BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

322 related articles for article (PubMed ID: 9027481)

  • 21. A family with 3460G>A and 11778G>A mutations and haplogroup analysis of Polish Leber hereditary optic neuropathy patients.
    Tonska K; Kurzawa M; Ambroziak AM; Korwin-Rujna M; Szaflik JP; Grabowska E; Szaflik J; Bartnik E
    Mitochondrion; 2008 Dec; 8(5-6):383-8. PubMed ID: 18801464
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].
    Mao YJ; Qu J; Guan MX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Feb; 25(1):45-9. PubMed ID: 18247303
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The influence of nuclear background on the biochemical expression of 3460 Leber's hereditary optic neuropathy.
    Cock HR; Tabrizi SJ; Cooper JM; Schapira AH
    Ann Neurol; 1998 Aug; 44(2):187-93. PubMed ID: 9708540
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Leber hereditary optic neuropathy: mitochondrial mutations and degeneration of the optic nerve.
    Howell N
    Vision Res; 1997 Dec; 37(24):3495-507. PubMed ID: 9425526
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Diagnostic and differential diagnostic potential of mitochondrial DNA assessment in patients with Leber's hereditary optic neuropathy].
    Feng X; Pu W; Gao D
    Zhonghua Yan Ke Za Zhi; 2001 May; 37(3):174-7. PubMed ID: 11864415
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Characterization of the mitochondrial genome in childhood multiple sclerosis. I. Optic neuritis and LHON mutations.
    Ohlenbusch A; Wilichowski E; Hanefeld F
    Neuropediatrics; 1998 Aug; 29(4):175-9. PubMed ID: 9762692
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. [Analysis of mutations and heteroplasmy at mitochondrial DNA 11778 using non-RI single strand conformation polymorphisms in Leber's hereditary optic neuropathy].
    Toyo-Oka Y; Wada C; Yamabe H; Inoue M; Ishigaki M; Matsuyama N; Ohnuki Y; Ichibe Y; Wakakura M; Ohtani H
    Rinsho Byori; 1996 Jul; 44(7):676-80. PubMed ID: 8741498
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Spectrum of the mitochondrial DNA mutations of Leber's hereditary optic neuropathy in Koreans.
    Kim JY; Hwang JM; Chang BL; Park SS
    J Neurol; 2003 Mar; 250(3):278-81. PubMed ID: 12638016
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Detection of mtDNA*LHON G11778A mutation by real-time polymerase chain reaction using TaqMan-MGB probe technology].
    Li YM; Wang JY; Chen Y; Shao JB; Wang J; Tong Y
    Zhonghua Yan Ke Za Zhi; 2006 Aug; 42(8):728-32. PubMed ID: 17081446
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Sporadic bilateral optic neuropathy in children: the role of mitochondrial abnormalities.
    Bosley TM; Brodsky MC; Glasier CM; Abu-Amero KK
    Invest Ophthalmol Vis Sci; 2008 Dec; 49(12):5250-6. PubMed ID: 18676632
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mitochondrial DNA mutation m.3635G>A may be associated with Leber hereditary optic neuropathy in Chinese.
    Zhang AM; Zou Y; Guo X; Jia X; Zhang Q; Yao YG
    Biochem Biophys Res Commun; 2009 Aug; 386(2):392-5. PubMed ID: 19527690
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Haplogroup heterogeneity of LHON patients carrying the m.14484T>C mutation in India.
    Khan NA; Govindaraj P; Soumittra N; Srilekha S; Ambika S; Vanniarajan A; Meena AK; Uppin MS; Sundaram C; Taly AB; Bindu PS; Gayathri N; Thangaraj K
    Invest Ophthalmol Vis Sci; 2013 Jun; 54(6):3999-4005. PubMed ID: 23674761
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Spectrum of pathogenic mtDNA mutations in Leber hereditary optic neuropathy families from Siberia].
    Volod'ko NV; L'vova MA; Starikovskaia EB; Derbeneva OA; Bychkov IIu; Mikhaĭlovskaia IE; Pogozheva IV; Fedotov FF; Soyan GV; Procaccio V; Wallace DC; Sukernik RI
    Genetika; 2006 Jan; 42(1):89-97. PubMed ID: 16523671
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G>A point mutation--A case report.
    Grazina MM; Diogo LM; Garcia PC; Silva ED; Garcia TD; Robalo CB; Oliveira CR
    Eur J Paediatr Neurol; 2007 Mar; 11(2):115-8. PubMed ID: 17254817
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations.
    Ferré M; Bonneau D; Milea D; Chevrollier A; Verny C; Dollfus H; Ayuso C; Defoort S; Vignal C; Zanlonghi X; Charlin JF; Kaplan J; Odent S; Hamel CP; Procaccio V; Reynier P; Amati-Bonneau P
    Hum Mutat; 2009 Jul; 30(7):E692-705. PubMed ID: 19319978
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Leber's hereditary optic neuropathy].
    Konrádová V; Zeman J; Stratilová L; Hermanská J; Vseticka I; Misovicová N; Kurca E; Gerinec A; Houstĕk J
    Cas Lek Cesk; 1999 Oct; 138(18):565-8. PubMed ID: 10596473
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mitochondrial tRNA gene mutations in patients having mitochondrial disease with lactic acidosis.
    Ueki I; Koga Y; Povalko N; Akita Y; Nishioka J; Yatsuga S; Fukiyama R; Matsuishi T
    Mitochondrion; 2006 Feb; 6(1):29-36. PubMed ID: 16337222
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.
    Brown MD; Sun F; Wallace DC
    Am J Hum Genet; 1997 Feb; 60(2):381-7. PubMed ID: 9012411
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [An analysis of 6 Leber mutations in 31 individuals with optic atrophy. A study of its transmission in 5 families].
    Gómez Zaera M; Barrientos A; Arias L; Rojas I; Arruga J; Estivill X; Casademont J; Nunes V
    Med Clin (Barc); 1999 Mar; 112(9):326-9. PubMed ID: 10220763
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.