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Journal Abstract Search

162 related items for PubMed ID: 30114697

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  • 2. 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; 91(11):1118-1122. PubMed ID: 27501013
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  • 3. 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; 54(3):224-30. PubMed ID: 25703683
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  • 4. 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; 51(1):22-6. PubMed ID: 23465615
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  • 9. 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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  • 10. The influence of fetal hemoglobin on the clinical expression of sickle cell anemia.
    Powars DR, Chan L, Schroeder WA.
    Ann N Y Acad Sci; 1989 Jul; 565():262-78. PubMed ID: 2476064
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  • 13. Original Research: A case-control genome-wide association study identifies genetic modifiers of fetal hemoglobin in sickle cell disease.
    Liu L, Pertsemlidis A, Ding LH, Story MD, Steinberg MH, Sebastiani P, Hoppe C, Ballas SK, Pace BS.
    Exp Biol Med (Maywood); 2016 Apr; 241(7):706-18. PubMed ID: 27022141
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  • 16. 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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  • 18. 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 Aug 04; 35(3):437-43. PubMed ID: 26849705
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  • 19. Hydroxyurea in sickle cell disease--a study of clinico-pharmacological efficacy in the Indian haplotype.
    Italia K, Jain D, Gattani S, Jijina F, Nadkarni A, Sawant P, Nair S, Mohanty D, Ghosh K, Colah R.
    Blood Cells Mol Dis; 2009 Aug 04; 42(1):25-31. PubMed ID: 18954999
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