These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

209 related articles for article (PubMed ID: 8527802)

  • 1. 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]  

  • 2. 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]  

  • 3. A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa.
    Rosenfeld PJ; Cowley GS; McGee TL; Sandberg MA; Berson EL; Dryja TP
    Nat Genet; 1992 Jun; 1(3):209-13. PubMed ID: 1303237
    [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. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. [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]  

  • 9. 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]  

  • 10. 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]  

  • 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. 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. 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]  

  • 14. 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]  

  • 15. Mutation of human retinal fascin gene (FSCN2) causes autosomal dominant retinitis pigmentosa.
    Wada Y; Abe T; Takeshita T; Sato H; Yanashima K; Tamai M
    Invest Ophthalmol Vis Sci; 2001 Sep; 42(10):2395-400. PubMed ID: 11527955
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. [A recurrent rhodopsin gene missense mutation in a Chinese family with autosomal dominant retinitis pigmentosa].
    Wang S; Zhang R; Shi Z; Ren L; Ren J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr; 22(2):192-4. PubMed ID: 15793783
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.