Williamson RA - Search Results

1

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

2

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

3

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: williamson ra. Neuron. 2003 Jun 5;38(5):747-58. doi: 10.1016/s0896-6273(03)00301-5. Neuron. 2003. PMID: 12797959 Free article.

4

Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice.

Williamson RA, Henry MD, Daniels KJ, Hrstka RF, Lee JC, Sunada Y, Ibraghimov-Beskrovnaya O, Campbell KP. Williamson RA, et al. Hum Mol Genet. 1997 Jun;6(6):831-41. doi: 10.1093/hmg/6.6.831. Hum Mol Genet. 1997. PMID: 9175728

5

Analysis of the role of dystroglycan in early postimplantation mouse development.

Henry MD, Williamson RA, Campbell KP. Henry MD, et al. Among authors: williamson ra. Ann N Y Acad Sci. 1998 Oct 23;857:256-9. doi: 10.1111/j.1749-6632.1998.tb10126.x. Ann N Y Acad Sci. 1998. PMID: 9917851 No abstract available.

6

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: williamson ra. Mol Cell. 2000 Jan;5(1):141-51. doi: 10.1016/s1097-2765(00)80410-4. Mol Cell. 2000. PMID: 10678176 Free article.

7

Defective membrane repair in dysferlin-deficient muscular dystrophy.

Bansal D, Miyake K, Vogel SS, Groh S, Chen CC, Williamson R, McNeil PL, Campbell KP. Bansal D, et al. Nature. 2003 May 8;423(6936):168-72. doi: 10.1038/nature01573. Nature. 2003. PMID: 12736685

8

Sarcospan-deficient mice maintain normal muscle function.

Lebakken CS, Venzke DP, Hrstka RF, Consolino CM, Faulkner JA, Williamson RA, Campbell KP. Lebakken CS, et al. Among authors: williamson ra. Mol Cell Biol. 2000 Mar;20(5):1669-77. doi: 10.1128/MCB.20.5.1669-1677.2000. Mol Cell Biol. 2000. PMID: 10669744 Free PMC article.

9

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: williamson ra. Science. 2003 Nov 21;302(5649):1416-8. doi: 10.1126/science.1089268. Science. 2003. PMID: 14631046

10

Muscles of mice deficient in alpha-sarcoglycan maintain large masses and near control force values throughout the life span.

Consolino CM, Duclos F, Lee J, Williamson RA, Campbell KP, Brooks SV. Consolino CM, et al. Among authors: williamson ra. Physiol Genomics. 2005 Jul 14;22(2):244-56. doi: 10.1152/physiolgenomics.00311.2004. Epub 2005 May 10. Physiol Genomics. 2005. PMID: 15886330

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