Wang N - Search Results

1

Association of Common Variants in the Glucocerebrosidase Gene with High Susceptibility to Parkinson's Disease among Chinese.

Zhang X, Bao QQ, Zhuang XS, Gan SR, Zhao D, Liu Y, Hu Q, Chen Y, Zhu F, Wang L, Wang N. Zhang X, et al. Among authors: wang l, wang n. Chin J Physiol. 2012 Dec 31;55(6):398-404. doi: 10.4077/CJP.2011.AMM076. Chin J Physiol. 2012. PMID: 23286447

2

Screening for FMR1 expanded alleles in patients with parkinsonism in mainland China.

Zhang X, Zhuang X, Gan S, Wu Z, Chen W, Hu Y, Wang N. Zhang X, et al. Among authors: wang n. Neurosci Lett. 2012 Apr 11;514(1):16-21. doi: 10.1016/j.neulet.2012.02.036. Epub 2012 Feb 22. Neurosci Lett. 2012. PMID: 22387066

3

High frequency of Machado-Joseph disease identified in southeastern Chinese kindreds with spinocerebellar ataxia.

Gan SR, Shi SS, Wu JJ, Wang N, Zhao GX, Weng ST, Murong SX, Lu CZ, Wu ZY. Gan SR, et al. Among authors: wang n. BMC Med Genet. 2010 Mar 25;11:47. doi: 10.1186/1471-2350-11-47. BMC Med Genet. 2010. PMID: 20334689 Free PMC article.

4

Additional evidence supports association of common genetic variants in VTI1A and ETFA with increased risk of glioma susceptibility.

Wang N, Deng Z, Wang M, Li R, Xu G, Bao G. Wang N, et al. Among authors: wang m. J Neurol Sci. 2017 Apr 15;375:282-288. doi: 10.1016/j.jns.2017.02.013. Epub 2017 Feb 8. J Neurol Sci. 2017. PMID: 28320150

5

The R219K polymorphism in the ATP-binding cassette transporter 1 gene has a protective effect on atherothrombotic cerebral infarction in Chinese Han ethnic population.

Wang N, Xue XH, Lin Y, Fang L, Murong S, Wu ZY. Wang N, et al. Neurobiol Aging. 2010 Apr;31(4):647-53. doi: 10.1016/j.neurobiolaging.2008.05.032. Epub 2008 Jul 14. Neurobiol Aging. 2010. PMID: 18621447

6

Kukoamine A attenuates insulin resistance and fatty liver through downregulation of Srebp-1c.

Li G, Zhou F, Chen Y, Zhang W, Wang N. Li G, et al. Among authors: wang n. Biomed Pharmacother. 2017 May;89:536-543. doi: 10.1016/j.biopha.2017.02.024. Epub 2017 Feb 28. Biomed Pharmacother. 2017. PMID: 28254666

7

Distinguishing the 4qA and 4qB variants is essential for the diagnosis of facioscapulohumeral muscular dystrophy in the Chinese population.

Wang ZQ, Wang N, van der Maarel S, Murong SX, Wu ZY. Wang ZQ, et al. Among authors: wang n. Eur J Hum Genet. 2011 Jan;19(1):64-9. doi: 10.1038/ejhg.2010.143. Epub 2010 Aug 25. Eur J Hum Genet. 2011. PMID: 20736973 Free PMC article.

8

Mutation analysis of 218 Chinese patients with Wilson disease revealed no correlation between the canine copper toxicosis gene MURR1 and Wilson disease.

Wu ZY, Zhao GX, Chen WJ, Wang N, Wan B, Lin MT, Murong SX, Yu L. Wu ZY, et al. Among authors: wang n. J Mol Med (Berl). 2006 May;84(5):438-42. doi: 10.1007/s00109-005-0036-y. Epub 2006 Jan 28. J Mol Med (Berl). 2006. PMID: 16649058

9

Genetic variants of CYP4F12 gene are associated with glioma susceptibility.

Li N, Shi H, Hou P, Gao L, Shi Y, Mi W, Zhang G, Wang N, Dai W, Wei L, Jin T, Shi Y, Guo S. Li N, et al. Among authors: wang n. Int J Cancer. 2021 Dec 1;149(11):1910-1915. doi: 10.1002/ijc.33755. Epub 2021 Aug 28. Int J Cancer. 2021. PMID: 34319593

10

Association between the activities of daily living and clinical outcomes in patients with heart failure.

Li HQ, Wang N, Chen Y. Li HQ, et al. Among authors: wang n. J Cardiol. 2019 Nov;74(5):473. doi: 10.1016/j.jjcc.2019.05.013. Epub 2019 Jul 9. J Cardiol. 2019. PMID: 31300269 Free article. No abstract available.

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