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MicroRNA expression patterns in HbE/β-thalassemia patients: The passwords to unlock fetal hemoglobin expression in β-hemoglobinopathies

  • Published:2021-03 Issue: Volume:87 Page:102523
  • ISSN:1079-9796
  • Container-title:Blood Cells, Molecules, and Diseases
  • language:en
  • Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Das Sankha Subhra,Das Subhayan,Byram Prasanna Kumar,Rahaman Motiur,Dolai Tuphan Kanti,Chatterjee Anish,Chakravorty Nishant

Funder

Indian Institute of Technology Kharagpur

Council of Scientific and Industrial Research, India

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference56 articles.

1. Hb E/beta-thalassaemia: a common & clinically diverse disorder;Olivieri;Indian J. Med. Res.,2011

2. Treatment strategies for hemoglobin E beta-thalassemia;Olivieri;Blood Rev.,2012

3. Ineffective erythropoiesis and thalassemias;Rivella;Curr. Opin. Hematol.,2009

4. Hemoglobin E beta-thalassemia: an increasingly common disease with some diagnostic pitfalls;Weatherall;J. Pediatr.,1998

5. HbF in HbE/beta-thalassemia: a clinical and laboratory correlation;Lim;Hematology,2015

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