Characterization of DRP2, a novel human dystrophin homologue
about
Sequence analysis of LRPPRC and its SEC1 domain interaction partners suggests roles in cytoskeletal organization, vesicular trafficking, nucleocytosolic shuttling, and chromosome activityBrain dystrophin-glycoprotein complex: persistent expression of beta-dystroglycan, impaired oligomerization of Dp71 and up-regulation of utrophins in animal models of muscular dystrophyDystrophins and dystrobrevins.Absence of Dystrophin Related Protein-2 disrupts Cajal bands in a patient with Charcot-Marie-Tooth disease.Profound human/mouse differences in alpha-dystrobrevin isoforms: a novel syntrophin-binding site and promoter missing in mouse and rat.The dystrotelin, dystrophin and dystrobrevin superfamily: new paralogues and old isoforms.Regulation and functional significance of utrophin expression at the mammalian neuromuscular synapse.Dystrophins, utrophins, and associated scaffolding complexes: role in mammalian brain and implications for therapeutic strategies.Harnessing the potential of dystrophin-related proteins for ameliorating Duchenne's muscular dystrophy.Viral-mediated gene therapy for the muscular dystrophies: successes, limitations and recent advancesSubtle neuromuscular defects in utrophin-deficient mice.A PDZ-containing scaffold related to the dystrophin complex at the basolateral membrane of epithelial cells.Differential membrane localization and intermolecular associations of alpha-dystrobrevin isoforms in skeletal muscleBex1 knock out mice show altered skeletal muscle regeneration.Activation of utrophin promoter by heregulin via the ets-related transcription factor complex GA-binding protein alpha/beta.The roles of the dystrophin-associated glycoprotein complex at the synapsePathoproteomic profiling of the skeletal muscle matrisome in dystrophinopathy associated myofibrosis.Evidence of a Conserved Molecular Response to Selection for Increased Brain Size in Primates.ABC of multifaceted dystrophin glycoprotein complex (DGC).The 3'-untranslated region of the dystrophin gene - conservation and consequences of loss.Novel hemizygous nonsense mutation in DRP2 is associated with inherited neuropathy.Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes.
P2860
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P2860
Characterization of DRP2, a novel human dystrophin homologue
description
1996 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի հունիսին հրատարակված գիտական հոդված
@hy
articolo scientifico
@it
artículu científicu espublizáu en 1996
@ast
im Juni 1996 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1996/06/01)
@sk
vědecký článek publikovaný v roce 1996
@cs
wetenschappelijk artikel (gepubliceerd op 1996/06/01)
@nl
наукова стаття, опублікована в червні 1996
@uk
name
Characterization of DRP2, a novel human dystrophin homologue
@ast
Characterization of DRP2, a novel human dystrophin homologue
@en
Characterization of DRP2, a novel human dystrophin homologue
@nl
type
label
Characterization of DRP2, a novel human dystrophin homologue
@ast
Characterization of DRP2, a novel human dystrophin homologue
@en
Characterization of DRP2, a novel human dystrophin homologue
@nl
prefLabel
Characterization of DRP2, a novel human dystrophin homologue
@ast
Characterization of DRP2, a novel human dystrophin homologue
@en
Characterization of DRP2, a novel human dystrophin homologue
@nl
P2093
P50
P356
P1433
P1476
Characterization of DRP2, a novel human dystrophin homologue
@en
P2093
P2888
P304
P356
10.1038/NG0696-223
P407
P577
1996-06-01T00:00:00Z