Zhao X - Search Results

1

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

2

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

3

[Molecular biological study of glycoprotein IX gene defect in Bernard-Soulier syndrome].

Zhao XJ, Wang ZY, Duan WM, Fu JX, Lu ME, Wang JM, Bai X, Ruan CG. Zhao XJ, et al. Zhonghua Xue Ye Xue Za Zhi. 2003 Sep;24(9):480-3. Zhonghua Xue Ye Xue Za Zhi. 2003. PMID: 14575593 Chinese.

4

Kasabach-Merritt syndrome caused by giant hemangiomas of the spleen in patients with Proteus syndrome.

Wang Z, Yu Z, Su Y, Yang H, Cao L, Zhao X, Hu H, Zhan S, Ruan C. Wang Z, et al. Among authors: zhao x. Blood Coagul Fibrinolysis. 2007 Jul;18(5):505-8. doi: 10.1097/MBC.0b013e32814203af. Blood Coagul Fibrinolysis. 2007. PMID: 17581327

5

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.

6

Hyperfibrinogenemia and prolonged clotting times in a Turner syndrome patient with hepatocellular carcinoma.

Zhao X, Wang Z, Cao L, Zhang W, Bai X, Dong N, Yu Z, Ruan C. Zhao X, et al. Blood Coagul Fibrinolysis. 2010 Jul;21(5):398-405. doi: 10.1097/MBC.0b013e328336578c. Blood Coagul Fibrinolysis. 2010. PMID: 20410814

7

[Establishment and characterization of leukemic cell line U937 stably expressing exogenous RbAp46].

Duan WM, Chen ZX, Wang W, Fu JX, Bai X, Zhao XJ, Yao L. Duan WM, et al. Among authors: zhao xj. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2004 Aug;12(4):416-9. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2004. PMID: 15363122 Chinese.

8

[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.

9

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.

10

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.

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

51,963 results

Search Page

Filters