- MT-ND2
NADH dehydrogenase subunit 2, also known as ND2, is a human
gene .PBB_Summary
section_title =
summary_text =Further reading
PBB_Further_reading
citations =
*cite journal | author=Torroni A, Achilli A, Macaulay V, "et al." |title=Harvesting the fruit of the human mtDNA tree. |journal=Trends Genet. |volume=22 |issue= 6 |pages= 339–45 |year= 2006 |pmid= 16678300 |doi= 10.1016/j.tig.2006.04.001
*cite journal | author=Bodenteich A, Mitchell LG, Polymeropoulos MH, Merril CR |title=Dinucleotide repeat in the human mitochondrial D-loop. |journal=Hum. Mol. Genet. |volume=1 |issue= 2 |pages= 140 |year= 1993 |pmid= 1301157 |doi=
*cite journal | author=Lin FH, Lin R, Wisniewski HM, "et al." |title=Detection of point mutations in codon 331 of mitochondrial NADH dehydrogenase subunit 2 in Alzheimer's brains. |journal=Biochem. Biophys. Res. Commun. |volume=182 |issue= 1 |pages= 238–46 |year= 1992 |pmid= 1370613 |doi=
*cite journal | author=Lu X, Walker T, MacManus JP, Seligy VL |title=Differentiation of HT-29 human colonic adenocarcinoma cells correlates with increased expression of mitochondrial RNA: effects of trehalose on cell growth and maturation. |journal=Cancer Res. |volume=52 |issue= 13 |pages= 3718–25 |year= 1992 |pmid= 1377597 |doi=
*cite journal | author=Brown MD, Voljavec AS, Lott MT, "et al." |title=Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy. |journal=Genetics |volume=130 |issue= 1 |pages= 163–73 |year= 1992 |pmid= 1732158 |doi=
*cite journal | author=Marzuki S, Noer AS, Lertrit P, "et al." |title=Normal variants of human mitochondrial DNA and translation products: the building of a reference data base. |journal=Hum. Genet. |volume=88 |issue= 2 |pages= 139–45 |year= 1992 |pmid= 1757091 |doi=
*cite journal | author=Johns DR, Berman J |title=Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy. |journal=Biochem. Biophys. Res. Commun. |volume=174 |issue= 3 |pages= 1324–30 |year= 1991 |pmid= 1900003 |doi=
*cite journal | author=Moraes CT, Andreetta F, Bonilla E, "et al." |title=Replication-competent human mitochondrial DNA lacking the heavy-strand promoter region. |journal=Mol. Cell. Biol. |volume=11 |issue= 3 |pages= 1631–7 |year= 1991 |pmid= 1996112 |doi=
*cite journal | author=Attardi G, Chomyn A, Doolittle RF, "et al." |title=Seven unidentified reading frames of human mitochondrial DNA encode subunits of the respiratory chain NADH dehydrogenase. |journal=Cold Spring Harb. Symp. Quant. Biol. |volume=51 Pt 1 |issue= |pages= 103–14 |year= 1987 |pmid= 3472707 |doi=
*cite journal | author=Chomyn A, Cleeter MW, Ragan CI, "et al." |title=URF6, last unidentified reading frame of human mtDNA, codes for an NADH dehydrogenase subunit. |journal=Science |volume=234 |issue= 4776 |pages= 614–8 |year= 1986 |pmid= 3764430 |doi=
*cite journal | author=Chomyn A, Mariottini P, Cleeter MW, "et al." |title=Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase. |journal=Nature |volume=314 |issue= 6012 |pages= 592–7 |year= 1985 |pmid= 3921850 |doi=
*cite journal | author=Sanger F, Coulson AR, Barrell BG, "et al." |title=Cloning in single-stranded bacteriophage as an aid to rapid DNA sequencing. |journal=J. Mol. Biol. |volume=143 |issue= 2 |pages= 161–78 |year= 1981 |pmid= 6260957 |doi=
*cite journal | author=Anderson S, Bankier AT, Barrell BG, "et al." |title=Sequence and organization of the human mitochondrial genome. |journal=Nature |volume=290 |issue= 5806 |pages= 457–65 |year= 1981 |pmid= 7219534 |doi=
*cite journal | author=Montoya J, Ojala D, Attardi G |title=Distinctive features of the 5'-terminal sequences of the human mitochondrial mRNAs. |journal=Nature |volume=290 |issue= 5806 |pages= 465–70 |year= 1981 |pmid= 7219535 |doi=
*cite journal | author=Horai S, Hayasaka K, Kondo R, "et al." |title=Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=92 |issue= 2 |pages= 532–6 |year= 1995 |pmid= 7530363 |doi=
*cite journal | author=Rieder MJ, Taylor SL, Tobe VO, Nickerson DA |title=Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome. |journal=Nucleic Acids Res. |volume=26 |issue= 4 |pages= 967–73 |year= 1998 |pmid= 9461455 |doi=
*cite journal | author=Wise CA, Sraml M, Easteal S |title=Departure from neutrality at the mitochondrial NADH dehydrogenase subunit 2 gene in humans, but not in chimpanzees. |journal=Genetics |volume=148 |issue= 1 |pages= 409–21 |year= 1998 |pmid= 9475751 |doi=
*cite journal | author=Andrews RM, Kubacka I, Chinnery PF, "et al." |title=Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA. |journal=Nat. Genet. |volume=23 |issue= 2 |pages= 147 |year= 1999 |pmid= 10508508 |doi= 10.1038/13779
*cite journal | author=Ingman M, Kaessmann H, Pääbo S, Gyllensten U |title=Mitochondrial genome variation and the origin of modern humans. |journal=Nature |volume=408 |issue= 6813 |pages= 708–13 |year= 2001 |pmid= 11130070 |doi= 10.1038/35047064
*cite journal | author=Finnilä S, Lehtonen MS, Majamaa K |title=Phylogenetic network for European mtDNA. |journal=Am. J. Hum. Genet. |volume=68 |issue= 6 |pages= 1475–84 |year= 2001 |pmid= 11349229 |doi=PBB_Controls
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