Tesarova M - Search Results

1

A novel insertion of a rearranged L1 element in exon 44 of the dystrophin gene: further evidence for possible bias in retroposon integration.

Musova Z, Hedvicakova P, Mohrmann M, Tesarova M, Krepelova A, Zeman J, Sedlacek Z. Musova Z, et al. Among authors: tesarova m. Biochem Biophys Res Commun. 2006 Aug 18;347(1):145-9. doi: 10.1016/j.bbrc.2006.06.071. Epub 2006 Jun 21. Biochem Biophys Res Commun. 2006. PMID: 16808900

2

Case report: A rare variant m.4135T>C in the MT-ND1 gene leads to Leber hereditary optic neuropathy and altered respiratory chain supercomplexes.

Rákosníková T, Kelifová S, Štufková H, Lokvencová K, Lišková P, Kousal B, Honzík T, Hansíková H, Martínek V, Tesařová M. Rákosníková T, et al. Among authors: tesarova m. Front Genet. 2023 May 18;14:1182288. doi: 10.3389/fgene.2023.1182288. eCollection 2023. Front Genet. 2023. PMID: 37274791 Free PMC article.

3

Polarographic evaluation of mitochondrial enzymes activity in isolated mitochondria and in permeabilized human muscle cells with inherited mitochondrial defects.

Wenchich L, Drahota Z, Honzík T, Hansíková H, Tesarová M, Zeman J, Houstek J. Wenchich L, et al. Among authors: tesarova m. Physiol Res. 2003;52(6):781-8. Physiol Res. 2003. PMID: 14640901 Free article.

4

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

5

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. Neuropediatrics. 2004 Aug;35(4):217-23. doi: 10.1055/s-2004-821081. Neuropediatrics. 2004. PMID: 15328560

6

Clinical, biochemical and molecular analyses of six patients with isolated cytochrome c oxidase deficiency due to mutations in the SCO2 gene.

Vesela K, Hansikova H, Tesarova M, Martasek P, Elleder M, Houstek J, Zeman J. Vesela K, et al. Among authors: tesarova m. Acta Paediatr. 2004 Oct;93(10):1312-7. doi: 10.1080/08035250410008761. Acta Paediatr. 2004. PMID: 15499950

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

8

Retrospective, multicentric study of 180 children with cytochrome C oxidase deficiency.

Böhm M, Pronicka E, Karczmarewicz E, Pronicki M, Piekutowska-Abramczuk D, Sykut-Cegielska J, Mierzewska H, Hansikova H, Vesela K, Tesarova M, Houstkova H, Houstek J, Zeman J. Böhm M, et al. Among authors: tesarova m. Pediatr Res. 2006 Jan;59(1):21-6. doi: 10.1203/01.pdr.0000190572.68191.13. Epub 2005 Dec 2. Pediatr Res. 2006. PMID: 16326995

9

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: tesarova m. Ultrastruct Pathol. 2006 Jul-Aug;30(4):239-45. doi: 10.1080/01913120600820112. Ultrastruct Pathol. 2006. PMID: 16971348

10

Biogenesis of eukaryotic cytochrome c oxidase.

Stiburek L, Hansikova H, Tesarova M, Cerna L, Zeman J. Stiburek L, et al. Among authors: tesarova m. Physiol Res. 2006;55 Suppl 2:S27-41. doi: 10.33549/physiolres.930000.55.S2.27. Physiol Res. 2006. PMID: 17298220 Free article. Review.

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