Literature DB >> 7207866

Absence of receptor outer segments in the retina of rds mutant mice.

S Sanyal, H G Jansen.   

Abstract

In mice homozygous for the newly reported rds (retinal degeneration slow) gene, a progressive loss of visual cells occurs throughout life. Histogenesis of the retina proceeds normally with the exception of the receptor layer which remains rudimentary. Electron microscopic observations of the retina at different stages of development have revealed that the outer segments of the visual cells in this mutant fail to develop and that the receptor layer consists of inner segments only. In the absorption spectra of the retinal extract from the mutant the characteristic rhodopsin peak is lacking.

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Year:  1981        PMID: 7207866     DOI: 10.1016/0304-3940(81)90051-3

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  66 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.  Characterization of peripherin/rds and rom-1 transport in rod photoreceptors of transgenic and knockout animals.

Authors:  Edwin S Lee; Beth Burnside; John G Flannery
Journal:  Invest Ophthalmol Vis Sci       Date:  2006-05       Impact factor: 4.799

Review 3.  Photoreceptors at a glance.

Authors:  Robert S Molday; Orson L Moritz
Journal:  J Cell Sci       Date:  2015-11-15       Impact factor: 5.285

4.  Three-dimensional organization of nascent rod outer segment disk membranes.

Authors:  Stefanie Volland; Louise C Hughes; Christina Kong; Barry L Burgess; Kenneth A Linberg; Gabriel Luna; Z Hong Zhou; Steven K Fisher; David S Williams
Journal:  Proc Natl Acad Sci U S A       Date:  2015-11-17       Impact factor: 11.205

5.  ROM-1 potentiates photoreceptor specific membrane fusion processes.

Authors:  Kathleen Boesze-Battaglia; Frank P Stefano; Catherine Fitzgerald; Susan Muller-Weeks
Journal:  Exp Eye Res       Date:  2006-10-20       Impact factor: 3.467

6.  Identification of photoreceptor genes affected by PRPF31 mutations associated with autosomal dominant retinitis pigmentosa.

Authors:  Daniel Mordes; Liya Yuan; Lili Xu; Mariko Kawada; Robert S Molday; Jane Y Wu
Journal:  Neurobiol Dis       Date:  2007-03-09       Impact factor: 5.996

7.  Genetic supplementation of RDS alleviates a loss-of-function phenotype in C214S model of retinitis pigmentosa.

Authors:  May Nour; Steven J Fliesler; Muna I Naash
Journal:  Adv Exp Med Biol       Date:  2008       Impact factor: 2.622

8.  Transgenic expression of constitutively active RAC1 disrupts mouse rod morphogenesis.

Authors:  Hongman Song; Ronald A Bush; Camasamudram Vijayasarathy; Robert N Fariss; Sten Kjellstrom; Paul A Sieving
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-04-25       Impact factor: 4.799

9.  Uncoupling of photoreceptor peripherin/rds fusogenic activity from biosynthesis, subunit assembly, and targeting: a potential mechanism for pathogenic effects.

Authors:  Linda M Ritter; Kathleen Boesze-Battaglia; Beatrice M Tam; Orson L Moritz; Nidhi Khattree; Shu-Chu Chen; Andrew F X Goldberg
Journal:  J Biol Chem       Date:  2004-07-13       Impact factor: 5.157

10.  Insights into the mechanisms of macular degeneration associated with the R172W mutation in RDS.

Authors:  Shannon M Conley; Michael W Stuck; Justin L Burnett; Dibyendu Chakraborty; Seifollah Azadi; Steven J Fliesler; Muna I Naash
Journal:  Hum Mol Genet       Date:  2014-01-25       Impact factor: 6.150

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