Wright AF - Search Results

1

Lifespan and mitochondrial control of neurodegeneration.

Wright AF, Jacobson SG, Cideciyan AV, Roman AJ, Shu X, Vlachantoni D, McInnes RR, Riemersma RA. Wright AF, et al. Nat Genet. 2004 Nov;36(11):1153-8. doi: 10.1038/ng1448. Nat Genet. 2004. PMID: 15514669 Review.

2

Evidence of severe mitochondrial oxidative stress and a protective effect of low oxygen in mouse models of inherited photoreceptor degeneration.

Vlachantoni D, Bramall AN, Murphy MP, Taylor RW, Shu X, Tulloch B, Van Veen T, Turnbull DM, McInnes RR, Wright AF. Vlachantoni D, et al. Among authors: wright af. Hum Mol Genet. 2011 Jan 15;20(2):322-35. doi: 10.1093/hmg/ddq467. Epub 2010 Nov 3. Hum Mol Genet. 2011. PMID: 21051333

3

Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration.

Hayward C, Shu X, Cideciyan AV, Lennon A, Barran P, Zareparsi S, Sawyer L, Hendry G, Dhillon B, Milam AH, Luthert PJ, Swaroop A, Hastie ND, Jacobson SG, Wright AF. Hayward C, et al. Among authors: wright af. Hum Mol Genet. 2003 Oct 15;12(20):2657-67. doi: 10.1093/hmg/ddg289. Epub 2003 Aug 27. Hum Mol Genet. 2003. PMID: 12944416

4

Disease mechanisms in late-onset retinal macular degeneration associated with mutation in C1QTNF5.

Shu X, Tulloch B, Lennon A, Vlachantoni D, Zhou X, Hayward C, Wright AF. Shu X, et al. Among authors: wright af. Hum Mol Genet. 2006 May 15;15(10):1680-9. doi: 10.1093/hmg/ddl091. Epub 2006 Apr 6. Hum Mol Genet. 2006. PMID: 16600989

5

Biochemical characterisation of the C1QTNF5 gene associated with late-onset retinal degeneration. A genetic model of age-related macular degeneration.

Shu X, Tulloch B, Lennon A, Hayward C, O'Connell M, Cideciyan AV, Jacobson SG, Wright AF. Shu X, et al. Among authors: wright af. Adv Exp Med Biol. 2006;572:41-8. doi: 10.1007/0-387-32442-9_7. Adv Exp Med Biol. 2006. PMID: 17249553 No abstract available.

6

Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome.

Wright AF, Reddick AC, Schwartz SB, Ferguson JS, Aleman TS, Kellner U, Jurklies B, Schuster A, Zrenner E, Wissinger B, Lennon A, Shu X, Cideciyan AV, Stone EM, Jacobson SG, Swaroop A. Wright AF, et al. Hum Mutat. 2004 Nov;24(5):439. doi: 10.1002/humu.9285. Hum Mutat. 2004. PMID: 15459973

7

Focus on Molecules: RPGR.

Wright AF, Shu X. Wright AF, et al. Exp Eye Res. 2007 Jul;85(1):1-2. doi: 10.1016/j.exer.2006.03.006. Epub 2006 Jun 12. Exp Eye Res. 2007. PMID: 16769054 Review. No abstract available.

8

Zebrafish Rpgr is required for normal retinal development and plays a role in dynein-based retrograde transport processes.

Shu X, Zeng Z, Gautier P, Lennon A, Gakovic M, Patton EE, Wright AF. Shu X, et al. Among authors: wright af. Hum Mol Genet. 2010 Feb 15;19(4):657-70. doi: 10.1093/hmg/ddp533. Epub 2009 Dec 1. Hum Mol Genet. 2010. PMID: 19955120

9

The genomic, biochemical, and cellular responses of the retina in inherited photoreceptor degenerations and prospects for the treatment of these disorders.

Bramall AN, Wright AF, Jacobson SG, McInnes RR. Bramall AN, et al. Among authors: wright af. Annu Rev Neurosci. 2010;33:441-72. doi: 10.1146/annurev-neuro-060909-153227. Annu Rev Neurosci. 2010. PMID: 20572772 Review.

10

Late-onset retinal degeneration caused by C1QTNF5 mutation: sub-retinal pigment epithelium deposits and visual consequences.

Jacobson SG, Cideciyan AV, Sumaroka A, Roman AJ, Wright AF. Jacobson SG, et al. Among authors: wright af. JAMA Ophthalmol. 2014 Oct;132(10):1252-5. doi: 10.1001/jamaophthalmol.2014.2059. JAMA Ophthalmol. 2014. PMID: 25010528 Free PMC article. No abstract available.

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