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1 to 25 of 44  Show
  1. 1
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 12 other entries.

  2. 2
    "Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs."
    Horai S., Hayasaka K., Kondo R., Tsugane K., Takahata N.
    Proc. Natl. Acad. Sci. U.S.A. 92:532-536(1995) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA], VARIANTS ALA-87 AND ALA-168.
    Category: Sequences.
    Tissue: Placenta.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 76 other entries.

  3. 3
    "Lineage-specific selection in human mtDNA: lack of polymorphisms in a segment of MTND5 gene in haplogroup J."
    Moilanen J.S., Finnila S., Majamaa K.
    Mol. Biol. Evol. 20:2132-2142(2003) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 97 other entries.

  4. 4
    "Mitochondrial genome variation and the origin of modern humans."
    Ingman M., Kaessmann H., Paeaebo S., Gyllensten U.
    Nature 408:708-713(2000) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 98 other entries.

  5. 5
    "Mitochondrial genome variation and evolutionary history of Australian and New Guinean aborigines."
    Ingman M., Gyllensten U.
    Genome Res. 13:1600-1606(2003) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 97 other entries.

  6. 6
    "Single nucleotide polymorphisms over the entire mtDNA genome that increase the power of forensic testing in Caucasians."
    Coble M.D., Just R.S., O'Callaghan J.E., Letmanyi I.H., Peterson C.T., Irwin J.A., Parsons T.J.
    Int. J. Legal Med. 118:137-146(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 125 other entries.

  7. 7
    Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 7 other entries.

  8. 8
    "Cloning in single-stranded bacteriophage as an aid to rapid DNA sequencing."
    Sanger F., Coulson A.R., Barrell B.G., Smith A.J.H., Roe B.A.
    J. Mol. Biol. 143:161-178(1980) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 130-318.
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 2 other entries.

  9. 9
    "Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase."
    Chomyn A., Mariottini P., Cleeter M.W.J., Ragan C.I., Matsuno-Yagi A., Hatefi Y., Doolittle R.F., Attardi G.
    Nature 314:592-597(1985) [PubMed] [Europe PMC] [Abstract]
    Cited for: IDENTIFICATION OF PROTEIN.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 5 other entries.

  10. 10
    "The subunit composition of the human NADH dehydrogenase obtained by rapid one-step immunopurification."
    Murray J., Zhang B., Taylor S.W., Oglesbee D., Fahy E., Marusich M.F., Ghosh S.S., Capaldi R.A.
    J. Biol. Chem. 278:13619-13622(2003) [PubMed] [Europe PMC] [Abstract]
    Cited for: IDENTIFICATION IN THE NADH-UBIQUINONE OXIDOREDUCTASE COMPLEX, IDENTIFICATION BY MASS SPECTROMETRY.
    Category: Interaction, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 41 other entries.

  11. 11
    "Relationship between mutations of mitochondrial DNA ND1 gene and type 2 diabetes."
    Yu P., Yu D.M., Liu D.M., Wang K., Tang X.Z.
    Chin. Med. J. 117:985-989(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: POSSIBLE INVOLVEMENT IN SUSCEPTIBILITY TO NIDDM.
    Category: Pathology & Biotech.
    Source: UniProtKB/Swiss-Prot (reviewed).
  12. 12
    "Whole-exome sequencing identifies a variant of the mitochondrial MT-ND1 gene associated with epileptic encephalopathy: west syndrome evolving to Lennox-Gastaut syndrome."
    Delmiro A., Rivera H., Garcia-Silva M.T., Garcia-Consuegra I., Martin-Hernandez E., Quijada-Fraile P., de Las Heras R.S., Moreno-Izquierdo A., Martin M.A., Arenas J., Martinez-Azorin F.
    Hum. Mutat. 34:1623-1627(2013) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANT LYS-214.
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  13. 13
    Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 6426 other entries.

  14. 14
    "Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees."
    Howell N., Bindoff L.A., McCullough D.A., Kubacka I., Poulton J., Mackey D., Taylor L., Turnbull D.M.
    Am. J. Hum. Genet. 49:939-950(1991) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANT LHON THR-52.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  15. 15
    "A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy."
    Huoponen K., Vilkki J., Aula P., Nikoskelainen E.K., Savontaus M.L.
    Am. J. Hum. Genet. 48:1147-1153(1991) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANT LHON THR-52.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  16. 16
    "Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation."
    Howell N., Kubacka I., Xu M., McCullough D.A.
    Am. J. Hum. Genet. 48:935-942(1991) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANT LHON PRO-285, VARIANT CYS-277.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  17. 17
    "Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy."
    Johns D.R., Berman J.
    Biochem. Biophys. Res. Commun. 174:1324-1330(1991) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANT LHON HIS-304.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 2 other entries.

  18. 18
    "Electron transfer properties of NADH:ubiquinone reductase in the ND1/3460 and the ND4/11778 mutations of the Leber hereditary optic neuroretinopathy (LHON)."
    Majander A., Huoponen K., Savontaus M.-L., Nikoskelainen E., Wikstroem M.
    FEBS Lett. 292:289-292(1991) [PubMed] [Europe PMC] [Abstract]
    Cited for: CHARACTERIZATION OF VARIANT LHON THR-52.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 other entry.

  19. 19
    "Normal variants of human mitochondrial DNA and translation products: the building of a reference data base."
    Marzuki S., Noer A.S., Lertrit P., Thyagarajan D., Kapsa R., Utthanaphol P., Byrne E.
    Hum. Genet. 88:139-145(1991) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANTS PRO-205; CYS-255 AND PRO-288.
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 12 other entries.

  20. 20
    "An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy."
    Johns D.R., Neufeld M.J., Park R.D.
    Biochem. Biophys. Res. Commun. 187:1551-1557(1992) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANT LHON HIS-30.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 other entry.

  21. 21
    Cited for: POSSIBLE INVOLVEMENT IN AD-MT, VARIANT AD-MT VAL-31.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  22. 22
    "A novel combination of mitochondrial tRNA and ND1 gene mutations in a syndrome with MELAS, cardiomyopathy, and diabetes mellitus."
    Jaksch M., Hofmann S., Kaufhold P., Obermaier-Kusser B., Zierz S., Gerbitz K.-D.
    Hum. Mutat. 7:358-360(1996) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANT MELAS THR-31.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  23. 23
    "A new mitochondrial DNA mutation associated with non-insulin-dependent diabetes mellitus."
    Nakagawa Y., Ikegami H., Yamato E., Takekawa K., Fujisawa T., Hamada Y., Ueda H., Uchigata Y., Miki T., Kumahara Y.
    Biochem. Biophys. Res. Commun. 209:664-668(1995) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANT THR-4, POSSIBLE INVOLVEMENT IN SUSCEPTIBILITY TO NIDDM.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  24. 24
    "A novel m.3395A>G missense mutation in the mitochondrial ND1 gene associated with the new tRNA(Ile) m.4316A>G mutation in a patient with hypertrophic cardiomyopathy and profound hearing loss."
    Chamkha I., Mkaouar-Rebai E., Aloulou H., Chabchoub I., Kifagi C., Fendri-Kriaa N., Kammoun T., Hachicha M., Fakhfakh F.
    Biochem. Biophys. Res. Commun. 404:504-510(2011) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANT CYS-30.
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  25. 25
    "Human NADH:ubiquinone oxidoreductase."
    Smeitink J., Sengers R., Trijbels F., van den Heuvel L.
    J. Bioenerg. Biomembr. 33:259-266(2001) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Annotation: PathwayImported.
    Source: Reactome:R-HSA-60551.

    This publication is mapped to 44 other entries.

1 to 25 of 44  Show
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