Citations for
1NDUFS1, NDUFS2, NDUFS4, NDUFS7, NDUFS8
Pathogenetic mechanisms in hereditary dysfunctions of complex I of the respiratory chain in neurological diseases.
Papa S, Petruzzella V, Scacco S, Sardanelli AM, Iuso A, Panelli D, Vitale R, Trentadue R, De Rasmo D, Capitanio N, Piccoli C, Papa F, Scivetti M, Bertini E, Rizza T, De Michele G.
Biochim Biophys Acta 1787(5):502-17. Epub 2009 Jan 10. Review.PMID: 19210954 2009
2NDUFS1, NDUFS2, NDUFS3, NDUFS4, NDUFS5, NDUFS6, NDUFS7, NDUFS8
Sequence analysis of nuclear genes encoding functionally important complex I subunits in children with encephalomyopathy.
Hinttala R, Uusimaa J, Remes AM, Rantala H, Hassinen IE, Majamaa K.
J Mol Med 83(10):786-94. Epub 2005 Sep 3. 2005
3CMTND1, NDUFS2, NDUFS4, NDUFS7, NDUFS8
Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiency.
Ugalde C, Janssen RJ, Van Den Heuvel LP, Smeitink JA, Nijtmans LG.
Hum Mol Genet 13(6):659-67. Epub 2004 Jan 28. 2004
4NDUFS8
YY1 and Sp1 activate transcription of the human NDUFS8 gene encoding the mitochondrial complex I TYKY subunit.
Lescuyer P, Martinez P, Lunardi J.
Biochim Biophys Acta 1574(2):164-74. 2002
5BCS1L, C10orf2, COX10, COX10D, COX17, DSPP, FRDA, MNGIE, NARP, NDUFS1, NDUFS2, NDUFS4, NDUFS7, NDUFS8, NDUFV1, NF1, OPA1, PGL1, PGL2, PGL3, POLG, SCO1, SCO2, SDHA, SDHB, SDHC, SDHD, SLC25A4, SPG7, SURF1, VHL
Nuclear genetic defects of oxidative phosphorylation.
Shoubridge EA.
Hum Mol Genet 10(20):2277-84. Review. 2001
6NDUFA1, NDUFA6, NDUFA7, NDUFB8, NDUFS8
Mapping of the NDUFA2, NDUFA6, NDUFA7, NDUFB8, and NDUFS8 electron transport chain genes by intron based radiation hybrid mapping.
Emahazion T, et al.
Cytogenet Cell Genet 82 : 114. 1998
7NDUFS8
Genomic structure of the human NDUFS8 gene coding for the iron-sulfur TYKY subunit of the mitochondrial NADH : ubiquinone oxidoreductase.
De Sury R, et al.
Gene 215 : 1-10. 1998
8NDUFS8
The first nuclear-encoded complex I mutation in a patient with Leigh syndrome.
Loeffen J, Smeitink J, Triepels R, Smeets R, Schuelke M, Sengers R, Trijbels F, Hamel B, Mullaart R, van den Heuvel L.
Am J Hum Genet 63 : 1598-1608. 1998
9MT-ND1, MT-ND2, MT-ND3, MT-ND4L, MT-ND5, NDUFA10, NDUFA3, NDUFA7, NDUFA9, NDUFB10, NDUFB4, NDUFB5, NDUFB8, NDUFC2, NDUFS1, NDUFS7, NDUFS8, NDUFV2, NDUFV3
cDNA of eight nuclear encoded subunits of NADH:ubiquinone oxidoreductase: human complex I cDNA characterization completed.
Loeffen JL, et al.
Biochem Biophys Res Commun 253(2):415-22. 1998
10NDUFS8
cDNA sequence and chromosomal localization of the NDUFS8 human gene coding for the 23 kDa subunit of the mitochondrial complex I.
Procaccio V, et al.
Biochim Biophys Acta 1351 : 37-41. 1997
11NDUFA2, NDUFA6, NDUFA7, NDUFB8, NDUFS8
In situ hybridisation mapping of genomic clones for five human respiratory chain complex I genes.
Dunbar DR, Shibasaki Y, Dobbie L, Andersson B, Brookes AJ.
Cytogenet Cell Genet 78(1):21-4. 1997