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Journal Abstract Search

260 related items for PubMed ID: 26849705

  • 1. Genetic variants associated with fetal hemoglobin levels show the diverse ethnic origin in Colombian patients with sickle cell anemia.
    Fong C, Menzel S, Lizarralde MA, Barreto G.
    Biomedica; 2015; 35(3):437-43. PubMed ID: 26849705
    [Abstract] [Full Text] [Related]

  • 2. 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; 53(4):176-9. PubMed ID: 25084696
    [Abstract] [Full Text] [Related]

  • 3. Association between BCL11A, HSB1L-MYB, and XmnI γG-158 (C/T) gene polymorphism and hemoglobin F level in Egyptian sickle cell disease patients.
    El-Ghamrawy M, Yassa ME, Tousson AMS, El-Hady MA, Mikhaeil E, Mohamed NB, Khorshied MM.
    Ann Hematol; 2020 Oct; 99(10):2279-2288. PubMed ID: 32772141
    [Abstract] [Full Text] [Related]

  • 4. Fetal hemoglobin in sickle cell anemia: molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans.
    Akinsheye I, Solovieff N, Ngo D, Malek A, Sebastiani P, Steinberg MH, Chui DH.
    Am J Hematol; 2012 Feb; 87(2):217-9. PubMed ID: 22139998
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Association of variants at BCL11A and HBS1L-MYB with hemoglobin F and hospitalization rates among sickle cell patients in Cameroon.
    Wonkam A, Ngo Bitoungui VJ, Vorster AA, Ramesar R, Cooper RS, Tayo B, Lettre G, Ngogang J.
    PLoS One; 2014 Jun 12; 9(3):e92506. PubMed ID: 24667352
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  • 8. DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease.
    Lettre G, Sankaran VG, Bezerra MA, Araújo AS, Uda M, Sanna S, Cao A, Schlessinger D, Costa FF, Hirschhorn JN, Orkin SH.
    Proc Natl Acad Sci U S A; 2008 Aug 19; 105(33):11869-74. PubMed ID: 18667698
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. 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 04; 21(7):425-9. PubMed ID: 27077760
    [Abstract] [Full Text] [Related]

  • 11. BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia.
    Sebastiani P, Farrell JJ, Alsultan A, Wang S, Edward HL, Shappell H, Bae H, Milton JN, Baldwin CT, Al-Rubaish AM, Naserullah Z, Al-Muhanna F, Alsuliman A, Patra PK, Farrer LA, Ngo D, Vathipadiekal V, Chui DH, Al-Ali AK, Steinberg MH.
    Blood Cells Mol Dis; 2015 Mar 04; 54(3):224-30. PubMed ID: 25703683
    [Abstract] [Full Text] [Related]

  • 12. 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 04; 41(1):87-93. PubMed ID: 30216683
    [Abstract] [Full Text] [Related]

  • 13. 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 04; 99(7):1453-1463. PubMed ID: 32447424
    [Abstract] [Full Text] [Related]

  • 14. Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype.
    Ngo D, Bae H, Steinberg MH, Sebastiani P, Solovieff N, Baldwin CT, Melista E, Safaya S, Farrer LA, Al-Suliman AM, Albuali WH, Al Bagshi MH, Naserullah Z, Akinsheye I, Gallagher P, Luo HY, Chui DH, Farrell JJ, Al-Ali AK, Alsultan A.
    Blood Cells Mol Dis; 2013 Jun 04; 51(1):22-6. PubMed ID: 23465615
    [Abstract] [Full Text] [Related]

  • 15. Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia.
    Makani J, Menzel S, Nkya S, Cox SE, Drasar E, Soka D, Komba AN, Mgaya J, Rooks H, Vasavda N, Fegan G, Newton CR, Farrall M, Thein SL.
    Blood; 2011 Jan 27; 117(4):1390-2. PubMed ID: 21068433
    [Abstract] [Full Text] [Related]

  • 16. A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia.
    Vathipadiekal V, Farrell JJ, Wang S, Edward HL, Shappell H, Al-Rubaish AM, Al-Muhanna F, Naserullah Z, Alsuliman A, Qutub HO, Simkin I, Farrer LA, Jiang Z, Luo HY, Huang S, Mostoslavsky G, Murphy GJ, Patra PK, Chui DH, Alsultan A, Al-Ali AK, Sebastiani P, Steinberg MH.
    Am J Hematol; 2016 Nov 27; 91(11):1118-1122. PubMed ID: 27501013
    [Abstract] [Full Text] [Related]

  • 17. Genetic variants at HbF-modifier loci moderate anemia and leukocytosis in sickle cell disease in Tanzania.
    Mtatiro SN, Makani J, Mmbando B, Thein SL, Menzel S, Cox SE.
    Am J Hematol; 2015 Jan 27; 90(1):E1-4. PubMed ID: 25263325
    [Abstract] [Full Text] [Related]

  • 18. Polymorphic variations influencing fetal hemoglobin levels: association study in beta-thalassemia carriers and in normal individuals of Portuguese origin.
    Pereira C, Relvas L, Bento C, Abade A, Ribeiro ML, Manco L.
    Blood Cells Mol Dis; 2015 Apr 27; 54(4):315-20. PubMed ID: 25842369
    [Abstract] [Full Text] [Related]

  • 19. The association between four SNPs (rs7482144, rs4671393, rs28384513 and rs4895441) and fetal hemoglobin levels in Chinese Zhuang β-thalassemia intermedia patients.
    Lai Y, Zhou L, Yi S, Chen Y, Tang Y, Yi S, Yang Z, Wei H, Zheng C, He S.
    Blood Cells Mol Dis; 2017 Mar 27; 63():52-57. PubMed ID: 28160732
    [Abstract] [Full Text] [Related]

  • 20. The genetics of hemoglobin A2 regulation in sickle cell anemia.
    Griffin PJ, Sebastiani P, Edward H, Baldwin CT, Gladwin MT, Gordeuk VR, Chui DH, Steinberg MH.
    Am J Hematol; 2014 Nov 27; 89(11):1019-23. PubMed ID: 25042611
    [Abstract] [Full Text] [Related]

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