Wright AF - Search Results

1

Mutations of RPGR in X-linked retinitis pigmentosa (RP3).

Vervoort R, Wright AF. Vervoort R, et al. Among authors: wright af. Hum Mutat. 2002 May;19(5):486-500. doi: 10.1002/humu.10057. Hum Mutat. 2002. PMID: 11968081 Review.

2

A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa.

Breuer DK, Yashar BM, Filippova E, Hiriyanna S, Lyons RH, Mears AJ, Asaye B, Acar C, Vervoort R, Wright AF, Musarella MA, Wheeler P, MacDonald I, Iannaccone A, Birch D, Hoffman DR, Fishman GA, Heckenlively JR, Jacobson SG, Sieving PA, Swaroop A. Breuer DK, et al. Among authors: wright af. Am J Hum Genet. 2002 Jun;70(6):1545-54. doi: 10.1086/340848. Epub 2002 Apr 30. Am J Hum Genet. 2002. PMID: 11992260 Free PMC article.

3

Different RPGR exon ORF15 mutations in Canids provide insights into photoreceptor cell degeneration.

Zhang Q, Acland GM, Wu WX, Johnson JL, Pearce-Kelling S, Tulloch B, Vervoort R, Wright AF, Aguirre GD. Zhang Q, et al. Among authors: wright af. Hum Mol Genet. 2002 May 1;11(9):993-1003. doi: 10.1093/hmg/11.9.993. Hum Mol Genet. 2002. PMID: 11978759

4

RPGR mutation analysis and disease: an update.

Shu X, Black GC, Rice JM, Hart-Holden N, Jones A, O'Grady A, Ramsden S, Wright AF. Shu X, et al. Among authors: wright af. Hum Mutat. 2007 Apr;28(4):322-8. doi: 10.1002/humu.20461. Hum Mutat. 2007. PMID: 17195164

5

The human retinitis pigmentosa GTPase regulator gene variant database.

Shu X, McDowall E, Brown AF, Wright AF. Shu X, et al. Among authors: wright af. Hum Mutat. 2008 May;29(5):605-8. doi: 10.1002/humu.20733. Hum Mutat. 2008. PMID: 18361418

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

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

8

Evolutionary Characterization of the Retinitis Pigmentosa GTPase Regulator Gene.

Raghupathy RK, Gautier P, Soares DC, Wright AF, Shu X. Raghupathy RK, et al. Among authors: wright af. Invest Ophthalmol Vis Sci. 2015 Oct;56(11):6255-64. doi: 10.1167/iovs.15-17726. Invest Ophthalmol Vis Sci. 2015. PMID: 26431479 Free PMC article.

9

A microdeletion in Xp11.3 accounts for co-segregation of retinitis pigmentosa and mental retardation in a large kindred.

Zhang L, Wang T, Wright AF, Suri M, Schwartz CE, Stevenson RE, Valle D. Zhang L, et al. Among authors: wright af. Am J Med Genet A. 2006 Feb 15;140(4):349-57. doi: 10.1002/ajmg.a.31080. Am J Med Genet A. 2006. PMID: 16419135

10

Gelsolin dysfunction causes photoreceptor loss in induced pluripotent cell and animal retinitis pigmentosa models.

Megaw R, Abu-Arafeh H, Jungnickel M, Mellough C, Gurniak C, Witke W, Zhang W, Khanna H, Mill P, Dhillon B, Wright AF, Lako M, Ffrench-Constant C. Megaw R, et al. Among authors: wright af. Nat Commun. 2017 Aug 16;8(1):271. doi: 10.1038/s41467-017-00111-8. Nat Commun. 2017. PMID: 28814713 Free PMC article.

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