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Molecular Therapy : the Journal of the American Society of Gene Therapy|August 10, 2000
Inclusion of the hepatic locus control region, an intron, and untranslated region increases and stabilizes hepatic factor IX gene expression in vivo but not in vitroC H Miao, K Ohashi, G A Patijn, et al.Nature Genetics|October 1, 1995
Long-term hepatic adenovirus-mediated gene expression in mice following CTLA4Ig administrationM 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 administrationC B Wilson, L J Embree, D 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 transductionC 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 liverM A Kay, L Meuse, A M Gown, et al.Transplantation Proceedings|January 3, 2006
Heterotopically transplanted hepatocyte survival depends on extracellular matrix componentsK Ohashi, M A Kay, H Kuge, et al.Genetics|September 20, 2014
Wild sex in zebrafish: loss of the natural sex determinant in domesticated strainsCatherine A Wilson, Samantha K High, Braedan M McCluskey, 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 hepatocytesM 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 MertkD 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 dogsM A Kay, C N Landen, S R Rothenberg, et al.Pageof 11