McKenzie M - Search Results

1

Deletion of the Complex I Subunit NDUFS4 Adversely Modulates Cellular Differentiation.

Johnson J, Lee W, Frazier AE, Vaghjiani V, Laskowski A, Rodriguez AL, Cagnone GL, McKenzie M, White SJ, Nisbet DR, Thorburn DR, St John JC. Johnson J, et al. Among authors: mckenzie m. Stem Cells Dev. 2016 Feb 1;25(3):239-50. doi: 10.1089/scd.2015.0211. Epub 2016 Jan 7. Stem Cells Dev. 2016. PMID: 26608563

2

Mitochondrial respiratory chain supercomplexes are destabilized in Barth Syndrome patients.

McKenzie M, Lazarou M, Thorburn DR, Ryan MT. McKenzie M, et al. J Mol Biol. 2006 Aug 18;361(3):462-9. doi: 10.1016/j.jmb.2006.06.057. Epub 2006 Jul 5. J Mol Biol. 2006. PMID: 16857210

3

Analysis of mitochondrial subunit assembly into respiratory chain complexes using Blue Native polyacrylamide gel electrophoresis.

McKenzie M, Lazarou M, Thorburn DR, Ryan MT. McKenzie M, et al. Anal Biochem. 2007 May 15;364(2):128-37. doi: 10.1016/j.ab.2007.02.022. Epub 2007 Feb 24. Anal Biochem. 2007. PMID: 17391635

4

Analysis of the assembly profiles for mitochondrial- and nuclear-DNA-encoded subunits into complex I.

Lazarou M, McKenzie M, Ohtake A, Thorburn DR, Ryan MT. Lazarou M, et al. Among authors: mckenzie m. Mol Cell Biol. 2007 Jun;27(12):4228-37. doi: 10.1128/MCB.00074-07. Epub 2007 Apr 16. Mol Cell Biol. 2007. PMID: 17438127 Free PMC article.

5

Human CIA30 is involved in the early assembly of mitochondrial complex I and mutations in its gene cause disease.

Dunning CJ, McKenzie M, Sugiana C, Lazarou M, Silke J, Connelly A, Fletcher JM, Kirby DM, Thorburn DR, Ryan MT. Dunning CJ, et al. Among authors: mckenzie m. EMBO J. 2007 Jul 11;26(13):3227-37. doi: 10.1038/sj.emboj.7601748. Epub 2007 Jun 7. EMBO J. 2007. PMID: 17557076 Free PMC article.

6

Assembly of mitochondrial complex I and defects in disease.

Lazarou M, Thorburn DR, Ryan MT, McKenzie M. Lazarou M, et al. Among authors: mckenzie m. Biochim Biophys Acta. 2009 Jan;1793(1):78-88. doi: 10.1016/j.bbamcr.2008.04.015. Epub 2008 May 4. Biochim Biophys Acta. 2009. PMID: 18501715 Free article. Review.

7

Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease.

Sugiana C, Pagliarini DJ, McKenzie M, Kirby DM, Salemi R, Abu-Amero KK, Dahl HH, Hutchison WM, Vascotto KA, Smith SM, Newbold RF, Christodoulou J, Calvo S, Mootha VK, Ryan MT, Thorburn DR. Sugiana C, et al. Among authors: mckenzie m. Am J Hum Genet. 2008 Oct;83(4):468-78. doi: 10.1016/j.ajhg.2008.09.009. Am J Hum Genet. 2008. PMID: 18940309 Free PMC article.

8

Assembly of nuclear DNA-encoded subunits into mitochondrial complex IV, and their preferential integration into supercomplex forms in patient mitochondria.

Lazarou M, Smith SM, Thorburn DR, Ryan MT, McKenzie M. Lazarou M, et al. Among authors: mckenzie m. FEBS J. 2009 Nov;276(22):6701-13. doi: 10.1111/j.1742-4658.2009.07384.x. Epub 2009 Oct 16. FEBS J. 2009. PMID: 19843159 Free article.

9

Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia--MLASA syndrome.

Riley LG, Cooper S, Hickey P, Rudinger-Thirion J, McKenzie M, Compton A, Lim SC, Thorburn D, Ryan MT, Giegé R, Bahlo M, Christodoulou J. Riley LG, et al. Among authors: mckenzie m. Am J Hum Genet. 2010 Jul 9;87(1):52-9. doi: 10.1016/j.ajhg.2010.06.001. Am J Hum Genet. 2010. PMID: 20598274 Free PMC article.

10

Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation.

Tucker EJ, Hershman SG, Köhrer C, Belcher-Timme CA, Patel J, Goldberger OA, Christodoulou J, Silberstein JM, McKenzie M, Ryan MT, Compton AG, Jaffe JD, Carr SA, Calvo SE, RajBhandary UL, Thorburn DR, Mootha VK. Tucker EJ, et al. Among authors: mckenzie m. Cell Metab. 2011 Sep 7;14(3):428-34. doi: 10.1016/j.cmet.2011.07.010. Cell Metab. 2011. PMID: 21907147 Free PMC article.

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