady-state levels facioscapulohumeral muscular dystrophy duchenne muscular dystrophy isoprenoid synthase domain pre-mrna splicing analyses variable n-terminal domain membrane-bound intracellular vesicles recruits dysferlin-carrying vesicles contraction-induced membrane injuries congenital muscular dystrophy c-terminal domain interacts becker muscular dystrophy toxic transcription factor fukutin-related protein gene increased ca2+ concentration α7β1 integrin dimer protein-o-mannosyltransferase 1
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Analytics and Tracking {📊}
- Google Analytics
- Google Analytics 4
- Google Tag Manager
Libraries {📚}
- Foundation
- jQuery
- jQuery module (jquery-3.6.0)
- Zoom.js
Emails and Hosting {✉️}
Mail Servers:
- nihcesxway.hub.nih.gov
- nihcesxway2.hub.nih.gov
- nihcesxway3.hub.nih.gov
- nihcesxway4.hub.nih.gov
- nihcesxway5.hub.nih.gov
Name Servers:
- dns1-ncbi.ncbi.nlm.nih.gov
- dns2-ncbi.ncbi.nlm.nih.gov
- lhcns1.nlm.nih.gov
- lhcns2.nlm.nih.gov
CDN Services {📦}
- Ncbi