ADAMTS13 phenotype in plasma from normal individuals and patients with thrombotic thrombocytopenic purpura - Wikidata - wikimedia - TriplyDB

ADAMTS13 phenotype in plasma from normal individuals and patients with thrombotic thrombocytopenic purpura

ADAMTS13 phenotype in plasma from normal individuals and patients with thrombotic thrombocytopenic purpura

http://www.wikidata.org/entity/Q33373698

about

Pathophysiology of thrombotic thrombocytopenic purpura Proteolytic processing of von Willebrand factor by adamts13 and leukocyte proteases Podocytes express ADAMTS13 in normal renal cortex and in patients with thrombotic thrombocytopenic purpura.Atypical haemolytic uremic syndrome complicated by microangiopathic antiphospholipid-associated syndrome.Escherichia coli Shiga Toxin Mechanisms of Action in Renal Disease.Natural history of Upshaw-Schulman syndrome based on ADAMTS13 gene analysis in Japan.Complement activation associated with ADAMTS13 deficiency in human and murine thrombotic microangiopathy Congenital thrombotic thrombocytopenic purpura caused by new compound heterozygous mutations of the ADAMTS13 gene.Congenital thrombotic thrombocytopenic purpura: Upshaw-Schulman syndrome: a cause of neonatal death and review of literature.High prevalence of hereditary thrombotic thrombocytopenic purpura in central Norway: from clinical observation to evidence.Phenotypic expression of ADAMTS13 in glomerular endothelial cells von Willebrand factor-cleaving protease ADAMTS13 reduces ischemic brain injury in experimental stroke.Biological variations of ADAMTS13 and von Willebrand factor in human adults.ADAMTS13 and Von Willebrand factor in patients undergoing hemodialysis.

P2860

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P2860

ADAMTS13 phenotype in plasma from normal individuals and patients with thrombotic thrombocytopenic purpura

http://www.wikidata.org/entity/Q33373698

description

2006 nî lūn-bûn

@nan

2006 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2006年の論文

@ja

2006年論文

@yue

2006年論文

@zh-hant

2006年論文

@zh-hk

2006年論文

@zh-mo

2006年論文

@zh-tw

2006年论文

@wuu

name

ADAMTS13 phenotype in plasma f ...... botic thrombocytopenic purpura

@ast

ADAMTS13 phenotype in plasma f ...... botic thrombocytopenic purpura

@en

type

label

ADAMTS13 phenotype in plasma f ...... botic thrombocytopenic purpura

@ast

ADAMTS13 phenotype in plasma f ...... botic thrombocytopenic purpura

@en

prefLabel

ADAMTS13 phenotype in plasma f ...... botic thrombocytopenic purpura

@ast

ADAMTS13 phenotype in plasma f ...... botic thrombocytopenic purpura

@en

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European Journal of Pediatrics

P1476

ADAMTS13 phenotype in plasma f ...... botic thrombocytopenic purpura

@en

P2093

AnnCharlotte Kristoffersson

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

Han-Mou Tsai

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

Ingemar Winqvist

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

Lars Holmberg

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

Minola Manea

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

Peter Björk

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Rolf Billström

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Wenhua Zhou

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

P2860

Purification of human von Willebrand factor-cleaving protease and its identification as a new member of the metalloproteinase family

Lipopolysaccharide from enterohemorrhagic Escherichia coli binds to platelets through TLR4 and CD62 and is detected on circulating platelets in patients with hemolytic uremic syndrome

Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura

A rapid test for the diagnosis of thrombotic thrombocytopenic purpura using surface enhanced laser desorption/ionization time-of-flight (SELDI-TOF)-mass spectrometry.

Estimation of the von Willebrand factor-cleaving protease in plasma using monoclonal antibodies to vWF.

Assay of von Willebrand factor (vWF)-cleaving protease based on decreased collagen binding affinity of degraded vWF: a tool for the diagnosis of thrombotic thrombocytopenic purpura (TTP)

von Willebrand factor and von Willebrand factor-cleaving metalloprotease activity in Escherichia coli O157:H7-associated hemolytic uremic syndrome.

Pathogenesis of Shiga toxin-associated hemolytic uremic syndrome.

Partial amino acid sequence of purified von Willebrand factor-cleaving protease.

Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura.

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3

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thrombocytopenia

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