Wang J - Search Results

1

The phenotypic spectrum of Kabuki syndrome in patients of Chinese descent: A case series.

Wang Y, Li N, Su Z, Xu Y, Liu S, Chen Y, Li X, Shen Y, Hung C, Wang J, Wang X, Bodamer O. Wang Y, et al. Among authors: wang x, wang j. Am J Med Genet A. 2020 Apr;182(4):640-651. doi: 10.1002/ajmg.a.61467. Epub 2019 Dec 28. Am J Med Genet A. 2020. PMID: 31883305

2

Endothelial nitric oxide synthase gene sequence variations and vascular disease.

Wang XL, Wang J. Wang XL, et al. Among authors: wang j. Mol Genet Metab. 2000 Aug;70(4):241-51. doi: 10.1006/mgme.2000.3033. Mol Genet Metab. 2000. PMID: 10993711 Review.

3

Cigarette smoke activates caspase-3 to induce apoptosis of human umbilical venous endothelial cells.

Wang J, Wilcken DE, Wang XL. Wang J, et al. Among authors: wang xl. Mol Genet Metab. 2001 Jan;72(1):82-8. doi: 10.1006/mgme.2000.3115. Mol Genet Metab. 2001. PMID: 11161833

4

[Neuropsychological study of dementia severity in Alzheimer's disease].

Wang J, Wang Y. Wang J, et al. Among authors: wang y. Zhonghua Nei Ke Za Zhi. 1999 Oct;38(10):663-5. Zhonghua Nei Ke Za Zhi. 1999. PMID: 11798702 Chinese.

5

A simple technique for a new working heterotopic heart transplantation model in rats.

Wen P, Wang X, Wang J, Zhang B, Qiu G, Fan Y, Xu Y, Tang H, Sun X, Peng Z. Wen P, et al. Among authors: wang x, wang j. Transplant Proc. 2013 Jul-Aug;45(6):2522-6. doi: 10.1016/j.transproceed.2013.03.036. Transplant Proc. 2013. PMID: 23953574

6

Kabuki syndrome: a Chinese case series and systematic review of the spectrum of mutations.

Liu S, Hong X, Shen C, Shi Q, Wang J, Xiong F, Qiu Z. Liu S, et al. Among authors: wang j. BMC Med Genet. 2015 Apr 21;16:26. doi: 10.1186/s12881-015-0171-4. BMC Med Genet. 2015. PMID: 25896430 Free PMC article. Review.

7

A New Subtype of Multiple Synostoses Syndrome Is Caused by a Mutation in GDF6 That Decreases Its Sensitivity to Noggin and Enhances Its Potency as a BMP Signal.

Wang J, Yu T, Wang Z, Ohte S, Yao RE, Zheng Z, Geng J, Cai H, Ge Y, Li Y, Xu Y, Zhang Q, Gusella JF, Fu Q, Pregizer S, Rosen V, Shen Y. Wang J, et al. Among authors: wang z. J Bone Miner Res. 2016 Apr;31(4):882-9. doi: 10.1002/jbmr.2761. Epub 2015 Dec 28. J Bone Miner Res. 2016. PMID: 26643732 Free PMC article.

8

Novel mutations in the CYP11B2 gene causing aldosterone synthase deficiency.

Li N, Li J, Ding Y, Yu T, Shen Y, Fu Q, Shen Y, Huang X, Wang J. Li N, et al. Among authors: wang j. Mol Med Rep. 2016 Apr;13(4):3127-32. doi: 10.3892/mmr.2016.4906. Epub 2016 Feb 18. Mol Med Rep. 2016. PMID: 26936515

9

X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism: Identification and in vitro study of a novel small indel in the NR0B1 gene.

Yu T, Wang J, Yu Y, Huang X, Fu Q, Shen Y, Chen F. Yu T, et al. Among authors: wang j. Mol Med Rep. 2016 May;13(5):4039-45. doi: 10.3892/mmr.2016.5006. Epub 2016 Mar 18. Mol Med Rep. 2016. PMID: 27035099

10

Exome sequencing identifies a novel nonsense mutation of HOXD13 in a Chinese family with synpolydactyly.

Wang B, Li N, Geng J, Wang Z, Fu Q, Wang J, Xu Y. Wang B, et al. Among authors: wang z, wang j. Congenit Anom (Kyoto). 2017 Jan;57(1):4-7. doi: 10.1111/cga.12173. Congenit Anom (Kyoto). 2017. PMID: 27254532

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