Literature DB >> 31416513

[Research advances in limb-girdle muscular dystrophy type 2Q].

Min Zhang1, Dan Lan.   

Abstract

Limb-girdle muscular dystrophy (LGMD) is a group of muscular dystrophies with predominantly proximal muscular weakness, and some genes associated with this disease have been identified at present. LGMD type 2Q (LGMD2Q) is a subtype of LGMD and is associated with PLEC gene mutation. Major phenotypes of PLEC gene mutation include epidermolysis bullosa with late-onset muscular dystrophy and epidermolysis bullosa with other lesions. LGMD2Q without skin lesions is rarely reported. This article reviews the pathogenic gene PLEC and clinical manifestations of LGMD2Q, so as to deepen the understanding of the pathogenic gene and phenotype of LGMD2Q.

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Year:  2019        PMID: 31416513      PMCID: PMC7389895     

Source DB:  PubMed          Journal:  Zhongguo Dang Dai Er Ke Za Zhi        ISSN: 1008-8830


  41 in total

Review 1.  Networking and anchoring through plectin: a key to IF functionality and mechanotransduction.

Authors:  Gerhard Wiche; Selma Osmanagic-Myers; Maria J Castañón
Journal:  Curr Opin Cell Biol       Date:  2014-10-29       Impact factor: 8.382

2.  Laryngeal lesion associated with epidermolysis bullosa secondary to congenital plectin deficiency.

Authors:  T Bourhis; S Buche; S Fraitag; P Fayoux
Journal:  Eur Ann Otorhinolaryngol Head Neck Dis       Date:  2019-03-15       Impact factor: 2.080

Review 3.  The Limb-Girdle Muscular Dystrophies and the Dystrophinopathies.

Authors:  Stanley Jones P Iyadurai; John T Kissel
Journal:  Continuum (Minneap Minn)       Date:  2016-12

Review 4.  Update on muscle disease.

Authors:  J Witherick; S Brady
Journal:  J Neurol       Date:  2018-04-18       Impact factor: 4.849

5.  Report of a patient with limb-girdle muscular dystrophy, ptosis and ophthalmoparesis caused by plectinopathy.

Authors:  Zohreh Fattahi; Kimia Kahrizi; Shahriar Nafissi; Mahsa Fadaee; Seyedeh Sedigheh Abedini; Ariana Kariminejad; Mohammad R Akbari; Hossein Najmabadi
Journal:  Arch Iran Med       Date:  2015-01       Impact factor: 1.354

6.  Defective expression of plectin/HD1 in epidermolysis bullosa simplex with muscular dystrophy.

Authors:  Y Gache; S Chavanas; J P Lacour; G Wiche; K Owaribe; G Meneguzzi; J P Ortonne
Journal:  J Clin Invest       Date:  1996-05-15       Impact factor: 14.808

7.  Targeted ablation of plectin isoform 1 uncovers role of cytolinker proteins in leukocyte recruitment.

Authors:  Christina Abrahamsberg; Peter Fuchs; Selma Osmanagic-Myers; Irmgard Fischer; Friedrich Propst; Adelheid Elbe-Bürger; Gerhard Wiche
Journal:  Proc Natl Acad Sci U S A       Date:  2005-12-12       Impact factor: 11.205

8.  Plectin deficiency leads to both muscular dystrophy and pyloric atresia in epidermolysis bullosa simplex.

Authors:  Ken Natsuga; Wataru Nishie; Satoru Shinkuma; Ken Arita; Hideki Nakamura; Makiko Ohyama; Hitoshi Osaka; Takeshi Kambara; Yoshiaki Hirako; Hiroshi Shimizu
Journal:  Hum Mutat       Date:  2010-10       Impact factor: 4.878

Review 9.  Advances in understanding the molecular basis of skin fragility.

Authors:  Cristina Has
Journal:  F1000Res       Date:  2018-03-06

10.  Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy.

Authors:  Lilli Winter; Matthias Türk; Patrick N Harter; Michel Mittelbronn; Cornelia Kornblum; Fiona Norwood; Heinz Jungbluth; Christian T Thiel; Ursula Schlötzer-Schrehardt; Rolf Schröder
Journal:  Acta Neuropathol Commun       Date:  2016-04-27       Impact factor: 7.801

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