Kochanek S - Search Results

1

Viral gene delivery to skeletal muscle: insights on maturation-dependent loss of fiber infectivity for adenovirus and herpes simplex type 1 viral vectors.

Feero WG, Rosenblatt JD, Huard J, Watkins SC, Epperly M, Clemens PR, Kochanek S, Glorioso JC, Partridge TA, Hoffman EP. Feero WG, et al. Among authors: kochanek s. Hum Gene Ther. 1997 Mar 1;8(4):371-80. doi: 10.1089/hum.1997.8.4-371. Hum Gene Ther. 1997. PMID: 9054512

2

Sustained muscle expression of dystrophin from a high-capacity adenoviral vector with systemic gene transfer of T cell costimulatory blockade.

Jiang Z, Schiedner G, van Rooijen N, Liu CC, Kochanek S, Clemens PR. Jiang Z, et al. Among authors: kochanek s. Mol Ther. 2004 Oct;10(4):688-96. doi: 10.1016/j.ymthe.2004.07.020. Mol Ther. 2004. PMID: 15451453 Free article.

3

Systemic delivery of a high-capacity adenoviral vector expressing mouse CTLA4Ig improves skeletal muscle gene therapy.

Jiang Z, Feingold E, Kochanek S, Clemens PR. Jiang Z, et al. Among authors: kochanek s. Mol Ther. 2002 Sep;6(3):369-76. doi: 10.1006/mthe.2002.0676. Mol Ther. 2002. PMID: 12231173 Free article.

4

Fetal muscle gene transfer is not enhanced by an RGD capsid modification to high-capacity adenoviral vectors.

Bilbao R, Reay DP, Hughes T, Biermann V, Volpers C, Goldberg L, Bergelson J, Kochanek S, Clemens PR. Bilbao R, et al. Among authors: kochanek s. Gene Ther. 2003 Oct;10(21):1821-9. doi: 10.1038/sj.gt.3302084. Gene Ther. 2003. PMID: 12960972

5

CTLA4Ig delivered by high-capacity adenoviral vector induces stable expression of dystrophin in mdx mouse muscle.

Jiang Z, Schiedner G, Gilchrist SC, Kochanek S, Clemens PR. Jiang Z, et al. Among authors: kochanek s. Gene Ther. 2004 Oct;11(19):1453-61. doi: 10.1038/sj.gt.3302315. Gene Ther. 2004. PMID: 15269713

6

Comparison of high-capacity and first-generation adenoviral vector gene delivery to murine muscle in utero.

Bilbao R, Reay DP, Wu E, Zheng H, Biermann V, Kochanek S, Clemens PR. Bilbao R, et al. Among authors: kochanek s. Gene Ther. 2005 Jan;12(1):39-47. doi: 10.1038/sj.gt.3302392. Gene Ther. 2005. PMID: 15483668

7

In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genes.

Clemens PR, Kochanek S, Sunada Y, Chan S, Chen HH, Campbell KP, Caskey CT. Clemens PR, et al. Among authors: kochanek s. Gene Ther. 1996 Nov;3(11):965-72. Gene Ther. 1996. PMID: 8940636

8

Ex vivo gene transfer using adenovirus-mediated full-length dystrophin delivery to dystrophic muscles.

Floyd SS Jr, Clemens PR, Ontell MR, Kochanek S, Day CS, Yang J, Hauschka SD, Balkir L, Morgan J, Moreland MS, Feero GW, Epperly M, Huard J. Floyd SS Jr, et al. Among authors: kochanek s. Gene Ther. 1998 Jan;5(1):19-30. doi: 10.1038/sj.gt.3300549. Gene Ther. 1998. PMID: 9536261

9

DNA from both high-capacity and first-generation adenoviral vectors remains intact in skeletal muscle.

Chen HH, Mack LM, Choi SY, Ontell M, Kochanek S, Clemens PR. Chen HH, et al. Among authors: kochanek s. Hum Gene Ther. 1999 Feb 10;10(3):365-73. doi: 10.1089/10430349950018814. Hum Gene Ther. 1999. PMID: 10048389

10

Local high-capacity adenovirus-mediated mCTLA4Ig and mCD40Ig expression prolongs recombinant gene expression in skeletal muscle.

Jiang ZL, Reay D, Kreppel F, Gambotto A, Feingold E, Kochanek S, McCarthy SA, Clemens PR. Jiang ZL, et al. Among authors: kochanek s. Mol Ther. 2001 Jun;3(6):892-900. doi: 10.1006/mthe.2001.0331. Mol Ther. 2001. PMID: 11407903 Free article.

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