Fetal hemoglobin regulation in β-thalassemia: heterogeneity, modifiers and therapeutic approaches
Author:
Funder
Mahidol University
National Science and Technology Development Agency (NSTDA)
Thailand Research Fund
Publisher
Informa UK Limited
Subject
Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1080/17474086.2016.1255142
Reference103 articles.
1. Pathophysiology and Clinical Manifestations of the -Thalassemias
2. Survival in Medically Treated Patients with Homozygous β-Thalassemia
3. IthaGenes: An Interactive Database for Haemoglobin Variations and Epidemiology
4. Hemoglobinopathies in Southeast Asia: Molecular Biology and Clinical Medicine
Cited by 44 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. α-Globin mutations and Genetic Variants in γ-globin Promoters are Associated with Unelevated Hemoglobin F Expression of Atypical β0-thalassemia/HbE;Archives of Medical Research;2024-09
2. Pharmacogenomics of Drugs Used in β-Thalassemia and Sickle-Cell Disease: From Basic Research to Clinical Applications;International Journal of Molecular Sciences;2024-04-12
3. A Population-Oriented Genetic Scoring System to Predict Phenotype: A Pathway to Personalized Medicine in Iraqis With β-Thalassemia;Hemoglobin;2024-02-23
4. A 6-Year Follow-up of a Chinese Child with Homozygous β 0 -Thalaasemia and a Heterozygous KLF1 Mutation;Hemoglobin;2024-01-02
5. New Synthetic Isoxazole Derivatives Acting as Potent Inducers of Fetal Hemoglobin in Erythroid Precursor Cells Isolated from β-Thalassemic Patients;Molecules;2023-12-19
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3