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Journal Abstract Search

251 related items for PubMed ID: 21068433

  • 1. 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
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  • 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 27; 53(4):176-9. PubMed ID: 25084696
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  • 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 Dec 27; 9(3):e92506. PubMed ID: 24667352
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  • 6. Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania.
    Mtatiro SN, Singh T, Rooks H, Mgaya J, Mariki H, Soka D, Mmbando B, Msaki E, Kolder I, Thein SL, Menzel S, Cox SE, Makani J, Barrett JC.
    PLoS One; 2014 Dec 27; 9(11):e111464. PubMed ID: 25372704
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  • 7. 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 Dec 27; 35(3):437-43. PubMed ID: 26849705
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  • 10. 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
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  • 11. 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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  • 12. Prediction of fetal hemoglobin in sickle cell anemia using an ensemble of genetic risk prediction models.
    Milton JN, Gordeuk VR, Taylor JG, Gladwin MT, Steinberg MH, Sebastiani P.
    Circ Cardiovasc Genet; 2014 Apr 19; 7(2):110-5. PubMed ID: 24585758
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  • 13. 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 19; 99(10):2279-2288. PubMed ID: 32772141
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  • 17. Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation.
    Galarneau G, Palmer CD, Sankaran VG, Orkin SH, Hirschhorn JN, Lettre G.
    Nat Genet; 2010 Dec 19; 42(12):1049-51. PubMed ID: 21057501
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  • 18. 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 19; 91(11):1118-1122. PubMed ID: 27501013
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  • 19. Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania.
    Nkya S, Mwita L, Mgaya J, Kumburu H, van Zwetselaar M, Menzel S, Mazandu GK, Sangeda R, Chimusa E, Makani J.
    BMC Med Genet; 2020 Jun 05; 21(1):125. PubMed ID: 32503527
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  • 20. 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
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