Sequence and organization of the human mitochondrial genome.Anderson S., Bankier A.T., Barrell B.G., de Bruijn M.H.L., Coulson A.R., Drouin J., Eperon I.C., Nierlich D.P., Roe B.A.[...], Young I.G.View abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNature 290:457-465 (1981)Cited in15
Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs.Horai S., Hayasaka K., Kondo R., Tsugane K., Takahata N.View abstractCited forNUCLEOTIDE SEQUENCE [GENOMIC DNA]TissuePlacentaCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 92:532-536 (1995)Cited in5918
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.View abstractCited forNUCLEOTIDE SEQUENCE [GENOMIC DNA]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCMol. Biol. Evol. 20:2132-2142 (2003)Cited in1187
Mitochondrial genome variation and the origin of modern humans.Ingman M., Kaessmann H., Paeaebo S., Gyllensten U.View abstractCited forNUCLEOTIDE SEQUENCE [GENOMIC DNA]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNature 408:708-713 (2000)Cited in1287
Mitochondrial genome variation and evolutionary history of Australian and New Guinean aborigines.Ingman M., Gyllensten U.View abstractCited forNUCLEOTIDE SEQUENCE [GENOMIC DNA]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCGenome Res. 13:1600-1606 (2003)Cited in1187
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.View abstractCited forNUCLEOTIDE SEQUENCE [GENOMIC DNA]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCInt. J. Legal Med. 118:137-146 (2004)Cited in1199+
Initial characterization of the human central proteome.Burkard T.R., Planyavsky M., Kaupe I., Breitwieser F.P., Buerckstuemmer T., Bennett K.L., Superti-Furga G., Colinge J.View abstractCited forIDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCBMC Syst. Biol. 5:17-17 (2011)Cited in99+99+
N-terminome analysis of the human mitochondrial proteome.Vaca Jacome A.S., Rabilloud T., Schaeffer-Reiss C., Rompais M., Ayoub D., Lane L., Bairoch A., Van Dorsselaer A., Carapito C.View abstractCited forIDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCProteomics 15:2519-2524 (2015)Cited in99+99+
PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathy.Yu J., Liang X., Ji Y., Ai C., Liu J., Zhu L., Nie Z., Jin X., Wang C.[...], Guan M.X.View abstractCited forINTERACTION WITH PRICKLE3CategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Clin. Invest. 130:4935-4946 (2020)Cited in3Mapped to8
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.View abstractCited forVARIANTS PRO-17 AND SER-21CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCHum. Genet. 88:139-145 (1991)Cited in13
Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome.Rieder M.J., Taylor S.L., Tobe V.O., Nickerson D.A.View abstractCited forVARIANT THR-28CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNucleic Acids Res. 26:967-973 (1998)Cited in5
Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genes.Ware S.M., El-Hassan N., Kahler S.G., Zhang Q., Ma Y.W., Miller E., Wong B., Spicer R.L., Craigen W.J.[...], Wong L.J.View abstractCited forVARIANT MC5DM2 ARG-55, INVOLVEMENT IN CMHI, VARIANT CMHI ARG-55CategoriesSequences, Disease & VariantsSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Med. Genet. 46:308-314 (2009)Cited in2
A new concept for energy coupling in oxidative phosphorylation based on a molecular explanation of the oxygen exchange reactions.Boyer P.D., Cross R.L., Momsen W.View abstractAnnotationPathwayCategoriesFunctionSourceReactome: R-HSA-50500PubMedEurope PMCProc Natl Acad Sci U S A 70:2837-2839 (1973)Mapped to20
Structure of the human ATP synthase.Lai Y., Zhang Y., Zhou S., Xu J., Du Z., Feng Z., Yu L., Zhao Z., Wang W.[...], Gong H.View abstractCategoriesStructureSourcePDB: 8H9F, PDB: 8H9J, PDB: 8H9M, PDB: 8H9Q, PDB: 8H9S, PDB: 8H9T, PDB: 8H9U, PDB: 8H9VPubMedEurope PMCMol Cell 83:2137-2147.e4 (2023)Mapped to17
A human interactome in three quantitative dimensions organized by stoichiometries and abundances.Hein M.Y., Hubner N.C., Poser I., Cox J., Nagaraj N., Toyoda Y., Gak I.A., Weisswange I., Mansfeld J.[...], Mann M.View abstractCategoriesInteractionSourceIntAct: P03928PubMedEurope PMCCell 163:712-723 (2015)Mapped to99+
Inhibition of the Mitochondrial Protease ClpP as a Therapeutic Strategy for Human Acute Myeloid Leukemia.Cole A., Wang Z., Coyaud E., Voisin V., Gronda M., Jitkova Y., Mattson R., Hurren R., Babovic S.[...], Schimmer A.D.View abstractCategoriesInteractionSourceIntAct: P03928PubMedEurope PMCCancer Cell 27:864-876 (2015)Mapped to82
Visualization of ATP synthase dimers in mitochondria by electron cryo- tomography.Davies K.M., Daum B., Gold V.A., Muhleip A.W., Brandt T., Blum T.B., Mills D.J., Kuhlbrandt W.View abstractAnnotationPathwayCategoriesFunctionSourceReactome: R-HSA-50500PubMedEurope PMCJ Vis Exp 0:51228-51228 (2014)Mapped to20
Human F1F0 ATP synthase, mitochondrial ultrastructure and OXPHOS impairment: a (super-)complex matter?Habersetzer J., Larrieu I., Priault M., Salin B., Rossignol R., Brethes D., Paumard P.View abstractAnnotationPathwayCategoriesFunctionSourceReactome: R-HSA-50500PubMedEurope PMCPLoS One 8:e75429-e75429 (2013)Mapped to20
Structure of the yeast F1Fo-ATP synthase dimer and its role in shaping the mitochondrial cristae.Davies K.M., Anselmi C., Wittig I., Faraldo-Gomez J.D., Kuhlbrandt W.View abstractAnnotationPathwayCategoriesFunctionSourceReactome: R-HSA-50500PubMedEurope PMCProc Natl Acad Sci U S A 109:13602-13607 (2012)Mapped to33
Macromolecular organization of ATP synthase and complex I in whole mitochondria.Davies K.M., Strauss M., Daum B., Kief J.H., Osiewacz H.D., Rycovska A., Zickermann V., Kuhlbrandt W.View abstractAnnotationPathwayCategoriesFunctionSourceReactome: R-HSA-50500PubMedEurope PMCProc Natl Acad Sci U S A 108:14121-14126 (2011)Mapped to20
A human MAP kinase interactome.Bandyopadhyay S., Chiang C.Y., Srivastava J., Gersten M., White S., Bell R., Kurschner C., Martin C., Smoot M.[...], Ideker T.View abstractCategoriesInteractionSourceIntAct: P03928PubMedEurope PMCNat Methods 7:801-805 (2010)Mapped to99+
Structure of dimeric F1F0-ATP synthase.Couoh-Cardel S.J., Uribe-Carvajal S., Wilkens S., Garcia-Trejo J.J.View abstractAnnotationPathwayCategoriesFunctionSourceReactome: R-HSA-50500PubMedEurope PMCJ Biol Chem 285:36447-36455 (2010)Mapped to20
Dimer ribbons of ATP synthase shape the inner mitochondrial membrane.Strauss M., Hofhaus G., Schroder R.R., Kuhlbrandt W.View abstractAnnotationPathwayCategoriesFunctionSourceReactome: R-HSA-50500PubMedEurope PMCEMBO J 27:1154-1160 (2008)Mapped to20
ATP6 homoplasmic mutations inhibit and destabilize the human F1F0-ATP synthase without preventing enzyme assembly and oligomerization.Cortes-Hernandez P., Vazquez-Memije M.E., Garcia J.J.View abstractAnnotationPathwayCategoriesFunctionSourceReactome: R-HSA-50500PubMedEurope PMCJ Biol Chem 282:1051-1058 (2007)Mapped to20