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Showing results (31-40 of 35) with videos related to

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Gene Therapy|December 19, 2003
Widespread and efficient marker gene expression in the airway epithelia of fetal sheep after minimally invasive tracheal application of recombinant adenovirus in uteroD Peebles, L G Gregory, A David, et al.
Gene Therapy|January 16, 2004
Reduced toxicity of F-deficient Sendai virus vector in the mouse fetusS N Waddington, S M K Buckley, C Bernloehr, et al.
Gene Therapy|July 15, 2003
Long-term transgene expression by administration of a lentivirus-based vector to the fetal circulation of immuno-competent miceS N Waddington, K A Mitrophanous, F M Ellard, et al.
Gene Therapy|May 14, 2004
Highly efficient EIAV-mediated in utero gene transfer and expression in the major muscle groups affected by Duchenne muscular dystrophyL G Gregory, S N Waddington, M V Holder, et al.
Gene Therapy|September 16, 2005
Permanent partial phenotypic correction and tolerance in a mouse model of hemophilia B by stem cell gene delivery of human factor IXB W Bigger, E K Siapati, A Mistry, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Gene Therapy|December 19, 2003
Widespread and efficient marker gene expression in the airway epithelia of fetal sheep after minimally invasive tracheal application of recombinant adenovirus in uteroD Peebles, L G Gregory, A David, et al.
Gene Therapy|January 16, 2004
Reduced toxicity of F-deficient Sendai virus vector in the mouse fetusS N Waddington, S M K Buckley, C Bernloehr, et al.
Gene Therapy|July 15, 2003
Long-term transgene expression by administration of a lentivirus-based vector to the fetal circulation of immuno-competent miceS N Waddington, K A Mitrophanous, F M Ellard, et al.
Gene Therapy|May 14, 2004
Highly efficient EIAV-mediated in utero gene transfer and expression in the major muscle groups affected by Duchenne muscular dystrophyL G Gregory, S N Waddington, M V Holder, et al.
Gene Therapy|September 16, 2005
Permanent partial phenotypic correction and tolerance in a mouse model of hemophilia B by stem cell gene delivery of human factor IXB W Bigger, E K Siapati, A Mistry, et al.
Pageof 4