Yang N - Search Results

1

Nemaline myopathy caused by mutations in the muscle alpha-skeletal-actin gene.

Ilkovski B, Cooper ST, Nowak K, Ryan MM, Yang N, Schnell C, Durling HJ, Roddick LG, Wilkinson I, Kornberg AJ, Collins KJ, Wallace G, Gunning P, Hardeman EC, Laing NG, North KN. Ilkovski B, et al. Among authors: yang n. Am J Hum Genet. 2001 Jun;68(6):1333-43. doi: 10.1086/320605. Epub 2001 Apr 27. Am J Hum Genet. 2001. PMID: 11333380 Free PMC article.

2

Hypertrophy and dietary tyrosine ameliorate the phenotypes of a mouse model of severe nemaline myopathy.

Nguyen MA, Joya JE, Kee AJ, Domazetovska A, Yang N, Hook JW, Lemckert FA, Kettle E, Valova VA, Robinson PJ, North KN, Gunning PW, Mitchell CA, Hardeman EC. Nguyen MA, et al. Among authors: yang n. Brain. 2011 Dec;134(Pt 12):3516-29. doi: 10.1093/brain/awr274. Epub 2011 Nov 8. Brain. 2011. PMID: 22067542

3

A mutation in alpha-tropomyosin(slow) affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathy.

Corbett MA, Robinson CS, Dunglison GF, Yang N, Joya JE, Stewart AW, Schnell C, Gunning PW, North KN, Hardeman EC. Corbett MA, et al. Among authors: yang n. Hum Mol Genet. 2001 Feb 15;10(4):317-28. doi: 10.1093/hmg/10.4.317. Hum Mol Genet. 2001. PMID: 11157795

4

ACTN3 genotype is associated with human elite athletic performance.

Yang N, MacArthur DG, Gulbin JP, Hahn AG, Beggs AH, Easteal S, North K. Yang N, et al. Am J Hum Genet. 2003 Sep;73(3):627-31. doi: 10.1086/377590. Epub 2003 Jul 23. Am J Hum Genet. 2003. PMID: 12879365 Free PMC article.

5

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: yang n. 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

6

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: yang n. J Neuropathol Exp Neurol. 2005 Apr;64(4):350-61. doi: 10.1093/jnen/64.4.350. J Neuropathol Exp Neurol. 2005. PMID: 15835271

7

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: yang n. 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

8

Loss of ACTN3 gene function alters mouse muscle metabolism and shows evidence of positive selection in humans.

MacArthur DG, Seto JT, Raftery JM, Quinlan KG, Huttley GA, Hook JW, Lemckert FA, Kee AJ, Edwards MR, Berman Y, Hardeman EC, Gunning PW, Easteal S, Yang N, North KN. MacArthur DG, et al. Among authors: yang n. Nat Genet. 2007 Oct;39(10):1261-5. doi: 10.1038/ng2122. Epub 2007 Sep 9. Nat Genet. 2007. PMID: 17828264

9

An Actn3 knockout mouse provides mechanistic insights into the association between alpha-actinin-3 deficiency and human athletic performance.

MacArthur DG, Seto JT, Chan S, Quinlan KG, Raftery JM, Turner N, Nicholson MD, Kee AJ, Hardeman EC, Gunning PW, Cooney GJ, Head SI, Yang N, North KN. MacArthur DG, et al. Among authors: yang n. Hum Mol Genet. 2008 Apr 15;17(8):1076-86. doi: 10.1093/hmg/ddm380. Epub 2008 Jan 4. Hum Mol Genet. 2008. PMID: 18178581

10

Alpha-actinin-3 deficiency results in reduced glycogen phosphorylase activity and altered calcium handling in skeletal muscle.

Quinlan KG, Seto JT, Turner N, Vandebrouck A, Floetenmeyer M, Macarthur DG, Raftery JM, Lek M, Yang N, Parton RG, Cooney GJ, North KN. Quinlan KG, et al. Among authors: yang n. Hum Mol Genet. 2010 Apr 1;19(7):1335-46. doi: 10.1093/hmg/ddq010. Epub 2010 Jan 20. Hum Mol Genet. 2010. PMID: 20089531

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