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Page 1
Primary and secondary CoQ(10) deficiencies in humans.
Quinzii CM, Hirano M. Quinzii CM, et al. Biofactors. 2011 Sep-Oct;37(5):361-5. doi: 10.1002/biof.155. Epub 2011 Oct 11. Biofactors. 2011. PMID: 21990098 Free PMC article. Review.
Extensive screening system using suspension array technology to detect mitochondrial DNA point mutations.
Nishigaki Y, Ueno H, Coku J, Koga Y, Fujii T, Sahashi K, Nakano K, Yoneda M, Nonaka M, Tang L, Liou CW, Paquis-Flucklinger V, Harigaya Y, Ibi T, Goto Y, Hosoya H, DiMauro S, Hirano M, Tanaka M. Nishigaki Y, et al. Mitochondrion. 2010 Apr;10(3):300-8. doi: 10.1016/j.mito.2010.01.003. Epub 2010 Jan 11. Mitochondrion. 2010. PMID: 20064630 Free PMC article.
Nuclear genome transfer in human oocytes eliminates mitochondrial DNA variants.
Paull D, Emmanuele V, Weiss KA, Treff N, Stewart L, Hua H, Zimmer M, Kahler DJ, Goland RS, Noggle SA, Prosser R, Hirano M, Sauer MV, Egli D. Paull D, et al. Nature. 2013 Jan 31;493(7434):632-7. doi: 10.1038/nature11800. Epub 2012 Dec 19. Nature. 2013. PMID: 23254936 Free PMC article.
27 results