BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 1395084)

  • 1. Leber hereditary optic neuropathy: estimation of number of embryonic precursor cells and disease threshold in heterozygous affected females at the X-linked locus.
    Bu X; Rotter JI
    Clin Genet; 1992 Sep; 42(3):143-8. PubMed ID: 1395084
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. The two locus control of Leber hereditary optic neuropathy and a high penetrance in Japanese pedigrees.
    Nakamura M; Fujiwara Y; Yamamoto M
    Hum Genet; 1993 May; 91(4):339-41. PubMed ID: 8500789
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Leber hereditary optic neuropathy (LHON): a mitochondrial disease with unresolved complexities.
    Went LN
    Cytogenet Cell Genet; 1999; 86(2):153-6. PubMed ID: 10545708
    [No Abstract]   [Full Text] [Related]  

  • 6. X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinant.
    Pegoraro E; Carelli V; Zeviani M; Cortelli P; Montagna P; Barboni P; Angelini C; Hoffman EP
    Am J Med Genet; 1996 Feb; 61(4):356-62. PubMed ID: 8834048
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. X-chromosomal gene in Leber hereditary optic neuroretinopathy.
    Chen JD; Denton MJ
    Am J Hum Genet; 1991 Sep; 49(3):692-3. PubMed ID: 1882847
    [No Abstract]   [Full Text] [Related]  

  • 9. X-Inactivation patterns in females harboring mtDNA mutations that cause Leber hereditary optic neuropathy.
    Hudson G; Carelli V; Horvath R; Zeviani M; Smeets HJ; Chinnery PF
    Mol Vis; 2007 Dec; 13():2339-43. PubMed ID: 18199976
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. No evidence for 'skewed' inactivation of the X-chromosome as cause of Leber's hereditary optic neuropathy in female carriers.
    Oostra RJ; Kemp S; Bolhuis PA; Bleeker-Wagemakers EM
    Hum Genet; 1996 Apr; 97(4):500-5. PubMed ID: 8834251
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Genetic characteristics of Japanese pedigrees with Leber's hereditary optic neuropathy].
    Nakamura M; Yamamoto M
    Nippon Ganka Gakkai Zasshi; 1994 Apr; 98(4):319-26. PubMed ID: 8165962
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Preliminary exclusion of an X-linked gene in Leber optic atrophy by linkage analysis.
    Chen JD; Cox I; Denton MJ
    Hum Genet; 1989 Jun; 82(3):203-7. PubMed ID: 2731932
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. [Leber's optic nerve atrophy; a mitochondrial hereditary disease].
    Oostra RJ; Bolhuis PA; Wijburg FA; Bleeker-Wagemakers EM
    Ned Tijdschr Geneeskd; 1995 Jul; 139(26):1327-31. PubMed ID: 7617050
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Leber hereditary optic neuropathy 14,484 mutation and X-linked adrenoleukodystrophy: a possible modifier of phenotypic expression?
    Gray RG; Green SH; Davies P; Alger S; Green A
    J Inherit Metab Dis; 1999 Aug; 22(6):760-1. PubMed ID: 10472539
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.