BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 27707011)

  • 1. A Multi-locus Approach to Characterization of Major Quantitative Trait Loci Influencing Hb F Regulation in Chinese β-thalassemia Carriers.
    Chan NC; Lau KM; Cheng KC; Chan NP; Ng MH
    Hemoglobin; 2016 Nov; 40(6):400-404. PubMed ID: 27707011
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 40(6):405-410. PubMed ID: 28361591
    [TBL] [Abstract][Full Text] [Related]  

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

  • 4. Annotated definition of BCL11A and HMIP-2 haplotypes through the analysis of sicilian β-thalassemia patients with high levels of fetal hemoglobin.
    Buccheri MA; Spina S; Ruberto C; Lombardo T; Labie D; Ragusa AA
    Hemoglobin; 2013; 37(5):423-34. PubMed ID: 23777413
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Multi-Locus Models to Address Hb F Variability in Portuguese β-Thalassemia Carriers.
    Manco L; Bento C; Relvas L; Cunha E; Pereira J; Moreira V; Alvarez M; Maia T; Ribeiro ML
    Hemoglobin; 2020 Mar; 44(2):113-117. PubMed ID: 32319326
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 9(3):e92506. PubMed ID: 24667352
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 40(3):198-201. PubMed ID: 27117569
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Utility of the multivariate approach in predicting β-thalassemia intermedia or β-thalassemia major types In Iranian patients.
    Banan M; Bayat H; Namdar-Aligoodarzi P; Azarkeivan A; Kamali K; Daneshmand P; Zaker-Kandjani B; Najmabadi H
    Hemoglobin; 2013; 37(5):413-22. PubMed ID: 23805990
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 39(3):156-61. PubMed ID: 25806420
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults.
    Thein SL; Menzel S; Peng X; Best S; Jiang J; Close J; Silver N; Gerovasilli A; Ping C; Yamaguchi M; Wahlberg K; Ulug P; Spector TD; Garner C; Matsuda F; Farrall M; Lathrop M
    Proc Natl Acad Sci U S A; 2007 Jul; 104(27):11346-51. PubMed ID: 17592125
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association Between Genetic Polymorphisms and Hb F Levels in Heterozygous β-Thalassemia 3.5 kb Deletions.
    Tepakhan W; Kanjanaopas S; Srewaradachpisal K
    Hemoglobin; 2020 Sep; 44(5):338-343. PubMed ID: 32878504
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The association between four SNPs (rs7482144, rs4671393, rs28384513 and rs4895441) and fetal hemoglobin levels in Chinese Zhuang β-thalassemia intermedia patients.
    Lai Y; Zhou L; Yi S; Chen Y; Tang Y; Yi S; Yang Z; Wei H; Zheng C; He S
    Blood Cells Mol Dis; 2017 Mar; 63():52-57. PubMed ID: 28160732
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hb F Levels in β-Thalassemia Carriers and Normal Individuals: Known and Unknown Quantitative Trait Loci in the β-Globin Gene Cluster.
    Manco L; Santos R; Rocha C; Relvas L; Bento C; Maia T; Gomes V; Amorim A; Prata MJ
    Hemoglobin; 2022 May; 46(3):168-175. PubMed ID: 35635444
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association of SNP in exon 1 of HBS1L with hemoglobin F level in beta0-thalassemia/hemoglobin E.
    Pandit RA; Svasti S; Sripichai O; Munkongdee T; Triwitayakorn K; Winichagoon P; Fucharoen S; Peerapittayamongkol C
    Int J Hematol; 2008 Nov; 88(4):357-361. PubMed ID: 18839276
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Existence of HbF Enhancer Haplotypes at
    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; 2017():1972429. PubMed ID: 28280727
    [No Abstract]   [Full Text] [Related]  

  • 17. The HBS1L-MYB intergenic region on chromosome 6q23 is a quantitative trait locus controlling fetal haemoglobin level in carriers of beta-thalassaemia.
    So CC; Song YQ; Tsang ST; Tang LF; Chan AY; Ma ES; Chan LC
    J Med Genet; 2008 Nov; 45(11):745-51. PubMed ID: 18697826
    [TBL] [Abstract][Full Text] [Related]  

  • 18. HBS1L-MYB intergenic variants modulate fetal hemoglobin via long-range MYB enhancers.
    Stadhouders R; Aktuna S; Thongjuea S; Aghajanirefah A; Pourfarzad F; van Ijcken W; Lenhard B; Rooks H; Best S; Menzel S; Grosveld F; Thein SL; Soler E
    J Clin Invest; 2014 Apr; 124(4):1699-710. PubMed ID: 24614105
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 84():102442. PubMed ID: 32387854
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genotyping of BCL11A and HBS1L-MYB SNPs associated with fetal haemoglobin levels: a SNaPshot minisequencing approach.
    Fanis P; Kousiappa I; Phylactides M; Kleanthous M
    BMC Genomics; 2014 Feb; 15():108. PubMed ID: 24502199
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.