Kay MA - Search Results

1

Epstein-Barr virus/human vector provides high-level, long-term expression of alpha1-antitrypsin in mice.

Stoll SM, Sclimenti CR, Baba EJ, Meuse L, Kay MA, Calos MP. Stoll SM, et al. Among authors: kay ma. Mol Ther. 2001 Aug;4(2):122-9. doi: 10.1006/mthe.2001.0429. Mol Ther. 2001. PMID: 11482983 Free article.

2

Hepatic gene therapy: persistent expression of human alpha 1-antitrypsin in mice after direct gene delivery in vivo.

Kay MA, Li Q, Liu TJ, Leland F, Toman C, Finegold M, Woo SL. Kay MA, et al. Hum Gene Ther. 1992 Dec;3(6):641-7. doi: 10.1089/hum.1992.3.6-641. Hum Gene Ther. 1992. PMID: 1482704

3

Long-term hepatic adenovirus-mediated gene expression in mice following CTLA4Ig administration.

Kay MA, Holterman AX, Meuse L, Gown A, Ochs HD, Linsley PS, Wilson CB. Kay MA, et al. Nat Genet. 1995 Oct;11(2):191-7. doi: 10.1038/ng1095-191. Nat Genet. 1995. PMID: 7550348

4

Adenovirus-mediated urokinase gene transfer induces liver regeneration and allows for efficient retrovirus transduction of hepatocytes in vivo.

Lieber A, Vrancken Peeters MJ, Meuse L, Fausto N, Perkins J, Kay MA. Lieber A, et al. Among authors: kay ma. Proc Natl Acad Sci U S A. 1995 Jun 20;92(13):6210-4. doi: 10.1073/pnas.92.13.6210. Proc Natl Acad Sci U S A. 1995. PMID: 7597103 Free PMC article.

5

Adenovirus-mediated expression of ribozymes in mice.

Lieber A, Kay MA. Lieber A, et al. Among authors: kay ma. J Virol. 1996 May;70(5):3153-8. doi: 10.1128/JVI.70.5.3153-3158.1996. J Virol. 1996. PMID: 8627795 Free PMC article.

6

Adenovirus-mediated hepatic gene transfer in mice: comparison of intravascular and biliary administration.

Peeters MJ, Patijn GA, Lieber A, Meuse L, Kay MA. Peeters MJ, et al. Among authors: kay ma. Hum Gene Ther. 1996 Sep 10;7(14):1693-9. doi: 10.1089/hum.1996.7.14-1693. Hum Gene Ther. 1996. PMID: 8886840

7

Adenovirus-mediated gene therapy in a mouse model of hereditary tyrosinemia type I.

Overturf K, al-Dhalimy M, Ou CN, Finegold M, Tanguay R, Lieber A, Kay M, Grompe M. Overturf K, et al. Hum Gene Ther. 1997 Mar 20;8(5):513-21. doi: 10.1089/hum.1997.8.5-513. Hum Gene Ther. 1997. PMID: 9095403

8

Transient immunomodulation with anti-CD40 ligand antibody and CTLA4Ig enhances persistence and secondary adenovirus-mediated gene transfer into mouse liver.

Kay MA, Meuse L, Gown AM, Linsley P, Hollenbaugh D, Aruffo A, Ochs HD, Wilson CB. Kay MA, et al. Proc Natl Acad Sci U S A. 1997 Apr 29;94(9):4686-91. doi: 10.1073/pnas.94.9.4686. Proc Natl Acad Sci U S A. 1997. PMID: 9114052 Free PMC article.

9

Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors.

Snyder RO, Miao CH, Patijn GA, Spratt SK, Danos O, Nagy D, Gown AM, Winther B, Meuse L, Cohen LK, Thompson AR, Kay MA. Snyder RO, et al. Among authors: kay ma. Nat Genet. 1997 Jul;16(3):270-6. doi: 10.1038/ng0797-270. Nat Genet. 1997. PMID: 9207793

10

Constitutive expression of murine CTLA4Ig from a recombinant adenovirus vector results in prolonged transgene expression.

Schowalter DB, Meuse L, Wilson CB, Linsley PS, Kay MA. Schowalter DB, et al. Among authors: kay ma. Gene Ther. 1997 Aug;4(8):853-60. doi: 10.1038/sj.gt.3300466. Gene Ther. 1997. PMID: 9338015

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