Davies KE - Search Results

1

Prevention of dystrophic pathology in severely affected dystrophin/utrophin-deficient mice by morpholino-oligomer-mediated exon-skipping.

Goyenvalle A, Babbs A, Powell D, Kole R, Fletcher S, Wilton SD, Davies KE. Goyenvalle A, et al. Among authors: davies ke. Mol Ther. 2010 Jan;18(1):198-205. doi: 10.1038/mt.2009.248. Epub 2009 Oct 20. Mol Ther. 2010. PMID: 19844193 Free PMC article.

2

Expression of the dystrophin-related protein (utrophin) gene during mouse embryogenesis.

Schofield J, Houzelstein D, Davies K, Buckingham M, Edwards YH. Schofield J, et al. Dev Dyn. 1993 Dec;198(4):254-64. doi: 10.1002/aja.1001980403. Dev Dyn. 1993. PMID: 8130373 Free article.

3

Expression of full-length utrophin prevents muscular dystrophy in mdx mice.

Tinsley J, Deconinck N, Fisher R, Kahn D, Phelps S, Gillis JM, Davies K. Tinsley J, et al. Nat Med. 1998 Dec;4(12):1441-4. doi: 10.1038/4033. Nat Med. 1998. PMID: 9846586

4

Function and genetics of dystrophin and dystrophin-related proteins in muscle.

Blake DJ, Weir A, Newey SE, Davies KE. Blake DJ, et al. Among authors: davies ke. Physiol Rev. 2002 Apr;82(2):291-329. doi: 10.1152/physrev.00028.2001. Physiol Rev. 2002. PMID: 11917091 Free article. Review.

5

The role of utrophin in the potential therapy of Duchenne muscular dystrophy.

Perkins KJ, Davies KE. Perkins KJ, et al. Among authors: davies ke. Neuromuscul Disord. 2002 Oct;12 Suppl 1:S78-89. doi: 10.1016/s0960-8966(02)00087-1. Neuromuscul Disord. 2002. PMID: 12206801 Review.

6

A- and B-utrophin have different expression patterns and are differentially up-regulated in mdx muscle.

Weir AP, Burton EA, Harrod G, Davies KE. Weir AP, et al. Among authors: davies ke. J Biol Chem. 2002 Nov 22;277(47):45285-90. doi: 10.1074/jbc.M205177200. Epub 2002 Sep 15. J Biol Chem. 2002. PMID: 12235137 Free article.

7

A-utrophin up-regulation in mdx skeletal muscle is independent of regeneration.

Weir AP, Morgan JE, Davies KE. Weir AP, et al. Among authors: davies ke. Neuromuscul Disord. 2004 Jan;14(1):19-23. doi: 10.1016/j.nmd.2003.09.004. Neuromuscul Disord. 2004. PMID: 14659408

8

Gene expression profiling studies on Caenorhabditis elegans dystrophin mutants dys-1(cx-35) and dys-1(cx18).

Towers PR, Lescure P, Baban D, Malek JA, Duarte J, Jones E, Davies KE, Ségalat L, Sattelle DB. Towers PR, et al. Among authors: davies ke. Genomics. 2006 Nov;88(5):642-9. doi: 10.1016/j.ygeno.2006.07.014. Epub 2006 Sep 7. Genomics. 2006. PMID: 16962739 Free article.

9

A dominant mutation in Snap25 causes impaired vesicle trafficking, sensorimotor gating, and ataxia in the blind-drunk mouse.

Jeans AF, Oliver PL, Johnson R, Capogna M, Vikman J, Molnár Z, Babbs A, Partridge CJ, Salehi A, Bengtsson M, Eliasson L, Rorsman P, Davies KE. Jeans AF, et al. Among authors: davies ke. Proc Natl Acad Sci U S A. 2007 Feb 13;104(7):2431-6. doi: 10.1073/pnas.0610222104. Epub 2007 Feb 5. Proc Natl Acad Sci U S A. 2007. PMID: 17283335 Free PMC article.

10

Microarray analysis of mdx mice expressing high levels of utrophin: therapeutic implications for dystrophin deficiency.

Baban D, Davies KE. Baban D, et al. Among authors: davies ke. Neuromuscul Disord. 2008 Mar;18(3):239-47. doi: 10.1016/j.nmd.2007.11.011. Epub 2008 Mar 14. Neuromuscul Disord. 2008. PMID: 18343112

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