Selak M - Search Results

1

Primary coenzyme Q deficiency in Pdss2 mutant mice causes isolated renal disease.

Peng M, Falk MJ, Haase VH, King R, Polyak E, Selak M, Yudkoff M, Hancock WW, Meade R, Saiki R, Lunceford AL, Clarke CF, Gasser DL. Peng M, et al. Among authors: selak m. PLoS Genet. 2008 Apr 25;4(4):e1000061. doi: 10.1371/journal.pgen.1000061. PLoS Genet. 2008. PMID: 18437205 Free PMC article.

2

Hypoxia-inducible factor 2 regulates hepatic lipid metabolism.

Rankin EB, Rha J, Selak MA, Unger TL, Keith B, Liu Q, Haase VH. Rankin EB, et al. Mol Cell Biol. 2009 Aug;29(16):4527-38. doi: 10.1128/MCB.00200-09. Epub 2009 Jun 15. Mol Cell Biol. 2009. PMID: 19528226 Free PMC article.

3

Mitochondrial DNA variant in COX1 subunit significantly alters energy metabolism of geographically divergent wild isolates in Caenorhabditis elegans.

Dingley SD, Polyak E, Ostrovsky J, Srinivasan S, Lee I, Rosenfeld AB, Tsukikawa M, Xiao R, Selak MA, Coon JJ, Hebert AS, Grimsrud PA, Kwon YJ, Pagliarini DJ, Gai X, Schurr TG, Hüttemann M, Nakamaru-Ogiso E, Falk MJ. Dingley SD, et al. Among authors: selak ma. J Mol Biol. 2014 May 29;426(11):2199-216. doi: 10.1016/j.jmb.2014.02.009. Epub 2014 Feb 14. J Mol Biol. 2014. PMID: 24534730 Free PMC article.

4

Dynamic regulation of metabolism and respiration by endogenously produced nitric oxide protects against oxidative stress.

Paxinou E, Weisse M, Chen Q, Souza JM, Hertkorn C, Selak M, Daikhin E, Yudkoff M, Sowa G, Sessa WC, Ischiropoulos H. Paxinou E, et al. Among authors: selak m. Proc Natl Acad Sci U S A. 2001 Sep 25;98(20):11575-80. doi: 10.1073/pnas.201293198. Epub 2001 Sep 18. Proc Natl Acad Sci U S A. 2001. PMID: 11562476 Free PMC article.

5

Mitochondrial activity in Pompe's disease.

Selak MA, de Chadarevian JP, Melvin JJ, Grover WD, Salganicoff L, Kaye EM. Selak MA, et al. Pediatr Neurol. 2000 Jul;23(1):54-7. doi: 10.1016/s0887-8994(00)00145-4. Pediatr Neurol. 2000. PMID: 10963971

6

Mechanisms underlying metabolic and neural defects in zebrafish and human multiple acyl-CoA dehydrogenase deficiency (MADD).

Song Y, Selak MA, Watson CT, Coutts C, Scherer PC, Panzer JA, Gibbs S, Scott MO, Willer G, Gregg RG, Ali DW, Bennett MJ, Balice-Gordon RJ. Song Y, et al. PLoS One. 2009 Dec 17;4(12):e8329. doi: 10.1371/journal.pone.0008329. PLoS One. 2009. PMID: 20020044 Free PMC article.

7

Impaired oxidative phosphorylation in hepatic mitochondria in growth-retarded rats.

Peterside IE, Selak MA, Simmons RA. Peterside IE, et al. Am J Physiol Endocrinol Metab. 2003 Dec;285(6):E1258-66. doi: 10.1152/ajpendo.00437.2002. Am J Physiol Endocrinol Metab. 2003. PMID: 14607783 Free article.

8

Erythroid dysplasia, megaloblastic anemia, and impaired lymphopoiesis arising from mitochondrial dysfunction.

Chen ML, Logan TD, Hochberg ML, Shelat SG, Yu X, Wilding GE, Tan W, Kujoth GC, Prolla TA, Selak MA, Kundu M, Carroll M, Thompson JE. Chen ML, et al. Among authors: selak ma. Blood. 2009 Nov 5;114(19):4045-53. doi: 10.1182/blood-2008-08-169474. Epub 2009 Sep 4. Blood. 2009. PMID: 19734452 Free PMC article.

9

Progressive accumulation of mitochondrial DNA mutations and decline in mitochondrial function lead to beta-cell failure.

Simmons RA, Suponitsky-Kroyter I, Selak MA. Simmons RA, et al. J Biol Chem. 2005 Aug 5;280(31):28785-91. doi: 10.1074/jbc.M505695200. Epub 2005 Jun 9. J Biol Chem. 2005. PMID: 15946949 Free article.

10

Blood cells from Friedreich ataxia patients harbor frataxin deficiency without a loss of mitochondrial function.

Selak MA, Lyver E, Micklow E, Deutsch EC, Onder O, Selamoglu N, Yager C, Knight S, Carroll M, Daldal F, Dancis A, Lynch DR, Sarry JE. Selak MA, et al. Mitochondrion. 2011 Mar;11(2):342-50. doi: 10.1016/j.mito.2010.12.003. Epub 2010 Dec 13. Mitochondrion. 2011. PMID: 21147271 Free PMC article.

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