Why patients with THBD c.1611C>A (p.Cys537X) nonsense mutation have high levels of soluble thrombomodulin?

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Why patients with THBD c.1611C>A (p.Cys537X) nonsense mutation have high levels of soluble thrombomodulin?

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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Why patients with THBD c.1611C ...... els of soluble thrombomodulin?

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Why patients with THBD c.1611C>A

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Item

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Why patients with THBD c.1611C ...... els of soluble thrombomodulin?

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Why patients with THBD c.1611C>A

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Why patients with THBD c.1611C ...... els of soluble thrombomodulin?

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Why patients with THBD c.1611C>A

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P1476

Why patients with THBD c.1611C ...... els of soluble thrombomodulin?

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P2093

Jean Claude Bordet

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P2860

Human thrombomodulin: complete cDNA sequence and chromosome localization of the gene

Structure and expression of human thrombomodulin, a thrombin receptor on endothelium acting as a cofactor for protein C activation

The calibrated automated thrombogram (CAT): a universal routine test for hyper- and hypocoagulability

TAFI, or plasma procarboxypeptidase B, couples the coagulation and fibrinolytic cascades through the thrombin-thrombomodulin complex

Thrombomodulin mutations in atypical hemolytic-uremic syndrome.

Functions of rhomboid family protease RHBDL2 and thrombomodulin in wound healing.

A hereditary bleeding disorder resulting from a premature stop codon in thrombomodulin (p.Cys537Stop)

Characterization of an autosomal dominant bleeding disorder caused by a thrombomodulin mutation.

Thrombomodulin.

Identification of an endothelial cell cofactor for thrombin-catalyzed activation of protein C.

P304

e0188213

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scholarly article

P356

10.1371/JOURNAL.PONE.0188213

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English

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P478

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P50

Christine Vinciguerra

P577

2017-11-16T00:00:00Z

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P698

29145514

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P932

5690669

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