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Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1996
[Gene therapy in lysosomal diseases]P Moullier, A Salvetti, D Bohl, et al.Nouvelle Revue Francaise D'Hematologie|January 1, 1994
Gene therapy for lysosomal disordersN Naffakh, D Bohl, A Salvetti, et al.Nature Genetics|June 1, 1993
Correction of lysosomal storage in the liver and spleen of MPS VII mice by implantation of genetically modified skin fibroblastsP Moullier, D Bohl, J M Heard, et al.Blood|August 26, 1998
Control of erythropoietin delivery by doxycycline in mice after intramuscular injection of adeno-associated vectorD Bohl, A Salvetti, P Moullier, et al.Nature Medicine|April 1, 1995
Long-term delivery of a lysosomal enzyme by genetically modified fibroblasts in dogsP Moullier, D Bohl, J Cardoso, et al.British Medical Bulletin|January 1, 1995
Gene therapy of lysosomal storage disordersA Salvetti, J M Heard, O DanosHuman Gene Therapy|September 1, 1995
In vivo delivery of human alpha-L-iduronidase in mice implanted with neo-organsA Salvetti, P Moullier, V Cornet, et al.Transplantation|August 1, 1993
Continuous systemic secretion of a lysosomal enzyme by genetically modified mouse skin fibroblastsP Moullier, V Maréchal, O Danos, et al.Nouvelle Revue Francaise D'Hematologie|January 1, 1991
Gene transfer to somatic tissues using retroviral vectorsP Moullier, V Marechal, N Ferry, et al.Gene Therapy|May 1, 1995
Continuous secretion of human soluble CD4 in mice transplanted with genetically modified cellsT Valere, D Bohl, D Klatzmann, et al.Pageof 68