Residual plasmatic activity of ADAMTS13 is correlated with phenotype severity in congenital thrombotic thrombocytopenic purpura (Q33400891)

26 July 2017

title

Residual plasmatic activity of ADAMTS13 is correlated with phenotype severity in congenital thrombotic thrombocytopenic purpura (English)

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thrombotic thrombocytopenic purpura

26 July 2017

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1 reference

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Luca A Lotta

1

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Khaled M. Musallam

Khaled M Musallam

16

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Flora Peyvandi

Flora Peyvandi

17

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Giuseppe Remuzzi

Giuseppe Remuzzi

7

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Marina Noris

4

Marina Noris

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26 July 2017

8

Paul Coppo

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6

Marie A Scully

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12

Richard A Gibbs

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26 July 2017

Haifeng M Wu

2

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26 July 2017

Ian J Mackie

3

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26 July 2017

Agnes Veyradier

5

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26 July 2017

Ri Liesner

9

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26 July 2017

Roberta Donadelli

10

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26 July 2017

Chantal Loirat

11

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April Horne

13

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Shangbin Yang

14

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Isabella Garagiola

15

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26 July 2017

language of work or name

English

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publication date

23 April 2012

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26 July 2017

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26 July 2017

volume

120

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26 July 2017

issue

2

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26 July 2017

page(s)

440-448

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Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes

26 July 2017

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21 June 2018

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Platelet reactive conformation and multimeric pattern of von Willebrand factor in acquired thrombotic thrombocytopenic purpura during acute disease and remission.

21 June 2018

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Different clinical severity of first episodes and recurrences of thrombotic thrombocytopenic purpura

21 June 2018

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Predictive features of severe acquired ADAMTS13 deficiency in idiopathic thrombotic microangiopathies: the French TMA reference center experience

21 June 2018

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Multiple domains of ADAMTS13 are targeted by autoantibodies against ADAMTS13 in patients with acquired idiopathic thrombotic thrombocytopenic purpura

21 June 2018

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21 June 2018

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21 June 2018

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The first deletion mutation in the TSP1-6 repeat domain of ADAMTS13 in a family with inherited thrombotic thrombocytopenic purpura

21 June 2018

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

21 June 2018

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Nonsense-mediated mRNA decay in the ADAMTS13 gene caused by a 29-nucleotide deletion

21 June 2018

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Second international collaborative study evaluating performance characteristics of methods measuring the von Willebrand factor cleaving protease (ADAMTS-13).

21 June 2018

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Regional UK TTP registry: correlation with laboratory ADAMTS 13 analysis and clinical features

21 June 2018

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Relationship between ADAMTS13 activity in clinical remission and the risk of TTP relapse

21 June 2018

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ADAMTS13 and anti-ADAMTS13 antibodies as markers for recurrence of acquired thrombotic thrombocytopenic purpura during remission

21 June 2018

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Prevalence of the ADAMTS-13 missense mutation R1060W in late onset adult thrombotic thrombocytopenic purpura

21 June 2018

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In-vitro and in-vivo consequences of mutations in the von Willebrand factor cleaving protease ADAMTS13 in thrombotic thrombocytopenic purpura

21 June 2018

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Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome

21 June 2018

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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

21 June 2018

1 reference

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

21 June 2018

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FRETS-VWF73, a first fluorogenic substrate for ADAMTS13 assay

21 June 2018

1 reference

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

21 June 2018

1 reference

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

21 June 2018

1 reference

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Measurement of von Willebrand factor cleaving protease (ADAMTS-13): results of an international collaborative study involving 11 methods testing the same set of coded plasmas

21 June 2018

1 reference

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

21 June 2018

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Studies on thrombopoiesis. I. A factor in normal human plasma required for platelet production; chronic thrombocytopenia due to its deficiency

21 June 2018

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

21 June 2018

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

21 June 2018

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Mutation analysis and clinical implications of von Willebrand factor-cleaving protease deficiency

21 June 2018

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von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP.

21 June 2018

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

21 June 2018

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

21 June 2018

1 reference

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3721603

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)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3721603

Cysteine residues in CUB-1 domain are critical for ADAMTS13 secretion and stability.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3721603

Essential role of the disintegrin-like domain in ADAMTS13 function.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3721603

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

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3721603

Cleavage of ultralarge multimers of von Willebrand factor by C-terminal-truncated mutants of ADAMTS-13 under flow

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3721603

Polymorphisms and mutations of ADAMTS13 in the Japanese population and estimation of the number of patients with Upshaw-Schulman syndrome

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22529288

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1182/BLOOD-2012-01-403113

1 reference

26 July 2017

1 reference

26 July 2017

1 reference