Amelioration of Sardinian 0 thalassemia by genetic modifiers-Reference-Cited by-同舟云学术

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Amelioration of Sardinian 0 thalassemia by genetic modifiers

Published:2009-08-20 Issue:18 Volume:114 Page:3935-3937
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:Blood

Author:

Galanello R.,Sanna S.,Perseu L.,Sollaino M. C.,Satta S.,Lai M. E.,Barella S.,Uda M.,Usala G.,Abecasis G. R.,Cao A.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference11 articles.

1. Genotype-phenotype correlations in β-thalassemias

2. Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults

3. A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15

4. Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of -thalassemia

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1. Anemia and iron overload as prognostic markers of outcomes in β-thalassemia;Expert Review of Hematology;2024-07-26

2. EVALUATION OF FREE THYROXINE LEVEL AND BCL11A GENE POLYMORPHISM WITH BETA-THALASSEMIA;Military Medical Science Letters;2024-06-03

3. Characterization and Clinical Assessment of a Peculiar Case of Hemolytic Anemia;Journal of Hematology;2024-06

4. Impact of genotype on multi-organ iron and complications in patients with non-transfusion-dependent β-thalassemia intermedia;Annals of Hematology;2024-04-06

5. A Population-Oriented Genetic Scoring System to Predict Phenotype: A Pathway to Personalized Medicine in Iraqis With β-Thalassemia;Hemoglobin;2024-02-23

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