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Results: 1 to 20 of 200

Similar articles for PubMed (Select 9295268)

1.

Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration.

Allikmets R, Shroyer NF, Singh N, Seddon JM, Lewis RA, Bernstein PS, Peiffer A, Zabriskie NA, Li Y, Hutchinson A, Dean M, Lupski JR, Leppert M.

Science. 1997 Sep 19;277(5333):1805-7.

2.

Analysis of the Stargardt disease gene (ABCR) in age-related macular degeneration.

De La Paz MA, Guy VK, Abou-Donia S, Heinis R, Bracken B, Vance JM, Gilbert JR, Gass JD, Haines JL, Pericak-Vance MA.

Ophthalmology. 1999 Aug;106(8):1531-6.

PMID:
10442900
3.

The rod photoreceptor ATP-binding cassette transporter gene, ABCR, and retinal disease: from monogenic to multifactorial.

Shroyer NF, Lewis RA, Allikmets R, Singh N, Dean M, Leppert M, Lupski JR.

Vision Res. 1999 Jul;39(15):2537-44. Review.

4.

The ABCR gene in recessive and dominant Stargardt diseases: a genetic pathway in macular degeneration.

Zhang K, Kniazeva M, Hutchinson A, Han M, Dean M, Allikmets R.

Genomics. 1999 Sep 1;60(2):234-7.

PMID:
10486215
5.

New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease.

Simonelli F, Testa F, de Crecchio G, Rinaldi E, Hutchinson A, Atkinson A, Dean M, D'Urso M, Allikmets R.

Invest Ophthalmol Vis Sci. 2000 Mar;41(3):892-7.

PMID:
10711710
6.

Age-related macular degeneration in grandparents of patients with Stargardt disease: genetic study.

Souied EH, Ducroq D, Gerber S, Ghazi I, Rozet JM, Perrault I, Munnich A, Dufier JL, Coscas G, Soubrane G, Kaplan J.

Am J Ophthalmol. 1999 Aug;128(2):173-8.

PMID:
10458172
7.

A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt disease.

Zhang K, Garibaldi DC, Kniazeva M, Albini T, Chiang MF, Kerrigan M, Sunness JS, Han M, Allikmets R.

Am J Ophthalmol. 1999 Dec;128(6):720-4.

PMID:
10612508
8.

Genotype-phenotype analysis of ABCR variants in macular degeneration probands and siblings.

Bernstein PS, Leppert M, Singh N, Dean M, Lewis RA, Lupski JR, Allikmets R, Seddon JM.

Invest Ophthalmol Vis Sci. 2002 Feb;43(2):466-73.

PMID:
11818392
9.
10.

Mutations in ABCR (ABCA4) in patients with Stargardt macular degeneration or cone-rod degeneration.

Briggs CE, Rucinski D, Rosenfeld PJ, Hirose T, Berson EL, Dryja TP.

Invest Ophthalmol Vis Sci. 2001 Sep;42(10):2229-36.

PMID:
11527935
12.

ABCR gene analysis in familial exudative age-related macular degeneration.

Souied EH, Ducroq D, Rozet JM, Gerber S, Perrault I, Munnich A, Coscas G, Soubrane G, Kaplan J.

Invest Ophthalmol Vis Sci. 2000 Jan;41(1):244-7.

PMID:
10634626
13.

Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt disease.

Lewis RA, Shroyer NF, Singh N, Allikmets R, Hutchinson A, Li Y, Lupski JR, Leppert M, Dean M.

Am J Hum Genet. 1999 Feb;64(2):422-34.

14.

Molecular genetic analysis of ABCR gene in Japanese dry form age-related macular degeneration.

Fuse N, Suzuki T, Wada Y, Yoshida M, Shimura M, Abe T, Nakazawa M, Tamai M.

Jpn J Ophthalmol. 2000 May-Jun;44(3):245-9.

PMID:
10913642
15.

A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degeneration.

Rivera A, White K, Stöhr H, Steiner K, Hemmrich N, Grimm T, Jurklies B, Lorenz B, Scholl HP, Apfelstedt-Sylla E, Weber BH.

Am J Hum Genet. 2000 Oct;67(4):800-13. Epub 2000 Aug 24.

16.

Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR.

Cremers FP, van de Pol DJ, van Driel M, den Hollander AI, van Haren FJ, Knoers NV, Tijmes N, Bergen AA, Rohrschneider K, Blankenagel A, Pinckers AJ, Deutman AF, Hoyng CB.

Hum Mol Genet. 1998 Mar;7(3):355-62.

17.

Analysis of the Arg345Trp disease-associated allele of the EFEMP1 gene in individuals with early onset drusen or familial age-related macular degeneration.

Guymer RH, McNeil R, Cain M, Tomlin B, Allen PJ, Dip CL, Baird PN.

Clin Experiment Ophthalmol. 2002 Dec;30(6):419-23.

PMID:
12427233
18.

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy.

Allikmets R, Singh N, Sun H, Shroyer NF, Hutchinson A, Chidambaram A, Gerrard B, Baird L, Stauffer D, Peiffer A, Rattner A, Smallwood P, Li Y, Anderson KL, Lewis RA, Nathans J, Leppert M, Dean M, Lupski JR.

Nat Genet. 1997 Mar;15(3):236-46. Erratum in: Nat Genet. 1997 Sep;17(1):122.

PMID:
9054934
19.

Genetic susceptibility to age related macular degeneration.

Yates JR, Moore AT.

J Med Genet. 2000 Feb;37(2):83-7. Review.

20.

The gene for Stargardt disease, ABCA4, is a major retinal gene: a mini-review.

Koenekoop RK.

Ophthalmic Genet. 2003 Jun;24(2):75-80. Review. Erratum in: Ophthalmic Genet. 2003 Dec;24(4):253.

PMID:
12789571
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