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Journal Abstract Search

332 related items for PubMed ID: 32447424

  • 1. Functional polymorphisms of BCL11A and HBS1L-MYB genes affect both fetal hemoglobin level and clinical outcomes in a cohort of children with sickle cell anemia.
    Sales RR, Belisário AR, Faria G, Mendes F, Luizon MR, Viana MB.
    Ann Hematol; 2020 Jul; 99(7):1453-1463. PubMed ID: 32447424
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  • 3. Fetal hemoglobin regulating genetic variants identified in homozygous (HbSS) and heterozygous (HbSA) subjects from South Mexico.
    Rizo-de la Torre LC, Borrayo-López FJ, Perea-Díaz FJ, Aquino E, Venegas M, Hernández-Carbajal C, Espinoza-Mata LL, Ibarra-Cortés B.
    J Trop Pediatr; 2022 Aug 04; 68(5):. PubMed ID: 36130307
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  • 7. 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.
    Friedrisch JR, Sheehan V, Flanagan JM, Baldan A, Summarell CC, Bittar CM, Friedrisch BK, Wilke II, Ribeiro CB, Daudt LE, da Rocha Silla LM.
    Blood Cells Mol Dis; 2016 Nov 04; 62():32-37. PubMed ID: 27838552
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  • 8. DNA polymorphisms at BCL11A, HBS1L-MYB and Xmn1-HBG2 site loci associated with fetal hemoglobin levels in sickle cell anemia patients from Northern Brazil.
    Cardoso GL, Diniz IG, Silva AN, Cunha DA, Silva Junior JS, Uchôa CT, Santos SE, Trindade SM, Cardoso Mdo S, Guerreiro JF.
    Blood Cells Mol Dis; 2014 Dec 04; 53(4):176-9. PubMed ID: 25084696
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  • 9. Genotyping the BCL11A Single Nucleotide Polymorphism and Associated Levels of Fetal Hemoglobin in Mauritanian Sickle Cell Patients.
    Taleb Brahim A, Taleb M, Soumaré H, Ghaber SM, Mohamed A, Ould Mohamed Salem Boukhary A.
    Front Biosci (Schol Ed); 2024 Jun 12; 16(2):11. PubMed ID: 38939975
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  • 10. The association of HBG2, BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease.
    Al-Allawi N, Qadir SMA, Puehringer H, Chui DHK, Farrell JJ, Oberkanins C.
    Int J Lab Hematol; 2019 Feb 12; 41(1):87-93. PubMed ID: 30216683
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  • 13. A survey of genetic fetal-haemoglobin modifiers in Nigerian patients with sickle cell anaemia.
    Adeyemo TA, Ojewunmi OO, Oyetunji IA, Rooks H, Rees DC, Akinsulie AO, Akanmu AS, Thein SL, Menzel S.
    PLoS One; 2018 Feb 12; 13(6):e0197927. PubMed ID: 29879141
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  • 16. The XmnI (G)gamma polymorphism influences hemoglobin F synthesis contrary to BCL11A and HBS1L-MYB SNPs in a cohort of 57 beta-thalassemia intermedia patients.
    Nguyen TK, Joly P, Bardel C, Moulsma M, Bonello-Palot N, Francina A.
    Blood Cells Mol Dis; 2010 Aug 15; 45(2):124-7. PubMed ID: 20472475
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  • 18. rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients.
    Chaouch L, Moumni I, Ouragini H, Darragi I, Kalai M, Chaouachi D, Boudrigua I, Hafsia R, Abbes S.
    Hematology; 2016 Aug 15; 21(7):425-9. PubMed ID: 27077760
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