Zeman J - Search Results

1

Mitochondrial membrane potential and ATP production in primary disorders of ATP synthase.

Vojtísková A, Jesina P, Kalous M, Kaplanová V, Houstek J, Tesarová M, Fornůsková D, Zeman J, Dubot A, Godinot C. Vojtísková A, et al. Among authors: zeman j. Toxicol Mech Methods. 2004;14(1-2):7-11. doi: 10.1080/15376520490257347. Toxicol Mech Methods. 2004. PMID: 20021115

2

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: zeman j. Biochem J. 2004 Nov 1;383(Pt. 3):561-71. doi: 10.1042/BJ20040407. Biochem J. 2004. PMID: 15265003 Free PMC article.

3

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. Among authors: zeman j. Biochim Biophys Acta. 2003 Sep 1;1639(1):53-63. doi: 10.1016/s0925-4439(03)00127-3. Biochim Biophys Acta. 2003. PMID: 12943968 Free article.

4

Mitochondrial diseases and ATPase defects of nuclear origin.

Houstek J, Mrácek T, Vojtísková A, Zeman J. Houstek J, et al. Among authors: zeman j. Biochim Biophys Acta. 2004 Jul 23;1658(1-2):115-21. doi: 10.1016/j.bbabio.2004.04.012. Biochim Biophys Acta. 2004. PMID: 15282182 Free article. Review.

5

The impact of mitochondrial tRNA mutations on the amount of ATP synthase differs in the brain compared to other tissues.

Fornuskova D, Brantova O, Tesarova M, Stiburek L, Honzik T, Wenchich L, Tietzeova E, Hansikova H, Zeman J. Fornuskova D, et al. Among authors: zeman j. Biochim Biophys Acta. 2008 May;1782(5):317-25. doi: 10.1016/j.bbadis.2008.02.001. Epub 2008 Feb 15. Biochim Biophys Acta. 2008. PMID: 18319067 Free article.

6

TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy.

Cízková A, Stránecký V, Mayr JA, Tesarová M, Havlícková V, Paul J, Ivánek R, Kuss AW, Hansíková H, Kaplanová V, Vrbacký M, Hartmannová H, Nosková L, Honzík T, Drahota Z, Magner M, Hejzlarová K, Sperl W, Zeman J, Houstek J, Kmoch S. Cízková A, et al. Among authors: zeman j. Nat Genet. 2008 Nov;40(11):1288-90. doi: 10.1038/ng.246. Epub 2008 Oct 26. Nat Genet. 2008. PMID: 18953340

7

TMEM70 protein - a novel ancillary factor of mammalian ATP synthase.

Houstek J, Kmoch S, Zeman J. Houstek J, et al. Among authors: zeman j. Biochim Biophys Acta. 2009 May;1787(5):529-32. doi: 10.1016/j.bbabio.2008.11.013. Epub 2008 Dec 6. Biochim Biophys Acta. 2009. PMID: 19103153 Free article.

8

Reply to Comment on: Sideroblastic anemia associated with multisystem mitochondrial disorders.

Tesarova M, Zeman J. Tesarova M, et al. Among authors: zeman j. Pediatr Blood Cancer. 2019 Dec;66(12):e28007. doi: 10.1002/pbc.28007. Epub 2019 Sep 18. Pediatr Blood Cancer. 2019. PMID: 31535449 No abstract available.

9

[Hereditary disorders of mitochondrial ATP synthase].

Houstĕk J, Zeman J. Houstĕk J, et al. Among authors: zeman j. Cas Lek Cesk. 2004;143(8):517-20. Cas Lek Cesk. 2004. PMID: 15446454 Review. Czech.

10

Clinical Heterogeneity, Tissue Distribution, and Intergenerational Segregation of mtDNA Mutation A3243G.

Tesarova M, Hansikova H, Kytnarova J, Houstkova H, Bohm M, Cerna L, Zeman J, Houstek J. Tesarova M, et al. Among authors: zeman j. Toxicol Mech Methods. 2004;14(1-2):79-84. doi: 10.1080/15376520490257527. Toxicol Mech Methods. 2004. PMID: 20021128

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