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T Bienvenu

Showing results (31-40 of 92) with videos related to

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European Journal of Human Genetics : EJHG|April 21, 2001
Parental origin of de novo MECP2 mutations in Rett syndromeM Girard, P Couvert, A Carrié, et al.
Human Genetics|June 1, 1995
Three novel sequence variations in the 5' upstream region of the cystic fibrosis transmembrane conductance regulator (CFTR) gene: two polymorphisms and one putative molecular defectT Bienvenu, V Lacronique, M Raymondjean, et al.
European Journal of Clinical Nutrition|September 16, 2004
Malnutrition in adults with cystic fibrosisX Dray, R Kanaan, T Bienvenu, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Analysis of alternative splicing patterns in the cystic fibrosis transmembrane conductance regulator gene using mRNA derived from lymphoblastoid cells of cystic fibrosis patientsT Bienvenu, C Beldjord, J Chelly, et al.
Human Mutation|January 29, 2000
A novel missense mutation D513G in exon 10 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in a French CBAVD patient. Mutations in brief no. 175. OnlineT Bienvenu, S Bousquet, D Vidaud, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patientsP Vourc'h, T Bienvenu, C Beldjord, et al.
European Journal of Clinical Pharmacology|January 1, 1996
Non invasive in vivo study of the maturation of CYP IIIA in neonates and infantsF Vauzelle-Kervroedan, E Rey, A Pariente-Khayat, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|May 1, 1990
Effect of growth hormone on caffeine metabolism in hypophysectomized ratsT Bienvenu, G Pons, E Rey, et al.
Human Genetics|August 4, 2005
Maternal mosaicism for mutations in the ARX gene in a family with X linked mental retardationK Poirier, J Abriol, I Souville, et al.
Haemostasis|January 1, 1991
Antithrombin III activity is not related to plasma homocysteine concentrationsT Bienvenu, B Chadefaux, A Ankri, et al.
Pageof 10

Showing results (31-40 of 92) with videos related to

Sort By:
Pageof 10
European Journal of Human Genetics : EJHG|April 21, 2001
Parental origin of de novo MECP2 mutations in Rett syndromeM Girard, P Couvert, A Carrié, et al.
Human Genetics|June 1, 1995
Three novel sequence variations in the 5' upstream region of the cystic fibrosis transmembrane conductance regulator (CFTR) gene: two polymorphisms and one putative molecular defectT Bienvenu, V Lacronique, M Raymondjean, et al.
European Journal of Clinical Nutrition|September 16, 2004
Malnutrition in adults with cystic fibrosisX Dray, R Kanaan, T Bienvenu, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Analysis of alternative splicing patterns in the cystic fibrosis transmembrane conductance regulator gene using mRNA derived from lymphoblastoid cells of cystic fibrosis patientsT Bienvenu, C Beldjord, J Chelly, et al.
Human Mutation|January 29, 2000
A novel missense mutation D513G in exon 10 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in a French CBAVD patient. Mutations in brief no. 175. OnlineT Bienvenu, S Bousquet, D Vidaud, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patientsP Vourc'h, T Bienvenu, C Beldjord, et al.
European Journal of Clinical Pharmacology|January 1, 1996
Non invasive in vivo study of the maturation of CYP IIIA in neonates and infantsF Vauzelle-Kervroedan, E Rey, A Pariente-Khayat, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|May 1, 1990
Effect of growth hormone on caffeine metabolism in hypophysectomized ratsT Bienvenu, G Pons, E Rey, et al.
Human Genetics|August 4, 2005
Maternal mosaicism for mutations in the ARX gene in a family with X linked mental retardationK Poirier, J Abriol, I Souville, et al.
Haemostasis|January 1, 1991
Antithrombin III activity is not related to plasma homocysteine concentrationsT Bienvenu, B Chadefaux, A Ankri, et al.
Pageof 10