Immune Modulatory Cell Therapy for Hemophilia B Based on CD20-Targeted Lentiviral Gene Transfer to Primary B Cells-Reference-Cited by-同舟云学术

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Immune Modulatory Cell Therapy for Hemophilia B Based on CD20-Targeted Lentiviral Gene Transfer to Primary B Cells

Published:2017-06 Issue: Volume:5 Page:76-82
ISSN:2329-0501
Container-title:Molecular Therapy - Methods & Clinical Development
language:en
Short-container-title:Molecular Therapy - Methods & Clinical Development

Author:

Wang Xiaomei,Herzog Roland W.,Byrne Barry J.,Kumar Sandeep R.P.,Zhou Qi,Buchholz Christian J.,Biswas Moanaro

Funder

Pfizer Inc

NIH

LOEWE Center for Cell and Gene Therapy Frankfurt

Hessisches Ministerium für Wissenschaft und Kunst

Publisher

Elsevier BV

Subject

Genetics,Molecular Biology,Molecular Medicine

Reference43 articles.

1. Gene therapy for hemophilia;Rogers;Front. Biosci. (Landmark Ed.),2015

2. Inhibitor development in haemophilia B: an orphan disease in need of attention;DiMichele;Br. J. Haematol.,2007

3. Immune tolerance in haemophilia: the long journey to the fork in the road;DiMichele;Br. J. Haematol.,2012

4. Inhibitors in factor IX deficiency a report of the ISTH-SSC international FIX inhibitor registry (1997-2006);Chitlur;Haemophilia,2009

5. Inhibitors in Hemophilia B;Warrier,2005

Cited by 15 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. Envelope protein-specific B cell receptors direct lentiviral vector tropism in vivo;Molecular Therapy;2024-05

2. Gene Therapy Approaches for the Treatment of Hemophilia B;International Journal of Molecular Sciences;2023-06-28

3. Challenges and opportunities in gene editing of B cells;Biochemical Pharmacology;2022-12

4. Genomic Designs of rAAVs Contribute to Pathological Changes in the Livers and Spleens of Mice;Advances in Cell and Gene Therapy;2022-03-20

5. Genome edited B cells: a new frontier in immune cell therapies;Molecular Therapy;2021-11

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