146 related articles for article (PubMed ID: 26547501)
1. A novel mutation, c.494C>A (p.Ala165Asp), in the GPR143 gene causes a mild phenotype in a Chinese X-linked ocular albinism patient.
Pan Q; Yi C; Xu T; Liu J; Jing X; Hu B; Wang Y
Acta Ophthalmol; 2016 Jun; 94(4):417-8. PubMed ID: 26547501
[No Abstract] [Full Text] [Related]
2. 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]
3. A novel splicing site mutation of the GPR143 gene in a Chinese X-linked ocular albinism pedigree.
Cai CY; Zhu H; Shi W; Su L; Shi O; Cai CQ; Ling C; Li WD
Genet Mol Res; 2013 Nov; 12(4):5673-9. PubMed ID: 24301936
[TBL] [Abstract][Full Text] [Related]
4. [Identification of a novel GPR143 mutation in a Chinese family affected with X-linked ocular albinism].
Zhao Q; Guan M; Wang L; Liao Y; Li-Ling J; Wan H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr; 34(2):224-227. PubMed ID: 28397224
[TBL] [Abstract][Full Text] [Related]
5. Identification of a novel mutation in a Chinese family with X-linked ocular albinism.
Wang Y; Guo X; Wei A; Zhu W; Li W; Lian S
Eur J Ophthalmol; 2009; 19(1):124-8. PubMed ID: 19123159
[TBL] [Abstract][Full Text] [Related]
6.
Zhong J; You B; Xu K; Zhang X; Xie Y; Li Y
Ophthalmic Genet; 2021 Dec; 42(6):717-724. PubMed ID: 34346269
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Iris hyperpigmentation in a Chinese family with ocular albinism and the GPR143 mutation.
Xiao X; Zhang Q
Am J Med Genet A; 2009 Aug; 149A(8):1786-8. PubMed ID: 19610097
[TBL] [Abstract][Full Text] [Related]
9. A novel nonsense mutation of the GPR143 gene identified in a Chinese pedigree with ocular albinism.
Yan N; Liao X; Cai SP; Lan C; Wang Y; Zhou X; Yin Y; Yu W; Liu X
PLoS One; 2012; 7(8):e43177. PubMed ID: 22916221
[TBL] [Abstract][Full Text] [Related]
10. Identification of a novel
Jung JH; Oh EH; Shin JH; Kim HS; Choi SY; Choi KD; Lee C; Choi JH
J Genet; 2018 Dec; 97(5):1479-1484. PubMed ID: 30555098
[TBL] [Abstract][Full Text] [Related]
11. Case of Japanese patient with x-linked ocular albinism associated with GPR143 gene mutation.
Ohtsubo M; Sato M; Hikoya A; Hosono K; Minoshima S; Hotta Y
Jpn J Ophthalmol; 2010 Nov; 54(6):624-6. PubMed ID: 21348135
[No Abstract] [Full Text] [Related]
12. GPR143 Gene Mutations in Five Chinese Families with X-linked Congenital Nystagmus.
Han R; Wang X; Wang D; Wang L; Yuan Z; Ying M; Li N
Sci Rep; 2015 Jul; 5():12031. PubMed ID: 26160353
[TBL] [Abstract][Full Text] [Related]
13. Molecular genetic and clinical evaluation of three Chinese families with X-linked ocular albinism.
Zou X; Li H; Yang L; Sun Z; Yuan Z; Li H; Sui R
Sci Rep; 2017 Feb; 7():33713. PubMed ID: 28211458
[TBL] [Abstract][Full Text] [Related]
14. Identification of Novel G Protein-Coupled Receptor 143 Ligands as Pharmacologic Tools for Investigating X-Linked Ocular Albinism.
De Filippo E; Manga P; Schiedel AC
Invest Ophthalmol Vis Sci; 2017 Jun; 58(7):3118-3126. PubMed ID: 28632878
[TBL] [Abstract][Full Text] [Related]
15. A novel GPR143 splicing mutation in a Chinese family with X-linked congenital nystagmus.
Hu J; Liang D; Xue J; Liu J; Wu L
Mol Vis; 2011 Mar; 17():715-22. PubMed ID: 21423867
[TBL] [Abstract][Full Text] [Related]
16. A novel GPR143 mutation in a Chinese family with X‑linked ocular albinism type 1.
Gao X; Liu T; Cheng X; Dai A; Liu W; Li R; Zhang M
Mol Med Rep; 2020 Jan; 21(1):240-248. PubMed ID: 31746431
[TBL] [Abstract][Full Text] [Related]
17.
Xu J; Zheng Y; Cheng L; Sun H; Yu X; Gu F; Song E
Mol Vis; 2023; 29():234-244. PubMed ID: 38222445
[TBL] [Abstract][Full Text] [Related]
18. Molecular genetic analysis of patients with sporadic and X-linked infantile nystagmus.
Zhao H; Huang XF; Zheng ZL; Deng WL; Lei XL; Xing DJ; Ye L; Xu SZ; Chen J; Zhang F; Yu XP; Jin ZB
BMJ Open; 2016 Apr; 6(4):e010649. PubMed ID: 27036142
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Deep intronic GPR143 mutation in a Japanese family with ocular albinism.
Naruto T; Okamoto N; Masuda K; Endo T; Hatsukawa Y; Kohmoto T; Imoto I
Sci Rep; 2015 Jun; 5():11334. PubMed ID: 26061757
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
