These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 1764087)

  • 1. Cytochrome b mutations in Leber hereditary optic neuropathy.
    Johns DR; Neufeld MJ
    Biochem Biophys Res Commun; 1991 Dec; 181(3):1358-64. PubMed ID: 1764087
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy.
    Johns DR; Berman J
    Biochem Biophys Res Commun; 1991 Feb; 174(3):1324-30. PubMed ID: 1900003
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cytochrome c oxidase mutations in Leber hereditary optic neuropathy.
    Johns DR; Neufeld MJ
    Biochem Biophys Res Commun; 1993 Oct; 196(2):810-5. PubMed ID: 8240356
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy.
    Johns DR; Neufeld MJ; Park RD
    Biochem Biophys Res Commun; 1992 Sep; 187(3):1551-7. PubMed ID: 1417830
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.
    Brown MD; Voljavec AS; Lott MT; Torroni A; Yang CC; Wallace DC
    Genetics; 1992 Jan; 130(1):163-73. PubMed ID: 1732158
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia.
    De Vries DD; Went LN; Bruyn GW; Scholte HR; Hofstra RM; Bolhuis PA; van Oost BA
    Am J Hum Genet; 1996 Apr; 58(4):703-11. PubMed ID: 8644732
    [TBL] [Abstract][Full Text] [Related]  

  • 7. High frequency of mutations at position 11778 in mitochondrial ND4 gene in Japanese families with Leber's hereditary optic neuropathy.
    Mashima Y; Hiida Y; Oguchi Y; Kudoh J; Shimizu N
    Hum Genet; 1993 Aug; 92(1):101-2. PubMed ID: 8103501
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. The mitochondrial DNA mutation ND6*14,484C associated with leber hereditary optic neuropathy, leads to deficiency of complex I of the respiratory chain.
    Oostra RJ; Van Galen MJ; Bolhuis PA; Bleeker-Wagemakers EM; Van den Bogert C
    Biochem Biophys Res Commun; 1995 Oct; 215(3):1001-5. PubMed ID: 7488023
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Allelic mutations of the fourth subunit of NADH dehydrogenase are not pathogenetically important in 11778-negative Leber hereditary optic neuropathy.
    Johns DR
    Am J Hum Genet; 1991 Jun; 48(6):1209-13. PubMed ID: 2035540
    [No Abstract]   [Full Text] [Related]  

  • 11. [A case of Leber optic neuropathy with a new point mutation in the cytochrome b gene].
    Besch D; Wissinger B; Zrenner E; Leo-Kotter B
    Ophthalmologe; 2000 Jan; 97(1):22-6. PubMed ID: 10663786
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia.
    Jun AS; Brown MD; Wallace DC
    Proc Natl Acad Sci U S A; 1994 Jun; 91(13):6206-10. PubMed ID: 8016139
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial encephalomyopathies.
    DiMauro S; Moraes CT
    Arch Neurol; 1993 Nov; 50(11):1197-208. PubMed ID: 8215979
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes.
    Hofmann S; Bezold R; Jaksch M; Obermaier-Kusser B; Mertens S; Kaufhold P; Rabl W; Hecker W; Gerbitz KD
    Genomics; 1997 Jan; 39(1):8-18. PubMed ID: 9027481
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An example of Leber hereditary optic neuropathy not involving a mutation in the mitochondrial ND4 gene.
    Howell N; McCullough D
    Am J Hum Genet; 1990 Oct; 47(4):629-34. PubMed ID: 2121024
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A family with Leber's hereditary optic neuropathy with mitochondrial 11778/ND4 and 4216/ND1 mutations.
    Hwang JM
    Korean J Ophthalmol; 2000 Jun; 14(1):45-8. PubMed ID: 10933019
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees.
    Howell N; Bindoff LA; McCullough DA; Kubacka I; Poulton J; Mackey D; Taylor L; Turnbull DM
    Am J Hum Genet; 1991 Nov; 49(5):939-50. PubMed ID: 1928099
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I.
    Brown MD; Yang CC; Trounce I; Torroni A; Lott MT; Wallace DC
    Am J Hum Genet; 1992 Aug; 51(2):378-85. PubMed ID: 1322638
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of the human SDHD gene encoding the small subunit of cytochrome b (cybS) in mitochondrial succinate-ubiquinone oxidoreductase.
    Hirawake H; Taniwaki M; Tamura A; Amino H; Tomitsuka E; Kita K
    Biochim Biophys Acta; 1999 Aug; 1412(3):295-300. PubMed ID: 10482792
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.