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B Mousson

Showing results (21-30 of 48) with videos related to

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In Vitro Cellular & Developmental Biology. Animal|May 1, 1993
Failure to obtain hybridomas between human macrophages and human tumoral U-937 cells is probably due to parental macrophagesA Bohbot, F Uttwiller, R Fujita, et al.
Neurology|April 25, 2007
NARP mitochondriopathy: an unusual cause of progressive myoclonic epilepsyJ Jung, F Mauguière, P Clerc-Renaud, et al.
Acta Neuropathologica|January 1, 1996
Molecular histology of mitochondrial and nuclear transcripts in the muscle of patients harbouring a single mitochondrial DNA deletionH Carrier, B Burt-Pichat, F Flocard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 6, 2004
[Mitochondrial cytopathy: an unusual infantile cause of total villous atrophy]C Bonnemains, J Berthelot, B Mousson de Camaret, et al.
Mitochondrion|August 27, 2005
Induction of ANT2 gene expression in liver of patients with mitochondrial DNA depletionC Bonod-Bidaud, A Chevrollier, I Bourasseau, et al.
La Revue De Medecine Interne|January 1, 1992
[Diagnosis of muscular intolerance during exercise caused by enzyme deficiency in adults]B Mousson, A Fléchaire, I Maire, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1997
Identification of a large-scale mitochondrial deoxyribonucleic acid deletion in endocrinopathies and deafness: report of two unrelated cases with diabetes mellitus and adrenal insufficiency, respectivelyM Nicolino, T Ferlin, M Forest, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 10, 1998
Metabolic studies in a patient with severe carnitine palmitoyltransferase type II deficiencyM Fontaine, G Briand, C Largillière, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Cardiac transplantation in an incomplete Kearns-Sayre syndrome with mitochondrial DNA deletionC Tranchant, B Mousson, M Mohr, et al.
Molecular and Cellular Biochemistry|March 1, 1997
Expression of oxidative phosphorylation genes in muscle cell cultures from patients with mitochondrial myopathiesJ M Collombet, H Faure-Vigny, G Mandon, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
In Vitro Cellular & Developmental Biology. Animal|May 1, 1993
Failure to obtain hybridomas between human macrophages and human tumoral U-937 cells is probably due to parental macrophagesA Bohbot, F Uttwiller, R Fujita, et al.
Neurology|April 25, 2007
NARP mitochondriopathy: an unusual cause of progressive myoclonic epilepsyJ Jung, F Mauguière, P Clerc-Renaud, et al.
Acta Neuropathologica|January 1, 1996
Molecular histology of mitochondrial and nuclear transcripts in the muscle of patients harbouring a single mitochondrial DNA deletionH Carrier, B Burt-Pichat, F Flocard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 6, 2004
[Mitochondrial cytopathy: an unusual infantile cause of total villous atrophy]C Bonnemains, J Berthelot, B Mousson de Camaret, et al.
Mitochondrion|August 27, 2005
Induction of ANT2 gene expression in liver of patients with mitochondrial DNA depletionC Bonod-Bidaud, A Chevrollier, I Bourasseau, et al.
La Revue De Medecine Interne|January 1, 1992
[Diagnosis of muscular intolerance during exercise caused by enzyme deficiency in adults]B Mousson, A Fléchaire, I Maire, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1997
Identification of a large-scale mitochondrial deoxyribonucleic acid deletion in endocrinopathies and deafness: report of two unrelated cases with diabetes mellitus and adrenal insufficiency, respectivelyM Nicolino, T Ferlin, M Forest, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 10, 1998
Metabolic studies in a patient with severe carnitine palmitoyltransferase type II deficiencyM Fontaine, G Briand, C Largillière, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Cardiac transplantation in an incomplete Kearns-Sayre syndrome with mitochondrial DNA deletionC Tranchant, B Mousson, M Mohr, et al.
Molecular and Cellular Biochemistry|March 1, 1997
Expression of oxidative phosphorylation genes in muscle cell cultures from patients with mitochondrial myopathiesJ M Collombet, H Faure-Vigny, G Mandon, et al.
Pageof 5