Michele DE - Search Results

1

Limb-girdle muscular dystrophy in the United States.

Moore SA, Shilling CJ, Westra S, Wall C, Wicklund MP, Stolle C, Brown CA, Michele DE, Piccolo F, Winder TL, Stence A, Barresi R, King N, King W, Florence J, Campbell KP, Fenichel GM, Stedman HH, Kissel JT, Griggs RC, Pandya S, Mathews KD, Pestronk A, Serrano C, Darvish D, Mendell JR. Moore SA, et al. Among authors: michele de. J Neuropathol Exp Neurol. 2006 Oct;65(10):995-1003. doi: 10.1097/01.jnen.0000235854.77716.6c. J Neuropathol Exp Neurol. 2006. PMID: 17021404

2

Myoglobinuria and muscle pain are common in patients with limb-girdle muscular dystrophy 2I.

Mathews KD, Stephan CM, Laubenthal K, Winder TL, Michele DE, Moore SA, Campbell KP. Mathews KD, et al. Among authors: michele de. Neurology. 2011 Jan 11;76(2):194-5. doi: 10.1212/WNL.0b013e3182061ad4. Neurology. 2011. PMID: 21220724 Free PMC article. No abstract available.

3

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.

Moore SA, Saito F, Chen J, Michele DE, Henry MD, Messing A, Cohn RD, Ross-Barta SE, Westra S, Williamson RA, Hoshi T, Campbell KP. Moore SA, et al. Among authors: michele de. Nature. 2002 Jul 25;418(6896):422-5. doi: 10.1038/nature00838. Nature. 2002. PMID: 12140559

4

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

Michele DE, Campbell KP. Michele DE, et al. J Biol Chem. 2003 May 2;278(18):15457-60. doi: 10.1074/jbc.R200031200. Epub 2003 Jan 29. J Biol Chem. 2003. PMID: 12556455 Free article. Review. No abstract available.

5

Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophy.

Durbeej M, Sawatzki SM, Barresi R, Schmainda KM, Allamand V, Michele DE, Campbell KP. Durbeej M, et al. Among authors: michele de. Proc Natl Acad Sci U S A. 2003 Jul 22;100(15):8910-5. doi: 10.1073/pnas.1537554100. Epub 2003 Jul 8. Proc Natl Acad Sci U S A. 2003. PMID: 12851463 Free PMC article.

6

Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies.

Michele DE, Barresi R, Kanagawa M, Saito F, Cohn RD, Satz JS, Dollar J, Nishino I, Kelley RI, Somer H, Straub V, Mathews KD, Moore SA, Campbell KP. Michele DE, et al. Nature. 2002 Jul 25;418(6896):417-22. doi: 10.1038/nature00837. Nature. 2002. PMID: 12140558

7

ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies.

Cirak S, Foley AR, Herrmann R, Willer T, Yau S, Stevens E, Torelli S, Brodd L, Kamynina A, Vondracek P, Roper H, Longman C, Korinthenberg R, Marrosu G, Nürnberg P; UK10K Consortium; Michele DE, Plagnol V, Hurles M, Moore SA, Sewry CA, Campbell KP, Voit T, Muntoni F. Cirak S, et al. Among authors: michele de. Brain. 2013 Jan;136(Pt 1):269-81. doi: 10.1093/brain/aws312. Epub 2013 Jan 3. Brain. 2013. PMID: 23288328 Free PMC article.

8

Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration.

Cohn RD, Henry MD, Michele DE, Barresi R, Saito F, Moore SA, Flanagan JD, Skwarchuk MW, Robbins ME, Mendell JR, Williamson RA, Campbell KP. Cohn RD, et al. Among authors: michele de. Cell. 2002 Sep 6;110(5):639-48. doi: 10.1016/s0092-8674(02)00907-8. Cell. 2002. PMID: 12230980 Free article.

9

LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies.

Barresi R, Michele DE, Kanagawa M, Harper HA, Dovico SA, Satz JS, Moore SA, Zhang W, Schachter H, Dumanski JP, Cohn RD, Nishino I, Campbell KP. Barresi R, et al. Among authors: michele de. Nat Med. 2004 Jul;10(7):696-703. doi: 10.1038/nm1059. Epub 2004 Jun 6. Nat Med. 2004. PMID: 15184894 Free article.

10

Dystroglycan matrix receptor function in cardiac myocytes is important for limiting activity-induced myocardial damage.

Michele DE, Kabaeva Z, Davis SL, Weiss RM, Campbell KP. Michele DE, et al. Circ Res. 2009 Nov 6;105(10):984-93. doi: 10.1161/CIRCRESAHA.109.199489. Epub 2009 Sep 24. Circ Res. 2009. PMID: 19797173 Free PMC article.

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