These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

369 related items for PubMed ID: 27009595

  • 1. Modifying effect of XmnI, BCL11A, and HBS1L-MYB on clinical appearances: A study on β-thalassemia and hemoglobin E/β-thalassemia patients in Indonesia.
    Rujito L, Basalamah M, Siswandari W, Setyono J, Wulandari G, Mulatsih S, Sofro AS, Sadewa AH, Sutaryo S.
    Hematol Oncol Stem Cell Ther; 2016 Jun; 9(2):55-63. PubMed ID: 27009595
    [Abstract] [Full Text] [Related]

  • 2. Polymorphic variations influencing fetal hemoglobin levels: association study in beta-thalassemia carriers and in normal individuals of Portuguese origin.
    Pereira C, Relvas L, Bento C, Abade A, Ribeiro ML, Manco L.
    Blood Cells Mol Dis; 2015 Apr; 54(4):315-20. PubMed ID: 25842369
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. The Impact of XmnI-HBG2, BCL11A and HBS1L-MYB Single Nucleotide Polymorphisms on Hb F Variation of Hematologically Normal Iranian Individuals.
    Keyhani E, Jafari Vesiehsari M, Talebi Kakroodi S, Darabi E, Zamani F, Karimlou M, Kamali K, Neishabury M.
    Hemoglobin; 2016 Jun 15; 40(3):198-201. PubMed ID: 27117569
    [Abstract] [Full Text] [Related]

  • 5. Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island.
    Muszlak M, Pissard S, Badens C, Chamouine A, Maillard O, Thuret I.
    Hemoglobin; 2015 Jun 15; 39(3):156-61. PubMed ID: 25806420
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. [Correlation between hemoglobin F levels and single nucleotide polymorphism at BCL11A gene rs11886868 locus in β-thalassemia patients].
    Chen QR, Sun SC, Peng YS, Wang Q, Mo BM.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2012 Jun 15; 20(3):650-3. PubMed ID: 22739175
    [Abstract] [Full Text] [Related]

  • 8. Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang β-Thalassemia Intermedia Patients.
    Lai Y, Chen Y, Chen B, Zheng H, Yi S, Li G, Wei H, He S, Zheng C.
    Hemoglobin; 2016 Nov 15; 40(6):405-410. PubMed ID: 28361591
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. Existence of HbF Enhancer Haplotypes at HBS1L-MYB Intergenic Region in Transfusion-Dependent Saudi β-Thalassemia Patients.
    Cyrus C, Vatte C, Borgio JF, Al-Rubaish A, Chathoth S, Nasserullah ZA, Jarrash SA, Sulaiman A, Qutub H, Alsaleem H, Alzahrani AJ, Steinberg MH, Ali AK.
    Biomed Res Int; 2017 Aug 04; 2017():1972429. PubMed ID: 28280727
    [Abstract] [Full Text] [Related]

  • 12. 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 04; 99(10):2279-2288. PubMed ID: 32772141
    [Abstract] [Full Text] [Related]

  • 13. The influence of the BCL11A polymorphism on the phenotype of patients with beta thalassemia could be affected by the beta globin locus control region and/or the Xmn1-HBG2 genotypic background.
    Neishabury M, Zamani F, Keyhani E, Azarkeivan A, Abedini SS, Eslami MS, Kakroodi ST, Vesiehsari MJ, Najmabadi H.
    Blood Cells Mol Dis; 2013 Aug 04; 51(2):80-4. PubMed ID: 23541515
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Essential genetic modifiers and their measurable impact in a community-recruited population analysis for non-severe hemoglobin E/β-thalassemia prenatal genetic counseling.
    Wong P, Chitsobhak T, Jittasathian S, Sirichantharawat C, Cherdchoo N, Prangcharoen W, Jongautchariyakul P, Jampachaisri K, Tapprom A, Deoisares R, Chumnumsiriwath P.
    Blood Cells Mol Dis; 2023 Nov 19; 103():102765. PubMed ID: 37353362
    [Abstract] [Full Text] [Related]

  • 16. The correlation of α-globin gene mutations and the XmnI polymorphism with clinical severity of Hb E/β-thalassemia.
    Charoenkwan P, Teerachaimahit P, Sanguansermsri T.
    Hemoglobin; 2014 Nov 19; 38(5):335-8. PubMed ID: 25238043
    [Abstract] [Full Text] [Related]

  • 17. Modulatory effect of single nucleotide polymorphism in Xmn1, BCL11A and HBS1L-MYB loci on foetal haemoglobin levels in β-thalassemia major and Intermedia patients.
    Bashir S, Mahmood S, Mohsin S, Tabassum I, Ghafoor M, Sajjad O.
    J Pak Med Assoc; 2021 May 19; 71(5):1394-1398. PubMed ID: 34091621
    [Abstract] [Full Text] [Related]

  • 18. The association of HBG2, BCL11A, and HBS1L-MYB polymorphisms to thalidomide response in Chinese β-thalassemia patients.
    Yang K, Wu Y, Ma Y, Xiao J, Zhou Y, Yin X.
    Blood Cells Mol Dis; 2020 Sep 19; 84():102442. PubMed ID: 32387854
    [Abstract] [Full Text] [Related]

  • 19. Influence of BCL11A, HBS1L-MYB, HBBP1 single nucleotide polymorphisms and the HBG2 XmnI polymorphism On Hb F levels.
    Roy P, Bhattacharya G, Mandal A, Dasgupta UB, Banerjee D, Chandra S, Das M.
    Hemoglobin; 2012 Sep 19; 36(6):592-9. PubMed ID: 23094636
    [Abstract] [Full Text] [Related]

  • 20. Molecular understanding of unusual HbE-β+-thalassemia with Hb phenotype similar to HbE heterozygote: simple and rapid differentiation using HbE levels.
    Jomoui W, Satthakarn S, Panyasai S.
    Ann Med; 2023 Sep 19; 55(2):2267054. PubMed ID: 37816374
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 19.