Abnormal von Willebrand factor secretion, factor VIII stabilization and thrombus dynamics in type 2N von Willebrand disease mice.

about

Abnormal von Willebrand factor secretion, factor VIII stabilization and thrombus dynamics in type 2N von Willebrand disease mice.

Item

http://www.wikidata.org/entity/Q50959137

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Abnormal von Willebrand factor ...... N von Willebrand disease mice.

@en

Abnormal von Willebrand factor ...... N von Willebrand disease mice.

@nl

type

Item

label

Abnormal von Willebrand factor ...... N von Willebrand disease mice.

@en

Abnormal von Willebrand factor ...... N von Willebrand disease mice.

@nl

prefLabel

Abnormal von Willebrand factor ...... N von Willebrand disease mice.

@en

Abnormal von Willebrand factor ...... N von Willebrand disease mice.

@nl

P1476

Abnormal von Willebrand factor ...... N von Willebrand disease mice.

@en

P2093

C Brown

http://www.w3.org/2001/XMLSchema#string

C Dwyer

http://www.w3.org/2001/XMLSchema#string

C Notley

http://www.w3.org/2001/XMLSchema#string

D Lillicrap

http://www.w3.org/2001/XMLSchema#string

I Georgescu

http://www.w3.org/2001/XMLSchema#string

J Mewburn

http://www.w3.org/2001/XMLSchema#string

K Hebert

http://www.w3.org/2001/XMLSchema#string

K Nesbitt

http://www.w3.org/2001/XMLSchema#string

L L Swystun

http://www.w3.org/2001/XMLSchema#string

M Deforest

http://www.w3.org/2001/XMLSchema#string

P2860

Solution structure of the major factor VIII binding region on von Willebrand factor

A mouse model of severe von Willebrand disease: defects in hemostasis and thrombosis

Analysis of the spatial and temporal characteristics of platelet-delivered factor VIII-based clots

In vivo imaging visualizes discoid platelet aggregations without endothelium disruption and implicates contribution of inflammatory cytokine and integrin signaling.

Mutation-specific hemostatic variability in mice expressing common type 2B von Willebrand disease substitutions.

A von Willebrand factor fragment containing the D'D3 domains is sufficient to stabilize coagulation factor VIII in mice

Analysis of the role of von Willebrand factor, platelet glycoprotein VI-, and α2β1-mediated collagen binding in thrombus formation.

Biologic response to desmopressin in patients with severe type 1 and type 2 von Willebrand disease: results of a multicenter European study.

Congenital von Willebrand disease type 3: clinical manifestations, pathophysiology and molecular biology.

The mutational spectrum of type 1 von Willebrand disease: Results from a Canadian cohort study.

P304

1607-1619

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1111/JTH.13749

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2017-06-05T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

28581694

http://www.w3.org/2001/XMLSchema#string