Wang B - Search Results

1

Lack of an association between CYP1A1 gene Ile462Val polymorphism and polycystic ovary syndrome in Chinese.

Wang B, Wang J, Liu J, Ni F, Yan J, Zhou S, Mu Y, Cao Y, Ma X. Wang B, et al. Among authors: wang j. Endocrine. 2009 Aug;36(1):16-9. doi: 10.1007/s12020-009-9205-z. Epub 2009 Jun 9. Endocrine. 2009. PMID: 19507064

2

Association between Alzheimer's disease and the NOS3 gene Glu298Asp polymorphism in Chinese.

Wang B, Tan S, Yang Z, Xie YC, Wang J, Zhou S, Li S, Zheng C, Ma X. Wang B, et al. Among authors: wang j. J Mol Neurosci. 2008 Feb;34(2):173-6. doi: 10.1007/s12031-007-9026-6. Epub 2008 Jan 9. J Mol Neurosci. 2008. PMID: 18183499

3

The association of mitochondrial aldehyde dehydrogenase gene (ALDH2) polymorphism with susceptibility to late-onset Alzheimer's disease in Chinese.

Wang B, Wang J, Zhou S, Tan S, He X, Yang Z, Xie YC, Li S, Zheng C, Ma X. Wang B, et al. Among authors: wang j. J Neurol Sci. 2008 May 15;268(1-2):172-5. doi: 10.1016/j.jns.2007.12.006. Epub 2008 Jan 16. J Neurol Sci. 2008. PMID: 18201725

4

Genetic analysis of tumor necrosis factor-alpha (TNF-alpha) G-308A and Saitohin Q7R polymorphisms with Alzheimer's disease.

Wang B, Zhou S, Yang Z, Xie YC, Wang J, Zhang P, Lv Z, Zheng C, Ma X. Wang B, et al. Among authors: wang j. J Neurol Sci. 2008 Jul 15;270(1-2):148-51. doi: 10.1016/j.jns.2008.02.021. Epub 2008 Apr 8. J Neurol Sci. 2008. PMID: 18396294

5

Lack of an association between Alzheimer's disease and the cystatin C (CST3) gene G73A polymorphism in Mainland Chinese.

Wang B, Xie YC, Yang Z, Peng D, Wang J, Zhou S, Li S, Ma X. Wang B, et al. Among authors: wang j. Dement Geriatr Cogn Disord. 2008;25(5):461-4. doi: 10.1159/000125670. Epub 2008 Apr 11. Dement Geriatr Cogn Disord. 2008. PMID: 18408364

6

Lack of association between interleukin-1a gene (IL-1a) C (-889) T variant and polycystic ovary syndrome in Chinese women.

Wang B, Zhou S, Wang J, Liu J, Ni F, Liu C, Yan J, Mu Y, Cao Y, Ma X. Wang B, et al. Among authors: wang j. Endocrine. 2009 Apr;35(2):198-203. doi: 10.1007/s12020-009-9152-8. Epub 2009 Feb 4. Endocrine. 2009. PMID: 19191034

7

TAQIB and I405V polymorphisms of CETP are moderately associated with obesity risk in the Chinese adult population.

Ruan X, Ma L, Wang S, Lindpaintner K, Liu X, Wang B, Peng Z, Ma X, Cheng M, Zhang J, Liu L, Wang X. Ruan X, et al. Among authors: wang x, wang s, wang b. Acta Diabetol. 2010 Sep;47(3):217-24. doi: 10.1007/s00592-009-0117-4. Epub 2009 Apr 10. Acta Diabetol. 2010. PMID: 19360375

8

Analyses of growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) mutation in Chinese women with premature ovarian failure.

Wang B, Wen Q, Ni F, Zhou S, Wang J, Cao Y, Ma X. Wang B, et al. Among authors: wang j. Clin Endocrinol (Oxf). 2010 Jan;72(1):135-6. doi: 10.1111/j.1365-2265.2009.03613.x. Epub 2009 May 4. Clin Endocrinol (Oxf). 2010. PMID: 19438907 No abstract available.

9

Association of two CETP polymorphisms with HDL levels in the Chinese obese population.

Ruan X, Ma L, Wang S, Lindpaintner K, Liu X, Wang B, Peng Z, Ma X, Cheng M, Zhang J, Liu L, Wang X. Ruan X, et al. Among authors: wang x, wang s, wang b. Obesity (Silver Spring). 2009 Dec;17(12):2196-201. doi: 10.1038/oby.2009.138. Epub 2009 May 14. Obesity (Silver Spring). 2009. PMID: 19444232 Free article.

10

Forkhead box H1 (FOXH1) sequence variants in ventricular septal defect.

Wang B, Yan J, Mi R, Zhou S, Xie X, Wang J, Ma X. Wang B, et al. Among authors: wang j. Int J Cardiol. 2010 Nov 5;145(1):83-5. doi: 10.1016/j.ijcard.2009.05.030. Epub 2009 Jun 13. Int J Cardiol. 2010. PMID: 19525021

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