282 related articles for article (PubMed ID: 8025068)
1. Ocular manifestations in autosomal dominant retinitis pigmentosa with a Lys-296-Glu rhodopsin mutation at the retinal binding site.
Owens SL; Fitzke FW; Inglehearn CF; Jay M; Keen TJ; Arden GB; Bhattacharya SS; Bird AC
Br J Ophthalmol; 1994 May; 78(5):353-8. PubMed ID: 8025068
[TBL] [Abstract][Full Text] [Related]
2. Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucine.
Berson EL; Rosner B; Sandberg MA; Weigel-DiFranco C; Dryja TP
Am J Ophthalmol; 1991 May; 111(5):614-23. PubMed ID: 2021172
[TBL] [Abstract][Full Text] [Related]
3. Ocular findings in a family with autosomal dominant retinitis pigmentosa and a frameshift mutation altering the carboxyl terminal sequence of rhodopsin.
Apfelstedt-Sylla E; Kunisch M; Horn M; Rüther K; Gerding H; Gal A; Zrenner E
Br J Ophthalmol; 1993 Aug; 77(8):495-501. PubMed ID: 8025047
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Diffuse loss of rod function in autosomal dominant retinitis pigmentosa with pro-347-leu mutation of rhodopsin.
Apfelstedt-Sylla E; Kunisch M; Horn M; Rüther K; Gal A; Zrenner E
Ger J Ophthalmol; 1992; 1(5):319-27. PubMed ID: 1477634
[TBL] [Abstract][Full Text] [Related]
6. Thr4Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch family.
van den Born LI; van Schooneveld MJ; de Jong LA; Riemslag FC; de Jong PT; Gal A; Bleeker-Wagemakers EM
Ophthalmic Genet; 1994 Jun; 15(2):51-60. PubMed ID: 7850269
[TBL] [Abstract][Full Text] [Related]
7. A new codon 15 rhodopsin gene mutation in autosomal dominant retinitis pigmentosa is associated with sectorial disease.
Sullivan LJ; Makris GS; Dickinson P; Mulhall LE; Forrest S; Cotton RG; Loughnan MS
Arch Ophthalmol; 1993 Nov; 111(11):1512-7. PubMed ID: 8240107
[TBL] [Abstract][Full Text] [Related]
8. Ocular findings associated with rhodopsin gene codon 17 and codon 182 transition mutations in dominant retinitis pigmentosa.
Fishman GA; Stone EM; Sheffield VC; Gilbert LD; Kimura AE
Arch Ophthalmol; 1992 Jan; 110(1):54-62. PubMed ID: 1731723
[TBL] [Abstract][Full Text] [Related]
9. Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His).
Berson EL; Rosner B; Sandberg MA; Dryja TP
Arch Ophthalmol; 1991 Jan; 109(1):92-101. PubMed ID: 1987956
[TBL] [Abstract][Full Text] [Related]
10. Early-onset autosomal dominant retinitis pigmentosa with severe hyperopia.
Lam BL; Judisch GF
Am J Ophthalmol; 1991 Apr; 111(4):454-6. PubMed ID: 2012147
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Phenotypic expression of autosomal dominant retinitis pigmentosa in a Swedish family expressing a Phe-211-Leu variant of peripherin/RDS.
Ekström U; Ponjavic V; Abrahamson M; Nilsson-Ehle P; Andrëasson S; Stenström I; Ehinger B
Ophthalmic Genet; 1998 Mar; 19(1):27-37. PubMed ID: 9587927
[TBL] [Abstract][Full Text] [Related]
13. Disruption of conserved rhodopsin disulfide bond by Cys187Tyr mutation causes early and severe autosomal dominant retinitis pigmentosa.
Richards JE; Scott KM; Sieving PA
Ophthalmology; 1995 Apr; 102(4):669-77. PubMed ID: 7724183
[TBL] [Abstract][Full Text] [Related]
14. Rhodopsin gene codon 106 mutation (Gly-to-Arg) in a Japanese family with autosomal dominant retinitis pigmentosa.
Budu ; Matsumoto M; Hayasaka S; Yamada T; Hayasaka Y
Jpn J Ophthalmol; 2000; 44(6):610-4. PubMed ID: 11094174
[TBL] [Abstract][Full Text] [Related]
15. Low incidence of retinitis pigmentosa among heterozygous carriers of a specific rhodopsin splice site mutation.
Rosenfeld PJ; Hahn LB; Sandberg MA; Dryja TP; Berson EL
Invest Ophthalmol Vis Sci; 1995 Oct; 36(11):2186-92. PubMed ID: 7558711
[TBL] [Abstract][Full Text] [Related]
16. Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsin.
Heckenlively JR; Rodriguez JA; Daiger SP
Arch Ophthalmol; 1991 Jan; 109(1):84-91. PubMed ID: 1987955
[TBL] [Abstract][Full Text] [Related]
17. Abnormal rod dark adaptation in autosomal dominant retinitis pigmentosa with proline-23-histidine rhodopsin mutation.
Kemp CM; Jacobson SG; Roman AJ; Sung CH; Nathans J
Am J Ophthalmol; 1992 Feb; 113(2):165-74. PubMed ID: 1550184
[TBL] [Abstract][Full Text] [Related]
18. Autosomal dominant retinitis pigmentosa. A mutation in codon 181 (Glu-->Lys) of the rhodopsin gene in a Japanese family.
Saga M; Mashima Y; Akeo K; Oguchi Y; Kudoh J; Shimizu N
Ophthalmic Genet; 1994 Jun; 15(2):61-7. PubMed ID: 7850270
[TBL] [Abstract][Full Text] [Related]
19. Ocular findings associated with rhodopsin gene codon 267 and codon 190 mutations in dominant retinitis pigmentosa.
Fishman GA; Vandenburgh K; Stone EM; Gilbert LD; Alexander KR; Sheffield VC
Arch Ophthalmol; 1992 Nov; 110(11):1582-8. PubMed ID: 1444916
[TBL] [Abstract][Full Text] [Related]
20. Ocular findings associated with a rhodopsin gene codon 58 transversion mutation in autosomal dominant retinitis pigmentosa.
Fishman GA; Stone EM; Gilbert LD; Kenna P; Sheffield VC
Arch Ophthalmol; 1991 Oct; 109(10):1387-93. PubMed ID: 1929926
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]