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182 related items for PubMed ID: 38339995

  • 1. 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
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  • 7. 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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  • 12. Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer.
    Mtatiro SN, Mgaya J, Singh T, Mariki H, Rooks H, Soka D, Mmbando B, Thein SL, Barrett JC, Makani J, Cox SE, Menzel S.
    BMC Med Genet; 2015 Feb 10; 16():4. PubMed ID: 25928412
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  • 13. Foetal haemoglobin elevation, unfavourable prognosis, and protective role of genetic variants HBG2 rs7482144, HBS1L-MYB rs9399137 and BCL11A rs4671393 in children with ALL.
    Borrayo-LóPez FJ, Ibarra-Cortés B, Perea-Díaz F, MuñOz-Zúñiga AI, Montoya-Fuentes H, Soto-Padilla JM, Rizo-De La Torre LDC.
    J Genet; 2024 Feb 10; 103():. PubMed ID: 38736250
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  • 14. Genetic variant in the BCL11A (rs1427407), but not HBS1-MYB (rs6934903) loci associate with fetal hemoglobin levels in Indian sickle cell disease patients.
    Bhanushali AA, Patra PK, Nair D, Verma H, Das BR.
    Blood Cells Mol Dis; 2015 Jan 10; 54(1):4-8. PubMed ID: 25457385
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  • 16. 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 10; 41(1):87-93. PubMed ID: 30216683
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  • 18. 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 10; 165(6):696-703. PubMed ID: 25651163
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  • 19. 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 10; 54(3):224-30. PubMed ID: 25703683
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  • 20. 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
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