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M A Kay

Showing results (11-20 of 110) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|September 1, 1999
Gene therapy for the hemophiliasM A Kay, K High
Methods in Molecular Medicine|February 5, 2014
Methods for delivery of genes to hepatocytes in vivo using recombinant adenovirus vectorsD Barr, M A Kay
Current Gene Therapy|July 23, 2003
From virus evolution to vector revolution: use of naturally occurring serotypes of adeno-associated virus (AAV) as novel vectors for human gene therapyD Grimm, M A Kay
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 8, 2001
Modified HIV-1 based lentiviral vectors have an effect on viral transduction efficiency and gene expression in vitro and in vivoF Park, M A Kay
Human Gene Therapy|December 16, 1998
Efficient construction of a recombinant adenovirus vector by an improved in vitro ligation methodH Mizuguchi, M A Kay
Nature Medicine|September 1, 1995
Immunomodulation to enhance gene therapyC Wilson, M A Kay
Journal of Virology|May 1, 1996
Adenovirus-mediated expression of ribozymes in miceA Lieber, M A Kay
Molecular Medicine Today|March 1, 1997
Liver regeneration: prospects for therapy based on new technologiesM A Kay, N Fausto
Transplantation Proceedings|November 25, 2004
Extracellular matrix component cotransplantation prolongs survival of heterotopically transplanted human hepatocytes in miceK Ohashi, M A Kay
Gene Therapy|February 3, 2006
Therapeutic short hairpin RNA expression in the liver: viral targets and vectorsD Grimm, M A Kay
Pageof 11

Showing results (11-20 of 110) with videos related to

Sort By:
Pageof 11
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1999
Gene therapy for the hemophiliasM A Kay, K High
Methods in Molecular Medicine|February 5, 2014
Methods for delivery of genes to hepatocytes in vivo using recombinant adenovirus vectorsD Barr, M A Kay
Current Gene Therapy|July 23, 2003
From virus evolution to vector revolution: use of naturally occurring serotypes of adeno-associated virus (AAV) as novel vectors for human gene therapyD Grimm, M A Kay
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 8, 2001
Modified HIV-1 based lentiviral vectors have an effect on viral transduction efficiency and gene expression in vitro and in vivoF Park, M A Kay
Human Gene Therapy|December 16, 1998
Efficient construction of a recombinant adenovirus vector by an improved in vitro ligation methodH Mizuguchi, M A Kay
Nature Medicine|September 1, 1995
Immunomodulation to enhance gene therapyC Wilson, M A Kay
Journal of Virology|May 1, 1996
Adenovirus-mediated expression of ribozymes in miceA Lieber, M A Kay
Molecular Medicine Today|March 1, 1997
Liver regeneration: prospects for therapy based on new technologiesM A Kay, N Fausto
Transplantation Proceedings|November 25, 2004
Extracellular matrix component cotransplantation prolongs survival of heterotopically transplanted human hepatocytes in miceK Ohashi, M A Kay
Gene Therapy|February 3, 2006
Therapeutic short hairpin RNA expression in the liver: viral targets and vectorsD Grimm, M A Kay
Pageof 11