Characterization of a genetically engineered mouse model of hemophilia A with complete deletion of the F8 gene-Reference-Cited by-同舟云学术

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Characterization of a genetically engineered mouse model of hemophilia A with complete deletion of the F8 gene

Published:2016-01-08 Issue:2 Volume:14 Page:346-355
ISSN:1538-7933
Container-title:Journal of Thrombosis and Haemostasis
language:en
Short-container-title:J Thromb Haemost

Author:

Chao B. N.¹,Baldwin W. H.²,Healey J. F.²,Parker E. T.²,Shafer-Weaver K.¹,Cox C.²,Jiang P.¹,Kanellopoulou C.¹,Lollar P.²,Meeks S. L.²,Lenardo M. J.¹

Affiliation:

1. Laboratory of Immunology; National Institute of Allergy and Infectious Diseases (NIAID); National Institutes of Health; Bethesda MD USA

2. Department of Pediatrics; Aflac Cancer and Blood Disorders Center; Children's Healthcare of Atlanta; Emory University; Atlanta GA USA

Funder

National Institutes of Health

Hemophilia of Georgia, Inc.

National Institute of Allergy and Infectious Diseases

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jth.13202/fullpdf

Reference42 articles.

1. Mechanisms of action of immune tolerance induction against factor VIII in patients with congenital haemophilia A and factor VIII inhibitors;Reipert;Br J Haematol,2007

2. F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis;Gouw;Blood,2012

3. Characterization of mutations within the factor VIII gene of 73 unrelated mild and moderate haemophiliacs;Schwaab;Br J Haematol,1995

4. Risk stratification for inhibitor development at first treatment for severe hemophilia A: a tool for clinical practice;Avest;J Thromb Haemost,2008

5. The genetic basis of inhibitor development in haemophilia A;Tuddenham;Haemophilia,1998

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. AAV mediated genome engineering with a bypass coagulation factor alleviates the bleeding phenotype in a murine model of hemophilia B;Thrombosis Research;2024-06

2. AAV mediated repression of Neat1 lncRNA combined with F8 gene augmentation mitigates pathological mediators of joint disease in haemophilia;Journal of Cellular and Molecular Medicine;2024-06

3. Generation of Mouse Model of Hemophilia A by Introducing Novel Mutations, Using CRISPR/Nickase Gene Targeting System;CELL J;2023

4. Adeno-associated virus-mediated expression of activated factor V (FVa) for hemophilia phenotypic correction;Frontiers in Medicine;2022-08-05

5. Engineering a Therapeutic Protein to Enhance the Study of Anti-Drug Immunity;Biomedicines;2022-07-18

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