182 related articles for article (PubMed ID: 8088850)
1. Further screening of the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa.
Vaithinathan R; Berson EL; Dryja TP
Genomics; 1994 May; 21(2):461-3. PubMed ID: 8088850
[No Abstract] [Full Text] [Related]
2. [Identification of Arg-135-Leu mutation in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa].
Reig C; Antich J; Gean E; Dante Heredia C; Valverde D; Baiget M; Carballo M
Med Clin (Barc); 1996 Feb; 106(6):219-21. PubMed ID: 8667664
[TBL] [Abstract][Full Text] [Related]
3. Missense mutation of rhodopsin gene codon 15 found in Japanese autosomal dominant retinitis pigmentosa.
Fujiki K; Hotta Y; Murakami A; Yoshii M; Hayakawa M; Ichikawa T; Takeda M; Akeo K; Okisaka S; Kanai A
Jpn J Hum Genet; 1995 Sep; 40(3):271-7. PubMed ID: 8527802
[TBL] [Abstract][Full Text] [Related]
4. Missense mutation A346P in the rhodopsin gene in one family with autosomal dominant retinitis pigmentosa.
Borrego S; Sánchez B; Ruiz A; Antiñolo G
Hum Mutat; 1996; 7(2):180-1. PubMed ID: 8829641
[No Abstract] [Full Text] [Related]
5. Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (ADRP).
Fujiki K; Hotta Y; Hayakawa M; Sakuma H; Shiono T; Noro M; Sakuma T; Tamai M; Hikiji K; Kawaguchi R
Jpn J Hum Genet; 1992 Jun; 37(2):125-32. PubMed ID: 1391967
[TBL] [Abstract][Full Text] [Related]
6. A novel null mutation in the rhodopsin gene causing late onset autosomal dominant retinitis pigmentosa.
Sánchez B; Borrego S; Chaparro P; Rueda T; López F; Antiñolo G
Hum Mutat; 1996; 7(2):180. PubMed ID: 8829640
[No Abstract] [Full Text] [Related]
7. A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.
Dryja TP; McGee TL; Reichel E; Hahn LB; Cowley GS; Yandell DW; Sandberg MA; Berson EL
Nature; 1990 Jan; 343(6256):364-6. PubMed ID: 2137202
[TBL] [Abstract][Full Text] [Related]
8. Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa.
Dryja TP; McGee TL; Hahn LB; Cowley GS; Olsson JE; Reichel E; Sandberg MA; Berson EL
N Engl J Med; 1990 Nov; 323(19):1302-7. PubMed ID: 2215617
[TBL] [Abstract][Full Text] [Related]
9. Autosomal dominant retinitis pigmentosa: a mutation in codon 178 of the rhodopsin gene in two families of Celtic origin.
Farrar GJ; Kenna P; Redmond R; Shiels D; McWilliam P; Humphries MM; Sharp EM; Jordan S; Kumar-Singh R; Humphries P
Genomics; 1991 Dec; 11(4):1170-1. PubMed ID: 1783387
[No Abstract] [Full Text] [Related]
10. [Screening of candidate genes in a family with autosomal dominant retinitis pigmentosa].
Teng Y; Tian H; Wang H; Hu X; Chen Y; Yang Z; Wang W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Apr; 20(2):164-6. PubMed ID: 12673590
[TBL] [Abstract][Full Text] [Related]
11. Different amino acid substitutions at the same position in rhodopsin lead to distinct phenotypes.
Neidhardt J; Barthelmes D; Farahmand F; Fleischhauer JC; Berger W
Invest Ophthalmol Vis Sci; 2006 Apr; 47(4):1630-5. PubMed ID: 16565402
[TBL] [Abstract][Full Text] [Related]
12. Ser186Pro mutation of RHO gene in a Spanish autosomal dominant retinitis pigmentosa (ADRP) family.
Trujillo MJ; Garcia-Sandoval B; Lorda-Sanchez I; Gimenez A; Sanz R; Rodriguez de Alba M ; Gonzalez-Gonzalez MC; Ibañez A; Ramos C; Ayuso C
Ophthalmic Genet; 2000 Dec; 21(4):251-6. PubMed ID: 11135497
[TBL] [Abstract][Full Text] [Related]
13. [A Chinese family with autosomal dominant retinitis pigmentosa and a pro347Leu rhodopsin gene mutation].
Yang H; Luo C; Zhou J; Yan M
Chin Med J (Engl); 2000 Jun; 113(6):574-6. PubMed ID: 11775885
[No Abstract] [Full Text] [Related]
14. A mild phenotype of autosomal dominant retinitis pigmentosa is associated with the rhodopsin mutation Pro-267-Leu.
Ponjavic V; Abrahamson M; Andréasson S; Ehinger B; Fex G; Polland W
Ophthalmic Genet; 1997 Jun; 18(2):63-70. PubMed ID: 9228242
[TBL] [Abstract][Full Text] [Related]
15. Clinical features of Japanese family with autosomal dominant retinitis pigmentosa caused by point mutation in codon 347 of rhodopsin gene.
Shiono T; Hotta Y; Noro M; Sakuma T; Tamai M; Hayakawa M; Hashimoto T; Fujiki K; Kanai A; Nakajima A
Jpn J Ophthalmol; 1992; 36(1):69-75. PubMed ID: 1635298
[TBL] [Abstract][Full Text] [Related]
16. A Thr17Met mutation is associated with an unusual retinochoroidopathy in an autosomal dominant pedigree.
Bass SJ; Noble KG
Retina; 2008; 28(7):1013-4. PubMed ID: 18698306
[TBL] [Abstract][Full Text] [Related]
17. Gly114Asp mutation of rhodopsin in autosomal dominant retinitis pigmentosa.
Millán JM; Fuchs S; Paricio N; Wedemann H; Gal A; Nájera C; Prieto F
Mol Cell Probes; 1995 Feb; 9(1):67-9. PubMed ID: 7760863
[TBL] [Abstract][Full Text] [Related]
18. Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Mutations in brief no. 208. Online.
Bessant DA; Khaliq S; Hameed A; Anwar K; Payne AM; Mehdi SQ; Bhattacharya SS
Hum Mutat; 1999; 13(1):83. PubMed ID: 10189219
[TBL] [Abstract][Full Text] [Related]
19. Two new rhodopsin transversion mutations (L40R; M216K) in families with autosomal dominant retinitis pigmentosa.
al-Maghtheh M; Inglehearn C; Lunt P; Jay M; Bird A; Bhattacharya S
Hum Mutat; 1994; 3(4):409-10. PubMed ID: 8081400
[No Abstract] [Full Text] [Related]
20. Identification of a new mutation at codon 171 of rhodopsin gene causing autosomal dominant retinitis pigmentosa.
Antiñolo G; Sánchez B; Borrego S; Rueda T; Chaparro P; Cabeza JC
Hum Mol Genet; 1994 Aug; 3(8):1421. PubMed ID: 7987326
[No Abstract] [Full Text] [Related]
[Next] [New Search]