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Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1993
[Transfer of genes in hematopoietic tissue: from research to applications by autografts]P LehnComptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1996
[Gene therapy in cystic fibrosis: molecular and cellular aspects]P LehnPathologie-Biologie|October 1, 1993
[General principles of the production and use of retroviral vectors]P LehnProceedings of the National Academy of Sciences of the United States of America|May 20, 2004
Dynamers: polyacylhydrazone reversible covalent polymers, component exchange, and constitutional diversityWilliams G Skene, Jean-Marie P LehnJournal of the American Chemical Society|February 20, 2014
Coupled nanomechanical motions: metal-ion-effected, pH-modulated, simultaneous extension/contraction motions of double-domain helical/linear molecular strandsAdrian-Mihail Stadler, Jean-Marie P LehnCellular and Molecular Life Sciences : CMLS|July 4, 2008
Atomic model of human cystic fibrosis transmembrane conductance regulator: membrane-spanning domains and coupling interfacesJ-P Mornon, P Lehn, I CallebautCellular and Molecular Life Sciences : CMLS|January 28, 2004
Nucleotide-binding domains of human cystic fibrosis transmembrane conductance regulator: detailed sequence analysis and three-dimensional modeling of the heterodimerI Callebaut, R Eudes, J-P Mornon, et al.Nouvelle Revue Francaise D'Hematologie|January 1, 1989
A randomized study comparing ciclosporin A and antithymocyte globulin for treatment of severe aplastic anemiaH Esperou, A Devergie, P Lehn, et al.Molecular Biology and Evolution|April 1, 1997
Phylogenetic analysis of cystic fibrosis transmembrane conductance regulator gene in mammalian species argues for the development of a rabbit model for cystic fibrosisS Vuillaumier, B Kaltenboeck, G Lecointre, et al.Cellular and Molecular Life Sciences : CMLS|September 1, 2005
Nucleotide binding domains of human CFTR: a structural classification of critical residues and disease-causing mutationsR Eudes, P Lehn, C Férec, et al.Pageof 4