Zhao X - Search Results

1

Mutations in the D1 domain of von Willebrand factor impair their propeptide-dependent multimerization, intracellular trafficking and secretion.

Yin J, Ma Z, Su J, Wang JW, Zhao X, Ling J, Bai X, Ouyang W, Wang Z, Yu Z, Ruan C. Yin J, et al. Among authors: zhao x. J Hematol Oncol. 2015 Jun 20;8:73. doi: 10.1186/s13045-015-0166-9. J Hematol Oncol. 2015. PMID: 26088471 Free PMC article.

2

Identification and functional analysis of a novel von Willebrand factor mutation in a family with type 2A von Willebrand disease.

Dong J, Zhao X, Shi S, Ma Z, Liu M, Wu Q, Ruan C, Dong N. Dong J, et al. Among authors: zhao x. PLoS One. 2012;7(3):e33263. doi: 10.1371/journal.pone.0033263. Epub 2012 Mar 27. PLoS One. 2012. PMID: 22479377 Free PMC article.

3

[Clinical studies of 162 patients with von Willebrand disease].

Ouyang W, Yu Z, Yin J, Zhao X, Wang Z, Zhang W, Ma Z, Su J, Bai X, Ruan C. Ouyang W, et al. Among authors: zhao x. Zhonghua Xue Ye Xue Za Zhi. 2014 Feb;35(2):152-6. doi: 10.3760/cma.j.issn.0253-2727.2014.02.020. Zhonghua Xue Ye Xue Za Zhi. 2014. PMID: 24606659 Chinese.

4

A novel fibrinogen B beta chain frameshift mutation causes congenital afibrinogenaemia.

Zhang J, Zhao X, Wang Z, Yu Z, Cao L, Zhang W, Bai X, Ruan C. Zhang J, et al. Among authors: zhao x. Thromb Haemost. 2013 Jul;110(1):76-82. doi: 10.1160/TH12-12-0934. Epub 2013 Jun 6. Thromb Haemost. 2013. PMID: 23740095

5

[Gene analysis of five inherited factor V deficiency cases].

Cao LJ, Wang ZY, Su YH, Yang HY, Zhao XJ, Zhang W, Yu ZQ, Bai X, Ruan CG. Cao LJ, et al. Among authors: zhao xj. Zhonghua Xue Ye Xue Za Zhi. 2008 Mar;29(3):145-8. Zhonghua Xue Ye Xue Za Zhi. 2008. PMID: 18788609 Chinese.

6

[Inherited dysfibrinogenemia caused by Arg16His mutation in alpha chain of fibrinogen.].

Zhao XJ, Wang ZY, Jiang MH, Zhang W, Cao LJ, Ma ZN, Dong NZ, Bai X, Yu ZQ, Ruan CG. Zhao XJ, et al. Zhonghua Xue Ye Xue Za Zhi. 2010 Mar;31(3):154-6. Zhonghua Xue Ye Xue Za Zhi. 2010. PMID: 20510102 Chinese.

7

[Congenital afibrinogenemia caused by a novel insertion mutation in the FGB gene].

Zhang J, Zhao XJ, Wang ZY, Yu ZQ, Cao LJ, Ma ZN, Zhang J, Zhang W, Bai X, Ruan CG. Zhang J, et al. Among authors: zhao xj. Zhonghua Xue Ye Xue Za Zhi. 2013 Sep;34(9):751-6. doi: 10.3760/cma.j.issn.0253-2727.2013.09.004. Zhonghua Xue Ye Xue Za Zhi. 2013. PMID: 24103871 Chinese.

8

[Isolation, culture and characterization of outgrowth endothelial cells from the human peripheral blood].

Yin J, Ma ZN, Zhao XJ, Ruan CG. Yin J, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2014 Dec;22(6):1711-5. doi: 10.7534/j.issn.1009-2137.2014.06.039. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2014. PMID: 25543502 Chinese.

9

A novel mutation in the transmembrane region of glyco-protein IX associated with Bernard-Soulier syndrome.

Wang Z, Zhao X, Duan W, Fu J, Lu M, Wang G, Bai X, Ruan C. Wang Z, et al. Among authors: zhao x. Thromb Haemost. 2004 Sep;92(3):606-13. doi: 10.1160/TH04-04-0240. Thromb Haemost. 2004. PMID: 15351858

10

Sepsis-induced disseminated intravascular coagulation with features of thrombotic thrombocytopenic purpura: a fatal fulminant syndrome.

Wang Z, Yu Z, Su J, Cao L, Zhao X, Ruan C. Wang Z, et al. Among authors: zhao x. Clin Appl Thromb Hemost. 2011 Jun;17(3):251-3. doi: 10.1177/1076029609357739. Epub 2010 Mar 8. Clin Appl Thromb Hemost. 2011. PMID: 20211920 Free article.

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