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J Houstek

Showing results (21-30 of 36) with videos related to

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Physiological Research|February 19, 2005
Tert-butyl hydroperoxide selectively inhibits mitochondrial respiratory-chain enzymes in isolated rat hepatocytesZ Drahota, P Kriváková, Z Cervinková, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 27, 2004
Clinical, biochemical and molecular analyses of six patients with isolated cytochrome c oxidase deficiency due to mutations in the SCO2 geneK Vesela, H Hansikova, M Tesarova, et al.
Biochimica Et Biophysica Acta|July 26, 2005
Time-course of hormonal induction of mitochondrial glycerophosphate dehydrogenase biogenesis in rat liverT Mrácek, P Jesina, P Kriváková, et al.
Biochemistry and Molecular Biology International|December 1, 1993
Deficiency of pyruvate dehydrogenase complex in tissues of an eight month old infantH Hansikova, J Zeman, P Klement, et al.
Placenta|June 14, 2005
Specific properties of heavy fraction of mitochondria from human-term placenta - glycerophosphate-dependent hydrogen peroxide productionT Honzík, Z Drahota, M Böhm, et al.
Toxicology Mechanisms and Methods|December 22, 2009
Clinical Heterogeneity, Tissue Distribution, and Intergenerational Segregation of mtDNA Mutation A3243GM Tesarova, H Hansikova, J Kytnarova, et al.
Molecular Genetics and Metabolism|August 18, 2001
A novel mutation in SURF1 causes skipping of exon 8 in a patient with cytochrome c oxidase-deficient leigh syndrome and hypertrichosisS L Williams, J W Taanman, H Hansíková, et al.
Prenatal Diagnosis|July 23, 1999
Complex approach to prenatal diagnosis of cytochrome c oxidase deficienciesJ Houstek, P Klement, J Hermanská, et al.
Pediatric Research|December 13, 1997
Tissue metabolism and plasma levels of thyroid hormones in critically ill very premature infantsS Pavelka, P Kopecký, B Bendlová, et al.
The Biochemical Journal|September 8, 1999
Defective kinetics of cytochrome c oxidase and alteration of mitochondrial membrane potential in fibroblasts and cytoplasmic hybrid cells with the mutation for myoclonus epilepsy with ragged-red fibres ('MERRF') at position 8344 ntH Antonická, D Floryk, P Klement, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Physiological Research|February 19, 2005
Tert-butyl hydroperoxide selectively inhibits mitochondrial respiratory-chain enzymes in isolated rat hepatocytesZ Drahota, P Kriváková, Z Cervinková, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 27, 2004
Clinical, biochemical and molecular analyses of six patients with isolated cytochrome c oxidase deficiency due to mutations in the SCO2 geneK Vesela, H Hansikova, M Tesarova, et al.
Biochimica Et Biophysica Acta|July 26, 2005
Time-course of hormonal induction of mitochondrial glycerophosphate dehydrogenase biogenesis in rat liverT Mrácek, P Jesina, P Kriváková, et al.
Biochemistry and Molecular Biology International|December 1, 1993
Deficiency of pyruvate dehydrogenase complex in tissues of an eight month old infantH Hansikova, J Zeman, P Klement, et al.
Placenta|June 14, 2005
Specific properties of heavy fraction of mitochondria from human-term placenta - glycerophosphate-dependent hydrogen peroxide productionT Honzík, Z Drahota, M Böhm, et al.
Toxicology Mechanisms and Methods|December 22, 2009
Clinical Heterogeneity, Tissue Distribution, and Intergenerational Segregation of mtDNA Mutation A3243GM Tesarova, H Hansikova, J Kytnarova, et al.
Molecular Genetics and Metabolism|August 18, 2001
A novel mutation in SURF1 causes skipping of exon 8 in a patient with cytochrome c oxidase-deficient leigh syndrome and hypertrichosisS L Williams, J W Taanman, H Hansíková, et al.
Prenatal Diagnosis|July 23, 1999
Complex approach to prenatal diagnosis of cytochrome c oxidase deficienciesJ Houstek, P Klement, J Hermanská, et al.
Pediatric Research|December 13, 1997
Tissue metabolism and plasma levels of thyroid hormones in critically ill very premature infantsS Pavelka, P Kopecký, B Bendlová, et al.
The Biochemical Journal|September 8, 1999
Defective kinetics of cytochrome c oxidase and alteration of mitochondrial membrane potential in fibroblasts and cytoplasmic hybrid cells with the mutation for myoclonus epilepsy with ragged-red fibres ('MERRF') at position 8344 ntH Antonická, D Floryk, P Klement, et al.
Pageof 4