BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 1415219)

  • 1. Evidence against an X-linked locus close to DXS7 determining visual loss susceptibility in British and Italian families with Leber hereditary optic neuropathy.
    Sweeney MG; Davis MB; Lashwood A; Brockington M; Toscano A; Harding AE
    Am J Hum Genet; 1992 Oct; 51(4):741-8. PubMed ID: 1415219
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy.
    Chalmers RM; Davis MB; Sweeney MG; Wood NW; Harding AE
    Am J Hum Genet; 1996 Jul; 59(1):103-8. PubMed ID: 8659512
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7.
    Vilkki J; Ott J; Savontaus ML; Aula P; Nikoskelainen EK
    Am J Hum Genet; 1991 Mar; 48(3):486-91. PubMed ID: 1998335
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Leber's hereditary optic neuroretinopathy and the X-chromosomal susceptibility factor: no linkage to DXs7.
    Carvalho MR; Müller B; Rötzer E; Berninger T; Kommerell G; Blankenagel A; Savontaus ML; Meitinger T; Lorenz B
    Hum Hered; 1992; 42(5):316-20. PubMed ID: 1360941
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Reevaluation of the linkage of an optic atrophy susceptibility gene to X-chromosomal markers in Finnish families with Leber hereditary optic neuroretinopathy (LHON).
    Juvonen V; Vilkki J; Aula P; Nikoskelainen E; Savontaus ML
    Am J Hum Genet; 1993 Jul; 53(1):289-92. PubMed ID: 8317495
    [No Abstract]   [Full Text] [Related]  

  • 6. Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation.
    Harding AE; Sweeney MG; Govan GG; Riordan-Eva P
    Am J Hum Genet; 1995 Jul; 57(1):77-86. PubMed ID: 7611298
    [TBL] [Abstract][Full Text] [Related]  

  • 7. High frequency of mitochondrial ND4 gene mutation in Japanese pedigrees with Leber hereditary optic neuropathy.
    Nakamura M; Ara F; Yamada M; Hotta Y; Hayakawa M; Fujiki K; Kanai A; Sakai J; Inoue M; Yamamoto M
    Jpn J Ophthalmol; 1992; 36(1):56-61. PubMed ID: 1635296
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Meiotic breakpoint mapping of a proposed X linked visual loss susceptibility locus in Leber's hereditary optic neuropathy.
    Handoko HY; Wirapati PJ; Sudoyo HA; Sitepu M; Marzuki S
    J Med Genet; 1998 Aug; 35(8):668-71. PubMed ID: 9719375
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic analysis of Japanese pedigrees with Leber's hereditary optic neuropathy.
    Nakamura M
    Kobe J Med Sci; 1993 Dec; 39(5-6):171-82. PubMed ID: 8182918
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism.
    Vilkki J; Savontaus ML; Nikoskelainen EK
    Am J Hum Genet; 1989 Aug; 45(2):206-11. PubMed ID: 2757028
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Evidence for a novel x-linked modifier locus for leber hereditary optic neuropathy.
    Shankar SP; Fingert JH; Carelli V; Valentino ML; King TM; Daiger SP; Salomao SR; Berezovsky A; Belfort R; Braun TA; Sheffield VC; Sadun AA; Stone EM
    Ophthalmic Genet; 2008 Mar; 29(1):17-24. PubMed ID: 18363168
    [TBL] [Abstract][Full Text] [Related]  

  • 12. mtDNA analysis of Leber hereditary optic neuropathy associated with spondyloepiphyseal dysplasia.
    Howell N; Kubacka I; McDonough B; Hodess AB; Harter DH
    Am J Med Genet; 2001 May; 100(3):219-22. PubMed ID: 11343307
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial DNA mutation in an Italian family with Leber hereditary optic neuropathy.
    Carducci C; Leuzzi V; Scuderi M; De Negri AM; Gabrieli CB; Antonozzi I; Pontecorvi A
    Hum Genet; 1991 Oct; 87(6):725-7. PubMed ID: 1937476
    [TBL] [Abstract][Full Text] [Related]  

  • 14. X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation.
    Bu XD; Rotter JI
    Proc Natl Acad Sci U S A; 1991 Sep; 88(18):8198-202. PubMed ID: 1896469
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Leber hereditary optic neuropathy: Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial DNA mutation?
    Chinnery PF; Andrews RM; Turnbull DM; Howell NN
    Am J Med Genet; 2001 Jan; 98(3):235-43. PubMed ID: 11169561
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology.
    Mackey D; Howell N
    Am J Hum Genet; 1992 Dec; 51(6):1218-28. PubMed ID: 1463007
    [TBL] [Abstract][Full Text] [Related]  

  • 17. No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHON.
    Gerbitz KD; Paprotta A; Obermaier-Kusser B; Rietschel M; Zerres K
    FEBS Lett; 1992 Dec; 314(3):251-5. PubMed ID: 1361456
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.
    Chinnery PF; Brown DT; Andrews RM; Singh-Kler R; Riordan-Eva P; Lindley J; Applegarth DA; Turnbull DM; Howell N
    Brain; 2001 Jan; 124(Pt 1):209-18. PubMed ID: 11133798
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy.
    Huoponen K; Vilkki J; Aula P; Nikoskelainen EK; Savontaus ML
    Am J Hum Genet; 1991 Jun; 48(6):1147-53. PubMed ID: 1674640
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mitochondrial DNA mutation and heteroplasmy in type I Leber hereditary optic neuropathy.
    Zhu DP; Economou EP; Antonarakis SE; Maumenee IH
    Am J Med Genet; 1992 Jan; 42(2):173-9. PubMed ID: 1346348
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.