Literature DB >> 9146999

Muscular dystrophies and the dystrophin-glycoprotein complex.

V Straub1, K P Campbell.   

Abstract

Efforts to understand the function of dystrophin, the protein product for the Duchenne muscular dystrophy gene, resulted in the purification of the dystrophin-glycoprotein complex. Over the past year several novel components of this complex have been identified. Recent studies have extended the number of muscular dystrophies associated with the oligomeric complex to six genetically distinct diseases, including three new forms of limb-girdle muscular dystrophy and one form of congenital muscular dystrophy.

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Year:  1997        PMID: 9146999     DOI: 10.1097/00019052-199704000-00016

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


  89 in total

Review 1.  Clustering of nicotinic acetylcholine receptors: from the neuromuscular junction to interneuronal synapses.

Authors:  Kyung-Hye Huh; Christian Fuhrer
Journal:  Mol Neurobiol       Date:  2002-02       Impact factor: 5.590

Review 2.  Duchenne muscular dystrophy and dystrophin: pathogenesis and opportunities for treatment.

Authors:  Kristen J Nowak; Kay E Davies
Journal:  EMBO Rep       Date:  2004-09       Impact factor: 8.807

3.  Computational Analysis of Muscular Dystrophy Sub-types Using A Novel Integrative Scheme.

Authors:  Chen Wang; Sook Ha; Jianhua Xuan; Yue Wang; Eric Hoffman
Journal:  Neurocomputing       Date:  2012-09-01       Impact factor: 5.719

4.  Alpha 7 integrin preserves the function of the extensor digitorum longus muscle in dystrophin-null mice.

Authors:  Chady H Hakim; Dean J Burkin; Dongsheng Duan
Journal:  J Appl Physiol (1985)       Date:  2013-08-29

5.  Increased catalase expression improves muscle function in mdx mice.

Authors:  Joshua T Selsby
Journal:  Exp Physiol       Date:  2010-11-01       Impact factor: 2.969

Review 6.  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

7.  Spatial distribution and molecular dynamics of dystrophin glycoprotein components at the neuromuscular junction in vivo.

Authors:  Mohamed Aittaleb; Isabel Martinez-Pena Y Valenzuela; Mohammed Akaaboune
Journal:  J Cell Sci       Date:  2017-03-31       Impact factor: 5.285

8.  Guanine analogues enhance antisense oligonucleotide-induced exon skipping in dystrophin gene in vitro and in vivo.

Authors:  Yihong Hu; Bo Wu; Allen Zillmer; Peijuan Lu; Ehsan Benrashid; Mingxing Wang; Timothy Doran; Mona Shaban; Xiaohua Wu; Qi Long Lu
Journal:  Mol Ther       Date:  2010-01-19       Impact factor: 11.454

9.  Nanotopography-responsive myotube alignment and orientation as a sensitive phenotypic biomarker for Duchenne Muscular Dystrophy.

Authors:  Bin Xu; Alessandro Magli; Yoska Anugrah; Steven J Koester; Rita C R Perlingeiro; Wei Shen
Journal:  Biomaterials       Date:  2018-08-21       Impact factor: 12.479

Review 10.  Animal models for genetic neuromuscular diseases.

Authors:  Mariz Vainzof; Danielle Ayub-Guerrieri; Paula C G Onofre; Poliana C M Martins; Vanessa F Lopes; Dinorah Zilberztajn; Lucas S Maia; Karen Sell; Lydia U Yamamoto
Journal:  J Mol Neurosci       Date:  2008-01-18       Impact factor: 3.444

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