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Genetic Complementation of ATP Synthase Deficiency Due to Dysfunction of TMEM70 Assembly Factor in Rat.
Marković A, Tauchmannová K, Šimáková M, Mlejnek P, Kaplanová V, Pecina P, Pecinová A, Papoušek F, Liška F, Šilhavý J, Mikešová J, Neckář J, Houštěk J, Pravenec M, Mráček T. Marković A, et al. Among authors: pecina p. Biomedicines. 2022 Jan 26;10(2):276. doi: 10.3390/biomedicines10020276. Biomedicines. 2022. PMID: 35203486 Free PMC article.
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 Free article. Review.
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 Free article. 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.
48 results