North KN - Search Results

1

The syntrophin-dystrobrevin subcomplex in human neuromuscular disorders.

Compton AG, Cooper ST, Hill PM, Yang N, Froehner SC, North KN. Compton AG, et al. Among authors: north kn. J Neuropathol Exp Neurol. 2005 Apr;64(4):350-61. doi: 10.1093/jnen/64.4.350. J Neuropathol Exp Neurol. 2005. PMID: 15835271

2

Single section Western blot: improving the molecular diagnosis of the muscular dystrophies.

Cooper ST, Lo HP, North KN. Cooper ST, et al. Among authors: north kn. Neurology. 2003 Jul 8;61(1):93-7. doi: 10.1212/01.wnl.0000069460.53438.38. Neurology. 2003. PMID: 12847163

3

Changes in skeletal muscle expression of AQP1 and AQP4 in dystrophinopathy and dysferlinopathy patients.

Au CG, Butler TL, Egan JR, Cooper ST, Lo HP, Compton AG, North KN, Winlaw DS. Au CG, et al. Among authors: north kn. Acta Neuropathol. 2008 Sep;116(3):235-46. doi: 10.1007/s00401-008-0369-z. Epub 2008 Apr 8. Acta Neuropathol. 2008. PMID: 18392839

4

Mutations in contactin-1, a neural adhesion and neuromuscular junction protein, cause a familial form of lethal congenital myopathy.

Compton AG, Albrecht DE, Seto JT, Cooper ST, Ilkovski B, Jones KJ, Challis D, Mowat D, Ranscht B, Bahlo M, Froehner SC, North KN. Compton AG, et al. Among authors: north kn. Am J Hum Genet. 2008 Dec;83(6):714-24. doi: 10.1016/j.ajhg.2008.10.022. Epub 2008 Nov 20. Am J Hum Genet. 2008. PMID: 19026398 Free PMC article.

5

Deficiency of the syntrophins and alpha-dystrobrevin in patients with inherited myopathy.

Jones KJ, Compton AG, Yang N, Mills MA, Peters MF, Mowat D, Kunkel LM, Froehner SC, North KN. Jones KJ, et al. Among authors: north kn. Neuromuscul Disord. 2003 Aug;13(6):456-67. doi: 10.1016/s0960-8966(03)00066-x. Neuromuscul Disord. 2003. PMID: 12899872

6

Expression of aquaporin 1 in human cardiac and skeletal muscle.

Au CG, Cooper ST, Lo HP, Compton AG, Yang N, Wintour EM, North KN, Winlaw DS. Au CG, et al. Among authors: north kn. J Mol Cell Cardiol. 2004 May;36(5):655-62. doi: 10.1016/j.yjmcc.2004.01.009. J Mol Cell Cardiol. 2004. PMID: 15135660

7

An alphaTropomyosin mutation alters dimer preference in nemaline myopathy.

Corbett MA, Akkari PA, Domazetovska A, Cooper ST, North KN, Laing NG, Gunning PW, Hardeman EC. Corbett MA, et al. Among authors: north kn. Ann Neurol. 2005 Jan;57(1):42-9. doi: 10.1002/ana.20305. Ann Neurol. 2005. PMID: 15562513

8

Defining alpha-skeletal and alpha-cardiac actin expression in human heart and skeletal muscle explains the absence of cardiac involvement in ACTA1 nemaline myopathy.

Ilkovski B, Clement S, Sewry C, North KN, Cooper ST. Ilkovski B, et al. Among authors: north kn. Neuromuscul Disord. 2005 Dec;15(12):829-35. doi: 10.1016/j.nmd.2005.08.004. Epub 2005 Nov 8. Neuromuscul Disord. 2005. PMID: 16288873

9

Dystrophinopathy carrier determination and detection of protein deficiencies in muscular dystrophy using lentiviral MyoD-forced myogenesis.

Cooper ST, Kizana E, Yates JD, Lo HP, Yang N, Wu ZH, Alexander IE, North KN. Cooper ST, et al. Among authors: north kn. Neuromuscul Disord. 2007 Apr;17(4):276-84. doi: 10.1016/j.nmd.2006.12.010. Epub 2007 Feb 15. Neuromuscul Disord. 2007. PMID: 17303423

10

Intranuclear rod myopathy: molecular pathogenesis and mechanisms of weakness.

Domazetovska A, Ilkovski B, Kumar V, Valova VA, Vandebrouck A, Hutchinson DO, Robinson PJ, Cooper ST, Sparrow JC, Peckham M, North KN. Domazetovska A, et al. Among authors: north kn. Ann Neurol. 2007 Dec;62(6):597-608. doi: 10.1002/ana.21200. Ann Neurol. 2007. PMID: 17705262

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