Showing results (71-80 of 94) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|January 1, 1997
The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann diseaseL Bürglen, T Seroz, P Miniou, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 1, 2011
The endocannabinoid 2-arachidonoyl-glycerol activates human neutrophils: critical role of its hydrolysis and de novo leukotriene B4 biosynthesisFrançois Chouinard, Julie S Lefebvre, Pauline Navarro, et al.
Annales De Biologie Clinique|September 6, 2024
[Implementation of edoxaban anti-Xa activity assay in a hospital laboratory and evaluation of its analytical performance]Corentin S Lefebvre, Sophie Luneau, Nûn Kalim Bentounes, 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.
Nature Genetics|November 1, 1995
A frame-shift deletion in the survival motor neuron gene in Spanish spinal muscular atrophy patientsE Bussaglia, O Clermont, E Tizzano, et al.
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.
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.
Pageof 10