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Neuromuscular Disorders : NMD
|
September 1, 1993
Transplantation of adult-derived myoblasts in mice following gene transfer
N Naffakh, C Pinset, D Montarras, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 12, 2000
A conserved mechanism of retrovirus restriction in mammals
G Towers, M Bock, S Martin, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1994
Gene therapy for lysosomal disorders
N Naffakh, D Bohl, A Salvetti, et al.
Journal of Virology
|
May 1, 1983
Comparative analysis of the human type 1a and bovine type 1 papillomavirus genomes
O Danos, L W Engel, E Y Chen, et al.
Virology
|
July 1, 1994
Role of N-linked glycosylation in the activity of the Friend murine leukemia virus SU protein receptor-binding domain
J L Battini, S C Kayman, A Pinter, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1991
Gene transfer to somatic tissues using retroviral vectors
P Moullier, V Marechal, N Ferry, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1990
Expression of human adenosine deaminase in mice reconstituted with retrovirus-transduced hematopoietic stem cells
J M Wilson, O Danos, M Grossman, et al.
Gene Therapy
|
August 19, 2005
Noninvasive monitoring of therapeutic gene transfer in animal models of muscular dystrophies
M Bartoli, J Poupiot, A Goyenvalle, et al.
Journal of Virology
|
February 11, 1999
Structure of adeno-associated virus vector DNA following transduction of the skeletal muscle
N Vincent-Lacaze, R O Snyder, R Gluzman, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 9, 2003
Identification of an HLA-A*0201-restricted epitopic peptide from human dystrophin: application in duchenne muscular dystrophy gene therapy
F Ginhoux, C Doucet, M Leboeuf, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 109) with videos related to
Sort By:
Page
of 11
Neuromuscular Disorders : NMD
|
September 1, 1993
Transplantation of adult-derived myoblasts in mice following gene transfer
N Naffakh, C Pinset, D Montarras, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 12, 2000
A conserved mechanism of retrovirus restriction in mammals
G Towers, M Bock, S Martin, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1994
Gene therapy for lysosomal disorders
N Naffakh, D Bohl, A Salvetti, et al.
Journal of Virology
|
May 1, 1983
Comparative analysis of the human type 1a and bovine type 1 papillomavirus genomes
O Danos, L W Engel, E Y Chen, et al.
Virology
|
July 1, 1994
Role of N-linked glycosylation in the activity of the Friend murine leukemia virus SU protein receptor-binding domain
J L Battini, S C Kayman, A Pinter, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1991
Gene transfer to somatic tissues using retroviral vectors
P Moullier, V Marechal, N Ferry, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1990
Expression of human adenosine deaminase in mice reconstituted with retrovirus-transduced hematopoietic stem cells
J M Wilson, O Danos, M Grossman, et al.
Gene Therapy
|
August 19, 2005
Noninvasive monitoring of therapeutic gene transfer in animal models of muscular dystrophies
M Bartoli, J Poupiot, A Goyenvalle, et al.
Journal of Virology
|
February 11, 1999
Structure of adeno-associated virus vector DNA following transduction of the skeletal muscle
N Vincent-Lacaze, R O Snyder, R Gluzman, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 9, 2003
Identification of an HLA-A*0201-restricted epitopic peptide from human dystrophin: application in duchenne muscular dystrophy gene therapy
F Ginhoux, C Doucet, M Leboeuf, et al.
Page
of 11