Chamberlain JS - Search Results

1

Functional capacity of dystrophins carrying deletions in the N-terminal actin-binding domain.

Banks GB, Gregorevic P, Allen JM, Finn EE, Chamberlain JS. Banks GB, et al. Among authors: chamberlain js. Hum Mol Genet. 2007 Sep 1;16(17):2105-13. doi: 10.1093/hmg/ddm158. Epub 2007 Jun 22. Hum Mol Genet. 2007. PMID: 17588958

2

Expression of full-length and truncated dystrophin mini-genes in transgenic mdx mice.

Phelps SF, Hauser MA, Cole NM, Rafael JA, Hinkle RT, Faulkner JA, Chamberlain JS. Phelps SF, et al. Among authors: chamberlain js. Hum Mol Genet. 1995 Aug;4(8):1251-8. doi: 10.1093/hmg/4.8.1251. Hum Mol Genet. 1995. PMID: 7581361

3

Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoform.

Rafael JA, Sunada Y, Cole NM, Campbell KP, Faulkner JA, Chamberlain JS. Rafael JA, et al. Among authors: chamberlain js. Hum Mol Genet. 1994 Oct;3(10):1725-33. doi: 10.1093/hmg/3.10.1725. Hum Mol Genet. 1994. PMID: 7849695

4

Dystrophin and utrophin influence fiber type composition and post-synaptic membrane structure.

Rafael JA, Townsend ER, Squire SE, Potter AC, Chamberlain JS, Davies KE. Rafael JA, et al. Among authors: chamberlain js. Hum Mol Genet. 2000 May 22;9(9):1357-67. doi: 10.1093/hmg/9.9.1357. Hum Mol Genet. 2000. PMID: 10814717

5

Suppression of revertant fibers in mdx mice by expression of a functional dystrophin.

Crawford GE, Lu QL, Partridge TA, Chamberlain JS. Crawford GE, et al. Among authors: chamberlain js. Hum Mol Genet. 2001 Nov 15;10(24):2745-50. doi: 10.1093/hmg/10.24.2745. Hum Mol Genet. 2001. PMID: 11734539

6

Modular flexibility of dystrophin: implications for gene therapy of Duchenne muscular dystrophy.

Harper SQ, Hauser MA, DelloRusso C, Duan D, Crawford RW, Phelps SF, Harper HA, Robinson AS, Engelhardt JF, Brooks SV, Chamberlain JS. Harper SQ, et al. Among authors: chamberlain js. Nat Med. 2002 Mar;8(3):253-61. doi: 10.1038/nm0302-253. Nat Med. 2002. PMID: 11875496

7

Expression of Dp260 in muscle tethers the actin cytoskeleton to the dystrophin-glycoprotein complex and partially prevents dystrophy.

Warner LE, DelloRusso C, Crawford RW, Rybakova IN, Patel JR, Ervasti JM, Chamberlain JS. Warner LE, et al. Among authors: chamberlain js. Hum Mol Genet. 2002 May 1;11(9):1095-105. doi: 10.1093/hmg/11.9.1095. Hum Mol Genet. 2002. PMID: 11978768

8

Spectrin-like repeats from dystrophin and alpha-actinin-2 are not functionally interchangeable.

Harper SQ, Crawford RW, DelloRusso C, Chamberlain JS. Harper SQ, et al. Among authors: chamberlain js. Hum Mol Genet. 2002 Aug 1;11(16):1807-15. doi: 10.1093/hmg/11.16.1807. Hum Mol Genet. 2002. PMID: 12140183

9

Viral vectors for gene transfer of micro-, mini-, or full-length dystrophin.

Scott JM, Li S, Harper SQ, Welikson R, Bourque D, DelloRusso C, Hauschka SD, Chamberlain JS. Scott JM, et al. Among authors: chamberlain js. Neuromuscul Disord. 2002 Oct;12 Suppl 1:S23-9. doi: 10.1016/s0960-8966(02)00078-0. Neuromuscul Disord. 2002. PMID: 12206791 Review.

10

Gene therapy of muscular dystrophy.

Chamberlain JS. Chamberlain JS. Hum Mol Genet. 2002 Oct 1;11(20):2355-62. doi: 10.1093/hmg/11.20.2355. Hum Mol Genet. 2002. PMID: 12351570 Review.

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