Moore SA - Search Results

1

Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy.

Coral-Vazquez R, Cohn RD, Moore SA, Hill JA, Weiss RM, Davisson RL, Straub V, Barresi R, Bansal D, Hrstka RF, Williamson R, Campbell KP. Coral-Vazquez R, et al. Among authors: moore sa. Cell. 1999 Aug 20;98(4):465-74. doi: 10.1016/s0092-8674(00)81975-3. Cell. 1999. PMID: 10481911 Free article.

2

Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice.

Duclos F, Straub V, Moore SA, Venzke DP, Hrstka RF, Crosbie RH, Durbeej M, Lebakken CS, Ettinger AJ, van der Meulen J, Holt KH, Lim LE, Sanes JR, Davidson BL, Faulkner JA, Williamson R, Campbell KP. Duclos F, et al. Among authors: moore sa. J Cell Biol. 1998 Sep 21;142(6):1461-71. doi: 10.1083/jcb.142.6.1461. J Cell Biol. 1998. PMID: 9744877 Free PMC article.

3

Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E.

Durbeej M, Cohn RD, Hrstka RF, Moore SA, Allamand V, Davidson BL, Williamson RA, Campbell KP. Durbeej M, et al. Among authors: moore sa. Mol Cell. 2000 Jan;5(1):141-51. doi: 10.1016/s1097-2765(00)80410-4. Mol Cell. 2000. PMID: 10678176 Free article.

4

Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions.

Crosbie RH, Lim LE, Moore SA, Hirano M, Hays AP, Maybaum SW, Collin H, Dovico SA, Stolle CA, Fardeau M, Tomé FM, Campbell KP. Crosbie RH, et al. Among authors: moore sa. Hum Mol Genet. 2000 Aug 12;9(13):2019-27. doi: 10.1093/hmg/9.13.2019. Hum Mol Genet. 2000. PMID: 10942431

5

Expression of gamma -sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complex.

Barresi R, Moore SA, Stolle CA, Mendell JR, Campbell KP. Barresi R, et al. Among authors: moore sa. J Biol Chem. 2000 Dec 8;275(49):38554-60. doi: 10.1074/jbc.M007799200. J Biol Chem. 2000. PMID: 10993904 Free article.

6

Intracellular accumulation and reduced sarcolemmal expression of dysferlin in limb--girdle muscular dystrophies.

Piccolo F, Moore SA, Ford GC, Campbell KP. Piccolo F, et al. Among authors: moore sa. Ann Neurol. 2000 Dec;48(6):902-12. Ann Neurol. 2000. PMID: 11117547

7

Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex.

Cohn RD, Durbeej M, Moore SA, Coral-Vazquez R, Prouty S, Campbell KP. Cohn RD, et al. Among authors: moore sa. J Clin Invest. 2001 Jan;107(2):R1-7. doi: 10.1172/JCI11642. J Clin Invest. 2001. PMID: 11160141 Free PMC article.

8

Limb-girdle muscular dystrophies.

Piccolo F, Moore SA, Mathews KD, Campbell KP. Piccolo F, et al. Among authors: moore sa. Adv Neurol. 2002;88:273-91. Adv Neurol. 2002. PMID: 11908231 Review. No abstract available.

9

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. Among authors: moore sa. Nature. 2002 Jul 25;418(6896):417-22. doi: 10.1038/nature00837. Nature. 2002. PMID: 12140558

10

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. Nature. 2002 Jul 25;418(6896):422-5. doi: 10.1038/nature00838. Nature. 2002. PMID: 12140559

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