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370 related items for PubMed ID: 32772141

  • 1. 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]

  • 2. 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]

  • 3. 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]

  • 4. 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 12; 99(7):1453-1463. PubMed ID: 32447424
    [Abstract] [Full Text] [Related]

  • 5. 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 Jul 12; 9(3):e92506. PubMed ID: 24667352
    [Abstract] [Full Text] [Related]

  • 6. Genotyping of BCL11A and HBS1L-MYB SNPs associated with fetal haemoglobin levels: a SNaPshot minisequencing approach.
    Fanis P, Kousiappa I, Phylactides M, Kleanthous M.
    BMC Genomics; 2014 Feb 06; 15():108. PubMed ID: 24502199
    [Abstract] [Full Text] [Related]

  • 7. 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 06; 53(4):176-9. PubMed ID: 25084696
    [Abstract] [Full Text] [Related]

  • 8. The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria.
    Ojewunmi OO, Adeyemo TA, Oyetunji AI, Inyang B, Akinrindoye A, Mkumbe BS, Gardner K, Rooks H, Brewin J, Patel H, Lee SH, Chung R, Rashkin S, Kang G, Chianumba R, Sangeda R, Mwita L, Isa H, Agumadu UN, Ekong R, Faruk JA, Jamoh BY, Adebiyi NM, Umar IA, Hassan A, Grace C, Goel A, Inusa BPD, Falchi M, Nkya S, Makani J, Ahmad HR, Nnodu O, Strouboulis J, Menzel S.
    Hum Mol Genet; 2024 May 04; 33(10):919-929. PubMed ID: 38339995
    [Abstract] [Full Text] [Related]

  • 9. A study on the genotype frequency of -158 Gγ (C→T) Xmn1 polymorphism in a sickle cell trait cohort from Siwa Oasis, Egypt.
    Moez P, Moftah R, Mahmoud HA.
    J Genet; 2018 Jun 04; 97(2):505-511. PubMed ID: 29932071
    [Abstract] [Full Text] [Related]

  • 10. 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 04; 87(2):217-9. PubMed ID: 22139998
    [Abstract] [Full Text] [Related]

  • 11. 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 04; 54(4):315-20. PubMed ID: 25842369
    [Abstract] [Full Text] [Related]

  • 12. Genetics of fetal hemoglobin in tribal Indian patients with sickle cell anemia.
    Bhanushali AA, Patra PK, Pradhan S, Khanka SS, Singh S, Das BR.
    Transl Res; 2015 Jun 04; 165(6):696-703. PubMed ID: 25651163
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. Fetal hemoglobin-boosting haplotypes of BCL11A gene and HBS1L-MYB intergenic region in the prediction of clinical and hematological outcomes in a cohort of children with sickle cell anemia.
    Sales RR, Nogueira BL, Belisário AR, Faria G, Mendes F, Viana MB, Luizon MR.
    J Hum Genet; 2022 Dec 15; 67(12):701-709. PubMed ID: 36167770
    [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 15; 90(1):E1-4. PubMed ID: 25263325
    [Abstract] [Full Text] [Related]

  • 18. Protective BCL11A and HBS1L-MYB polymorphisms in a cohort of 102 Congolese patients suffering from sickle cell anemia.
    Mikobi TM, Tshilobo Lukusa P, Aloni MN, Lumaka AZ, Kaba DK, Devriendt K, Matthijs G, Mbuyi Muamba JM, Race V.
    J Clin Lab Anal; 2018 Jan 15; 32(1):. PubMed ID: 28332727
    [Abstract] [Full Text] [Related]

  • 19. Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island.
    Muszlak M, Pissard S, Badens C, Chamouine A, Maillard O, Thuret I.
    Hemoglobin; 2015 Jan 15; 39(3):156-61. PubMed ID: 25806420
    [Abstract] [Full Text] [Related]

  • 20. 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 15; 51(1):22-6. PubMed ID: 23465615
    [Abstract] [Full Text] [Related]

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