Kay MA - Search Results

1

Ribosomal DNA integrating rAAV-rDNA vectors allow for stable transgene expression.

Lisowski L, Lau A, Wang Z, Zhang Y, Zhang F, Grompe M, Kay MA. Lisowski L, et al. Among authors: kay ma. Mol Ther. 2012 Oct;20(10):1912-23. doi: 10.1038/mt.2012.164. Epub 2012 Sep 18. Mol Ther. 2012. PMID: 22990671 Free PMC article.

2

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

3

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

4

Efficient construction of a recombinant adenovirus vector by an improved in vitro ligation method.

Mizuguchi H, Kay MA. Mizuguchi H, et al. Among authors: kay ma. Hum Gene Ther. 1998 Nov 20;9(17):2577-83. doi: 10.1089/hum.1998.9.17-2577. Hum Gene Ther. 1998. PMID: 9853524

5

Integrating adenovirus-adeno-associated virus hybrid vectors devoid of all viral genes.

Lieber A, Steinwaerder DS, Carlson CA, Kay MA. Lieber A, et al. Among authors: kay ma. J Virol. 1999 Nov;73(11):9314-24. doi: 10.1128/JVI.73.11.9314-9324.1999. J Virol. 1999. PMID: 10516040 Free PMC article.

6

Increasing the size of rAAV-mediated expression cassettes in vivo by intermolecular joining of two complementary vectors.

Nakai H, Storm TA, Kay MA. Nakai H, et al. Among authors: kay ma. Nat Biotechnol. 2000 May;18(5):527-32. doi: 10.1038/75390. Nat Biotechnol. 2000. PMID: 10802620

7

Somatic integration and long-term transgene expression in normal and haemophilic mice using a DNA transposon system.

Yant SR, Meuse L, Chiu W, Ivics Z, Izsvak Z, Kay MA. Yant SR, et al. Among authors: kay ma. Nat Genet. 2000 May;25(1):35-41. doi: 10.1038/75568. Nat Genet. 2000. PMID: 10802653

8

Therapeutic levels of human factor VIII and IX using HIV-1-based lentiviral vectors in mouse liver.

Park F, Ohashi K, Kay MA. Park F, et al. Among authors: kay ma. Blood. 2000 Aug 1;96(3):1173-6. Blood. 2000. PMID: 10910939 Free article.

9

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 vitro.

Miao CH, Ohashi K, Patijn GA, Meuse L, Ye X, Thompson AR, Kay MA. Miao CH, et al. Among authors: kay ma. Mol Ther. 2000 Jun;1(6):522-32. doi: 10.1006/mthe.2000.0075. Mol Ther. 2000. PMID: 10933977 Free article.

10

Recruitment of single-stranded recombinant adeno-associated virus vector genomes and intermolecular recombination are responsible for stable transduction of liver in vivo.

Nakai H, Storm TA, Kay MA. Nakai H, et al. Among authors: kay ma. J Virol. 2000 Oct;74(20):9451-63. doi: 10.1128/jvi.74.20.9451-9463.2000. J Virol. 2000. PMID: 11000214 Free PMC article.

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