Induction of fetal hemoglobin: Lentiviral shRNA knockdown of HBS1L in β<sup>0</sup>thalassemia/HbE erythroid cells
Imbalanced globin chain output contributes to thalassemia pathophysiology. Hence, induction of fetal hemoglobin in β-thalassemia and other β-hemoglobinopathies are of continuing interest for therapeutic approaches. Genome-wide association studies have identified three common genetic loci: namely β-g...
Saved in:
主要作者: | Chumchuen S. |
---|---|
其他作者: | Mahidol University |
格式: | Article |
出版: |
2023
|
主題: | |
在線閱讀: | https://repository.li.mahidol.ac.th/handle/123456789/82145 |
標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|
相似書籍
-
Down-regulation of the transcriptional repressor ZNF802 (JAZF1) reactivates fetal hemoglobin in β<sup>0</sup>-thalassemia/HbE
由: Chokdee Wongborisuth, et al.
出版: (2022) -
Impaired Terminal Erythroid Maturation in β<sup>0</sup>-Thalassemia/HbE Patients with Different Clinical Severity
由: Thunwarat Suriyun, et al.
出版: (2022) -
Impaired Terminal Erythroid Maturation in β<sup>0</sup>-Thalassemia/HbE Patients with Different Clinical Severity
由: Suriyun T.
出版: (2023) -
Down-regulation of the transcriptional repressor ZNF802 (JAZF1) reactivates fetal hemoglobin in β<sup>0</sup>-thalassemia/HbE
由: Wongborisuth C.
出版: (2023) -
Genetic variation of Krüppel-like factor 1 (KLF1) and fetal hemoglobin (HbF) levels in β<sup>0</sup>-thalassemia/HbE disease
由: Pinyaphat Khamphikham, et al.
出版: (2019)