BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

162 related articles for article (PubMed ID: 9143920)

  • 1. Tissue distribution of the ND4/11778 mutation in heteroplasmic lineages with Leber hereditary optic neuropathy.
    Juvonen V; Nikoskelainen E; Lamminen T; Penttinen M; Aula P; Savontaus ML
    Hum Mutat; 1997; 9(5):412-7. PubMed ID: 9143920
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Mitochondrial DNA mutation in Leber's hereditary optic neuropathy.
    Yen MY; Yen TC; Pang CY; Liu JH; Wei YH
    Invest Ophthalmol Vis Sci; 1992 Jul; 33(8):2561-6. PubMed ID: 1634353
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Quantitative determination of heteroplasmy in Leber's hereditary optic neuropathy by single-strand conformation polymorphism.
    Mashima Y; Saga M; Hiida Y; Oguchi Y; Wakakura M; Kudoh J; Shimizu N
    Invest Ophthalmol Vis Sci; 1995 Jul; 36(8):1714-20. PubMed ID: 7601652
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. 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]  

  • 7. Time-resolved fluorometry in the diagnosis of Leber hereditary optic neuroretinopathy.
    Huoponen K; Juvonen V; Iitiä A; Dahlen P; Siitari H; Aula P; Nikoskelainen E; Savontaus ML
    Hum Mutat; 1994; 3(1):29-36. PubMed ID: 8118464
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Leber's hereditary optic neuropathy (LHON) with mitochondrial ND4 gene mutation (11778) in a Thai patient.
    Lertrit P; Ruangvaravate N; Trongpanich Y; Imsumran A; Mungkornkarn C; Neungton N
    J Med Assoc Thai; 1999 Jan; 82(1):59-64. PubMed ID: 10087740
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A family with Leber's hereditary optic neuropathy with mitochondrial DNA heteroplasmy related to disease expression.
    Tanaka A; Kiyosawa M; Mashima Y; Tokoro T
    J Neuroophthalmol; 1998 Jun; 18(2):81-3. PubMed ID: 9621260
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].
    Pénisson-Besnier I; Moreau C; Jacques C; Roger JC; Dubas F; Reynier P
    Rev Neurol (Paris); 2001 May; 157(5):537-41. PubMed ID: 11438773
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation analysis of the ND6 gene in patients with Lebers hereditary optic neuropathy.
    Wissinger B; Besch D; Baumann B; Fauser S; Christ-Adler M; Jurklies B; Zrenner E; Leo-Kottler B
    Biochem Biophys Res Commun; 1997 May; 234(2):511-5. PubMed ID: 9177303
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rapid quantification of the heteroplasmy of mutant mitochondrial DNAs in Leber's hereditary optic neuropathy using the Invader technology.
    Mashima Y; Nagano M; Funayama T; Zhang Q; Egashira T; Kudho J; Shimizu N; Oguchi Y
    Clin Biochem; 2004 Apr; 37(4):268-76. PubMed ID: 15003728
    [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. Leber's hereditary optic neuropathy.
    Letchavanakul A; Dechphongsaphilas W; Dhamcharee V
    J Med Assoc Thai; 1999 Oct; 82(10):1051-5. PubMed ID: 10561972
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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]  

  • 18. Intrafamilial variation in Leber hereditary optic neuropathy revealed by direct mutation analysis.
    Cavelier L; Gyllensten U; Dahl N
    Clin Genet; 1993 Feb; 43(2):69-72. PubMed ID: 8448903
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A patient with two mitochondrial DNA mutations causing PEO and LHON.
    Melberg A; Moslemi AR; Palm O; Raininko R; Stålberg E; Oldfors A
    Eur J Med Genet; 2009; 52(1):47-8. PubMed ID: 19015050
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Penetrance of Leber hereditary optic neuropathy individuals with mitochondrial DNA 11778 mutation in the Shanxi area].
    Zheng ML; Zhang GL; Hua AL; Zhang YL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr; 21(2):166-7. PubMed ID: 15079802
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.