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Genetic defects of cytochrome c oxidase assembly.
Pecina P, Houstková H, Hansíková H, Zeman J, Houstek J. Pecina P, et al. Physiol Res. 2004;53 Suppl 1:S213-23. Physiol Res. 2004. PMID: 15119951 Review.
Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome.
Pecina P, Capková M, Chowdhury SK, Drahota Z, Dubot A, Vojtísková A, Hansíková H, Houst'ková H, Zeman J, Godinot C, Houstek J. Pecina P, et al. Biochim Biophys Acta. 2003 Sep 1;1639(1):53-63. doi: 10.1016/s0925-4439(03)00127-3. Biochim Biophys Acta. 2003. PMID: 12943968
Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochrome c oxidase due to the mtDNA 2 bp microdeletion of TA at positions 9205 and 9206.
Jesina P, Tesarová M, Fornůsková D, Vojtísková A, Pecina P, Kaplanová V, Hansíková H, Zeman J, Houstek J. Jesina P, et al. Among authors: pecina p. Biochem J. 2004 Nov 1;383(Pt. 3):561-71. doi: 10.1042/BJ20040407. Biochem J. 2004. PMID: 15265003 Free PMC article.
Decreased affinity for oxygen of cytochrome-c oxidase in Leigh syndrome caused by SURF1 mutations.
Pecina P, Gnaiger E, Zeman J, Pronicka E, Houstek J. Pecina P, et al. Am J Physiol Cell Physiol. 2004 Nov;287(5):C1384-8. doi: 10.1152/ajpcell.00286.2004. Epub 2004 Jul 21. Am J Physiol Cell Physiol. 2004. PMID: 15269007
Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1.
Stiburek L, Vesela K, Hansikova H, Pecina P, Tesarova M, Cerna L, Houstek J, Zeman J. Stiburek L, et al. Among authors: pecina p. Biochem J. 2005 Dec 15;392(Pt 3):625-32. doi: 10.1042/BJ20050807. Biochem J. 2005. PMID: 16083427 Free PMC article.
Polyunsaturated fatty acids of marine origin upregulate mitochondrial biogenesis and induce beta-oxidation in white fat.
Flachs P, Horakova O, Brauner P, Rossmeisl M, Pecina P, Franssen-van Hal N, Ruzickova J, Sponarova J, Drahota Z, Vlcek C, Keijer J, Houstek J, Kopecky J. Flachs P, et al. Among authors: pecina p. Diabetologia. 2005 Nov;48(11):2365-75. doi: 10.1007/s00125-005-1944-7. Epub 2005 Oct 5. Diabetologia. 2005. PMID: 16205884
Two components in pathogenic mechanism of mitochondrial ATPase deficiency: energy deprivation and ROS production.
Mrácek T, Pecina P, Vojtísková A, Kalous M, Sebesta O, Houstek J. Mrácek T, et al. Among authors: pecina p. Exp Gerontol. 2006 Jul;41(7):683-7. doi: 10.1016/j.exger.2006.02.009. Epub 2006 Apr 3. Exp Gerontol. 2006. PMID: 16581217
Mitochondrial diseases and genetic defects of ATP synthase.
Houstek J, Pícková A, Vojtísková A, Mrácek T, Pecina P, Jesina P. Houstek J, et al. Among authors: pecina p. Biochim Biophys Acta. 2006 Sep-Oct;1757(9-10):1400-5. doi: 10.1016/j.bbabio.2006.04.006. Epub 2006 Apr 19. Biochim Biophys Acta. 2006. PMID: 16730639 Review.
Direct linkage of mitochondrial genome variation to risk factors for type 2 diabetes in conplastic strains.
Pravenec M, Hyakukoku M, Houstek J, Zidek V, Landa V, Mlejnek P, Miksik I, Dudová-Mothejzikova K, Pecina P, Vrbacky M, Drahota Z, Vojtiskova A, Mracek T, Kazdova L, Oliyarnyk O, Wang J, Ho C, Qi N, Sugimoto K, Kurtz T. Pravenec M, et al. Among authors: pecina p. Genome Res. 2007 Sep;17(9):1319-26. doi: 10.1101/gr.6548207. Epub 2007 Aug 10. Genome Res. 2007. PMID: 17693571 Free PMC article.
Isolation of regulatory-competent, phosphorylated cytochrome C oxidase.
Lee I, Salomon AR, Yu K, Samavati L, Pecina P, Pecinova A, Hüttemann M. Lee I, et al. Among authors: pecina p. Methods Enzymol. 2009;457:193-210. doi: 10.1016/S0076-6879(09)05011-3. Methods Enzymol. 2009. PMID: 19426869
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