Zeman J - Search Results

1

Mitochondrial DNA depletion in Alpers syndrome.

Tesarova M, Mayr JA, Wenchich L, Hansikova H, Elleder M, Blahova K, Sperl W, Zeman J. Tesarova M, et al. Among authors: zeman j. Neuropediatrics. 2004 Aug;35(4):217-23. doi: 10.1055/s-2004-821081. Neuropediatrics. 2004. PMID: 15328560

2

Ultrastructural changes of mitochondria in the cultivated skin fibroblasts of patients with point mutations in mitochondrial DNA.

Brantová O, Tesarová M, Hansíková H, Elleder M, Zeman J, Sládková J. Brantová O, et al. Among authors: zeman j. Ultrastruct Pathol. 2006 Jul-Aug;30(4):239-45. doi: 10.1080/01913120600820112. Ultrastruct Pathol. 2006. PMID: 16971348

3

The developmental changes in mitochondrial DNA content per cell in human cord blood leukocytes during gestation.

Pejznochová M, Tesařová M, Honzík T, Hansíková H, Magner M, Zeman J. Pejznochová M, et al. Among authors: zeman j. Physiol Res. 2008;57(6):947-955. doi: 10.33549/physiolres.931246. Epub 2007 Nov 30. Physiol Res. 2008. PMID: 18052680 Free article.

4

Mitochondrial DNA content and expression of genes involved in mtDNA transcription, regulation and maintenance during human fetal development.

Pejznochova M, Tesarova M, Hansikova H, Magner M, Honzik T, Vinsova K, Hajkova Z, Havlickova V, Zeman J. Pejznochova M, et al. Among authors: zeman j. Mitochondrion. 2010 Jun;10(4):321-9. doi: 10.1016/j.mito.2010.01.006. Epub 2010 Jan 20. Mitochondrion. 2010. PMID: 20096380

5

Mitochondrial energy metabolism in very premature neonates.

Wenchich L, Zeman J, Hansíková H, Plavka R, Sperl W, Houstek J. Wenchich L, et al. Among authors: zeman j. Biol Neonate. 2002;81(4):229-35. doi: 10.1159/000056753. Biol Neonate. 2002. PMID: 12011566

6

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.

7

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: zeman j. Biochem J. 2005 Dec 15;392(Pt 3):625-32. doi: 10.1042/BJ20050807. Biochem J. 2005. PMID: 16083427 Free PMC article.

8

Activities of respiratory chain complexes in isolated platelets in females with anorexia nervosa.

Böhm M, Papezova H, Hansikova H, Wenchich L, Zeman J. Böhm M, et al. Among authors: zeman j. Int J Eat Disord. 2007 Nov;40(7):659-63. doi: 10.1002/eat.20403. Int J Eat Disord. 2007. PMID: 17584871

9

Knockdown of human Oxa1l impairs the biogenesis of F1Fo-ATP synthase and NADH:ubiquinone oxidoreductase.

Stiburek L, Fornuskova D, Wenchich L, Pejznochova M, Hansikova H, Zeman J. Stiburek L, et al. Among authors: zeman j. J Mol Biol. 2007 Nov 23;374(2):506-16. doi: 10.1016/j.jmb.2007.09.044. Epub 2007 Sep 20. J Mol Biol. 2007. PMID: 17936786

10

Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated F1Fo ATP synthase deficiency.

Cízková A, Stránecký V, Ivánek R, Hartmannová H, Nosková L, Piherová L, Tesarová M, Hansíková H, Honzík T, Zeman J, Divina P, Potocká A, Paul J, Sperl W, Mayr JA, Seneca S, Houstĕk J, Kmoch S. Cízková A, et al. Among authors: zeman j. BMC Genomics. 2008 Jan 25;9:38. doi: 10.1186/1471-2164-9-38. BMC Genomics. 2008. PMID: 18221507 Free PMC article.

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