About: Dystrophin: the protein product of the Duchenne muscular dystrophy locus

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scientific article (publication date: 24 December 1987)

Attributes	Values
rdf:type	Item
description	artículu científicu espublizáu en 1987 (ast) 1987 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած (hyw) наукова стаття, опублікована в грудні 1987 (uk) 1987 թվականի դեկտեմբերին հրատարակված գիտական հոդված (hy) article scientifique publié en 1987 (fr) im Dezember 1987 veröffentlichter wissenschaftlicher Artikel (de) wetenschappelijk artikel (gepubliceerd op 1987/12/24) (nl) scientific article (publication date: 24 December 1987) (en) مقالة علمية (نشرت في 24-12-1987) (ar)
publication date	wds:Q29618077-93BA7680-A261-4719-97EB-61FAC65C3601
publication date	1987-12-24 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q29618077-818396ED-77FB-479E-9420-6F21D1EAE478
language of work or name	English
author name string	wds:Q29618077-A81E58FD-5F90-4A22-A3F6-E1F183559A19 wds:Q29618077-C6F13E45-0FBC-407C-86B2-B5EEC56EDFDE
OpenCitations bibliographic resource ID	wds:Q29618077-74FF77E8-CCBF-4376-B2EF-DCCE133DFBC5
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/245453
author name string	Kunkel LM Brown RH Jr
OpenCitations bibliographic resource ID	245453
rdfs:label	Dystrophin: the protein product of the Duchenne muscular dystrophy locus (en) Dystrophin: the protein product of the Duchenne muscular dystrophy locus (ast)
skos:prefLabel	Dystrophin: the protein product of the Duchenne muscular dystrophy locus (en) Dystrophin: the protein product of the Duchenne muscular dystrophy locus (ast)
name	Dystrophin: the protein product of the Duchenne muscular dystrophy locus (en) Dystrophin: the protein product of the Duchenne muscular dystrophy locus (ast)
author	wds:Q29618077-F156FC92-422F-4A30-9BC3-53805B2EF1D6
author	Eric Hoffman
title	wds:Q29618077-8A89EDE1-E511-40BD-905C-22381C70BBB2
title	Dystrophin: the protein product of the Duchenne muscular dystrophy locus (en)
page(s)	wds:Q29618077-507047D0-71F4-44D1-92BE-A765AEA94135
page(s)	919-28
instance of	wds:Q29618077-6C63B04B-A0A5-4BCA-BE07-6F3D86E55CB3
instance of	scholarly article
main subject	wds:Q29618077-15D39DDB-E33C-44C9-AABB-7AFFB7691A11
main subject	Duchenne muscular dystrophy
PubMed ID	wds:Q29618077-00F28AED-0481-438C-850D-38816EB6A590
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3319190
PubMed ID	3319190
published in	wds:Q29618077-255030EE-FD37-42F6-8141-DC88CC7D19BA
published in	Cell
issue	wds:Q29618077-536E89EE-1458-49E9-9798-0B4AA99A6552
volume	wds:Q29618077-669F9B4B-5088-400E-A72C-8E4292BD4BF3
issue	6
volume	51
DOI	wds:Q29618077-89F2DBCE-4902-4D99-84C3-78C1E8DC258B
DOI	http://dx.doi.org/10.1016/0092-8674(87)90579-4
DOI	10.1016/0092-8674(87)90579-4
ResearchGate publication ID	wds:Q29618077-6FE50520-A3E4-48D2-B5C1-AC1FF15B3AF0
ResearchGate publication ID	19837505
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q29618077
is cites work of	Caveolin-3 directly interacts with the C-terminal tail of beta -dystroglycan. Identification of a central WW-like domain within caveolin family members Membrane Repair: Mechanisms and Pathophysiology. The Rap1 guanine nucleotide exchange factor C3G is required for preservation of larval muscle integrity in Drosophila melanogaster Preclinical drug trials in the mdx mouse: assessment of reliable and sensitive outcome measures Clonal isolation of muscle-derived cells capable of enhancing muscle regeneration and bone healing Zebrafish integrin-linked kinase is required in skeletal muscles for strengthening the integrin-ECM adhesion complex Diagnosing duchenne muscular dystrophy The subcellular distribution of chromosome 6-encoded dystrophin-related protein in the brain Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 1. Trends across the clinical groups Dystrophins, utrophins, and associated scaffolding complexes: role in mammalian brain and implications for therapeutic strategies Red-green color vision impairment in Duchenne muscular dystrophy Postsynaptic abnormalities at the neuromuscular junctions of utrophin-deficient mice The roles of the dystrophin-associated glycoprotein complex at the synapse Dystrophin is phosphorylated by endogenous protein kinases Facilitated NMDA receptor-mediated synaptic plasticity in the hippocampal CA1 area of dystrophin-deficient mice Alterations in dystrophin and utrophin expression parallel the reorganization of GABAergic synapses in a mouse model of temporal lobe epilepsy. Expression of dystrophin-associated proteins during neuronal differentiation of P19 embryonal carcinoma cells. The potassium channel Kir4.1 associates with the dystrophin-glycoprotein complex via alpha-syntrophin in glia Nitric oxide generated by muscle corrects defects in hippocampal neurogenesis and neural differentiation caused by muscular dystrophy Spatial discrimination learning and CA1 hippocampal synaptic plasticity in mdx and mdx3cv mice lacking dystrophin gene products. Behavioral characterization of mdx3cv mice deficient in C-terminal dystrophins. Cortical and brainstem neurons containing calcium-binding proteins in a murine model of Duchenne's muscular dystrophy: selective changes in the sensorimotor cortex. A splice variant of Dp71 lacking the syntrophin binding site is expressed in early stages of human neural development. Passive avoidance behaviour deficit in the mdx mouse Severe Mechanical Dysfunction in Pharyngeal Muscle from AdultmdxMice Activation and localization of matrix metalloproteinase-2 and -9 in the skeletal muscle of the muscular dystrophy dog (CXMDJ). Gamma1- and gamma2-syntrophins, two novel dystrophin-binding proteins localized in neuronal cells Noncoding RNAs, Emerging Regulators of Skeletal Muscle Development and Diseases Stem cell therapy. Use of differentiated pluripotent stem cells as replacement therapy for treating disease microRNA-206 promotes skeletal muscle regeneration and delays progression of Duchenne muscular dystrophy in mice Preclinical studies in the mdx mouse model of duchenne muscular dystrophy with the histone deacetylase inhibitor givinostat Regulation of IRS1/Akt insulin signaling by microRNA-128a during myogenesis MEF2C, a MADS/MEF2-family transcription factor expressed in a laminar distribution in cerebral cortex Muscular dystrophies: genes to pathogenesis Functional disruption of the dystrophin gene in rhesus monkey using CRISPR/Cas9. Plasmapheresis eliminates the negative impact of AAV antibodies on microdystrophin gene expression following vascular delivery. mXBP/CRE-BP2 and c-Jun form a complex which binds to the cyclic AMP, but not to the 12-O-tetradecanoylphorbol-13-acetate, response element Three mouse models of muscular dystrophy: the natural history of strength and fatigue in dystrophin-, dystrophin/utrophin-, and laminin α2-deficient mice Gene and cell-mediated therapies for muscular dystrophy. Mouse regenerating myofibers detected as false-positive donor myofibers with anti-human spectrin Critical Role of Intracellular RyR1 Calcium Release Channels in Skeletal Muscle Function and Disease Chronic administration of membrane sealant prevents severe cardiac injury and ventricular dilatation in dystrophic dogs Development of Duchenne-type cardiomyopathy. Morphologic studies in a canine model. Genetic aspects of Wilson's disease Hydrodynamic limb vein injection of adeno-associated virus serotype 8 vector carrying canine myostatin propeptide gene into normal dogs enhances muscle growth Duchenne's cardiomyopathy in a canine model: electrocardiographic and echocardiographic studies Generation of muscular dystrophy model rats with a CRISPR/Cas system Animal models for genetic neuromuscular diseases

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