Cheng L - Search Results

1

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: cheng l. PLoS One. 2012;7(2):e24561. doi: 10.1371/journal.pone.0024561. Epub 2012 Feb 29. PLoS One. 2012. PMID: 22393348 Free PMC article.

2

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: cheng l. 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

3

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: cheng z, cheng l. BMC Musculoskelet Disord. 2012 Apr 20;13:59. doi: 10.1186/1471-2474-13-59. BMC Musculoskelet Disord. 2012. PMID: 22520331 Free PMC article.

4

Two single-nucleotide polymorphisms in the DKK1 gene are associated with developmental dysplasia of the hip in the Chinese Han female population.

Liu S, Tian W, Wang J, Cheng L, Jia J, Ma X. Liu S, et al. Among authors: cheng l. Genet Test Mol Biomarkers. 2014 Aug;18(8):557-61. doi: 10.1089/gtmb.2014.0044. Epub 2014 Jun 13. Genet Test Mol Biomarkers. 2014. PMID: 24926963 Clinical Trial.

5

Variations of the COL1A1 gene promoter and the relation to developmental dysplasia of the hip.

Zhao L, Tian W, Pan H, Zhu X, Wang J, Cheng Z, Cheng L, Ma X, Wang B. Zhao L, et al. Among authors: cheng z, cheng l. Genet Test Mol Biomarkers. 2013 Nov;17(11):840-3. doi: 10.1089/gtmb.2013.0179. Epub 2013 Aug 13. Genet Test Mol Biomarkers. 2013. PMID: 23941072

6

Two single nucleotide polymorphisms in the GDF5 gene are associated with development dysplasia of the hip in Chinese female population.

Zhao L, Pan H, Wang J, Cheng Z, Cheng L, Wang B, Ma X. Zhao L, et al. Among authors: cheng z, cheng l. Sci China Life Sci. 2013 Nov;56(11):1063-5. doi: 10.1007/s11427-013-4514-0. Epub 2013 Oct 10. Sci China Life Sci. 2013. PMID: 24114442 No abstract available.

7

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

8

A novel mutation of HOXA10 in a Chinese woman with a Mullerian duct anomaly.

Cheng Z, Zhu Y, Su D, Wang J, Cheng L, Chen B, Wei Z, Zhou P, Wang B, Ma X, Cao Y. Cheng Z, et al. Among authors: cheng l. Hum Reprod. 2011 Nov;26(11):3197-201. doi: 10.1093/humrep/der290. Epub 2011 Sep 7. Hum Reprod. 2011. PMID: 21900391

9

Functional Analysis of Two Novel Mutations in TWIST1 Protein Motifs Found in Ventricular Septal Defect Patients.

Deng X, Pan H, Wang J, Wang B, Cheng Z, Cheng L, Zhao L, Li H, Ma X. Deng X, et al. Among authors: cheng z, cheng l. Pediatr Cardiol. 2015 Dec;36(8):1602-9. doi: 10.1007/s00246-015-1202-9. Epub 2015 May 19. Pediatr Cardiol. 2015. PMID: 25981568

10

HOXA1 gene is not potentially related to ventricular septal defect in Chinese children.

Liu J, Wang B, Chen X, Li H, Wang J, Cheng L, Ma X, Gao B. Liu J, et al. Among authors: cheng l. Pediatr Cardiol. 2013 Feb;34(2):226-30. doi: 10.1007/s00246-012-0418-1. Epub 2012 Jul 10. Pediatr Cardiol. 2013. PMID: 22777240

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

14,928 results

Search Page

Filters