Abnormal whole blood thrombi in humans with inherited platelet receptor defects. - Wikidata - wikimedia - TriplyDB

Abnormal whole blood thrombi in humans with inherited platelet receptor defects.

Abnormal whole blood thrombi in humans with inherited platelet receptor defects.

http://www.wikidata.org/entity/Q34541342

about

An overview of platelet indices and methods for evaluating platelet function in thrombocytopenic patients.Thromboelastography identifies children with rare bleeding disorders and predicts bleeding phenotype.

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Abnormal whole blood thrombi in humans with inherited platelet receptor defects.

http://www.wikidata.org/entity/Q34541342

description

2012 nî lūn-bûn

@nan

2012 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2012年の論文

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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

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2012年论文

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name

Abnormal whole blood thrombi in humans with inherited platelet receptor defects.

@ast

Abnormal whole blood thrombi in humans with inherited platelet receptor defects.

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Abnormal whole blood thrombi in humans with inherited platelet receptor defects.

@nl

type

label

Abnormal whole blood thrombi in humans with inherited platelet receptor defects.

@ast

Abnormal whole blood thrombi in humans with inherited platelet receptor defects.

@en

Abnormal whole blood thrombi in humans with inherited platelet receptor defects.

@nl

prefLabel

Abnormal whole blood thrombi in humans with inherited platelet receptor defects.

@ast

Abnormal whole blood thrombi in humans with inherited platelet receptor defects.

@en

Abnormal whole blood thrombi in humans with inherited platelet receptor defects.

@nl

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JOURNAL.PONE.0052878

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Abnormal whole blood thrombi in humans with inherited platelet receptor defects.

@en

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Deborah L Donahue

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

Denise L Smith

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Francis J Castellino

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Harsha Musunuru

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

Mayra J Sandoval-Cooper

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Patrick K Davis

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Rashna D Balsara

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

Victoria A Ploplis

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

Zhong Liang

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

P2860

Molecular cloning, genomic structure, chromosomal localization, and alternative splice forms of the platelet collagen receptor glycoprotein VI

Central role of the P2Y12 receptor in platelet activation

Generation and rescue of a murine model of platelet dysfunction: the Bernard-Soulier syndrome

Platelet membrane glycoproteins implicated in ristocetin-induced aggregation. Studies of the proteins on platelets from patients with Bernard-Soulier syndrome and von Willebrand's disease.

A novel platelet aggregating factor found in a patient with defective collagen-induced platelet aggregation and autoimmune thrombocytopenia.

Systematic screening for genetic polymorphism in human platelet glycoprotein Ibalpha.

The role of von Willebrand factor and fibrinogen in platelet aggregation under varying shear stress

Polymorphism of human glycoprotein Ib alpha results from a variable number of tandem repeats of a 13-amino acid sequence in the mucin-like macroglycopeptide region. Structure/function implications.

An accompanying genetic severe deficiency of tissue factor protects mice with a protein C deficiency from lethal endotoxemia.

Signaling events underlying thrombus formation.

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