Wang BB - Search Results

1

Discovery of CCDC188 gene as a novel genetic target for human acephalic spermatozoa syndrome.

Wang J, Jin HJ, Lu Y, Wang ZH, Li TY, Xia L, Li HJ, Wang BB, Chen SR. Wang J, et al. Among authors: wang bb. Protein Cell. 2024 Sep 1;15(9):704-709. doi: 10.1093/procel/pwae018. Protein Cell. 2024. PMID: 38616611 Free PMC article. No abstract available.

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. 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. 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. 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. 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. Endocrine. 2009 Apr;35(2):198-203. doi: 10.1007/s12020-009-9152-8. Epub 2009 Feb 4. Endocrine. 2009. PMID: 19191034

7

Genetic variation of SAL-Like 4 (SALL4) in ventricular septal defect.

Wang B, Li L, Xie X, Wang J, Yan J, Mu Y, Ma X. Wang B, et al. Int J Cardiol. 2010 Nov 19;145(2):224-226. doi: 10.1016/j.ijcard.2009.05.067. Epub 2009 Jul 19. Int J Cardiol. 2010. PMID: 19619907

8

FABP4: a novel candidate gene for polycystic ovary syndrome.

Wang J, Tang J, Wang B, Song J, Liu J, Wei Z, Zhang F, Ma X, Cao Y. Wang J, et al. Endocrine. 2009 Dec;36(3):392-6. doi: 10.1007/s12020-009-9228-5. Epub 2009 Oct 21. Endocrine. 2009. PMID: 19844814

9

Absence of association on aldehyde dehydrogenase 2 (ALDH2) polymorphism with Mongolian Alzheimer patients.

Zhou S, Huriletemuer, Wang J, Zhang C, Zhao S, Wang de S, Wang B, Ma X. Zhou S, et al. Neurosci Lett. 2010 Jan 14;468(3):312-5. doi: 10.1016/j.neulet.2009.11.022. Epub 2009 Nov 13. Neurosci Lett. 2010. PMID: 19914339

10

Genetic analysis of ABCG2 gene C421A polymorphism with gout disease in Chinese Han male population.

Wang B, Miao Z, Liu S, Wang J, Zhou S, Han L, Meng D, Wang Y, Li C, Ma X. Wang B, et al. Hum Genet. 2010 Feb;127(2):245-6. doi: 10.1007/s00439-009-0760-4. Epub 2009 Nov 17. Hum Genet. 2010. PMID: 19921266 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

353 results

Search Page

Filters