Literature DB >> 8885257

Inherited retinal degeneration: exceptional genetic and clinical heterogeneity.

L S Sullivan1, S P Daiger.   

Abstract

The function of the retina is to detect light and to send appropriate signals to the brain in response. Inherited diseases that cause the retina to degenerate, leading to either partial or total blindness, affect approximately 1 in 3000 people. Rapid progress is being made in identifying the genetic causes of common, inherited retinal diseases, such as retinitis pigmentosa and macular degeneration, as well as some of the rare forms of retinal disease. Linkage studies of large families and candidate-gene screening of known retinal genes have already identified 59 independent genetic loci that can cause retinal degeneration. The astounding genetic and clinical heterogeneity that is being revealed is a 'nightmare' for those interested in molecular diagnostics but, at the same time, provides great insight into functional aspects of the normal retina.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8885257     DOI: 10.1016/s1357-4310(96)10037-x

Source DB:  PubMed          Journal:  Mol Med Today        ISSN: 1357-4310


  18 in total

1.  Rescue from photoreceptor degeneration in the rd mouse by human immunodeficiency virus vector-mediated gene transfer.

Authors:  M Takahashi; H Miyoshi; I M Verma; F H Gage
Journal:  J Virol       Date:  1999-09       Impact factor: 5.103

Review 2.  Multiprotein complexes of Retinitis Pigmentosa GTPase regulator (RPGR), a ciliary protein mutated in X-linked Retinitis Pigmentosa (XLRP).

Authors:  Carlos Murga-Zamalloa; Anand Swaroop; Hemant Khanna
Journal:  Adv Exp Med Biol       Date:  2010       Impact factor: 2.622

3.  A gene map of the Best's vitelliform macular dystrophy region in chromosome 11q12-q13.1.

Authors:  H Stöhr; A Marquardt; A Rivera; P R Cooper; N J Nowak; T B Shows; D S Gerhard; B H Weber
Journal:  Genome Res       Date:  1998-01       Impact factor: 9.043

4.  Alternative pathway of cell death in Drosophila mediated by NF-κB transcription factor Relish.

Authors:  Yashodhan Chinchore; Gloria F Gerber; Patrick J Dolph
Journal:  Proc Natl Acad Sci U S A       Date:  2012-02-10       Impact factor: 11.205

5.  Mutation of CERKL, a novel human ceramide kinase gene, causes autosomal recessive retinitis pigmentosa (RP26).

Authors:  Miquel Tuson; Gemma Marfany; Roser Gonzàlez-Duarte
Journal:  Am J Hum Genet       Date:  2003-12-16       Impact factor: 11.025

6.  Regulation of sorting and post-Golgi trafficking of rhodopsin by its C-terminal sequence QVS(A)PA.

Authors:  D Deretic; S Schmerl; P A Hargrave; A Arendt; J H McDowell
Journal:  Proc Natl Acad Sci U S A       Date:  1998-09-01       Impact factor: 11.205

7.  Accumulation of rhodopsin in late endosomes triggers photoreceptor cell degeneration.

Authors:  Yashodhan Chinchore; Amitavo Mitra; Patrick J Dolph
Journal:  PLoS Genet       Date:  2009-02-13       Impact factor: 5.917

8.  The potential of stem cell-based therapy for retinal repair.

Authors:  Honghua Yu; Lin Cheng; Kin-Sang Cho
Journal:  Neural Regen Res       Date:  2014-06-01       Impact factor: 5.135

9.  A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa.

Authors:  Maleeha Azam; Muhammad Imran Khan; Andreas Gal; Alamdar Hussain; Syed Tahir Abbas Shah; Muhammad Shakil Khan; Ahmed Sadeque; Habib Bokhari; Rob W J Collin; Ulrike Orth; Maria M van Genderen; A I den Hollander; Frans P M Cremers; Raheel Qamar
Journal:  Mol Vis       Date:  2009-12-03       Impact factor: 2.367

10.  Stem Cell Ophthalmology Treatment Study: bone marrow derived stem cells in the treatment of Retinitis Pigmentosa.

Authors:  Jeffrey N Weiss; Steven Levy
Journal:  Stem Cell Investig       Date:  2018-06-06
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.