Multiplein silicotools predict phenotypic manifestations in congenital thrombotic thrombocytopenic purpura-Reference-Cited by-同舟云学术

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Multiplein silicotools predict phenotypic manifestations in congenital thrombotic thrombocytopenic purpura

Published:2013-01-24 Issue:6 Volume:160 Page:825-837
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Hing Zachary A.¹,Schiller Tal¹,Wu Andrew¹,Hamasaki-Katagiri Nobuko¹,Struble Evi Budo²,Russek-Cohen Estelle³,Kimchi-Sarfaty Chava¹

Affiliation:

1. Laboratory of Hemostasis; Division of Hematology; Center for Biologics Evaluation & Research; FDA; Bethesda MD USA

2. Laboratory of Plasma Derivatives; Division of Hematology; Center for Biologics Evaluation & Research; FDA; Bethesda MD USA

3. Division of Biostatistics; Office of Biostatistics and Epidemiology; Center for Biologics Evaluation & Research; FDA; Bethesda MD USA

Funder

Laboratory of Hemostasis

Center for Biologics Evaluation and Research, Food and Drug Administration

Food and Drug Administration

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.12214/fullpdf

Reference35 articles.

1. Crystal structures of the noncatalytic domains of ADAMTS13 reveal multiple discontinuous exosites for von Willebrand factor;Akiyama;Proceedings of the National Academy of Sciences of the United States of America,2009

2. A new ADAMTS13 missense mutation (D1362V) in thrombotic thrombocytopenic purpura diagnosed during pregnancy;Calderazzo;Thrombosis and Haemostasis,2012

3. A phenotype-genotype correlation of ADAMTS13 mutations in congenital TTP patients treated in the United Kingdom;Camilleri;Journal of Thrombosis and Haemostasis,2012

4. Characterization of coding synonymous and non-synonymous variants in ADAMTS13 using ex vivo and in silico approaches;Edwards;PLoS ONE,2012

5. Regulation of Alzheimer's disease amyloid-β formation by casein kinase I;Flajolet;Proceedings of the National Academy of Sciences,2007

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1. Global prevalence of hereditary thrombotic thrombocytopenic purpura determined by genetic analysis;Blood Advances;2024-08-16

2. An Examination of Mechanisms by which Synonymous Mutations may Alter Protein Levels, Structure and Functions;Single Nucleotide Polymorphisms;2022

3. De Novo Mutation of the ADAMTS13 Gene with Mesenteric Ischemia in an Infant with Congenital Thrombotic Thrombocytopenic Purpura;Case Reports in Hematology;2021-07-06

4. Congenital Thrombotic Thrombocytopenic Purpura With a Novel ADAMTS13 Gene Mutation;Cureus;2020-12-13

5. Thirty five novel nsSNPs may effect on ADAMTS13 protein leading to Thrombotic thrombocytopenic purpura (TTP) using bioinformatics approach;2019-09-05

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