151 related articles for article (PubMed ID: 16023414)
1. Amelioration of both functional and morphological abnormalities in the retina of a mouse model of ocular albinism following AAV-mediated gene transfer.
Surace EM; Domenici L; Cortese K; Cotugno G; Di Vicino U; Venturi C; Cellerino A; Marigo V; Tacchetti C; Ballabio A; Auricchio A
Mol Ther; 2005 Oct; 12(4):652-8. PubMed ID: 16023414
[TBL] [Abstract][Full Text] [Related]
2. Retinal function in X-linked ocular albinism (OA1).
Nusinowitz S; Sarraf D
Curr Eye Res; 2008 Sep; 33(9):789-803. PubMed ID: 18798082
[TBL] [Abstract][Full Text] [Related]
3. Oa1 knock-out: new insights on the pathogenesis of ocular albinism type 1.
Incerti B; Cortese K; Pizzigoni A; Surace EM; Varani S; Coppola M; Jeffery G; Seeliger M; Jaissle G; Bennett DC; Marigo V; Schiaffino MV; Tacchetti C; Ballabio A
Hum Mol Genet; 2000 Nov; 9(19):2781-8. PubMed ID: 11092754
[TBL] [Abstract][Full Text] [Related]
4. A constitutively active Gαi3 protein corrects the abnormal retinal pigment epithelium phenotype of Oa1-/- mice.
Young A; Wang Y; Ahmedli NB; Jiang M; Farber DB
PLoS One; 2013; 8(9):e76240. PubMed ID: 24098784
[TBL] [Abstract][Full Text] [Related]
5. Expression pattern of the ocular albinism type 1 (Oa1) gene in the murine retinal pigment epithelium.
Surace EM; Angeletti B; Ballabio A; Marigo V
Invest Ophthalmol Vis Sci; 2000 Dec; 41(13):4333-7. PubMed ID: 11095635
[TBL] [Abstract][Full Text] [Related]
6. New insights into ocular albinism type 1 (OA1): Mutations and polymorphisms of the OA1 gene.
Oetting WS
Hum Mutat; 2002 Feb; 19(2):85-92. PubMed ID: 11793467
[TBL] [Abstract][Full Text] [Related]
7. The ocular albinism type 1 (OA1) gene controls melanosome maturation and size.
Cortese K; Giordano F; Surace EM; Venturi C; Ballabio A; Tacchetti C; Marigo V
Invest Ophthalmol Vis Sci; 2005 Dec; 46(12):4358-64. PubMed ID: 16303920
[TBL] [Abstract][Full Text] [Related]
8. Involvement of OA1, an intracellular GPCR, and G alpha i3, its binding protein, in melanosomal biogenesis and optic pathway formation.
Young A; Powelson EB; Whitney IE; Raven MA; Nusinowitz S; Jiang M; Birnbaumer L; Reese BE; Farber DB
Invest Ophthalmol Vis Sci; 2008 Jul; 49(7):3245-52. PubMed ID: 18378571
[TBL] [Abstract][Full Text] [Related]
9. The ocular albinism type 1 protein, an intracellular G protein-coupled receptor, regulates melanosome transport in pigment cells.
Palmisano I; Bagnato P; Palmigiano A; Innamorati G; Rotondo G; Altimare D; Venturi C; Sviderskaya EV; Piccirillo R; Coppola M; Marigo V; Incerti B; Ballabio A; Surace EM; Tacchetti C; Bennett DC; Schiaffino MV
Hum Mol Genet; 2008 Nov; 17(22):3487-501. PubMed ID: 18697795
[TBL] [Abstract][Full Text] [Related]
10. Specific interaction of Gαi3 with the Oa1 G-protein coupled receptor controls the size and density of melanosomes in retinal pigment epithelium.
Young A; Jiang M; Wang Y; Ahmedli NB; Ramirez J; Reese BE; Birnbaumer L; Farber DB
PLoS One; 2011; 6(9):e24376. PubMed ID: 21931697
[TBL] [Abstract][Full Text] [Related]
11. Ocular albinism type 1: more than meets the eye.
Shen B; Samaraweera P; Rosenberg B; Orlow SJ
Pigment Cell Res; 2001 Aug; 14(4):243-8. PubMed ID: 11549106
[TBL] [Abstract][Full Text] [Related]
12. Mutational analysis of the OA1 gene in ocular albinism.
Camand O; Boutboul S; Arbogast L; Roche O; Sternberg C; Sutherland J; Levin A; Héon E; Menasche M; Dufier J; Abitbol M
Ophthalmic Genet; 2003 Sep; 24(3):167-73. PubMed ID: 12868035
[TBL] [Abstract][Full Text] [Related]
13. Novel GPR143 mutations and clinical characteristics in six Chinese families with X-linked ocular albinism.
Fang S; Guo X; Jia X; Xiao X; Li S; Zhang Q
Mol Vis; 2008; 14():1974-82. PubMed ID: 18978956
[TBL] [Abstract][Full Text] [Related]
14. Eight previously unidentified mutations found in the OA1 ocular albinism gene.
Mayeur H; Roche O; Vêtu C; Jaliffa C; Marchant D; Dollfus H; Bonneau D; Munier FL; Schorderet DF; Levin AV; Héon E; Sutherland J; Lacombe D; Said E; Mezer E; Kaplan J; Dufier JL; Marsac C; Menasche M; Abitbol M
BMC Med Genet; 2006 Apr; 7():41. PubMed ID: 16646960
[TBL] [Abstract][Full Text] [Related]
15. GPR143 mutational analysis in two Italian families with X-linked ocular albinism.
Micale L; Augello B; Fusco C; Turturo MG; Granatiero M; Piemontese MR; Zelante L; Cecconi A; Merla G
Genet Test Mol Biomarkers; 2009 Aug; 13(4):527-31. PubMed ID: 19604113
[TBL] [Abstract][Full Text] [Related]
16. The ocular albinism type 1 (OA1) protein and the evidence for an intracellular signal transduction system involved in melanosome biogenesis.
Schiaffino MV; Tacchetti C
Pigment Cell Res; 2005 Aug; 18(4):227-33. PubMed ID: 16029416
[TBL] [Abstract][Full Text] [Related]
17. GPR143 mutations in Chinese patients with ocular albinism type 1.
Jia X; Yuan J; Jia X; Ling S; Li S; Guo X
Mol Med Rep; 2017 May; 15(5):3069-3075. PubMed ID: 28339057
[TBL] [Abstract][Full Text] [Related]
18. The ocular albinism type 1 (OA1) G-protein-coupled receptor functions with MART-1 at early stages of melanogenesis to control melanosome identity and composition.
Giordano F; Bonetti C; Surace EM; Marigo V; Raposo G
Hum Mol Genet; 2009 Dec; 18(23):4530-45. PubMed ID: 19717472
[TBL] [Abstract][Full Text] [Related]
19. Abnormal crossing of the optic fibres shown by evoked magnetic fields in patients with ocular albinism with a novel mutation in the OA1 gene.
Lauronen L; Jalkanen R; Huttunen J; Carlsson E; Tuupanen S; Lindh S; Forsius H; Sankila EM; Alitalo T
Br J Ophthalmol; 2005 Jul; 89(7):820-4. PubMed ID: 15965158
[TBL] [Abstract][Full Text] [Related]
20. Identification of two novel mutations in families with X-linked ocular albinism.
Iannaccone A; Gallaher KT; Buchholz J; Jennings BJ; Neitz M; Sidjanin DJ
Mol Vis; 2007 Oct; 13():1856-61. PubMed ID: 17960122
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]