BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

113 related articles for article (PubMed ID: 1668242)

  • 1. Analysis of rhodopsin gene in patients with retinitis pigmentosa using allele-specific polymerase chain reaction.
    Nakazawa M; Kikawa-Araki E; Shiono T; Tamai M
    Jpn J Ophthalmol; 1991; 35(4):386-93. PubMed ID: 1668242
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. [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]  

  • 4. [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]  

  • 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. 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]  

  • 7. [Rapid demonstration of mutations previously identified in parents at risk of patients with autosomic dominant retinitis pigmentosa].
    Souied E; Rozet JM; Gerber S; Munnich A; Kaplan J
    J Fr Ophtalmol; 1996; 19(4):265-70. PubMed ID: 8734219
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Development of a diagnostic genetic test for simplex and autosomal recessive retinitis pigmentosa.
    Clark GR; Crowe P; Muszynska D; O'Prey D; O'Neill J; Alexander S; Willoughby CE; McKay GJ; Silvestri G; Simpson DA
    Ophthalmology; 2010 Nov; 117(11):2169-77.e3. PubMed ID: 20591486
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evaluation of the human gene encoding recoverin in patients with retinitis pigmentosa or an allied disease.
    Parminder AH; Murakami A; Inana G; Berson EL; Dryja TP
    Invest Ophthalmol Vis Sci; 1997 Mar; 38(3):704-9. PubMed ID: 9071225
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Homozygous and heterozygous gly-188-Arg mutation of the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa.
    Reig CM; Trujillo JM; Martinez-Gimeno MM; Garcia-Sandoval BM; Calvo TM; Ayuso C; Carballo M
    Ophthalmic Genet; 2000 Jun; 21(2):79-87. PubMed ID: 10916182
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Screening for point mutations in rhodopsin gene among one hundred Chinese patients with retinitis pigmentosa].
    Zhang X; Fu W; Pang CP; Yeung KY
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Dec; 19(6):463-6. PubMed ID: 12476415
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sequence variations in the retinal fascin FSCN2 gene in a Spanish population with autosomal dominant retinitis pigmentosa or macular degeneration.
    Gamundi MJ; Hernan I; Maseras M; Baiget M; Ayuso C; Borrego S; Antiñolo G; Millán JM; Valverde D; Carballo M
    Mol Vis; 2005 Nov; 11():922-8. PubMed ID: 16280978
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evaluation of the human arrestin gene in patients with retinitis pigmentosa and stationary night blindness.
    Sippel KC; DeStefano JD; Berson EL; Dryja TP
    Invest Ophthalmol Vis Sci; 1998 Mar; 39(3):665-70. PubMed ID: 9501883
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [Retinitis pigmentosa: results of rhodopsin gene analysis in the Galician population].
    Blanco MJ; Capeans C; Lareu MV; Carracedo A; Piñero A; Santos L; Copena MJ; Sánchez-Salorio M
    Arch Soc Esp Oftalmol; 2000 Aug; 75(8):547-53. PubMed ID: 11151217
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1).
    Berson EL; Grimsby JL; Adams SM; McGee TL; Sweklo E; Pierce EA; Sandberg MA; Dryja TP
    Invest Ophthalmol Vis Sci; 2001 Sep; 42(10):2217-24. PubMed ID: 11527933
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa.
    Dryja TP; McEvoy JA; McGee TL; Berson EL
    Invest Ophthalmol Vis Sci; 2000 Sep; 41(10):3124-7. PubMed ID: 10967073
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.