Literature DB >> 19165952

Update on Usher syndrome.

Zubin Saihan1, Andrew R Webster, Linda Luxon, Maria Bitner-Glindzicz.   

Abstract

PURPOSE OF REVIEW: The present review addresses the mechanisms, genetics and pathogenesis of Usher syndrome. RECENT
FINDINGS: Recent molecular findings have provided more information regarding the pathogenesis of this disorder and the wide phenotypic variation in both audiovestibular and/or visual systems. Evidence has begun to emerge supporting a theory of a protein interactome involving the Usher proteins in both the inner ear and the retina. This interactome appears to be important for hair cell development in the ear but its role in the retina remains unclear.
SUMMARY: Understanding clinical disease progression and molecular pathways is important in the progress towards developing gene therapy to prevent blindness due to Usher syndrome as well as delivering prognostic information to affected individuals.

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Year:  2009        PMID: 19165952     DOI: 10.1097/wco.0b013e3283218807

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


  48 in total

1.  Comorbid bipolar disorder and Usher syndrome.

Authors:  Naren P Rao; Vijay Danivas; Ganesan Venkatasubramanian; Rishikesh V Behere; Bangalore N Gangadhar
Journal:  Prim Care Companion J Clin Psychiatry       Date:  2010

2.  Identification of 28 novel mutations in the Bardet-Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease.

Authors:  Jean Muller; C Stoetzel; M C Vincent; C C Leitch; V Laurier; J M Danse; S Hellé; V Marion; V Bennouna-Greene; S Vicaire; A Megarbane; J Kaplan; V Drouin-Garraud; M Hamdani; S Sigaudy; C Francannet; J Roume; P Bitoun; A Goldenberg; N Philip; S Odent; J Green; M Cossée; E E Davis; N Katsanis; D Bonneau; A Verloes; O Poch; J L Mandel; H Dollfus
Journal:  Hum Genet       Date:  2010-02-23       Impact factor: 4.132

3.  Mutational screening of the USH2A gene in Spanish USH patients reveals 23 novel pathogenic mutations.

Authors:  Gema Garcia-Garcia; Maria J Aparisi; Teresa Jaijo; Regina Rodrigo; Ana M Leon; Almudena Avila-Fernandez; Fiona Blanco-Kelly; Sara Bernal; Rafael Navarro; Manuel Diaz-Llopis; Montserrat Baiget; Carmen Ayuso; Jose M Millan; Elena Aller
Journal:  Orphanet J Rare Dis       Date:  2011-10-17       Impact factor: 4.123

4.  Clinical utility gene card for: Usher syndrome.

Authors:  Hanno J Bolz; Anne-Françoise Roux
Journal:  Eur J Hum Genet       Date:  2011-03-09       Impact factor: 4.246

5.  Dual adeno-associated virus vectors result in efficient in vitro and in vivo expression of an oversized gene, MYO7A.

Authors:  Frank M Dyka; Sanford L Boye; Vince A Chiodo; William W Hauswirth; Shannon E Boye
Journal:  Hum Gene Ther Methods       Date:  2014-04       Impact factor: 2.396

6.  Photoreceptors in whirler mice show defective transducin translocation and are susceptible to short-term light/dark changes-induced degeneration.

Authors:  Mei Tian; Weimin Wang; Duane Delimont; Linda Cheung; Marisa Zallocchi; Dominic Cosgrove; You-Wei Peng
Journal:  Exp Eye Res       Date:  2013-11-07       Impact factor: 3.467

Review 7.  Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities.

Authors:  Pranav Mathur; Jun Yang
Journal:  Biochim Biophys Acta       Date:  2014-12-04

Review 8.  [Usher syndrome: clinical features, diagnostic options, and therapeutic prospects].

Authors:  M W Seeliger; M D Fischer; M Pfister
Journal:  Ophthalmologe       Date:  2009-06       Impact factor: 1.059

9.  Novel USH2A compound heterozygous mutations cause RP/USH2 in a Chinese family.

Authors:  Xiaowen Liu; Zhaohui Tang; Chang Li; Kangjuan Yang; Guanqi Gan; Zibo Zhang; Jingyu Liu; Fagang Jiang; Qing Wang; Mugen Liu
Journal:  Mol Vis       Date:  2010-03-17       Impact factor: 2.367

10.  CLRN1 is nonessential in the mouse retina but is required for cochlear hair cell development.

Authors:  Scott F Geller; Karen I Guerin; Meike Visel; Aaron Pham; Edwin S Lee; Amiel A Dror; Karen B Avraham; Toshinori Hayashi; Catherine A Ray; Thomas A Reh; Olivia Bermingham-McDonogh; William J Triffo; Shaowen Bao; Juha Isosomppi; Hanna Västinsalo; Eeva-Marja Sankila; John G Flannery
Journal:  PLoS Genet       Date:  2009-08-14       Impact factor: 5.917

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