Literature DB >> 8542044

Dystrophin-glycoprotein complex: molecular organization and critical roles in skeletal muscle.

Y Sunada1, K P Campbell.   

Abstract

Recent molecular and biochemical studies have disclosed the detailed molecular organization of the dystrophin-glycoprotein complex, which links the cytoskeleton to the extracellular matrix. Defects in several components of this complex cause different types of muscular dystrophy. This glycoprotein complex is also involved in clustering and anchoring acetylcholine receptors at the postsynaptic membrane.

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Year:  1995        PMID： 8542044

Source DB:  PubMed          Journal:  Curr Opin Neurol        ISSN： 1350-7540            Impact factor:   5.710


  24 in total

Review 1.  Understanding dystrophinopathies: an inventory of the structural and functional consequences of the absence of dystrophin in muscles of the mdx mouse.

Authors:  J M Gillis
Journal:  J Muscle Res Cell Motil       Date:  1999-10       Impact factor: 2.698

2.  Structural and functional roles of desmin in mouse skeletal muscle during passive deformation.

Authors:  Sameer B Shah; Jennifer Davis; Noah Weisleder; Ioanna Kostavassili; Andrew D McCulloch; Evelyn Ralston; Yassemi Capetanaki; Richard L Lieber
Journal:  Biophys J       Date:  2004-05       Impact factor: 4.033

3.  Α-Dystrobrevin-1 recruits Grb2 and α-catulin to organize neurotransmitter receptors at the neuromuscular junction.

Authors:  Jacinthe Gingras; Marta Gawor; Krzysztof M Bernadzki; R Mark Grady; Peter Hallock; David J Glass; Joshua R Sanes; Tomasz J Proszynski
Journal:  J Cell Sci       Date:  2016-01-14       Impact factor: 5.285

4.  Convergent regulation of skeletal muscle Ca2+ channels by dystrophin, the actin cytoskeleton, and cAMP-dependent protein kinase.

Authors:  Barry D Johnson; Todd Scheuer; William A Catterall
Journal:  Proc Natl Acad Sci U S A       Date:  2005-03-07       Impact factor: 11.205

Review 5.  Primary dystonia: molecules and mechanisms.

Authors:  Lauren M Tanabe; Connie E Kim; Noga Alagem; William T Dauer
Journal:  Nat Rev Neurol       Date:  2009-10-13       Impact factor: 42.937

6.  Malignant-hyperthermia susceptibility is associated with a mutation of the alpha 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in skeletal muscle.

Authors:  N Monnier; V Procaccio; P Stieglitz; J Lunardi
Journal:  Am J Hum Genet       Date:  1997-06       Impact factor: 11.025

7.  Sarcoglycan Alpha Mitigates Neuromuscular Junction Decline in Aged Mice by Stabilizing LRP4.

Authors:  Kai Zhao; Chengyong Shen; Lei Li; Haitao Wu; Guanglin Xing; Zhaoqi Dong; Hongyang Jing; Wenbing Chen; Hongsheng Zhang; Zhibing Tan; Jinxiu Pan; Lei Xiong; Hongsheng Wang; Wanpeng Cui; Xiang-Dong Sun; Shihua Li; Xinping Huang; Wen-Cheng Xiong; Lin Mei
Journal:  J Neurosci       Date:  2018-08-31       Impact factor: 6.167

Review 8.  Moving towards successful exon-skipping therapy for Duchenne muscular dystrophy.

Authors:  Akinori Nakamura
Journal:  J Hum Genet       Date:  2017-06-01       Impact factor: 3.172

Review 9.  Emerging common molecular pathways for primary dystonia.

Authors:  Mark S Ledoux; William T Dauer; Thomas T Warner
Journal:  Mov Disord       Date:  2013-06-15       Impact factor: 10.338

10.  Essential roles of the acetylcholine receptor gamma-subunit in neuromuscular synaptic patterning.

Authors:  Yun Liu; Daniel Padgett; Masazumi Takahashi; Hongqiao Li; Ayaz Sayeed; Russell W Teichert; Baldomero M Olivera; Joseph J McArdle; William N Green; Weichun Lin
Journal:  Development       Date:  2008-04-23       Impact factor: 6.868
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