Suo P - Search Results

1

Haplotype analysis of chemokine CXCL12 polymorphisms and susceptibility to premature ovarian failure in Chinese women.

Wang B, Suo P, Chen B, Wei Z, Yang L, Zhou S, Wang J, Cao Y, Ma X. Wang B, et al. Among authors: suo p. Hum Reprod. 2011 Apr;26(4):950-4. doi: 10.1093/humrep/der001. Epub 2011 Feb 4. Hum Reprod. 2011. PMID: 21296802

2

The ESR1 gene in unexplained recurrent spontaneous abortion.

Pan H, Suo P, Liu C, Wang J, Zhou S, Ma X, Wang B. Pan H, et al. Among authors: suo p. Syst Biol Reprod Med. 2014 Jun;60(3):161-4. doi: 10.3109/19396368.2013.877540. Epub 2014 Feb 25. Syst Biol Reprod Med. 2014. PMID: 24568551

3

New candidate gene POU5F1 associated with premature ovarian failure in Chinese patients.

Wang J, Wang B, Song J, Suo P, Ni F, Chen B, Ma X, Cao Y. Wang J, et al. Among authors: suo p. Reprod Biomed Online. 2011 Mar;22(3):312-6. doi: 10.1016/j.rbmo.2010.11.008. Epub 2010 Nov 20. Reprod Biomed Online. 2011. PMID: 21273125

4

Mutation analysis of the WNT4 gene in Han Chinese women with premature ovarian failure.

Chen B, Suo P, Wang B, Wang J, Yang L, Zhou S, Zhu Y, Ma X, Cao Y. Chen B, et al. Among authors: suo p. Reprod Biol Endocrinol. 2011 May 30;9:75. doi: 10.1186/1477-7827-9-75. Reprod Biol Endocrinol. 2011. PMID: 21624127 Free PMC article.

5

A novel GJA8 mutation (p.I31T) causing autosomal dominant congenital cataract in a Chinese family.

Wang K, Wang B, Wang J, Zhou S, Yun B, Suo P, Cheng J, Ma X, Zhu S. Wang K, et al. Among authors: suo p. Mol Vis. 2009 Dec 16;15:2813-20. Mol Vis. 2009. PMID: 20019893 Free PMC article.

6

Genetic association between BDNF gene polymorphisms and phobic disorders: a case-control study among mainland Han Chinese.

Xie B, Wang B, Suo P, Kou C, Wang J, Meng X, Cheng L, Ma X, Yu Y. Xie B, et al. Among authors: suo p. J Affect Disord. 2011 Jul;132(1-2):239-42. doi: 10.1016/j.jad.2010.12.017. Epub 2011 Feb 4. J Affect Disord. 2011. PMID: 21295349

7

Polymorphisms in the presumptive promoter region of the SLC2A9 gene are associated with gout in a Chinese male population.

Li C, Chu N, Wang B, Wang J, Luan J, Han L, Meng D, Wang Y, Suo P, Cheng L, Ma X, Miao Z, Liu S. Li C, et al. Among authors: suo p. PLoS One. 2012;7(2):e24561. doi: 10.1371/journal.pone.0024561. Epub 2012 Feb 29. PLoS One. 2012. PMID: 22393348 Free PMC article.

8

Association analysis between HOXD9 genes and the development of developmental dysplasia of the hip in Chinese female Han population.

Tian W, Zhao L, Wang J, Suo P, Wang J, Cheng L, Cheng Z, Jia J, Kan S, Wang B, Ma X. Tian W, et al. Among authors: suo p. BMC Musculoskelet Disord. 2012 Apr 20;13:59. doi: 10.1186/1471-2474-13-59. BMC Musculoskelet Disord. 2012. PMID: 22520331 Free PMC article.

9

The HHEX gene is not related to congenital heart disease in 296 Chinese patients.

Deng XP, Zhao LX, Wang BB, Wang J, Cheng LF, Cheng Z, Suo PS, Li H, Ma X. Deng XP, et al. World J Pediatr. 2013 Aug;9(3):278-80. doi: 10.1007/s12519-013-0430-4. Epub 2013 Aug 9. World J Pediatr. 2013. PMID: 23929257

10

Mutation analysis of Connexon43 gene in Chinese patients with congenital heart defects.

Wang B, Wen Q, Xie X, Liu S, Liu M, Tao Y, Li Z, Suo P, Shen A, Wang J, Ma X. Wang B, et al. Among authors: suo p. Int J Cardiol. 2010 Dec 3;145(3):487-9. doi: 10.1016/j.ijcard.2009.06.026. Epub 2009 Jul 16. Int J Cardiol. 2010. PMID: 19615768 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

72 results

Search Page

Filters