A novel transgenic mouse model produced from lentiviral germline integration for the study of -thalassemia gene therapy-Reference-Cited by-同舟云学术

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A novel transgenic mouse model produced from lentiviral germline integration for the study of -thalassemia gene therapy

Published:2008-03-01 Issue:3 Volume:93 Page:356-362
ISSN:0390-6078
Container-title:Haematologica
language:en
Short-container-title:Haematologica

Author:

Li W.,Xie S.,Guo X.,Gong X.,Wang S.,Lin D.,Zhang J.,Ren Z.,Huang S.,Zeng F.,Zeng Y.

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

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. Gene Editing of the Endogenous Cryptic 3′ Splice Site Corrects the RNA Splicing Defect in the β⁶⁵⁴-Thalassemia Mouse Model;Human Gene Therapy;2024-08-13

2. CRISPR Gene Therapy: A Promising One-Time Therapeutic Approach for Transfusion-Dependent β-Thalassemia—CRISPR-Cas9 Gene Editing for β-Thalassemia;Thalassemia Reports;2023-02-06

3. Correction of Beta-Thalassemia IVS-II-654 Mutation in a Mouse Model Using Prime Editing;International Journal of Molecular Sciences;2022-05-25

4. Nrf2 expands the intracellular pool of the chaperone AHSP in a cellular model of β-thalassemia;Redox Biology;2022-04

5. Correction of RNA splicing defect in β⁶⁵⁴-thalassemia mice using CRISPR/Cas9 gene-editing technology;Haematologica;2021-10-28

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