K. Vinšová

发表

YME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferation

J. Zeman, J. Houštěk, L. Wenchich, 2012, Molecular biology of the cell.

Two patients with clinically distinct manifestation of pyruvate dehydrogenase deficiency due to mutations in PDHA1 gene.

M. Tesařová, J. Zeman, M. Vaněčková, 2011, Prague medical report.

Novel insights into the assembly and function of human nuclear-encoded cytochrome c oxidase subunits 4, 5a, 6a, 7a and 7b.

J. Zeman, H. Hansíková, L. Wenchich, 2010, The Biochemical journal.

Novel insights into the assembly and function of human nuclear-encoded cytochrome c oxidase subunits 4 , 5 a , 6 a , 7 a and 7 b

J. Zeman, H. Hansíková, L. Wenchich, 2010 .

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

M. Tesařová, V. Havlíčková, J. Zeman, 2010, Mitochondrion.

Large copy number variations in combination with point mutations in the TYMP and SCO2 genes found in two patients with mitochondrial disorders

M. Tesařová, H. Kratochvílová, J. Zeman, 2013, European Journal of Human Genetics.

Novel mutations in the tyrosine hydroxylase gene in the first Czech patient with tyrosine hydroxylase deficiency.

M. Tesařová, J. Zeman, T. Honzík, 2012, Prague medical report.

Different laboratory and muscle biopsy findings in a family with an m.8851T>C mutation in the mitochondrial MTATP6 gene.

M. Tesařová, H. Kratochvílová, J. Zeman, 2013, Molecular genetics and metabolism.

Large heterozygous deletions on 22q13.33 in combination with TYMP or SCO2 point mutations in two patients with mitochondrial disorders

M. Tesařová, J. Zeman, V. Stránecký, 2012 .