Characterization of an autosomal dominant bleeding disorder caused by a thrombomodulin mutation.
about
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disordersAltered fibrinolysis in autosomal dominant thrombomodulin-associated coagulopathy.Thrombin generation assays for global evaluation of the hemostatic system: perspectives and limitations.Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet function.Why patients with THBD c.1611C>A (p.Cys537X) nonsense mutation have high levels of soluble thrombomodulin?Thrombotic and Hemorrhagic Conditions Due to a Gain of Function of Coagulation Proteins: A Special Type of Clotting Disorders.Effect of five therapeutic strategies on the coagulation defect induced by the thrombomodulin c.1611C>A mutation.
P2860
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P2860
Characterization of an autosomal dominant bleeding disorder caused by a thrombomodulin mutation.
description
2015 nî lūn-bûn
@nan
2015 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Characterization of an autosom ...... by a thrombomodulin mutation.
@ast
Characterization of an autosom ...... by a thrombomodulin mutation.
@en
type
label
Characterization of an autosom ...... by a thrombomodulin mutation.
@ast
Characterization of an autosom ...... by a thrombomodulin mutation.
@en
prefLabel
Characterization of an autosom ...... by a thrombomodulin mutation.
@ast
Characterization of an autosom ...... by a thrombomodulin mutation.
@en
P2093
P2860
P50
P1433
P1476
Characterization of an autosom ...... by a thrombomodulin mutation.
@en
P2093
Christine Trzeciak
Elisabetta Castoldi
Jean Yves Scoazec
Simone J H Wielders
Theo Lindhout
Tilman M Hackeng
P2860
P304
P356
10.1182/BLOOD-2014-10-604553
P407
P577
2015-01-06T00:00:00Z