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T Bourgeron

Showing results (11-20 of 50) with videos related to

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Human Molecular Genetics|August 1, 1995
Spectrum of mitochondrial DNA rearrangements in the Pearson marrow-pancreas syndromeA Rötig, T Bourgeron, D Chretien, et al.
Journal of Medical Genetics|September 8, 2001
Mitochondrial DNA inheritance in patients with deleted mtDNAL Quintana-Murci, A Rötig, A Munnich, et al.
European Journal of Pediatrics|March 1, 1993
Uridine preserves the expression of respiratory enzyme deficiencies in cultured fibroblastsB Gérard, T Bourgeron, D Chretien, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Expression of respiratory chain deficiencies in human cultured cellsT Bourgeron, D Chretien, P Amati, et al.
Cytogenetic and Genome Research|November 17, 2011
Disentangling the myriad genomics of complex disorders, specifically focusing on autism, epilepsy, and schizophreniaM Poot, J J van der Smagt, E H Brilstra, et al.
Biochimica Et Biophysica Acta|August 22, 1997
Inborn errors of the Krebs cycle: a group of unusual mitochondrial diseases in humanP Rustin, T Bourgeron, B Parfait, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 1, 1994
Reference charts for respiratory chain activities in human tissuesD Chretien, P Rustin, T Bourgeron, et al.
Annales De Biologie Clinique|June 23, 1999
[Genetic control of spermatogenesis: Y chromosome and male infertility]C Krausz, J Siffroi, N Souleyreau-Therville, et al.
Genomics|November 15, 2001
Transduction of the human gene FAM8A1 by endogenous retrovirus during primate evolutionS Jamain, M Girondot, P Leroy, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1995
An improved spectrophotometric assay of pyruvate dehydrogenase in lactate dehydrogenase contaminated mitochondrial preparations from human skeletal muscleD Chretien, M Pourrier, T Bourgeron, et al.
Pageof 5

Showing results (11-20 of 50) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|August 1, 1995
Spectrum of mitochondrial DNA rearrangements in the Pearson marrow-pancreas syndromeA Rötig, T Bourgeron, D Chretien, et al.
Journal of Medical Genetics|September 8, 2001
Mitochondrial DNA inheritance in patients with deleted mtDNAL Quintana-Murci, A Rötig, A Munnich, et al.
European Journal of Pediatrics|March 1, 1993
Uridine preserves the expression of respiratory enzyme deficiencies in cultured fibroblastsB Gérard, T Bourgeron, D Chretien, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Expression of respiratory chain deficiencies in human cultured cellsT Bourgeron, D Chretien, P Amati, et al.
Cytogenetic and Genome Research|November 17, 2011
Disentangling the myriad genomics of complex disorders, specifically focusing on autism, epilepsy, and schizophreniaM Poot, J J van der Smagt, E H Brilstra, et al.
Biochimica Et Biophysica Acta|August 22, 1997
Inborn errors of the Krebs cycle: a group of unusual mitochondrial diseases in humanP Rustin, T Bourgeron, B Parfait, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 1, 1994
Reference charts for respiratory chain activities in human tissuesD Chretien, P Rustin, T Bourgeron, et al.
Annales De Biologie Clinique|June 23, 1999
[Genetic control of spermatogenesis: Y chromosome and male infertility]C Krausz, J Siffroi, N Souleyreau-Therville, et al.
Genomics|November 15, 2001
Transduction of the human gene FAM8A1 by endogenous retrovirus during primate evolutionS Jamain, M Girondot, P Leroy, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1995
An improved spectrophotometric assay of pyruvate dehydrogenase in lactate dehydrogenase contaminated mitochondrial preparations from human skeletal muscleD Chretien, M Pourrier, T Bourgeron, et al.
Pageof 5