A comparative study of Greek nondeletional hereditary persistence of fetal hemoglobin and β-thalassemia compound heterozygotes-Reference-Cited by-同舟云学术

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A comparative study of Greek nondeletional hereditary persistence of fetal hemoglobin and β-thalassemia compound heterozygotes

Published:2001-12-18 Issue:4 Volume:80 Page:243-247
ISSN:0946-2716
Container-title:Journal of Molecular Medicine
language:en
Short-container-title:J Mol Med

Author:

Papadakis Manoussos N.,Patrinos George P.,Tsaftaridis Panayotis,Loutradi-Anagnostou Aphrodite

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Drug Discovery,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00109-001-0312-4.pdf

Cited by 21 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. Investigating the Efficacy and Safety of Thalidomide for Treating Patients With ß-Thalassemia: A Meta-Analysis;Frontiers in Pharmacology;2022-01-11

2. An erythroid-to-myeloid cell fate conversion is elicited by LSD1 inactivation;Blood;2021-11-04

3. The epigenetic eraser LSD1 lies at the apex of a reversible erythroid to myeloid cell fate decision;2021-01-14

4. Small molecule therapeutics to treat the β-globinopathies;Current Opinion in Hematology;2020-05

5. Synergistic effect of two β globin gene cluster mutations leading to the hereditary persistence of fetal hemoglobin (HPFH) phenotype;Molecular Biology Reports;2017-09-06

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