The role of BCL11A and HMIP-2 polymorphisms on endogenous and hydroxyurea induced levels of fetal hemoglobin in sickle cell anemia patients from southern Brazil
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference16 articles.
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2. Mortality in sickle cell disease. Life expectancy and risk factors for early death;Platt;N. Engl. J. Med.,1994
3. Anemia: progress in molecular mechanisms and therapies;Sankaran;Nat. Med.,2015
4. Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation;Galarneau;Nat. Genet.,2010
5. Control of fetal hemoglobin: new insights emerging from genomics and clinical implications;Thein;Hum. Mol. Genet.,2009
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1. Genetic Variation and Sickle Cell Disease Severity;JAMA Network Open;2023-10-18
2. Glomerular filtration rate abnormalities in sickle cell disease;Frontiers in Medicine;2022-10-21
3. Single Nucleotide Polymorphisms in XMN1-HBG2, HBS1L-MYB, and BCL11A and Their Relation to High Fetal Hemoglobin Levels That Alleviate Anemia;Diagnostics;2022-06-02
4. Association Between Selected Single Nucleotide Polymorphisms in Globin and Related Genes and Response to Hydroxyurea Therapy in Ghanaian Children with Sickle Cell Disease;Pharmacogenomics and Personalized Medicine;2022-03
5. Do Genetic Polymorphisms Affect Fetal Hemoglobin (HbF) Levels in Patients With Sickle Cell Anemia Treated With Hydroxyurea? A Systematic Review and Pathway Analysis;Frontiers in Pharmacology;2022-01-21
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