Hydroxyurea responsiveness in -thalassemic patients is determined by the stress response adaptation of erythroid progenitors and their differentiation propensity-Reference-Cited by-同舟云学术

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Hydroxyurea responsiveness in -thalassemic patients is determined by the stress response adaptation of erythroid progenitors and their differentiation propensity

Published:2012-10-25 Issue:5 Volume:98 Page:696-704
ISSN:0390-6078
Container-title:Haematologica
language:en
Short-container-title:Haematologica

Author:

Pourfarzad F.,von Lindern M.,Azarkeivan A.,Hou J.,Kia S. K.,Esteghamat F.,van IJcken W.,Philipsen S.,Najmabadi H.,Grosveld F.

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

Cited by 45 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

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2. Mitochondrial regulation of erythropoiesis in homeostasis and disease;British Journal of Haematology;2024-06-30

3. Elevated CDKN1A (P21) mediates β-thalassemia erythroid apoptosis, but its loss does not improve β-thalassemic erythropoiesis;Blood Advances;2023-11-16

4. Foetal haemoglobin inducers for reducing blood transfusion in non-transfusion-dependent beta-thalassaemias;Cochrane Database of Systematic Reviews;2023-01-13

5. Role of microRNA in hydroxyurea mediated HbF induction in sickle cell anaemia patients;Scientific Reports;2023-01-07

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