(Q37917779)

English

SNPs in ADAMTS13.

scientific article published on August 2011

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scholarly article

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Europe PubMed Central

PubMed publication ID

25 August 2017

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Europe PubMed Central

SNPs in ADAMTS13. (English)

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Europe PubMed Central

PubMed publication ID

25 August 2017

author name string

Sandra Chang Tseng

1

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Europe PubMed Central

PubMed publication ID

25 August 2017

Chava Kimchi-Sarfaty

2

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Europe PubMed Central

PubMed publication ID

25 August 2017

publication date

1 August 2011

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Europe PubMed Central

PubMed publication ID

25 August 2017

Pharmacogenomics

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Europe PubMed Central

PubMed publication ID

25 August 2017

12

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Europe PubMed Central

PubMed publication ID

25 August 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

25 August 2017

1147-1160

1 reference

Europe PubMed Central

PubMed publication ID

25 August 2017

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

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

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

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

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

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

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

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Identification of a cleavage site directing the immunochemical detection of molecular abnormalities in type IIA von Willebrand factor

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

ADAMTS-13 cysteine-rich/spacer domains are functionally essential for von Willebrand factor cleavage

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Cleavage of von Willebrand factor requires the spacer domain of the metalloprotease ADAMTS13.

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

The proximal carboxyl-terminal domains of ADAMTS13 determine substrate specificity and are all required for cleavage of von Willebrand factor.

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Registry of 919 patients with thrombotic microangiopathies across Japan: database of Nara Medical University during 1998-2008.

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

von Willebrand factor cleaving protease (ADAMTS-13) and ADAMTS-13 neutralizing autoantibodies in 100 patients with thrombotic thrombocytopenic purpura

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

ADAMTS13 activity in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: relation to presenting features and clinical outcomes in a prospective cohort of 142 patients

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

ADAMTS13 autoantibodies in patients with thrombotic microangiopathies and other immunomediated diseases

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Nonneutralizing IgM and IgG antibodies to von Willebrand factor-cleaving protease (ADAMTS-13) in a patient with thrombotic thrombocytopenic purpura

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Epitope mapping of ADAMTS13 autoantibodies in acquired thrombotic thrombocytopenic purpura

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Familial acquired thrombotic thrombocytopenic purpura: ADAMTS13 inhibitory autoantibodies in identical twins

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Acquired ADAMTS-13 deficiency in pediatric patients with severe sepsis

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Severe secondary deficiency of von Willebrand factor-cleaving protease (ADAMTS13) in patients with sepsis-induced disseminated intravascular coagulation: its correlation with development of renal failure.

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Ticlopidine- and clopidogrel-associated thrombotic thrombocytopenic purpura (TTP): review of clinical, laboratory, epidemiological, and pharmacovigilance findings (1989-2008).

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

ADAMTS-13 plasma level determination uncovers antigen absence in acquired thrombotic thrombocytopenic purpura and ethnic differences

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

ADAMTS13 and microvascular thrombosis

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Inherited thrombotic thrombocytopenic purpura

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Molecular basis of ADAMTS13 dysfunction in thrombotic thrombocytopenic purpura

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Evaluation and clinical application of a new method for measuring activity of von Willebrand factor-cleaving metalloprotease (ADAMTS13).

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

FRETS-VWF73, a first fluorogenic substrate for ADAMTS13 assay

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

ADAMTS-13 rapidly cleaves newly secreted ultralarge von Willebrand factor multimers on the endothelial surface under flowing conditions

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

The role of ADAMT-13 in platelet adhesion in flow: methods for diagnosis of thrombotic thrombocytopenic purpura

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

ADAMTS-13 assays in thrombotic thrombocytopenic purpura

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Integrating common and rare genetic variation in diverse human populations

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

A map of human genome variation from population-scale sequencing

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

ADAMTS13 P475S polymorphism causes a lowered enzymatic activity and urea lability in vitro

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Frequency of Pro475Ser polymorphism of ADAMTS13 gene and its association with ADAMTS-13 activity in the Korean population

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Absence of Pro475Ser polymorphism in ADAMTS-13 in Caucasians

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Association between ADAMTS13 polymorphisms and risk of cardiovascular events in chronic coronary disease

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Novel ADAMTS-13 mutations in an adult with delayed onset thrombotic thrombocytopenic purpura

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Modulation of ADAMTS13 secretion and specific activity by a combination of common amino acid polymorphisms and a missense mutation

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

ADAMTS13 gene defects in two brothers with constitutional thrombotic thrombocytopenic purpura and normalization of von Willebrand factor-cleaving protease activity by recombinant human ADAMTS13.

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Mutation of the H-bond acceptor S119 in the ADAMTS13 metalloprotease domain reduces secretion and substrate turnover in a patient with congenital thrombotic thrombocytopenic purpura

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Complement factor H mutation in familial thrombotic thrombocytopenic purpura with ADAMTS13 deficiency and renal involvement

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Mechanisms of the interaction between two ADAMTS13 gene mutations leading to severe deficiency of enzymatic activity.

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

ADAMTS13 and von Willebrand factor and the risk of myocardial infarction in men.

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

An amino acid polymorphism in von Willebrand factor correlates with increased susceptibility to proteolysis by ADAMTS13

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

A "silent" polymorphism in the MDR1 gene changes substrate specificity

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Silent (synonymous) SNPs: should we care about them?

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Transient ribosomal attenuation coordinates protein synthesis and co-translational folding.

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Novel compound heterozygote mutations (H234Q/R1206X) of the ADAMTS13 gene in an adult patient with Upshaw-Schulman syndrome showing predominant episodes of repeated acute renal failure

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Pregnancy-induced thrombocytopenia and TTP, and the risk of fetal death, in Upshaw-Schulman syndrome: a series of 15 pregnancies in 9 genotyped patients

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Amino acid residues Arg(659), Arg(660), and Tyr(661) in the spacer domain of ADAMTS13 are critical for cleavage of von Willebrand factor.

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

An autoantibody epitope comprising residues R660, Y661, and Y665 in the ADAMTS13 spacer domain identifies a binding site for the A2 domain of VWF

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Crystal structures of the noncatalytic domains of ADAMTS13 reveal multiple discontinuous exosites for von Willebrand factor

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Cloning, expression and functional characterization of the full-length murine ADAMTS13.

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Complete deficiency in ADAMTS13 is prothrombotic, but it alone is not sufficient to cause thrombotic thrombocytopenic purpura

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Shigatoxin triggers thrombotic thrombocytopenic purpura in genetically susceptible ADAMTS13-deficient mice

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Thrombotic Microangiopathies

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Enzymatically active ADAMTS13 variants are not inhibited by anti-ADAMTS13 autoantibodies: a novel therapeutic strategy?

1 reference

https://api.crossref.org/works/10.2217%2FPGS.11.66

21 January 2018

Identifiers

10.2217/PGS.11.66

1 reference

Europe PubMed Central

PubMed publication ID

25 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 August 2017

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