Search research articles
Contact Us
Filters
Showing results (91-100 of 110) with videos related to
Page
of 11
Sort By:
Nature Genetics
|
October 1, 1995
Long-term hepatic adenovirus-mediated gene expression in mice following CTLA4Ig administration
M A Kay, A X Holterman, L Meuse, et al.
Journal of Virology
|
August 8, 1998
Transient inhibition of CD28 and CD40 ligand interactions prolongs adenovirus-mediated transgene expression in the lung and facilitates expression after secondary vector administration
C B Wilson, L J Embree, D Schowalter, et al.
Nature Genetics
|
May 20, 1998
The kinetics of rAAV integration in the liver
C H Miao, R O Snyder, D B Schowalter, et al.
Journal of Virology
|
March 23, 2000
Nonrandom transduction of recombinant adeno-associated virus vectors in mouse hepatocytes in vivo: cell cycling does not influence hepatocyte transduction
C H Miao, H Nakai, A R Thompson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 29, 1997
Transient immunomodulation with anti-CD40 ligand antibody and CTLA4Ig enhances persistence and secondary adenovirus-mediated gene transfer into mouse liver
M A Kay, L Meuse, A M Gown, et al.
Transplantation Proceedings
|
January 3, 2006
Heterotopically transplanted hepatocyte survival depends on extracellular matrix components
K Ohashi, M A Kay, H Kuge, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1992
Expression of human alpha 1-antitrypsin in dogs after autologous transplantation of retroviral transduced hepatocytes
M A Kay, P Baley, S Rothenberg, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 11, 2001
Correction of the retinal dystrophy phenotype of the RCS rat by viral gene transfer of Mertk
D Vollrath, W Feng, J L Duncan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 15, 1994
In vivo hepatic gene therapy: complete albeit transient correction of factor IX deficiency in hemophilia B dogs
M A Kay, C N Landen, S R Rothenberg, et al.
Nature Medicine
|
March 4, 2000
Sustained survival of human hepatocytes in mice: A model for in vivo infection with human hepatitis B and hepatitis delta viruses
K Ohashi, P L Marion, H Nakai, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 110) with videos related to
Sort By:
Page
of 11
Nature Genetics
|
October 1, 1995
Long-term hepatic adenovirus-mediated gene expression in mice following CTLA4Ig administration
M A Kay, A X Holterman, L Meuse, et al.
Journal of Virology
|
August 8, 1998
Transient inhibition of CD28 and CD40 ligand interactions prolongs adenovirus-mediated transgene expression in the lung and facilitates expression after secondary vector administration
C B Wilson, L J Embree, D Schowalter, et al.
Nature Genetics
|
May 20, 1998
The kinetics of rAAV integration in the liver
C H Miao, R O Snyder, D B Schowalter, et al.
Journal of Virology
|
March 23, 2000
Nonrandom transduction of recombinant adeno-associated virus vectors in mouse hepatocytes in vivo: cell cycling does not influence hepatocyte transduction
C H Miao, H Nakai, A R Thompson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 29, 1997
Transient immunomodulation with anti-CD40 ligand antibody and CTLA4Ig enhances persistence and secondary adenovirus-mediated gene transfer into mouse liver
M A Kay, L Meuse, A M Gown, et al.
Transplantation Proceedings
|
January 3, 2006
Heterotopically transplanted hepatocyte survival depends on extracellular matrix components
K Ohashi, M A Kay, H Kuge, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1992
Expression of human alpha 1-antitrypsin in dogs after autologous transplantation of retroviral transduced hepatocytes
M A Kay, P Baley, S Rothenberg, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 11, 2001
Correction of the retinal dystrophy phenotype of the RCS rat by viral gene transfer of Mertk
D Vollrath, W Feng, J L Duncan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 15, 1994
In vivo hepatic gene therapy: complete albeit transient correction of factor IX deficiency in hemophilia B dogs
M A Kay, C N Landen, S R Rothenberg, et al.
Nature Medicine
|
March 4, 2000
Sustained survival of human hepatocytes in mice: A model for in vivo infection with human hepatitis B and hepatitis delta viruses
K Ohashi, P L Marion, H Nakai, et al.
Page
of 11