Caskey CT - Search Results

1

Correction of chromosomal mutation and random integration in embryonic stem cells with helper-dependent adenoviral vectors.

Ohbayashi F, Balamotis MA, Kishimoto A, Aizawa E, Diaz A, Hasty P, Graham FL, Caskey CT, Mitani K. Ohbayashi F, et al. Among authors: caskey ct. Proc Natl Acad Sci U S A. 2005 Sep 20;102(38):13628-33. doi: 10.1073/pnas.0506598102. Epub 2005 Sep 7. Proc Natl Acad Sci U S A. 2005. PMID: 16174752 Free PMC article.

2

Gene targeting in mouse embryonic stem cells with an adenoviral vector.

Mitani K, Wakamiya M, Hasty P, Graham FL, Bradley A, Caskey CT. Mitani K, et al. Among authors: caskey ct. Somat Cell Mol Genet. 1995 Jul;21(4):221-31. doi: 10.1007/BF02255777. Somat Cell Mol Genet. 1995. PMID: 8525428

3

Rescue, propagation, and partial purification of a helper virus-dependent adenovirus vector.

Mitani K, Graham FL, Caskey CT, Kochanek S. Mitani K, et al. Among authors: caskey ct. Proc Natl Acad Sci U S A. 1995 Apr 25;92(9):3854-8. doi: 10.1073/pnas.92.9.3854. Proc Natl Acad Sci U S A. 1995. PMID: 7731995 Free PMC article.

4

A new adenoviral vector: Replacement of all viral coding sequences with 28 kb of DNA independently expressing both full-length dystrophin and beta-galactosidase.

Kochanek S, Clemens PR, Mitani K, Chen HH, Chan S, Caskey CT. Kochanek S, et al. Among authors: caskey ct. Proc Natl Acad Sci U S A. 1996 Jun 11;93(12):5731-6. doi: 10.1073/pnas.93.12.5731. Proc Natl Acad Sci U S A. 1996. PMID: 8650161 Free PMC article.

5

An adenoviral vector deleted for all viral coding sequences results in enhanced safety and extended expression of a leptin transgene.

Morsy MA, Gu M, Motzel S, Zhao J, Lin J, Su Q, Allen H, Franlin L, Parks RJ, Graham FL, Kochanek S, Bett AJ, Caskey CT. Morsy MA, et al. Among authors: caskey ct. Proc Natl Acad Sci U S A. 1998 Jul 7;95(14):7866-71. doi: 10.1073/pnas.95.14.7866. Proc Natl Acad Sci U S A. 1998. PMID: 9653106 Free PMC article.

6

Transduction of human bone marrow by adenoviral vector.

Mitani K, Graham FL, Caskey CT. Mitani K, et al. Among authors: caskey ct. Hum Gene Ther. 1994 Aug;5(8):941-8. doi: 10.1089/hum.1994.5.8-941. Hum Gene Ther. 1994. PMID: 7948143

7

Efficient adenoviral-mediated ornithine transcarbamylase expression in deficient mouse and human hepatocytes.

Morsy MA, Alford EL, Bett A, Graham FL, Caskey CT. Morsy MA, et al. Among authors: caskey ct. J Clin Invest. 1993 Sep;92(3):1580-6. doi: 10.1172/JCI116739. J Clin Invest. 1993. PMID: 8376608 Free PMC article.

8

Recombinant truncated dystrophin minigenes: construction, expression, and adenoviral delivery.

Clemens PR, Krause TL, Chan S, Korb KE, Graham FL, Caskey CT. Clemens PR, et al. Among authors: caskey ct. Hum Gene Ther. 1995 Nov;6(11):1477-85. doi: 10.1089/hum.1995.6.11-1477. Hum Gene Ther. 1995. PMID: 8573620

9

Delivering therapeutic genes--matching approach and application.

Mitani K, Caskey CT. Mitani K, et al. Among authors: caskey ct. Trends Biotechnol. 1993 May;11(5):162-6. doi: 10.1016/0167-7799(93)90108-L. Trends Biotechnol. 1993. PMID: 7763805 Review. No abstract available.

10

Gene transfer therapy for heritable disease: cell and expression targeting.

Mitani K, Clemens PR, Moseley AB, Caskey CT. Mitani K, et al. Among authors: caskey ct. Philos Trans R Soc Lond B Biol Sci. 1993 Feb 27;339(1288):217-24. doi: 10.1098/rstb.1993.0019. Philos Trans R Soc Lond B Biol Sci. 1993. PMID: 8097051 Review.

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