ADAMTS13 is expressed in hepatic stellate cells. - Wikidata - awgldk - TriplyDB

ADAMTS13 is expressed in hepatic stellate cells.

ADAMTS13 is expressed in hepatic stellate cells.

http://www.wikidata.org/entity/Q36950896

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Pathophysiology of thrombotic thrombocytopenic purpura Current concepts in thrombotic thrombocytopenic purpura Pathogenesis of thrombotic microangiopathies Pathophysiological Function of ADAMTS Enzymes on Molecular Mechanism of Alzheimer's Disease Proteolytic processing of von Willebrand factor by adamts13 and leukocyte proteases Nxf1 natural variant E610G is a semi-dominant suppressor of IAP-induced RNA processing defects ADAMTS13 and von Willebrand factor in thrombotic thrombocytopenic purpura Hepatic stellate cell damage may lead to decreased plasma ADAMTS13 activity in rats Increased ADAMTS-13 proteolytic activity in rat hepatic stellate cells upon activation in vitro and in vivo ADAMTS13 reduces vascular inflammation and the development of early atherosclerosis in mice Molecular biology of ADAMTS13 and diagnostic utility of ADAMTS13 proteolytic activity and inhibitor assays.Systemic antithrombotic effects of ADAMTS13.ADAMTS13-binding IgG are present in patients with thrombotic thrombocytopenic purpura.Abnormal hemostasis tests and bleeding in chronic liver disease: are they related? No, but they need a careful look.ADAMTS13 and microvascular thrombosis An IAP retrotransposon in the mouse ADAMTS13 gene creates ADAMTS13 variant proteins that are less effective in cleaving von Willebrand factor multimers.Podocytes express ADAMTS13 in normal renal cortex and in patients with thrombotic thrombocytopenic purpura.Thrombotic thrombocytopenic purpura: a thrombotic disorder caused by ADAMTS13 deficiency The kidney in thrombotic thrombocytopenic purpura.Intensive plasma exchange increases a disintegrin and metalloprotease with thrombospondin motifs-13 activity and reverses organ dysfunction in children with thrombocytopenia-associated multiple organ failure Correction of ADAMTS13 deficiency by in utero gene transfer of lentiviral vector encoding ADAMTS13 genes.Effects of naturally occurring mutations in CUB-1 domain on synthesis, stability, and activity of ADAMTS-13.Mechanisms of microvascular thrombosis in thrombotic thrombocytopenic purpura.Thrombotic microangiopathies: multimers, metalloprotease, and beyond.Idiopathic noncirrhotic intrahepatic portal hypertension is associated with sustained ADAMTS13 Deficiency.[ADAMTS13, von Willebrand factor specific cleaving protease].Long term follow up of congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) on hemodialysis for 19 years: a case report.ADAMTS13 and von Willebrand factor interactions.Clinical-Pathological Conference Series from the Medical University of Graz Case No 155: 26-year-old woman in third trimester of pregnancy with epigastric pain and thrombocytopenia.Thrombocytopenia-Associated Multiple Organ Failure and Acute Kidney Injury.Characterization of conformation-sensitive antibodies to ADAMTS13, the von Willebrand cleavage protease In vivo imaging analysis of the interaction between unusually large von Willebrand factor multimers and platelets on the surface of vascular wall.Immortalized liver endothelial cells: a cell culture model for studies of motility and angiogenesis.Detection of a secreted metalloprotease within the nuclei of liver cells Increased expressions of ADAMTS-13, neuronal nitric oxide synthase, and neurofilament correlate with severity of neuropathology in Border disease virus-infected small ruminants.Probing ADAMTS13 substrate specificity using phage display The cooperative activity between the carboxyl-terminal TSP1 repeats and the CUB domains of ADAMTS13 is crucial for recognition of von Willebrand factor under flow.ADAMTS13 deficiency exacerbates VWF-dependent acute myocardial ischemia/reperfusion injury in mice Visualizing Trimming Dependence of Biodistribution and Kinetics with Homo- and Heterogeneous N-Glycoclusters on Fluorescent Albumin.Emerging Roles of ADAMTSs in Angiogenesis and Cancer.

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P2860

ADAMTS13 is expressed in hepatic stellate cells.

http://www.wikidata.org/entity/Q36950896

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2005 nî lūn-bûn

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ADAMTS13 is expressed in hepatic stellate cells.

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ADAMTS13 is expressed in hepatic stellate cells.

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ADAMTS13 is expressed in hepatic stellate cells.

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Laboratory Investigation

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ADAMTS13 is expressed in hepatic stellate cells.

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Daniel Benten

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Eric E Bouhassira

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Han-Mou Tsai

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Mari Inada

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Sanjeev Gupta

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Sergey Lyubsky

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Tai-Ping Lee

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Wenhua Zhou

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P2860

Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura

Advances in the pathogenesis, diagnosis, and treatment of thrombotic thrombocytopenic purpura

A disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motifs: the ADAMTS family

The amn gene product is required in extraembryonic tissues for the generation of middle primitive streak derivatives

Identification of strain-specific variants of mouse Adamts13 gene encoding von Willebrand factor-cleaving protease

High titers of inhibitors of von Willebrand factor-cleaving metalloproteinase in a fatal case of acute thrombotic thrombocytopenic purpura.

von Willebrand factor and von Willebrand factor-cleaving metalloprotease activity in Escherichia coli O157:H7-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.

Changes in health and disease of the metalloprotease that cleaves von Willebrand factor.

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