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Journal Abstract Search

176 related items for PubMed ID: 35303690

  • 1. Fetal hemoglobin modulates neurocognitive performance in sickle cell anemia✰,✰✰.
    Heitzer AM, Longoria J, Rampersaud E, Rashkin SR, Estepp JH, Okhomina VI, Wang WC, Raches D, Potter B, Steinberg MH, King AA, Kang G, Hankins JS.
    Curr Res Transl Med; 2022 Jul; 70(3):103335. PubMed ID: 35303690
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  • 3. 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
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  • 4. 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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  • 6. 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 04; 67(12):701-709. PubMed ID: 36167770
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  • 11. Catechol-O-methyltransferase gene (COMT) is associated with neurocognitive functioning in patients with sickle cell disease.
    Heitzer AM, Rashkin SR, Trpchevska A, Longoria JN, Rampersaud E, Olufadi Y, Wang WC, Raches D, Potter B, Steinberg MH, King AA, Kang G, Takemoto CM, Hankins JS.
    Curr Res Transl Med; 2024 Jun 04; 72(2):103433. PubMed ID: 38244277
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  • 12. 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
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  • 15. 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 04; 54(1):4-8. PubMed ID: 25457385
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  • 17. 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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  • 18. 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 12; 53(4):176-9. PubMed ID: 25084696
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  • 19. 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 Dec 12; 13(6):e0197927. PubMed ID: 29879141
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  • 20. 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 12; 54(3):224-30. PubMed ID: 25703683
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