Wang Z - Search Results

1

Identification of 8 Novel Mutations in Nephrogenesis-Related Genes in Chinese Han Patients with Unilateral Renal Agenesis.

Wu H, Xu Q, Xie J, Ma J, Qiao P, Zhang W, Yu H, Wang W, Qian Y, Zhang Q, Guo Y, Tang Y, Chen XN, Wang Z, Chen N. Wu H, et al. Among authors: wang w, wang z. Am J Nephrol. 2017;46(1):55-63. doi: 10.1159/000477590. Epub 2017 Jun 16. Am J Nephrol. 2017. PMID: 28618409

2

[Association of single nucleotide polymorphism of megsin gene with IgA nephropathy].

Wang ZH, Chen N, Pan XX, Ren H, Wang WM, Zhang W, Hao CL, Zhu J, Lu Y, Han B. Wang ZH, et al. Zhonghua Yi Xue Za Zhi. 2006 May 23;86(19):1337-41. Zhonghua Yi Xue Za Zhi. 2006. PMID: 16796905 Chinese.

3

[The association of single nucleotide P-selectin gene polymorphism with IgA nephropathy].

Wang ZH, Wang WM, Zhou T, Chen XN, Pan XX, Zhu J, Lu Y, Han B, Chen N. Wang ZH, et al. Zhonghua Nei Ke Za Zhi. 2006 Jul;45(7):559-64. Zhonghua Nei Ke Za Zhi. 2006. PMID: 17074110 Chinese.

4

Two brothers in one Chinese family with collagen type III glomerulopathy.

Chen N, Pan X, Xu Y, Wang Z, Shi H, Yan F, Dong X. Chen N, et al. Among authors: wang z. Am J Kidney Dis. 2007 Dec;50(6):1037-42. doi: 10.1053/j.ajkd.2007.08.021. Am J Kidney Dis. 2007. PMID: 18037106 No abstract available.

5

[Correlation between traditional Chinese medicine syndromes in primary immunoglobulin A nephropathy and A267G in 5'-untranslated region within exonal of megsin gene].

Zhong YF, Chen YP, Deng YY, Chen N, Wang ZH. Zhong YF, et al. Zhong Xi Yi Jie He Xue Bao. 2008 May;6(5):463-7. doi: 10.3736/jcim20080506. Zhong Xi Yi Jie He Xue Bao. 2008. PMID: 18471408 Chinese.

6

Identification and functional analysis of a novel TRPC6 mutation associated with late onset familial focal segmental glomerulosclerosis in Chinese patients.

Zhu B, Chen N, Wang ZH, Pan XX, Ren H, Zhang W, Wang WM. Zhu B, et al. Mutat Res. 2009 May 12;664(1-2):84-90. doi: 10.1016/j.mrfmmm.2008.11.021. Epub 2008 Dec 13. Mutat Res. 2009. PMID: 19124028

7

ACTN4 gene mutations and single nucleotide polymorphisms in idiopathic focal segmental glomerulosclerosis.

Dai S, Wang Z, Pan X, Chen X, Wang W, Ren H, Feng Q, He JC, Han B, Chen N. Dai S, et al. Among authors: wang w, wang z. Nephron Clin Pract. 2009;111(2):c87-94. doi: 10.1159/000191198. Epub 2009 Jan 13. Nephron Clin Pract. 2009. PMID: 19142020

8

Identification of five novel variants in the thiazide-sensitive NaCl co-transporter gene in Chinese patients with Gitelman syndrome.

Qin L, Shao L, Ren H, Wang W, Pan X, Zhang W, Wang Z, Shen P, Chen N. Qin L, et al. Among authors: wang w, wang z. Nephrology (Carlton). 2009 Feb;14(1):52-8. doi: 10.1111/j.1440-1797.2008.01042.x. Epub 2009 Jan 21. Nephrology (Carlton). 2009. PMID: 19207868

9

Serum proteome alteration of severe sepsis in the treatment of continuous renal replacement therapy.

Gong Y, Chen N, Wang FQ, Wang ZH, Xu HX. Gong Y, et al. Nephrol Dial Transplant. 2009 Oct;24(10):3108-14. doi: 10.1093/ndt/gfp231. Epub 2009 May 21. Nephrol Dial Transplant. 2009. PMID: 19461007

10

Functional analysis of promoter mutations in the ACTN4 and SYNPO genes in focal segmental glomerulosclerosis.

Dai S, Wang Z, Pan X, Wang W, Chen X, Ren H, Hao C, Han B, Chen N. Dai S, et al. Among authors: wang w, wang z. Nephrol Dial Transplant. 2010 Mar;25(3):824-35. doi: 10.1093/ndt/gfp394. Epub 2009 Aug 7. Nephrol Dial Transplant. 2010. PMID: 19666657

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