Spencer MJ - Search Results

1

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.

2

Absence of calpain 3 in a form of limb-girdle muscular dystrophy (LGMD2A).

Spencer MJ, Tidball JG, Anderson LV, Bushby KM, Harris JB, Passos-Bueno MR, Somer H, Vainzof M, Zatz M. Spencer MJ, et al. J Neurol Sci. 1997 Mar 10;146(2):173-8. doi: 10.1016/s0022-510x(96)00304-8. J Neurol Sci. 1997. PMID: 9077514

3

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.

4

Stable expression of calpain 3 from a muscle transgene in vivo: immature muscle in transgenic mice suggests a role for calpain 3 in muscle maturation.

Spencer MJ, Guyon JR, Sorimachi H, Potts A, Richard I, Herasse M, Chamberlain J, Dalkilic I, Kunkel LM, Beckmann JS. Spencer MJ, et al. Proc Natl Acad Sci U S A. 2002 Jun 25;99(13):8874-9. doi: 10.1073/pnas.132269299. Epub 2002 Jun 19. Proc Natl Acad Sci U S A. 2002. PMID: 12084932 Free PMC article.

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

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

9

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.

10

Identification of putative in vivo substrates of calpain 3 by comparative proteomics of overexpressing transgenic and nontransgenic mice.

Cohen N, Kudryashova E, Kramerova I, Anderson LV, Beckmann JS, Bushby K, Spencer MJ. Cohen N, et al. Among authors: spencer mj. Proteomics. 2006 Nov;6(22):6075-84. doi: 10.1002/pmic.200600199. Proteomics. 2006. PMID: 17051641

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