A novel type of macrothrombocytopenia associated with a defect in α2,3-sialylation. - Wikidata - wikimedia - TriplyDB

A novel type of macrothrombocytopenia associated with a defect in α2,3-sialylation.

A novel type of macrothrombocytopenia associated with a defect in α2,3-sialylation.

http://www.wikidata.org/entity/Q33396841

about

Progress in understanding the diagnosis and molecular genetics of macrothrombocytopenias.Human deficiencies of fucosylation and sialylation affecting selectin ligands.Recent advances in platelet proteomics.Congenital disorders of glycosylation: new defects and still counting.A functional splice variant of the human Golgi CMP-sialic acid transporter.PIGO deficiency: palmoplantar keratoderma and novel mutations Patterns and levels of platelet glycosylation in patients with coronary heart disease and type 2 diabetes mellitus.The class II PI 3-kinase, PI3KC2α, links platelet internal membrane structure to shear-dependent adhesive function.Encephalopathy caused by novel mutations in the CMP-sialic acid transporter, SLC35A1

P2860

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P2860

A novel type of macrothrombocytopenia associated with a defect in α2,3-sialylation.

http://www.wikidata.org/entity/Q33396841

description

2011 nî lūn-bûn

@nan

2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2011年の論文

@ja

2011年論文

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2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

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name

A novel type of macrothrombocytopenia associated with a defect in α2,3-sialylation.

@ast

A novel type of macrothrombocytopenia associated with a defect in α2,3-sialylation.

@en

type

label

A novel type of macrothrombocytopenia associated with a defect in α2,3-sialylation.

@ast

A novel type of macrothrombocytopenia associated with a defect in α2,3-sialylation.

@en

prefLabel

A novel type of macrothrombocytopenia associated with a defect in α2,3-sialylation.

@ast

A novel type of macrothrombocytopenia associated with a defect in α2,3-sialylation.

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J.AJPATH.2011.06.012

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The American Journal of Pathology

P1476

A novel type of macrothrombocytopenia associated with a defect in α2,3-sialylation.

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P2093

Annette G Beck-Sickinger

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Claire Jones

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Dagmar Zeuschner

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Dirk J Lefeber

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Dorothea Stahl

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Jonas Denecke

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Karen Strenge

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Kerstin Lühn

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Luca Gentile

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Martin K Wild

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

P2860

Molecular cloning of a novel alpha2,3-sialyltransferase (ST3Gal VI) that sialylates type II lactosamine structures on glycoproteins and glycolipids

Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy

The Ashwell receptor mitigates the lethal coagulopathy of sepsis

Five tumor necrosis factor-inducible cell adhesion mechanisms on the surface of mouse endothelioma cells mediate the binding of leukocytes

A defect in dolichol phosphate biosynthesis causes a new inherited disorder with death in early infancy

Improvement of interferon-gamma sialylation in Chinese hamster ovary cell culture by feeding of N-acetylmannosamine

Genetic abnormalities of Bernard-Soulier syndrome

Sialoadhesin, myelin-associated glycoprotein and CD22 define a new family of sialic acid-dependent adhesion molecules of the immunoglobulin superfamily

Recurrent Severe Infections Caused by a Novel Leukocyte Adhesion Deficiency

Rolling on E- or P-selectin induces the extended but not high-affinity conformation of LFA-1 in neutrophils

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1969-1977

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scholarly article

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10.1016/J.AJPATH.2011.06.012

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4

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179

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Alexander Zarbock

Judith Klumperman

Ronald Sträter

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2011-08-22T00:00:00Z

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51592912

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21864493

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Giant platelet disorder

P932

3181377

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