Shen J - Search Results

1

Familial nonsyndromic patent ductus arteriosus caused by mutations in TFAP2B.

Chen YW, Zhao W, Zhang ZF, Fu Q, Shen J, Zhang Z, Ji W, Wang J, Li F. Chen YW, et al. Among authors: shen j. Pediatr Cardiol. 2011 Oct;32(7):958-65. doi: 10.1007/s00246-011-0024-7. Epub 2011 Jun 4. Pediatr Cardiol. 2011. PMID: 21643846

2

[Effect of elastase inhibitor on pulmonary hypertension induced by monocrotaline].

Fu LJ, Zhou AQ, Shen J, Zhao W, Li F. Fu LJ, et al. Among authors: shen j. Zhonghua Er Ke Za Zhi. 2004 May;42(5):375-8. Zhonghua Er Ke Za Zhi. 2004. PMID: 15189699 Chinese.

3

A novel mutation in the BMPR2 gene in familial pulmonary arterial hypertension.

Fu LJ, Zhou AQ, Huang MR, Shen SH, Shen J, Zhang ZF, Li F. Fu LJ, et al. Among authors: shen sh, shen j. Chin Med J (Engl). 2008 Mar 5;121(5):399-404. Chin Med J (Engl). 2008. PMID: 18364108

4

GATA4 mutations in Chinese patients with congenital cardiac septal defects.

Chen MW, Pang YS, Guo Y, Pan JH, Liu BL, Shen J, Liu TW. Chen MW, et al. Among authors: shen j. Pediatr Cardiol. 2010 Jan;31(1):85-9. doi: 10.1007/s00246-009-9576-1. Epub 2009 Nov 14. Pediatr Cardiol. 2010. PMID: 19915893

5

Mutations in VEGFA are associated with congenital left ventricular outflow tract obstruction.

Zhao W, Wang J, Shen J, Sun K, Zhu J, Yu T, Ji W, Chen Y, Fu Q, Li F. Zhao W, et al. Among authors: shen j. Biochem Biophys Res Commun. 2010 May 28;396(2):483-8. doi: 10.1016/j.bbrc.2010.04.124. Epub 2010 Apr 24. Biochem Biophys Res Commun. 2010. PMID: 20420808

6

Novel CRELD1 gene mutations in patients with atrioventricular septal defect.

Guo Y, Shen J, Yuan L, Li F, Wang J, Sun K. Guo Y, et al. Among authors: shen j. World J Pediatr. 2010 Nov;6(4):348-52. doi: 10.1007/s12519-010-0235-7. Epub 2010 Nov 16. World J Pediatr. 2010. PMID: 21080147

7

A nonsense variation p.Arg325X in the vascular endothelial growth factor-A gene may be associated with congenital tricuspid aortic valve stenosis.

Zhao W, Wang J, Shen J, Sun K, Chen Y, Ji W, Fu L, Wu Y, Li F. Zhao W, et al. Among authors: shen j. Cardiol Young. 2012 Jun;22(3):316-22. doi: 10.1017/S104795111100151X. Epub 2011 Nov 9. Cardiol Young. 2012. PMID: 22067973

8

Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus.

Xu YJ, Wang J, Xu R, Zhao PJ, Wang XK, Sun HJ, Bao LM, Shen J, Fu QH, Li F, Sun K. Xu YJ, et al. Among authors: shen j. BMC Med Genet. 2011 Dec 21;12:169. doi: 10.1186/1471-2350-12-169. BMC Med Genet. 2011. PMID: 22185286 Free PMC article.

9

[Potential role of CRELD1 gene in the pathogenesis of atrioventricular septal defect].

Guo Y, Shen J, Li F, Wang J, Wang X, Guo A, Sun K. Guo Y, et al. Among authors: shen j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Jun;31(3):263-7. doi: 10.3760/cma.j.issn.1003-9406.2014.03.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 24927998 Chinese.

10

Vegfa Impacts Early Myocardium Development in Zebrafish.

Zhu D, Fang Y, Gao K, Shen J, Zhong TP, Li F. Zhu D, et al. Among authors: shen j. Int J Mol Sci. 2017 Feb 21;18(2):444. doi: 10.3390/ijms18020444. Int J Mol Sci. 2017. PMID: 28230770 Free PMC article.

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

20,994 results

Search Page

Filters