Hodges BL - Search Results

1

Strain-specific rate of shutdown of CMV enhancer activity in murine liver confirmed by use of persistent [E1(-), E2b(-)] adenoviral vectors.

Everett RS, Evans HK, Hodges BL, Ding EY, Serra DM, Amalfitano A. Everett RS, et al. Among authors: hodges bl. Virology. 2004 Jul 20;325(1):96-105. doi: 10.1016/j.virol.2004.04.032. Virology. 2004. PMID: 15231389 Free article.

2

Long-term efficacy after [E1-, polymerase-] adenovirus-mediated transfer of human acid-alpha-glucosidase gene into glycogen storage disease type II knockout mice.

Ding EY, Hodges BL, Hu H, McVie-Wylie AJ, Serra D, Migone FK, Pressley D, Chen YT, Amalfitano A. Ding EY, et al. Among authors: hodges bl. Hum Gene Ther. 2001 May 20;12(8):955-65. doi: 10.1089/104303401750195917. Hum Gene Ther. 2001. PMID: 11387060

3

Adenovirus vectors with the 100K gene deleted and their potential for multiple gene therapy applications.

Hodges BL, Evans HK, Everett RS, Ding EY, Serra D, Amalfitano A. Hodges BL, et al. J Virol. 2001 Jul;75(13):5913-20. doi: 10.1128/JVI.75.13.5913-5920.2001. J Virol. 2001. PMID: 11390592 Free PMC article.

4

Liver toxicities typically induced by first-generation adenoviral vectors can be reduced by use of E1, E2b-deleted adenoviral vectors.

Everett RS, Hodges BL, Ding EY, Xu F, Serra D, Amalfitano A. Everett RS, et al. Among authors: hodges bl. Hum Gene Ther. 2003 Dec 10;14(18):1715-26. doi: 10.1089/104303403322611737. Hum Gene Ther. 2003. PMID: 14670123

5

Efficacy of gene therapy for a prototypical lysosomal storage disease (GSD-II) is critically dependent on vector dose, transgene promoter, and the tissues targeted for vector transduction.

Ding E, Hu H, Hodges BL, Migone F, Serra D, Xu F, Chen YT, Amalfitano A. Ding E, et al. Among authors: hodges bl. Mol Ther. 2002 Apr;5(4):436-46. doi: 10.1006/mthe.2002.0563. Mol Ther. 2002. PMID: 11945071 Free article.

6

Multiply deleted [E1, polymerase-, and pTP-] adenovirus vector persists despite deletion of the preterminal protein.

Hodges BL, Serra D, Hu H, Begy CA, Chamberlain JS, Amalfitano A. Hodges BL, et al. J Gene Med. 2000 Jul-Aug;2(4):250-9. doi: 10.1002/1521-2254(200007/08)2:4<250::AID-JGM113>3.0.CO;2-3. J Gene Med. 2000. PMID: 10953916

7

Optimization of vaccine responses with an E1, E2b and E3-deleted Ad5 vector circumvents pre-existing anti-vector immunity.

Osada T, Yang XY, Hartman ZC, Glass O, Hodges BL, Niedzwiecki D, Morse MA, Lyerly HK, Amalfitano A, Clay TM. Osada T, et al. Among authors: hodges bl. Cancer Gene Ther. 2009 Sep;16(9):673-82. doi: 10.1038/cgt.2009.17. Epub 2009 Feb 20. Cancer Gene Ther. 2009. PMID: 19229288 Free PMC article.

8

Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for duchenne muscular dystrophy.

Ahmad A, Brinson M, Hodges BL, Chamberlain JS, Amalfitano A. Ahmad A, et al. Among authors: hodges bl. Hum Mol Genet. 2000 Oct 12;9(17):2507-15. doi: 10.1093/hmg/9.17.2507. Hum Mol Genet. 2000. PMID: 11030755

9

A modified adenovirus can transfect cochlear hair cells in vivo without compromising cochlear function.

Luebke AE, Steiger JD, Hodges BL, Amalfitano A. Luebke AE, et al. Among authors: hodges bl. Gene Ther. 2001 May;8(10):789-94. doi: 10.1038/sj.gt.3301445. Gene Ther. 2001. PMID: 11420643

10

Acute regression of advanced and retardation of early aortic atheroma in immunocompetent apolipoprotein-E (apoE) deficient mice by administration of a second generation [E1(-), E3(-), polymerase(-)] adenovirus vector expressing human apoE.

Harris JD, Graham IR, Schepelmann S, Stannard AK, Roberts ML, Hodges BL, Hill V, Amalfitano A, Hassall DG, Owen JS, Dickson G. Harris JD, et al. Among authors: hodges bl. Hum Mol Genet. 2002 Jan 1;11(1):43-58. doi: 10.1093/hmg/11.1.43. Hum Mol Genet. 2002. PMID: 11772998

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