Cohn RD - 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: cohn rd. 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. Cell. 2002 Sep 6;110(5):639-48. doi: 10.1016/s0092-8674(02)00907-8. Cell. 2002. PMID: 12230980 Free 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: cohn rd. 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 basis of muscular dystrophies.

Cohn RD, Campbell KP. Cohn RD, et al. Muscle Nerve. 2000 Oct;23(10):1456-71. doi: 10.1002/1097-4598(200010)23:10<1456::aid-mus2>3.0.co;2-t. Muscle Nerve. 2000. PMID: 11003781 Review.

5

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. J Clin Invest. 2001 Jan;107(2):R1-7. doi: 10.1172/JCI11642. J Clin Invest. 2001. PMID: 11160141 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. Among authors: cohn rd. Nature. 2002 Jul 25;418(6896):417-22. doi: 10.1038/nature00837. Nature. 2002. PMID: 12140558

7

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

8

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: cohn rd. Neuron. 2003 Jun 5;38(5):747-58. doi: 10.1016/s0896-6273(03)00301-5. Neuron. 2003. PMID: 12797959 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: cohn rd. Nat Med. 2004 Jul;10(7):696-703. doi: 10.1038/nm1059. Epub 2004 Jun 6. Nat Med. 2004. PMID: 15184894 Free article.

10

Congenital muscular dystrophy with rigid spine syndrome: a clinical, pathological, radiological, and genetic study.

Flanigan KM, Kerr L, Bromberg MB, Leonard C, Tsuruda J, Zhang P, Gonzalez-Gomez I, Cohn R, Campbell KP, Leppert M. Flanigan KM, et al. Ann Neurol. 2000 Feb;47(2):152-61. Ann Neurol. 2000. PMID: 10665485

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