Zhao Y - Search Results

1

Muscle injury induced by different types of contractions in dystrophic mdx mice.

Lou J, Bi W, Li W, Zhao Y, Liu S, Zheng J, Yan C. Lou J, et al. Among authors: zhao y. J Muscle Res Cell Motil. 2012 Mar;32(6):411-9. doi: 10.1007/s10974-012-9284-y. Epub 2012 Feb 11. J Muscle Res Cell Motil. 2012. PMID: 22327507

2

[Dysferlin expression in limb-girdle muscular dystrophy and Miyoshi myopathy: analysis of 45 cases].

Ren SC, Yan CZ, Li MX, Liu SP, Wu JL, Zhao YY, Li W, Li DN. Ren SC, et al. Zhonghua Yi Xue Za Zhi. 2007 Jun 5;87(21):1486-90. Zhonghua Yi Xue Za Zhi. 2007. PMID: 17785089 Chinese.

3

[Clinical and pathological features and prognosis of Chinese patients with distal myopathy with rimmed vacuoles: study of 17 cases].

Chen Q, Yan CZ, Liu SP, Zhao YY, Li W, Wu JL, Li DN. Chen Q, et al. Zhonghua Yi Xue Za Zhi. 2008 May 20;88(19):1313-7. Zhonghua Yi Xue Za Zhi. 2008. PMID: 18956699 Chinese.

4

[Clinical and biopsy-based myopathological features of 5 cases with centronuclear myopathy].

Li HH, Liu SP, Li W, Zhao YY, Wu JL, Li DN, Yan CZ. Li HH, et al. Zhonghua Er Ke Za Zhi. 2008 Nov;46(11):856-9. Zhonghua Er Ke Za Zhi. 2008. PMID: 19099905 Chinese.

5

Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations.

Wen B, Dai T, Li W, Zhao Y, Liu S, Zhang C, Li H, Wu J, Li D, Yan C. Wen B, et al. Among authors: zhao y. J Neurol Neurosurg Psychiatry. 2010 Feb;81(2):231-6. doi: 10.1136/jnnp.2009.176404. Epub 2009 Sep 15. J Neurol Neurosurg Psychiatry. 2010. PMID: 19758981

6

Clinical and molecular genetic analysis in Chinese patients with distal myopathy with rimmed vacuoles.

Li H, Chen Q, Liu F, Zhang X, Liu T, Li W, Liu S, Zhao Y, Wen B, Dai T, Lin P, Gong Y, Yan C. Li H, et al. Among authors: zhao y. J Hum Genet. 2011 Apr;56(4):335-8. doi: 10.1038/jhg.2011.15. Epub 2011 Feb 10. J Hum Genet. 2011. PMID: 21307865

7

Primary angiitis of the central nervous system: a case report.

Yu XL, Liu AF, Ma L, Yan CZ, Zhao YY, Shan PY. Yu XL, et al. Chin Med J (Engl). 2011 Sep;124(17):2782-5. Chin Med J (Engl). 2011. PMID: 22040443

8

Novel PNPLA2 gene mutations in Chinese Han patients causing neutral lipid storage disease with myopathy.

Lin P, Li W, Wen B, Zhao Y, Fenster DS, Wang Y, Gong Y, Yan C. Lin P, et al. Among authors: zhao y. J Hum Genet. 2012 Oct;57(10):679-81. doi: 10.1038/jhg.2012.84. Epub 2012 Jul 26. J Hum Genet. 2012. PMID: 22832386

9

Unfolded protein response and activated degradative pathways regulation in GNE myopathy.

Li H, Chen Q, Liu F, Zhang X, Li W, Liu S, Zhao Y, Gong Y, Yan C. Li H, et al. Among authors: zhao y. PLoS One. 2013;8(3):e58116. doi: 10.1371/journal.pone.0058116. Epub 2013 Mar 5. PLoS One. 2013. PMID: 23472144 Free PMC article.

10

Increased muscle coenzyme Q10 in riboflavin responsive MADD with ETFDH gene mutations due to secondary mitochondrial proliferation.

Wen B, Li D, Shan J, Liu S, Li W, Zhao Y, Lin P, Zheng J, Li D, Gong Y, Yan C. Wen B, et al. Among authors: zhao y. Mol Genet Metab. 2013 Jun;109(2):154-60. doi: 10.1016/j.ymgme.2013.04.007. Epub 2013 Apr 11. Mol Genet Metab. 2013. PMID: 23628458

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