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Journal Abstract Search

71 related items for PubMed ID: 8320863

  • 21. Stargardt's type maculopathy in a patient with 11778 Leber's optic neuropathy.
    Yen MY, Wei YH, Liu JH.
    J Neuroophthalmol; 1996 Jun; 16(2):120-3. PubMed ID: 8797169
    [Abstract] [Full Text] [Related]

  • 22. Analysis of the pathogenic human mitochondrial mutation ND1/3460, and mutations of strictly conserved residues in its vicinity, using the bacterium Paracoccus denitrificans.
    Zickermann V, Barquera B, Wikström M, Finel M.
    Biochemistry; 1998 Aug 25; 37(34):11792-6. PubMed ID: 9718301
    [Abstract] [Full Text] [Related]

  • 23. A 35 kDa NAD(P)H oxidase previously isolated from the archaeon Sulfolobus solfataricus is instead a thioredoxin reductase.
    Ruocco MR, Ruggiero A, Masullo L, Arcari P, Masullo M.
    Biochimie; 2004 Dec 25; 86(12):883-92. PubMed ID: 15667938
    [Abstract] [Full Text] [Related]

  • 24. 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 25; 44(2):187-93. PubMed ID: 9708540
    [Abstract] [Full Text] [Related]

  • 25. [Analysis on the effect of secondary mutations on Leber's hereditary optic neuropathy].
    Wang Y, Tong Y, Hu SX, Wang JY, Shao JB, Zhang HX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug 25; 24(4):397-400. PubMed ID: 17680528
    [Abstract] [Full Text] [Related]

  • 26. Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis.
    Kim JY, Hwang JM, Park SS.
    Ann Neurol; 2002 May 25; 51(5):630-4. PubMed ID: 12112111
    [Abstract] [Full Text] [Related]

  • 27. [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 25; 44(7):676-80. PubMed ID: 8741498
    [Abstract] [Full Text] [Related]

  • 28. The MELAS mutations 3946 and 3949 perturb the critical structure in a conserved loop of the ND1 subunit of mitochondrial complex I.
    Kervinen M, Hinttala R, Helander HM, Kurki S, Uusimaa J, Finel M, Majamaa K, Hassinen IE.
    Hum Mol Genet; 2006 Sep 01; 15(17):2543-52. PubMed ID: 16849371
    [Abstract] [Full Text] [Related]

  • 29. [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 20; 138(18):565-8. PubMed ID: 10596473
    [Abstract] [Full Text] [Related]

  • 30. A heteroplasmic LHON family: tissue distribution and transmission of the 11778 mutation.
    Howell N, Xu M, Halvorson S, Bodis-Wollner I, Sherman J.
    Am J Hum Genet; 1994 Jul 20; 55(1):203-6. PubMed ID: 8023847
    [No Abstract] [Full Text] [Related]

  • 31. Is the mitochondrial complex I ND5 gene a hot-spot for MELAS causing mutations?
    Liolitsa D, Rahman S, Benton S, Carr LJ, Hanna MG.
    Ann Neurol; 2003 Jan 20; 53(1):128-32. PubMed ID: 12509858
    [Abstract] [Full Text] [Related]

  • 32. [Optic atrophy/dystonia].
    Ishii A, Ohkoshi N.
    Ryoikibetsu Shokogun Shirizu; 2001 Jan 20; (36):203-8. PubMed ID: 11596371
    [No Abstract] [Full Text] [Related]

  • 33. Expression and characterization of a functional canine variant of cytochrome b5 reductase.
    Roma GW, Crowley LJ, Barber MJ.
    Arch Biochem Biophys; 2006 Aug 01; 452(1):69-82. PubMed ID: 16814740
    [Abstract] [Full Text] [Related]

  • 34. CIA30 complex I assembly factor: a candidate for human complex I deficiency?
    Janssen R, Smeitink J, Smeets R, van Den Heuvel L.
    Hum Genet; 2002 Mar 01; 110(3):264-70. PubMed ID: 11935339
    [Abstract] [Full Text] [Related]

  • 35. Platelet mitochondrial function in Leber's hereditary optic neuropathy.
    Smith PR, Cooper JM, Govan GG, Harding AE, Schapira AH.
    J Neurol Sci; 1994 Mar 01; 122(1):80-3. PubMed ID: 8195807
    [Abstract] [Full Text] [Related]

  • 36. The sugar beet mitochondrial genome contains an ORF sharing sequence homology with the gene for the 30 kDa subunit of bovine mitochondrial complex I.
    Kubo T, Mikami T, Kinoshita T.
    Mol Gen Genet; 1993 Nov 01; 241(3-4):479-81. PubMed ID: 8246903
    [Abstract] [Full Text] [Related]

  • 37. [Loss of visual acuity].
    Maeda K, Terada M, Mitsunami K.
    Nihon Rinsho; 2002 Apr 01; 60 Suppl 4():526-9. PubMed ID: 12013932
    [No Abstract] [Full Text] [Related]

  • 38. Immuno-purification of a dimeric subcomplex of the respiratory NADH-CoQ reductase of Rhodobacter capsulatus equivalent to the FP fraction of the mitochondrial complex I.
    Duborjal H, Dupuis A, Chapel A, Kieffer S, Lunardi J, Issartel JP.
    FEBS Lett; 1997 Apr 01; 405(3):345-50. PubMed ID: 9108316
    [Abstract] [Full Text] [Related]

  • 39. Two cases of hereditary optic atrophy associated with an enzymatic defect of the respiratory chain.
    Cahill M, Monavari A, Naughten E, O'Keefe M.
    Metab Pediatr Syst Ophthalmol (1985); 1997 Apr 01; 19-20():27-9. PubMed ID: 11548782
    [Abstract] [Full Text] [Related]

  • 40. Ubiquinone and inhibitor sites in complex I: one, two or three?
    Esposti MD, Ghelli A.
    Biochem Soc Trans; 1999 Aug 01; 27(4):606-9. PubMed ID: 10917651
    [No Abstract] [Full Text] [Related]

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