Barresi R - 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: barresi r. Cell. 1999 Aug 20;98(4):465-74. doi: 10.1016/s0092-8674(00)81975-3. Cell. 1999. PMID: 10481911 Free article.

2

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: barresi r. Cell. 2002 Sep 6;110(5):639-48. doi: 10.1016/s0092-8674(02)00907-8. Cell. 2002. PMID: 12230980 Free article.

3

Loss of sarcolemma nNOS in sarcoglycan-deficient muscle.

Crosbie RH, Barresi R, Campbell KP. Crosbie RH, et al. Among authors: barresi r. FASEB J. 2002 Nov;16(13):1786-91. doi: 10.1096/fj.02-0519com. FASEB J. 2002. PMID: 12409321

4

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. J Biol Chem. 2000 Dec 8;275(49):38554-60. doi: 10.1074/jbc.M007799200. J Biol Chem. 2000. PMID: 10993904 Free article.

5

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: barresi r. Nature. 2002 Jul 25;418(6896):417-22. doi: 10.1038/nature00837. Nature. 2002. PMID: 12140558

6

Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilization.

Saito F, Moore SA, Barresi R, Henry MD, Messing A, Ross-Barta SE, Cohn RD, Williamson RA, Sluka KA, Sherman DL, Brophy PJ, Schmelzer JD, Low PA, Wrabetz L, Feltri ML, Campbell KP. Saito F, et al. Among authors: barresi r. Neuron. 2003 Jun 5;38(5):747-58. doi: 10.1016/s0896-6273(03)00301-5. Neuron. 2003. PMID: 12797959 Free article.

7

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: barresi r. 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.

8

Abnormal coronary function in mice deficient in alpha1H T-type Ca2+ channels.

Chen CC, Lamping KG, Nuno DW, Barresi R, Prouty SJ, Lavoie JL, Cribbs LL, England SK, Sigmund CD, Weiss RM, Williamson RA, Hill JA, Campbell KP. Chen CC, et al. Among authors: barresi r. Science. 2003 Nov 21;302(5649):1416-8. doi: 10.1126/science.1089268. Science. 2003. PMID: 14631046

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. Nat Med. 2004 Jul;10(7):696-703. doi: 10.1038/nm1059. Epub 2004 Jun 6. Nat Med. 2004. PMID: 15184894 Free article.

10

Molecular recognition by LARGE is essential for expression of functional dystroglycan.

Kanagawa M, Saito F, Kunz S, Yoshida-Moriguchi T, Barresi R, Kobayashi YM, Muschler J, Dumanski JP, Michele DE, Oldstone MB, Campbell KP. Kanagawa M, et al. Among authors: barresi r. Cell. 2004 Jun 25;117(7):953-64. doi: 10.1016/j.cell.2004.06.003. Cell. 2004. PMID: 15210115 Free article.

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