405 related articles for article (PubMed ID: 26962691)
1. Genetic Analysis of the Rhodopsin Gene Identifies a Mosaic Dominant Retinitis Pigmentosa Mutation in a Healthy Individual.
Beryozkin A; Levy G; Blumenfeld A; Meyer S; Namburi P; Morad Y; Gradstein L; Swaroop A; Banin E; Sharon D
Invest Ophthalmol Vis Sci; 2016 Mar; 57(3):940-7. PubMed ID: 26962691
[TBL] [Abstract][Full Text] [Related]
2. New COL6A6 variant detected by whole-exome sequencing is linked to break points in intron 4 and 3'-UTR, deleting exon 5 of RHO, and causing adRP.
de Sousa Dias M; Hernan I; Delás B; Pascual B; Borràs E; Gamundi MJ; Mañé B; Fernández-San José P; Ayuso C; Carballo M
Mol Vis; 2015; 21():857-70. PubMed ID: 26321861
[TBL] [Abstract][Full Text] [Related]
3. Novel rhodopsin mutation in a Chinese family with autosomal dominant retinitis pigmentosa.
Zhao K; Xiong S; Wang L; Wang L; Cui Y; Wang Q
Ophthalmic Genet; 2001 Sep; 22(3):155-62. PubMed ID: 11559857
[TBL] [Abstract][Full Text] [Related]
4. [Genetic analysis of rhodopsin and peripherin genes in patients with autosomal dominant retinitis pigmentosa (adRP) in Polish families].
Brzeziańska E; Zdzieszyńska M; Goś R; Lewiński A
Klin Oczna; 2004; 106(6):743-8. PubMed ID: 15787173
[TBL] [Abstract][Full Text] [Related]
5. Prevalence of Rhodopsin mutations in autosomal dominant Retinitis Pigmentosa in Spain: clinical and analytical review in 200 families.
Fernandez-San Jose P; Blanco-Kelly F; Corton M; Trujillo-Tiebas MJ; Gimenez A; Avila-Fernandez A; Garcia-Sandoval B; Lopez-Molina MI; Hernan I; Carballo M; Riveiro-Alvarez R; Ayuso C
Acta Ophthalmol; 2015 Feb; 93(1):e38-44. PubMed ID: 25408095
[TBL] [Abstract][Full Text] [Related]
6. Genotype and Phenotype Studies in Autosomal Dominant Retinitis Pigmentosa (adRP) of the French Canadian Founder Population.
Coussa RG; Chakarova C; Ajlan R; Taha M; Kavalec C; Gomolin J; Khan A; Lopez I; Ren H; Waseem N; Kamenarova K; Bhattacharya SS; Koenekoop RK
Invest Ophthalmol Vis Sci; 2015 Dec; 56(13):8297-305. PubMed ID: 26720483
[TBL] [Abstract][Full Text] [Related]
7. Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 families.
Sullivan LS; Bowne SJ; Birch DG; Hughbanks-Wheaton D; Heckenlively JR; Lewis RA; Garcia CA; Ruiz RS; Blanton SH; Northrup H; Gire AI; Seaman R; Duzkale H; Spellicy CJ; Zhu J; Shankar SP; Daiger SP
Invest Ophthalmol Vis Sci; 2006 Jul; 47(7):3052-64. PubMed ID: 16799052
[TBL] [Abstract][Full Text] [Related]
8. Mutations P51U and G122E in retinal transcription factor NRL associated with autosomal dominant and sporadic retinitis pigmentosa.
Martinez-Gimeno M; Maseras M; Baiget M; Beneito M; Antiñolo G; Ayuso C; Carballo M
Hum Mutat; 2001 Jun; 17(6):520. PubMed ID: 11385710
[TBL] [Abstract][Full Text] [Related]
9. Rhodopsin gene mutation analysis in Iranian patients with autosomal dominant retinitis pigmentosa.
Roshandel D; Rafati M; Khorami S; Novin Baheran N; Jalali S; Tabatabaie R; Rezai S; Ahmadieh H; Ghaffari SR
Int Ophthalmol; 2019 Nov; 39(11):2523-2531. PubMed ID: 30972525
[TBL] [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. Mutational analysis of the rhodopsin gene in Chinese ADRP families by conformation sensitive gel electrophoresis.
Zhang XL; Liu M; Meng XH; Fu WL; Yin ZQ; Huang JF; Zhang X
Life Sci; 2006 Feb; 78(13):1494-8. PubMed ID: 16229860
[TBL] [Abstract][Full Text] [Related]
12. Molecular screening of rhodopsin and peripherin/RDS genes in Mexican families with autosomal dominant retinitis pigmentosa.
Matias-Florentino M; Ayala-Ramirez R; Graue-Wiechers F; Zenteno JC
Curr Eye Res; 2009 Dec; 34(12):1050-6. PubMed ID: 19958124
[TBL] [Abstract][Full Text] [Related]
13. A complete screen for mutations of the rhodopsin gene in a panel of Chinese patients with autosomal dominant retinitis pigmentosa.
Zhang XL; Liu M; Meng XH; Fu WL; Yin ZQ; Zhang X; Huang JF
Chin Med Sci J; 2005 Mar; 20(1):30-4. PubMed ID: 15844309
[TBL] [Abstract][Full Text] [Related]
14. Identification of novel rhodopsin mutations associated with retinitis pigmentosa by GC-clamped denaturing gradient gel electrophoresis.
Sheffield VC; Fishman GA; Beck JS; Kimura AE; Stone EM
Am J Hum Genet; 1991 Oct; 49(4):699-706. PubMed ID: 1897520
[TBL] [Abstract][Full Text] [Related]
15. Whole exome sequencing reveals GUCY2D as a major gene associated with cone and cone-rod dystrophy in Israel.
Lazar CH; Mutsuddi M; Kimchi A; Zelinger L; Mizrahi-Meissonnier L; Marks-Ohana D; Boleda A; Ratnapriya R; Sharon D; Swaroop A; Banin E
Invest Ophthalmol Vis Sci; 2014 Dec; 56(1):420-30. PubMed ID: 25515582
[TBL] [Abstract][Full Text] [Related]
16. Mutations in the gene coding for the pre-mRNA splicing factor, PRPF31, in patients with autosomal dominant retinitis pigmentosa.
Waseem NH; Vaclavik V; Webster A; Jenkins SA; Bird AC; Bhattacharya SS
Invest Ophthalmol Vis Sci; 2007 Mar; 48(3):1330-4. PubMed ID: 17325180
[TBL] [Abstract][Full Text] [Related]
17. Characterization of macular structure and function in two Swedish families with genetically identified autosomal dominant retinitis pigmentosa.
Abdulridha-Aboud W; Kjellström U; Andréasson S; Ponjavic V
Mol Vis; 2016; 22():362-73. PubMed ID: 27212874
[TBL] [Abstract][Full Text] [Related]
18. Transcriptional expression of cis-acting and trans-acting splicing mutations cause autosomal dominant retinitis pigmentosa.
Gamundi MJ; Hernan I; Muntanyola M; Maseras M; López-Romero P; Alvarez R; Dopazo A; Borrego S; Carballo M
Hum Mutat; 2008 Jun; 29(6):869-78. PubMed ID: 18412284
[TBL] [Abstract][Full Text] [Related]
19. Identification of two novel RHO mutations in Chinese retinitis pigmentosa patients.
Wang J; Xu D; Zhu T; Zhou Y; Chen X; Wang F; Zhang J; Tian H; Gao F; Zhang J; Jin C; Xu J; Lu L; Liu Q; Xu GT
Exp Eye Res; 2019 Nov; 188():107726. PubMed ID: 31319082
[TBL] [Abstract][Full Text] [Related]
20. Linkage analysis and mutation screening of the rhodopsin gene in a Chinese Bai family with autosomal dominant retinitis pigmentosa.
Guo H; Qin Y; Meng Q; Zhang H; Jin H; Chen Y
J Hum Genet; 2010 Sep; 55(9):571-6. PubMed ID: 20555336
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]