Phylogenetic network for European mtDNA.Finnila S., Lehtonen M.S., Majamaa K.View abstractCited forNUCLEOTIDE SEQUENCEStrainF11CategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCAm J Hum Genet 68:1475-1484 (2001)Cited in87
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 SEQUENCEStrainF11CategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCMol. Biol. Evol. 20:2132-2142 (2003)Cited in1187
Novel A14841G mutation is associated with high penetrance of LHON/C4171A family.Yang J., Zhu Y., Chen L., Zhang H., Tong Y., Huang D., Zhang Z., Chen S., Han X., Ma X.View abstractCited forNUCLEOTIDE SEQUENCEStrainLHON-008-IV-2CategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCBiochem Biophys Res Commun 386:693-696 (2009)Cited in8
Identification of the C4171A mutation in the mitochondrial ND1 gene as causative in one chinese LHON family.Yang J., Zhu Y., Ma X.Cited forNUCLEOTIDE SEQUENCEStrainLHON-008-IV-2CategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)Submission Submitted to EMBL/GenBank/DDBJ databases (APR-2009)Cited in4
A "Copernican" reassessment of the human mitochondrial DNA tree from its root.Behar D.M., van Oven M., Rosset S., Metspalu M., Loogvali E.L., Silva N.M., Kivisild T., Torroni A., Villems R.View abstractCited forNUCLEOTIDE SEQUENCECategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCAm J Hum Genet 90:675-684 (2012)Cited in99+
No title available.Loo J.-H., Trejaut J.A., Yen J.-C., Chen Z.-S., Ng W.-M., Huang C.-Y., Hsu K.-N., Hung K.-H., Hsiao Y.[...], Lin M.Cited forNUCLEOTIDE SEQUENCECategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)Submission Submitted to EMBL/GenBank/DDBJ databases (DEC-2012)Cited in99+
Mitochondrial DNA variant m.15218A>G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus.Soini H.K., Moilanen J.S., Vilmi-Kerala T., Finnila S., Majamaa K.Cited forNUCLEOTIDE SEQUENCECategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)Submission Submitted to EMBL/GenBank/DDBJ databases (MAR-2013)Cited in28
Mitochondrial DNA association study of type 2 diabetes with or without ischemic stroke in Taiwan.Loo J.H., Trejaut J.A., Yen J.C., Chen Z.S., Ng W.M., Huang C.Y., Hsu K.N., Hung K.H., Hsiao Y.[...], Lin M.View abstractCited forNUCLEOTIDE SEQUENCECategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCBMC Res Notes 7:223-223 (2014)Cited in99+
No title available.Afonso C.L., Miller P.J., Scott M.A., Spackman E., Goraichik I., Dimitrov K.M., Suarez D.L., Swayne D.E.Cited forNUCLEOTIDE SEQUENCECategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)Submission Submitted to EMBL/GenBank/DDBJ databases (APR-2017)Cited in199+
Mitochondrial Haplogroups N9 and G Are Associated with Metabolic Syndrome Among Human Immunodeficiency Virus-Infected Patients in China.Zhao D., Ding Y., Lin H., Chen X., Shen W., Gao M., Wei Q., Zhou S., Liu X., He N.View abstractCited forNUCLEOTIDE SEQUENCECategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCAIDS Res Hum Retroviruses 35:536-543 (2019)Cited in99+
Papuan mitochondrial genomes and the settlement of Sahul.Pedro N., Brucato N., Fernandes V., Andre M., Saag L., Pomat W., Besse C., Boland A., Deleuze J.F.[...], Ricaut F.X.View abstractCited forNUCLEOTIDE SEQUENCECategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCJ Hum Genet 65:875-887 (2020)Cited in99+