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J Demaille

Showing results (21-30 of 112) with videos related to

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Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1993
[Mice SI/Col: a study model in the research of genes involved in situs inversus]A de Meeus, S Alonso, J Demaille, et al.
Neuromuscular Disorders : NMD|September 1, 1994
Expression and subcellular localization of dystrophin in skeletal, cardiac and smooth muscles during the human developmentM P Chevron, F Girard, M Claustres, et al.
Human Mutation|October 26, 1999
Point mutations in the dystrophin gene: evidence for frequent use of cryptic splice sites as a result of splicing defectsS Tuffery-Giraud, S Chambert, J Demaille, et al.
European Journal of Biochemistry|August 1, 1975
The amino-acid sequence of the most acidic major parvalbumin from frog muscleJ P Capony, J Demaille, C Pina, et al.
Biology of the Neonate|January 1, 1995
Scanning gel densitometry of amniotic fluid acetylcholinesterase and butyrylcholinesterase: quantification of 'faint-positive' bands in fetal malformationsM Dupont, B Vallet, A Brun, et al.
Human Genetics|December 1, 1995
Four adult patients with the missense mutation L206W and a mild cystic fibrosis phenotypeM Desgeorges, M Rodier, M Piot, et al.
Human Genetics|December 1, 1990
Germinal mosaicism from grand-paternal origin in a family with Duchenne muscular dystrophyM Claustres, P Kjellberg, M Desgeorges, et al.
The Journal of Physiology|November 1, 1979
Mode of stimulation by injection of cyclic AMP and external acidification of the sodium efflux in barnacle muscle fibresE E Bittar, J Demaille, E H Fischer, et al.
Ophthalmic Genetics|November 15, 1997
A complex allele (1064delTC and IVS2 + 22ins7) in the peripherin/RDS gene in retinitis pigmentosa with macular dystrophyC Bareil, C Hamel, B Arnaud, et al.
Journal of Medical Genetics|January 1, 1994
Severe pulmonary and digestive disease in a cystic fibrosis child homozygous for G542XM Desgeorges, M Laussel, B Rollin, et al.
Pageof 12

Showing results (21-30 of 112) with videos related to

Sort By:
Pageof 12
Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1993
[Mice SI/Col: a study model in the research of genes involved in situs inversus]A de Meeus, S Alonso, J Demaille, et al.
Neuromuscular Disorders : NMD|September 1, 1994
Expression and subcellular localization of dystrophin in skeletal, cardiac and smooth muscles during the human developmentM P Chevron, F Girard, M Claustres, et al.
Human Mutation|October 26, 1999
Point mutations in the dystrophin gene: evidence for frequent use of cryptic splice sites as a result of splicing defectsS Tuffery-Giraud, S Chambert, J Demaille, et al.
European Journal of Biochemistry|August 1, 1975
The amino-acid sequence of the most acidic major parvalbumin from frog muscleJ P Capony, J Demaille, C Pina, et al.
Biology of the Neonate|January 1, 1995
Scanning gel densitometry of amniotic fluid acetylcholinesterase and butyrylcholinesterase: quantification of 'faint-positive' bands in fetal malformationsM Dupont, B Vallet, A Brun, et al.
Human Genetics|December 1, 1995
Four adult patients with the missense mutation L206W and a mild cystic fibrosis phenotypeM Desgeorges, M Rodier, M Piot, et al.
Human Genetics|December 1, 1990
Germinal mosaicism from grand-paternal origin in a family with Duchenne muscular dystrophyM Claustres, P Kjellberg, M Desgeorges, et al.
The Journal of Physiology|November 1, 1979
Mode of stimulation by injection of cyclic AMP and external acidification of the sodium efflux in barnacle muscle fibresE E Bittar, J Demaille, E H Fischer, et al.
Ophthalmic Genetics|November 15, 1997
A complex allele (1064delTC and IVS2 + 22ins7) in the peripherin/RDS gene in retinitis pigmentosa with macular dystrophyC Bareil, C Hamel, B Arnaud, et al.
Journal of Medical Genetics|January 1, 1994
Severe pulmonary and digestive disease in a cystic fibrosis child homozygous for G542XM Desgeorges, M Laussel, B Rollin, et al.
Pageof 12