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Dominique Chretien

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Current Medicinal Chemistry|February 3, 2004
Revisiting pitfalls, problems and tentative solutions for assaying mitochondrial respiratory chain complex III in human samplesDominique Chretien, Abdelhamid Slama, Jean-Jacques Brière, et al.
Journal of Hepatology|July 12, 2011
Mutation in the mitochondrial translation elongation factor EFTs results in severe infantile liver failureVanessa Vedrenne, Louise Galmiche, Dominique Chretien, et al.
Molecular Genetics and Metabolism|February 6, 2008
Mitochondrial respiratory chain complex assembly and function during human fetal developmentLimor Minai, Jelena Martinovic, Dominique Chretien, et al.
Biochemical and Biophysical Research Communications|January 22, 2003
Assay of mitochondrial respiratory chain complex I in human lymphocytes and cultured skin fibroblastsDominique Chretien, Paule Bénit, Marie Chol, et al.
American Journal of Medical Genetics. Part A|December 8, 2006
A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystoniaEmmanuelle Sarzi, Michael D Brown, Sophie Lebon, et al.
BMC Biochemistry|November 5, 2003
Mitochondrial activities in human cultured skin fibroblasts contaminated by Mycoplasma hyorhinisNiklas Darin, Norman Kadhom, Jean-Jacques Brière, et al.
Biochimica Et Biophysica Acta|April 23, 2013
Mutations in mitochondrial ribosomal protein MRPL12 leads to growth retardation, neurological deterioration and mitochondrial translation deficiencyValérie Serre, Agata Rozanska, Marine Beinat, et al.
European Journal of Human Genetics : EJHG|September 18, 2014
Unusual clinical expression and long survival of a pseudouridylate synthase (PUS1) mutation into adulthoodMetodi D Metodiev, Zahra Assouline, Pierre Landrieu, et al.
The Journal of Pediatrics|August 31, 2006
Mitochondrial respiratory chain deficiencies expressing the enzymatic deficiency in the hepatic tissue: a study of 31 patientsAngels Garcia-Cazorla, Pascale De Lonlay, Pierre Rustin, et al.
The Journal of Clinical Investigation|March 3, 2007
Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disordersJulie Mollet, Irina Giurgea, Dimitri Schlemmer, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Current Medicinal Chemistry|February 3, 2004
Revisiting pitfalls, problems and tentative solutions for assaying mitochondrial respiratory chain complex III in human samplesDominique Chretien, Abdelhamid Slama, Jean-Jacques Brière, et al.
Journal of Hepatology|July 12, 2011
Mutation in the mitochondrial translation elongation factor EFTs results in severe infantile liver failureVanessa Vedrenne, Louise Galmiche, Dominique Chretien, et al.
Molecular Genetics and Metabolism|February 6, 2008
Mitochondrial respiratory chain complex assembly and function during human fetal developmentLimor Minai, Jelena Martinovic, Dominique Chretien, et al.
Biochemical and Biophysical Research Communications|January 22, 2003
Assay of mitochondrial respiratory chain complex I in human lymphocytes and cultured skin fibroblastsDominique Chretien, Paule Bénit, Marie Chol, et al.
American Journal of Medical Genetics. Part A|December 8, 2006
A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystoniaEmmanuelle Sarzi, Michael D Brown, Sophie Lebon, et al.
BMC Biochemistry|November 5, 2003
Mitochondrial activities in human cultured skin fibroblasts contaminated by Mycoplasma hyorhinisNiklas Darin, Norman Kadhom, Jean-Jacques Brière, et al.
Biochimica Et Biophysica Acta|April 23, 2013
Mutations in mitochondrial ribosomal protein MRPL12 leads to growth retardation, neurological deterioration and mitochondrial translation deficiencyValérie Serre, Agata Rozanska, Marine Beinat, et al.
European Journal of Human Genetics : EJHG|September 18, 2014
Unusual clinical expression and long survival of a pseudouridylate synthase (PUS1) mutation into adulthoodMetodi D Metodiev, Zahra Assouline, Pierre Landrieu, et al.
The Journal of Pediatrics|August 31, 2006
Mitochondrial respiratory chain deficiencies expressing the enzymatic deficiency in the hepatic tissue: a study of 31 patientsAngels Garcia-Cazorla, Pascale De Lonlay, Pierre Rustin, et al.
The Journal of Clinical Investigation|March 3, 2007
Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disordersJulie Mollet, Irina Giurgea, Dimitri Schlemmer, et al.
Pageof 3