In vitro study of HAX1 gene therapy by retro viral transduction as a therapeutic target in severe congenital neutropenia-Reference-Cited by-同舟云学术

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In vitro study of HAX1 gene therapy by retro viral transduction as a therapeutic target in severe congenital neutropenia

Published:2018-10 Issue:4 Volume:29 Page:146-152
ISSN:1148-5493
Container-title:European Cytokine Network
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Author:

Farajifard Hamid,Zavvar Mahdi,Rajaei Taraneh,Noorbakhsh Farshid,Nikougoftar-zarif Mahin,Azadmanesh Kayhan,Kompani Farzad,Rezaei Nima

Publisher

John Libbey Eurotext

Subject

Clinical Biochemistry,Immunology,Immunology and Allergy

Cited by 5 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. Pediatric Bone Marrow Failure: A Broad Landscape in Need of Personalized Management;Journal of Clinical Medicine;2023-11-20

2. Gene therapy for inborn error of immunity – current status and future perspectives;Current Opinion in Allergy & Clinical Immunology;2022-12-06

3. Extracellular vesicles rich in HAX1 promote angiogenesis by modulating ITGB6 translation;Journal of Extracellular Vesicles;2022-05

4. Abnormal DNA methylation patterns in patients with infection‑caused leukocytopenia based on methylation microarrays;Molecular Medicine Reports;2020-04-08

5. Frataxin deficiency in Friedreich’s ataxia is associated with reduced levels of HAX-1, a regulator of cardiomyocyte death and survival;Human Molecular Genetics;2020-01-15

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