Effect of genetic variation in STXBP5 and STX2 on von Willebrand factor and bleeding phenotype in type 1 von Willebrand disease patients.
about
Syntaxin-binding protein STXBP5 inhibits endothelial exocytosis and promotes platelet secretion.The nuts and bolts of the platelet release reaction.Platelet secretion and hemostasis require syntaxin-binding protein STXBP5.Genome-wide association studies identify genetic loci for low von Willebrand factor levelsCurrent knowledge on the genetics of incident venous thrombosis.The secretion of von Willebrand factor from endothelial cells; an increasingly complicated story.Syntaxin-binding protein 5 exocytosis regulation: differential role in endothelial cells and platelets.Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients.Regulation of plasma von Willebrand factor.Novel Thrombotic Function of a Human SNP in STXBP5 Revealed by CRISPR/Cas9 Gene Editing in Mice.Von Willebrand disease in the elderly: clinical perspectives
P2860
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P2860
Effect of genetic variation in STXBP5 and STX2 on von Willebrand factor and bleeding phenotype in type 1 von Willebrand disease patients.
description
2012 nî lūn-bûn
@nan
2012 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Effect of genetic variation in ...... n Willebrand disease patients.
@ast
Effect of genetic variation in ...... n Willebrand disease patients.
@en
Effect of genetic variation in ...... n Willebrand disease patients.
@nl
type
label
Effect of genetic variation in ...... n Willebrand disease patients.
@ast
Effect of genetic variation in ...... n Willebrand disease patients.
@en
Effect of genetic variation in ...... n Willebrand disease patients.
@nl
prefLabel
Effect of genetic variation in ...... n Willebrand disease patients.
@ast
Effect of genetic variation in ...... n Willebrand disease patients.
@en
Effect of genetic variation in ...... n Willebrand disease patients.
@nl
P2093
P2860
P1433
P1476
Effect of genetic variation in ...... on Willebrand disease patients
@en
P2093
Eva M de Wee
Frank W G Leebeek
Janine E van Loon
Marieke J H A Kruip
Moniek P M de Maat
P2860
P304
P356
10.1371/JOURNAL.PONE.0040624
P407
P577
2012-07-06T00:00:00Z