Li Z - Search Results

1

Mutation profiles and clinical characteristics of Chinese males with isolated hypogonadotropic hypogonadism.

Zhou C, Niu Y, Xu H, Li Z, Wang T, Yang W, Wang S, Wang DW, Liu J. Zhou C, et al. Among authors: li z. Fertil Steril. 2018 Aug;110(3):486-495.e5. doi: 10.1016/j.fertnstert.2018.04.010. Fertil Steril. 2018. PMID: 30098700 Free article.

2

Novel URAT1 mutations caused acute renal failure after exercise in two Chinese families with renal hypouricemia.

Li Z, Ding H, Chen C, Chen Y, Wang DW, Lv Y. Li Z, et al. Gene. 2013 Jan 1;512(1):97-101. doi: 10.1016/j.gene.2012.09.115. Epub 2012 Oct 5. Gene. 2013. PMID: 23043931

3

Polymorphism of tumor necrosis factor alpha (TNF-alpha) gene promoter, circulating TNF-alpha level, and cardiovascular risk factor for ischemic stroke.

Cui G, Wang H, Li R, Zhang L, Li Z, Wang Y, Hui R, Ding H, Wang DW. Cui G, et al. Among authors: li z, li r. J Neuroinflammation. 2012 Oct 10;9:235. doi: 10.1186/1742-2094-9-235. J Neuroinflammation. 2012. PMID: 23050663 Free PMC article.

4

Association analysis of polymorphisms in ROCK2 with cardiovascular disease in a Chinese population.

Liu L, Cao Y, Cui G, Li Z, Sun J, Zhang L, Chen C, Wang Y, Wang P, Ding H, Wang DW. Liu L, et al. Among authors: li z. PLoS One. 2013;8(1):e53905. doi: 10.1371/journal.pone.0053905. Epub 2013 Jan 11. PLoS One. 2013. PMID: 23326532 Free PMC article.

5

Comparison of high-resolution melting analysis, TaqMan Allelic discrimination assay, and sanger sequencing for Clopidogrel efficacy genotyping in routine molecular diagnostics.

Zhang L, Cui G, Li Z, Wang H, Ding H, Wang DW. Zhang L, et al. Among authors: li z. J Mol Diagn. 2013 Sep;15(5):600-6. doi: 10.1016/j.jmoldx.2013.04.005. Epub 2013 Jun 28. J Mol Diagn. 2013. PMID: 23810503 Free article.

6

Rapid molecular genetic diagnosis of hypertrophic cardiomyopathy by semiconductor sequencing.

Li Z, Huang J, Zhao J, Chen C, Wang H, Ding H, Wang DW, Wang DW. Li Z, et al. J Transl Med. 2014 Jun 17;12:173. doi: 10.1186/1479-5876-12-173. J Transl Med. 2014. PMID: 24938736 Free PMC article.

7

A functional variant in APOA5/A4/C3/A1 gene cluster contributes to elevated triglycerides and severity of CAD by interfering with microRNA 3201 binding efficiency.

Cui G, Li Z, Li R, Huang J, Wang H, Zhang L, Ding H, Wang DW. Cui G, et al. Among authors: li z, li r. J Am Coll Cardiol. 2014 Jul 22;64(3):267-77. doi: 10.1016/j.jacc.2014.03.050. J Am Coll Cardiol. 2014. PMID: 25034063 Free article.

8

Next-generation sequencing identifies novel mutations in the FBN1 gene for two Chinese families with Marfan syndrome.

Ma M, Li Z, Wang DW, Wei X. Ma M, et al. Among authors: li z. Mol Med Rep. 2016 Jul;14(1):151-8. doi: 10.3892/mmr.2016.5229. Epub 2016 May 9. Mol Med Rep. 2016. PMID: 27175573 Free PMC article.

9

A novel nonsense mutation in LMNA gene identified by Exome Sequencing in an atrial fibrillation family.

Zhao J, Yao H, Li Z, Wang L, Liu G, Wang DW, Wang DW, Liang Z. Zhao J, et al. Among authors: li z. Eur J Med Genet. 2016 Aug;59(8):396-400. doi: 10.1016/j.ejmg.2016.06.006. Epub 2016 Jun 30. Eur J Med Genet. 2016. PMID: 27373676

10

Variants of genes encoding collagens and matrix metalloproteinase system increased the risk of aortic dissection.

Li Z, Zhou C, Tan L, Chen P, Cao Y, Li C, Li X, Yan J, Zeng H, Wang DW, Wang DW. Li Z, et al. Among authors: li c, li x. Sci China Life Sci. 2017 Jan;60(1):57-65. doi: 10.1007/s11427-016-0333-3. Epub 2016 Dec 13. Sci China Life Sci. 2017. PMID: 27975164

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