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S Lefebvre

Showing results (81-90 of 100) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|August 16, 2024
Pediatric reference values of NT-proBNP and Galectin-3 based on a French cohortVictor Gravrand, Corentin S Lefebvre, Fatma Hamza, et al.
Science (New York, N.Y.)|June 3, 1994
De novo and inherited deletions of the 5q13 region in spinal muscular atrophiesJ Melki, S Lefebvre, L Burglen, et al.
Journal of Reproductive Immunology|September 9, 1999
Molecular mechanisms controlling constitutive and IFN-gamma-inducible HLA-G expression in various cell typesS Lefebvre, P Moreau, V Guiard, et al.
The Journal of Biological Chemistry|June 22, 1999
Solution structure of substrate-based ligands when bound to hepatitis C virus NS3 protease domainS R LaPlante, D R Cameron, N Aubry, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1994
[Physical study of big fragments and search strategy of genes. Application to locus of infant spinal muscular atrophies]J Melki, S Lefebvre, L Burglen, et al.
American Journal of Human Genetics|April 1, 1994
Use of genetic and physical mapping to locate the spinal muscular atrophy locus between two new highly polymorphic DNA markersO Clermont, P Burlet, L Burglen, et al.
The Journal of Clinical Investigation|September 1, 1996
Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy associationL Bürglen, J Amiel, L Viollet, et al.
Genomics|February 15, 1997
cDNA isolation, expression, and chromosomal localization of the mouse survival motor neuron gene (Smn)L Viollet, S Bertrandy, A L Bueno Brunialti, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|April 21, 2012
Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomasS Lefebvre, F Borson-Chazot, N Boutry-Kryza, et al.
Human Molecular Genetics|November 13, 1998
The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophyP Burlet, C Huber, S Bertrandy, et al.
Pageof 10

Showing results (81-90 of 100) with videos related to

Sort By:
Pageof 10
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 16, 2024
Pediatric reference values of NT-proBNP and Galectin-3 based on a French cohortVictor Gravrand, Corentin S Lefebvre, Fatma Hamza, et al.
Science (New York, N.Y.)|June 3, 1994
De novo and inherited deletions of the 5q13 region in spinal muscular atrophiesJ Melki, S Lefebvre, L Burglen, et al.
Journal of Reproductive Immunology|September 9, 1999
Molecular mechanisms controlling constitutive and IFN-gamma-inducible HLA-G expression in various cell typesS Lefebvre, P Moreau, V Guiard, et al.
The Journal of Biological Chemistry|June 22, 1999
Solution structure of substrate-based ligands when bound to hepatitis C virus NS3 protease domainS R LaPlante, D R Cameron, N Aubry, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1994
[Physical study of big fragments and search strategy of genes. Application to locus of infant spinal muscular atrophies]J Melki, S Lefebvre, L Burglen, et al.
American Journal of Human Genetics|April 1, 1994
Use of genetic and physical mapping to locate the spinal muscular atrophy locus between two new highly polymorphic DNA markersO Clermont, P Burlet, L Burglen, et al.
The Journal of Clinical Investigation|September 1, 1996
Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy associationL Bürglen, J Amiel, L Viollet, et al.
Genomics|February 15, 1997
cDNA isolation, expression, and chromosomal localization of the mouse survival motor neuron gene (Smn)L Viollet, S Bertrandy, A L Bueno Brunialti, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|April 21, 2012
Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomasS Lefebvre, F Borson-Chazot, N Boutry-Kryza, et al.
Human Molecular Genetics|November 13, 1998
The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophyP Burlet, C Huber, S Bertrandy, et al.
Pageof 10