Literature DB >> 11180984

Coincident onset of expression of myosin VIIa and opsin in the cilium of the developing photoreceptor cell.

X Liu, D S Williams.   

Abstract

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Year:  2001        PMID： 11180984     DOI： 10.1006/exer.2000.0963

Source DB:  PubMed          Journal:  Exp Eye Res        ISSN： 0014-4835            Impact factor:   3.467


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  9 in total

Review 1.  Photoreceptor renewal: a role for peripherin/rds.

Authors:  Kathleen Boesze-Battaglia; Andrew F X Goldberg
Journal:  Int Rev Cytol       Date:  2002

2.  Tubby-like protein 1 (TULP1) interacts with F-actin in photoreceptor cells.

Authors:  Quansheng Xi; Gayle J T Pauer; Alan D Marmorstein; John W Crabb; Stephanie A Hagstrom
Journal:  Invest Ophthalmol Vis Sci       Date:  2005-12       Impact factor: 4.799

3.  Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.

Authors:  Z M Ahmed; S Riazuddin; S L Bernstein; Z Ahmed; S Khan; A J Griffith; R J Morell; T B Friedman; S Riazuddin; E R Wilcox
Journal:  Am J Hum Genet       Date:  2001-06-07       Impact factor: 11.025

Review 4.  Molecular basis for photoreceptor outer segment architecture.

Authors:  Andrew F X Goldberg; Orson L Moritz; David S Williams
Journal:  Prog Retin Eye Res       Date:  2016-06-01       Impact factor: 21.198

5.  Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.

Authors:  Samuel G Jacobson; Artur V Cideciyan; Tomas S Aleman; Alexander Sumaroka; Alejandro J Roman; Leigh M Gardner; Haydn M Prosser; Monalisa Mishra; N Torben Bech-Hansen; Waldo Herrera; Sharon B Schwartz; Xue-Zhong Liu; William J Kimberling; Karen P Steel; David S Williams
Journal:  Hum Mol Genet       Date:  2008-05-07       Impact factor: 6.150

6.  Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3.

Authors:  T Joensuu; R Hämäläinen; B Yuan; C Johnson; S Tegelberg; P Gasparini; L Zelante; U Pirvola; L Pakarinen; A E Lehesjoki; A de la Chapelle; E M Sankila
Journal:  Am J Hum Genet       Date:  2001-08-27       Impact factor: 11.025

7.  Myosin7a deficiency results in reduced retinal activity which is improved by gene therapy.

Authors:  Pasqualina Colella; Andrea Sommella; Elena Marrocco; Umberto Di Vicino; Elena Polishchuk; Marina Garcia Garrido; Mathias W Seeliger; Roman Polishchuk; Alberto Auricchio
Journal:  PLoS One       Date:  2013-08-26       Impact factor: 3.240

8.  Immunocytochemical evidence of the localization of the Crumbs homologue 3 protein (CRB3) in the developing and mature mouse retina.

Authors:  Saúl Herranz-Martín; David Jimeno; Antonio E Paniagua; Almudena Velasco; Juan M Lara; José Aijón; Concepción Lillo
Journal:  PLoS One       Date:  2012-11-30       Impact factor: 3.240

9.  Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2.

Authors:  Weining Rong; Xue Chen; Kanxing Zhao; Yani Liu; Xiaoxing Liu; Shaoping Ha; Wenzhou Liu; Xiaoli Kang; Xunlun Sheng; Chen Zhao
Journal:  PLoS One       Date:  2014-05-15       Impact factor: 3.240
  9 in total

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