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J Zeman

Showing results (221-230 of 311) with videos related to

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Human Mutation|July 5, 2001
Eight novel ABCD1 gene mutations and three polymorphisms in patients with X-linked adrenoleukodystrophy: The first polymorphism causing an amino acid exchangeL Dvoráková, G Storkánová, G Unterrainer, et al.
Infection|June 9, 2005
Epidemiology of severe sepsis in intensive care units in the Slovak RepublicR Záhorec, J Firment, J Straková, et al.
Ceskoslovenska Pediatrie|October 1, 1993
[Metabolic study in a child with Leigh's syndrome and deficient activity in complex I of the respiratory chain]J Zeman, P Klement, H Houst'ková, et al.
Folia Biologica|January 7, 2020
Stable COX17 Downregulation Leads to Alterations in Mitochondrial Ultrastructure, Decreased Copper Content and Impaired Cytochrome c Oxidase Biogenesis in HEK293 CellsM Vanišová, D Burská, J Křížová, et al.
Casopis Lekaru Ceskych|September 26, 2006
[Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)]T Honzík, M Tesarová, H Hansíková, et al.
Early Human Development|August 19, 2007
Activities of respiratory chain complexes and pyruvate dehydrogenase in isolated muscle mitochondria in premature neonatesT Honzik, L Wenchich, M Böhm, et al.
Biochimica Et Biophysica Acta|June 9, 1995
Altered properties of mitochondrial ATP-synthase in patients with a T-->G mutation in the ATPase 6 (subunit a) gene at position 8993 of mtDNAJ Houstĕk, P Klement, J Hermanská, et al.
Ceskoslovenska Pediatrie|November 1, 1990
[Non-ketotic hyperglycinemia]J Zeman, V Kozich, S Stastná, et al.
Ceskoslovenska Pediatrie|March 1, 1990
[Pneumococcal infectious endocarditis in an infant (case report)]Z Urbanová, J Zeman, J Skovránek, et al.
Ceskoslovenska Pediatrie|July 1, 1985
[Cystathioninuria]H Houst'ková, J Zeman, J Hyánek, et al.
Pageof 32

Showing results (221-230 of 311) with videos related to

Sort By:
Pageof 32
Human Mutation|July 5, 2001
Eight novel ABCD1 gene mutations and three polymorphisms in patients with X-linked adrenoleukodystrophy: The first polymorphism causing an amino acid exchangeL Dvoráková, G Storkánová, G Unterrainer, et al.
Infection|June 9, 2005
Epidemiology of severe sepsis in intensive care units in the Slovak RepublicR Záhorec, J Firment, J Straková, et al.
Ceskoslovenska Pediatrie|October 1, 1993
[Metabolic study in a child with Leigh's syndrome and deficient activity in complex I of the respiratory chain]J Zeman, P Klement, H Houst'ková, et al.
Folia Biologica|January 7, 2020
Stable COX17 Downregulation Leads to Alterations in Mitochondrial Ultrastructure, Decreased Copper Content and Impaired Cytochrome c Oxidase Biogenesis in HEK293 CellsM Vanišová, D Burská, J Křížová, et al.
Casopis Lekaru Ceskych|September 26, 2006
[Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)]T Honzík, M Tesarová, H Hansíková, et al.
Early Human Development|August 19, 2007
Activities of respiratory chain complexes and pyruvate dehydrogenase in isolated muscle mitochondria in premature neonatesT Honzik, L Wenchich, M Böhm, et al.
Biochimica Et Biophysica Acta|June 9, 1995
Altered properties of mitochondrial ATP-synthase in patients with a T-->G mutation in the ATPase 6 (subunit a) gene at position 8993 of mtDNAJ Houstĕk, P Klement, J Hermanská, et al.
Ceskoslovenska Pediatrie|November 1, 1990
[Non-ketotic hyperglycinemia]J Zeman, V Kozich, S Stastná, et al.
Ceskoslovenska Pediatrie|March 1, 1990
[Pneumococcal infectious endocarditis in an infant (case report)]Z Urbanová, J Zeman, J Skovránek, et al.
Ceskoslovenska Pediatrie|July 1, 1985
[Cystathioninuria]H Houst'ková, J Zeman, J Hyánek, et al.
Pageof 32