ADAMTS-13对血管性血友病因子的加工处理 - Suppr

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Processing of von Willebrand factor by ADAMTS-13.

作者信息

Chung Dominic W, Fujikawa Kazuo

机构信息

Department of Biochemistry, University of Washington, Seattle, Washington 98195, USA.

出版信息

Biochemistry. 2002 Sep 17;41(37):11065-70. doi: 10.1021/bi0204692.

DOI:10.1021/bi0204692

PMID:12220170

Abstract

摘要

相似文献

Processing of von Willebrand factor by ADAMTS-13.

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引用本文的文献

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Entropy (Basel). 2021 Apr 10;23(4):447. doi: 10.3390/e23040447.

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ADAMTS13 and von Willebrand factor interactions.

Curr Opin Hematol. 2015 Sep;22(5):452-9. doi: 10.1097/MOH.0000000000000169.

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Mediterr J Hematol Infect Dis. 2013 Sep 2;5(1):e2013058. doi: 10.4084/MJHID.2013.058.

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Fibrinogen-elongated gamma chain inhibits thrombin-induced platelet response, hindering the interaction with different receptors.

J Biol Chem. 2008 Oct 31;283(44):30193-204. doi: 10.1074/jbc.M803659200. Epub 2008 Sep 8.

Mechanistic studies on ADAMTS13 catalysis.

Biophys J. 2008 Sep;95(5):2450-61. doi: 10.1529/biophysj.108.131532. Epub 2008 May 23.

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相似文献

Processing of von Willebrand factor by ADAMTS-13.

Biochemistry. 2002 Sep 17;41(37):11065-70. doi: 10.1021/bi0204692.

von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome.

N Engl J Med. 1998 Nov 26;339(22):1578-84. doi: 10.1056/NEJM199811263392202.

[TTP/HUS and VWF/ADAMTS-13].

Rinsho Ketsueki. 2003 Dec;44(12):1144-53.

Molecular mechanisms in thrombotic thrombocytopenic purpura.

Semin Thromb Hemost. 2004 Oct;30(5):549-57. doi: 10.1055/s-2004-835675.

ADAMTS13, thrombotic thrombocytopenic purpura, and hemolytic uremic syndrome.

Curr Hematol Rep. 2005 May;4(3):167-9.

Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura.

J Mol Med (Berl). 2002 Oct;80(10):639-47. doi: 10.1007/s00109-002-0369-8. Epub 2002 Sep 5.

Report on the workshop: Von Willebrand factor and Thrombotic Thrombocytopenic Purpura.

Am J Hematol. 2001 Oct;68(2):122-6. doi: 10.1002/ajh.1163.

Moschcowitz, multimers, and metalloprotease.

N Engl J Med. 1998 Nov 26;339(22):1629-31. doi: 10.1056/NEJM199811263392210.

[Hereditary hemolytic uremic syndromes and thrombotic thrombocytopenic purpura].

Nephrol Ther. 2006 Jan;2 Suppl 2:S149-61.

Is ADAMTS-13 deficiency specific for thrombotic thrombocytopenic purpura? No.

J Thromb Haemost. 2003 Apr;1(4):632-4. doi: 10.1046/j.1538-7836.2003.00170.x.

引用本文的文献

Immune and Hereditary Thrombotic Thrombocytopenic Purpura: Can ADAMTS13 Deficiency Alone Explain the Different Clinical Phenotypes?

J Clin Med. 2023 Apr 25;12(9):3111. doi: 10.3390/jcm12093111.

Thrombotic microangiopathy in children.

Pediatr Nephrol. 2022 Sep;37(9):1967-1980. doi: 10.1007/s00467-021-05370-8. Epub 2022 Jan 18.

Von Willebrand Factor Multimers and the Relaxation Response: A One-Year Study.

Entropy (Basel). 2021 Apr 10;23(4):447. doi: 10.3390/e23040447.

Endothelial cell control of thrombosis.

BMC Cardiovasc Disord. 2015 Oct 19;15:130. doi: 10.1186/s12872-015-0124-z.

ADAMTS13 and von Willebrand factor interactions.

Curr Opin Hematol. 2015 Sep;22(5):452-9. doi: 10.1097/MOH.0000000000000169.

Proteolytic processing of von Willebrand factor by adamts13 and leukocyte proteases.

Mediterr J Hematol Infect Dis. 2013 Sep 2;5(1):e2013058. doi: 10.4084/MJHID.2013.058.

Blocking von Willebrand factor for treatment of cutaneous inflammation.

J Invest Dermatol. 2014 Jan;134(1):77-86. doi: 10.1038/jid.2013.292. Epub 2013 Jun 28.

Endothelial cell ADAMTS-13 and VWF: production, release, and VWF string cleavage.

Blood. 2009 Dec 3;114(24):5102-11. doi: 10.1182/blood-2009-07-231597. Epub 2009 Oct 12.

Fibrinogen-elongated gamma chain inhibits thrombin-induced platelet response, hindering the interaction with different receptors.

J Biol Chem. 2008 Oct 31;283(44):30193-204. doi: 10.1074/jbc.M803659200. Epub 2008 Sep 8.

Mechanistic studies on ADAMTS13 catalysis.

Biophys J. 2008 Sep;95(5):2450-61. doi: 10.1529/biophysj.108.131532. Epub 2008 May 23.