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 *

182 related articles for article (PubMed ID: 8364589)

  • 21. 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]  

  • 22. 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]  

  • 23. Description of a new mutation in rhodopsin, Pro23Ala, and comparison with electroretinographic and clinical characteristics of the Pro23His mutation.
    Oh KT; Weleber RG; Lotery A; Oh DM; Billingslea AM; Stone EM
    Arch Ophthalmol; 2000 Sep; 118(9):1269-76. PubMed ID: 10980774
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Clinical features of autosomal dominant retinitis pigmentosa with rhodopsin gene codon 17 mutation and retinal neovascularization in a Japanese patient.
    Hayakawa M; Hotta Y; Imai Y; Fujiki K; Nakamura A; Yanashima K; Kanai A
    Am J Ophthalmol; 1993 Feb; 115(2):168-73. PubMed ID: 7679248
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. 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]  

  • 27. 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]  

  • 28. Autosomal-dominant retinitis pigmentosa associated with an Arg-135-Trp point mutation of the rhodopsin gene. Clinical features and longitudinal observations.
    Pannarale MR; Grammatico B; Iannaccone A; Forte R; DeBernardo C; Flagiello L; Vingolo EM; Del Porto G
    Ophthalmology; 1996 Sep; 103(9):1443-52. PubMed ID: 8841304
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Autosomal dominant retinitis pigmentosa: absence of the rhodopsin proline----histidine substitution (codon 23) in pedigrees from Europe.
    Farrar GJ; Kenna P; Redmond R; McWilliam P; Bradley DG; Humphries MM; Sharp EM; Inglehearn CF; Bashir R; Jay M
    Am J Hum Genet; 1990 Dec; 47(6):941-5. PubMed ID: 2239971
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Autosomal dominant retinitis pigmentosa with rhodopsin, valine-345-methionine.
    Berson EL; Sandberg MA; Dryja TP
    Trans Am Ophthalmol Soc; 1991; 89():117-28; discussion 128-30. PubMed ID: 1808803
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [A novel rhodopsin E341ter mutation in patients with retinitis pigmentosa and corresponding clinical phenotype].
    Xiong S; Zhao K; Wang L; Wang L; Cui Y; Chen W; Wang L; Wang Q
    Zhonghua Yan Ke Za Zhi; 2002 Apr; 38(4):224-7. PubMed ID: 12133392
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Autosomal dominant retinitis pigmentosa: four new mutations in rhodopsin, one of them in the retinal attachment site.
    Keen TJ; Inglehearn CF; Lester DH; Bashir R; Jay M; Bird AC; Jay B; Bhattacharya SS
    Genomics; 1991 Sep; 11(1):199-205. PubMed ID: 1765377
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Phenotypes of stop codon and splice site rhodopsin mutations causing retinitis pigmentosa.
    Jacobson SG; Kemp CM; Cideciyan AV; Macke JP; Sung CH; Nathans J
    Invest Ophthalmol Vis Sci; 1994 Apr; 35(5):2521-34. PubMed ID: 8163341
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa.
    Dryja TP; Hahn LB; Cowley GS; McGee TL; Berson EL
    Proc Natl Acad Sci U S A; 1991 Oct; 88(20):9370-4. PubMed ID: 1833777
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. 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]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 10.