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Journal Abstract Search

162 related items for PubMed ID: 30114697

  • 21. Fetal hemoglobin in sickle cell anemia.
    Steinberg MH.
    Blood; 2020 Nov 19; 136(21):2392-2400. PubMed ID: 32808012
    [Abstract] [Full Text] [Related]

  • 22. Correlations between Multiple SNPs and HbF Levels in β-Thalassemia Carriers.
    Xu Q, Huang L, Jin T, Han Y, Liu J, Zhang W, Biao Y, An B, Huang S.
    Clin Lab; 2023 Sep 01; 69(9):. PubMed ID: 37702677
    [Abstract] [Full Text] [Related]

  • 23. 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 01; 70(3):103335. PubMed ID: 35303690
    [Abstract] [Full Text] [Related]

  • 24. 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 01; 7(2):110-5. PubMed ID: 24585758
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  • 25. Significance of heme oxygenase-1(HMOX1) gene on fetal hemoglobin induction in sickle cell anemia patients.
    Hariharan P, Chavan V, Nadkarni A.
    Sci Rep; 2020 Oct 28; 10(1):18506. PubMed ID: 33116199
    [Abstract] [Full Text] [Related]

  • 26. 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
    [Abstract] [Full Text] [Related]

  • 27. 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
    [Abstract] [Full Text] [Related]

  • 28. 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 10; 99(10):2279-2288. PubMed ID: 32772141
    [Abstract] [Full Text] [Related]

  • 29. Fetal hemoglobin in sickle cell anemia: molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans.
    Akinsheye I, Solovieff N, Ngo D, Malek A, Sebastiani P, Steinberg MH, Chui DH.
    Am J Hematol; 2012 Feb 10; 87(2):217-9. PubMed ID: 22139998
    [Abstract] [Full Text] [Related]

  • 30. Association of Xmn1 -158 γG variant with severity and HbF levels in β-thalassemia major and sickle cell anaemia.
    Dadheech S, Jain S, Madhulatha D, Sharma V, Joseph J, Jyothy A, Munshi A.
    Mol Biol Rep; 2014 May 10; 41(5):3331-7. PubMed ID: 24488321
    [Abstract] [Full Text] [Related]

  • 31. 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
    [Abstract] [Full Text] [Related]

  • 32. Biological impact of α genes, β haplotypes, and G6PD activity in sickle cell anemia at baseline and with hydroxyurea.
    Bernaudin F, Arnaud C, Kamdem A, Hau I, Lelong F, Epaud R, Pondarré C, Pissard S.
    Blood Adv; 2018 Mar 27; 2(6):626-637. PubMed ID: 29555644
    [Abstract] [Full Text] [Related]

  • 33. Beta-globin gene cluster haplotypes in sickle cell patients from southwest Iran.
    Rahimi Z, Karimi M, Haghshenass M, Merat A.
    Am J Hematol; 2003 Nov 27; 74(3):156-60. PubMed ID: 14587041
    [Abstract] [Full Text] [Related]

  • 34. Whole exome sequencing identifies novel genes for fetal hemoglobin response to hydroxyurea in children with sickle cell anemia.
    Sheehan VA, Crosby JR, Sabo A, Mortier NA, Howard TA, Muzny DM, Dugan-Perez S, Aygun B, Nottage KA, Boerwinkle E, Gibbs RA, Ware RE, Flanagan JM.
    PLoS One; 2014 Nov 27; 9(10):e110740. PubMed ID: 25360671
    [Abstract] [Full Text] [Related]

  • 35. g(HbF): a genetic model of fetal hemoglobin in sickle cell disease.
    Gardner K, Fulford T, Silver N, Rooks H, Angelis N, Allman M, Nkya S, Makani J, Howard J, Kesse-Adu R, Rees DC, Stuart-Smith S, Yeghen T, Awogbade M, Sangeda RZ, Mgaya J, Patel H, Newhouse S, Menzel S, Thein SL.
    Blood Adv; 2018 Feb 13; 2(3):235-239. PubMed ID: 29437638
    [Abstract] [Full Text] [Related]

  • 36. BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies.
    Sedgewick AE, Timofeev N, Sebastiani P, So JCC, Ma ESK, Chan LC, Fucharoen G, Fucharoen S, Barbosa CG, Vardarajan BN, Farrer LA, Baldwin CT, Steinberg MH, Chui DHK.
    Blood Cells Mol Dis; 2008 Feb 13; 41(3):255-258. PubMed ID: 18691915
    [Abstract] [Full Text] [Related]

  • 37. Genetic variants at HbF-modifier loci moderate anemia and leukocytosis in sickle cell disease in Tanzania.
    Mtatiro SN, Makani J, Mmbando B, Thein SL, Menzel S, Cox SE.
    Am J Hematol; 2015 Jan 13; 90(1):E1-4. PubMed ID: 25263325
    [Abstract] [Full Text] [Related]

  • 38. Relationship of foetal haemoglobin levels and beta s haplotypes in homozygous sickle cell disease.
    Falusi AG, Kulozik AE.
    Eur J Haematol; 1990 Jul 13; 45(1):1-4. PubMed ID: 1696209
    [Abstract] [Full Text] [Related]

  • 39. Fetal Haemoglobin and β-globin Gene Cluster Haplotypes among Sickle Cell Patients in Chhattisgarh.
    Bhagat S, Patra PK, Thakur AS.
    J Clin Diagn Res; 2013 Feb 13; 7(2):269-72. PubMed ID: 23542314
    [Abstract] [Full Text] [Related]

  • 40. Association between Variants at BCL11A Erythroid-Specific Enhancer and Fetal Hemoglobin Levels among Sickle Cell Disease Patients in Cameroon: Implications for Future Therapeutic Interventions.
    Pule GD, Ngo Bitoungui VJ, Chetcha Chemegni B, Kengne AP, Antonarakis S, Wonkam A.
    OMICS; 2015 Oct 13; 19(10):627-31. PubMed ID: 26393293
    [Abstract] [Full Text] [Related]

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