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Journal Abstract Search

189 related items for PubMed ID: 28499394

  • 1. SAR1a promoter polymorphisms are not associated with fetal hemoglobin in patients with sickle cell disease from Cameroon.
    Pule GD, Bitoungui VJN, Chemegni BC, Kengne AP, Wonkam A.
    BMC Res Notes; 2017 May 12; 10(1):183. PubMed ID: 28499394
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  • 2. 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 May 12; 9(3):e92506. PubMed ID: 24667352
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  • 3. Fetal haemoglobin response to hydroxycarbamide treatment and sar1a promoter polymorphisms in sickle cell anaemia.
    Kumkhaek C, Taylor JG, Zhu J, Hoppe C, Kato GJ, Rodgers GP.
    Br J Haematol; 2008 Apr 12; 141(2):254-9. PubMed ID: 18318767
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  • 4. Beta-globin gene haplotypes among cameroonians and review of the global distribution: is there a case for a single sickle mutation origin in Africa?
    Bitoungui VJ, Pule GD, Hanchard N, Ngogang J, Wonkam A.
    OMICS; 2015 Mar 12; 19(3):171-9. PubMed ID: 25748438
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  • 5. 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 12; 241(7):706-18. PubMed ID: 27022141
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  • 11. 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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  • 12. 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 Jun 05; 35(3):437-43. PubMed ID: 26849705
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