Spencer MJ - Search Results

1

Trim32 is a ubiquitin ligase mutated in limb girdle muscular dystrophy type 2H that binds to skeletal muscle myosin and ubiquitinates actin.

Kudryashova E, Kudryashov D, Kramerova I, Spencer MJ. Kudryashova E, et al. Among authors: spencer mj. J Mol Biol. 2005 Nov 25;354(2):413-24. doi: 10.1016/j.jmb.2005.09.068. Epub 2005 Oct 10. J Mol Biol. 2005. PMID: 16243356

2

Calpains and muscular dystrophies.

Tidball JG, Spencer MJ. Tidball JG, et al. Among authors: spencer mj. Int J Biochem Cell Biol. 2000 Jan;32(1):1-5. doi: 10.1016/s1357-2725(99)00095-3. Int J Biochem Cell Biol. 2000. PMID: 10661889 Review.

3

A nitric oxide synthase transgene ameliorates muscular dystrophy in mdx mice.

Wehling M, Spencer MJ, Tidball JG. Wehling M, et al. Among authors: spencer mj. J Cell Biol. 2001 Oct 1;155(1):123-31. doi: 10.1083/jcb.200105110. J Cell Biol. 2001. PMID: 11581289 Free PMC article.

4

Overexpression of a calpastatin transgene in mdx muscle reduces dystrophic pathology.

Spencer MJ, Mellgren RL. Spencer MJ, et al. Hum Mol Genet. 2002 Oct 1;11(21):2645-55. doi: 10.1093/hmg/11.21.2645. Hum Mol Genet. 2002. PMID: 12354790

5

Calpain 3 cleaves filamin C and regulates its ability to interact with gamma- and delta-sarcoglycans.

Guyon JR, Kudryashova E, Potts A, Dalkilic I, Brosius MA, Thompson TG, Beckmann JS, Kunkel LM, Spencer MJ. Guyon JR, et al. Among authors: spencer mj. Muscle Nerve. 2003 Oct;28(4):472-83. doi: 10.1002/mus.10465. Muscle Nerve. 2003. PMID: 14506720

6

Null mutation of calpain 3 (p94) in mice causes abnormal sarcomere formation in vivo and in vitro.

Kramerova I, Kudryashova E, Tidball JG, Spencer MJ. Kramerova I, et al. Among authors: spencer mj. Hum Mol Genet. 2004 Jul 1;13(13):1373-88. doi: 10.1093/hmg/ddh153. Epub 2004 May 11. Hum Mol Genet. 2004. PMID: 15138196

7

Calpain 3 participates in sarcomere remodeling by acting upstream of the ubiquitin-proteasome pathway.

Kramerova I, Kudryashova E, Venkatraman G, Spencer MJ. Kramerova I, et al. Among authors: spencer mj. Hum Mol Genet. 2005 Aug 1;14(15):2125-34. doi: 10.1093/hmg/ddi217. Epub 2005 Jun 16. Hum Mol Genet. 2005. PMID: 15961411

8

Mdm muscular dystrophy: interactions with calpain 3 and a novel functional role for titin's N2A domain.

Huebsch KA, Kudryashova E, Wooley CM, Sher RB, Seburn KL, Spencer MJ, Cox GA. Huebsch KA, et al. Among authors: spencer mj. Hum Mol Genet. 2005 Oct 1;14(19):2801-11. doi: 10.1093/hmg/ddi313. Epub 2005 Aug 22. Hum Mol Genet. 2005. PMID: 16115818 Free PMC article.

9

Molecular and cellular basis of calpainopathy (limb girdle muscular dystrophy type 2A).

Kramerova I, Beckmann JS, Spencer MJ. Kramerova I, et al. Among authors: spencer mj. Biochim Biophys Acta. 2007 Feb;1772(2):128-44. doi: 10.1016/j.bbadis.2006.07.002. Epub 2006 Jul 15. Biochim Biophys Acta. 2007. PMID: 16934440 Free article. Review.

10

Regulation of the M-cadherin-beta-catenin complex by calpain 3 during terminal stages of myogenic differentiation.

Kramerova I, Kudryashova E, Wu B, Spencer MJ. Kramerova I, et al. Among authors: spencer mj. Mol Cell Biol. 2006 Nov;26(22):8437-47. doi: 10.1128/MCB.01296-06. Epub 2006 Sep 18. Mol Cell Biol. 2006. PMID: 16982691 Free PMC article.

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