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J Demaille

Showing results (31-40 of 112) with videos related to

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Human Genetics|December 1, 1993
Rapid detection of single nucleotide deletions: application to the beta 6 (-A) mutation of the beta-globin gene and to cystic fibrosisM C Romey, P Aguilar-Martinez, J Demaille, et al.
Biochemical and Biophysical Research Communications|June 4, 1971
The amino acid sequence of the major parvalbumin from hake muscleJ F Pechere, J P Capony, L Ryden, et al.
European Journal of Biochemistry|January 3, 1973
The primary structure of the major parvalbumin from hake muscle. Overlapping peptides obtained with chemical and enzymatic methods. The complete amino-acid sequenceJ P Capony, L Rydèn, J Demaille, et al.
Human Genetics|December 1, 1992
Analysis of 30 known cystic fibrosis mutations: 10 mutations account for 27% of non-delta F508 chromosomes in southern FranceM Claustres, M Desgeorges, P Kjellberg, et al.
Genes and Immunity|February 22, 2002
Enhanced cytokine mRNA levels in attack-free patients with familial Mediterranean feverC Notarnicola, M N Didelot, F Seguret, et al.
Genomics|November 15, 2001
Comparative genomics of the SOX9 region in human and Fugu rubripes: conservation of short regulatory sequence elements within large intergenic regionsS Bagheri-Fam, C Ferraz, J Demaille, et al.
FEBS Letters|December 10, 1990
Evidence for aggregation of endothelin 1 in waterR Bennes, B Calas, P E Chabrier, et al.
Cytogenetics and Cell Genetics|July 15, 2000
Genomic sequencing reveals the structure of the Kcnk6 and map3k11 genes and their close vicinity to the sipa1 gene on mouse chromosome 19A Saridaki, C Ferraz, J Demaille, et al.
Genomics|July 27, 2001
The myosin light chain kinase gene is not duplicated in mouse: partial structure and chromosomal localization of MylkD Giorgi, C Ferraz, M G Mattéi, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Becker muscular dystrophy: demonstration of the carrier status of a female by immunoblotting and immunostainingM P Chevron, S Tuffery, B Echenne, et al.
Pageof 12

Showing results (31-40 of 112) with videos related to

Sort By:
Pageof 12
Human Genetics|December 1, 1993
Rapid detection of single nucleotide deletions: application to the beta 6 (-A) mutation of the beta-globin gene and to cystic fibrosisM C Romey, P Aguilar-Martinez, J Demaille, et al.
Biochemical and Biophysical Research Communications|June 4, 1971
The amino acid sequence of the major parvalbumin from hake muscleJ F Pechere, J P Capony, L Ryden, et al.
European Journal of Biochemistry|January 3, 1973
The primary structure of the major parvalbumin from hake muscle. Overlapping peptides obtained with chemical and enzymatic methods. The complete amino-acid sequenceJ P Capony, L Rydèn, J Demaille, et al.
Human Genetics|December 1, 1992
Analysis of 30 known cystic fibrosis mutations: 10 mutations account for 27% of non-delta F508 chromosomes in southern FranceM Claustres, M Desgeorges, P Kjellberg, et al.
Genes and Immunity|February 22, 2002
Enhanced cytokine mRNA levels in attack-free patients with familial Mediterranean feverC Notarnicola, M N Didelot, F Seguret, et al.
Genomics|November 15, 2001
Comparative genomics of the SOX9 region in human and Fugu rubripes: conservation of short regulatory sequence elements within large intergenic regionsS Bagheri-Fam, C Ferraz, J Demaille, et al.
FEBS Letters|December 10, 1990
Evidence for aggregation of endothelin 1 in waterR Bennes, B Calas, P E Chabrier, et al.
Cytogenetics and Cell Genetics|July 15, 2000
Genomic sequencing reveals the structure of the Kcnk6 and map3k11 genes and their close vicinity to the sipa1 gene on mouse chromosome 19A Saridaki, C Ferraz, J Demaille, et al.
Genomics|July 27, 2001
The myosin light chain kinase gene is not duplicated in mouse: partial structure and chromosomal localization of MylkD Giorgi, C Ferraz, M G Mattéi, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Becker muscular dystrophy: demonstration of the carrier status of a female by immunoblotting and immunostainingM P Chevron, S Tuffery, B Echenne, et al.
Pageof 12