BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

547 related articles for article (PubMed ID: 26897028)

  • 1. Structural and Functional Insights on an Uncharacterized Aγ-Globin-Gene Polymorphism Present in Four β0-Thalassemia Families with High Fetal Hemoglobin Levels.
    Bianchi N; Cosenza LC; Lampronti I; Finotti A; Breveglieri G; Zuccato C; Fabbri E; Marzaro G; Chilin A; De Angelis G; Borgatti M; Gallucci C; Alfieri C; Ribersani M; Isgrò A; Marziali M; Gaziev J; Morrone A; Sodani P; Lucarelli G; Gambari R; Paciaroni K
    Mol Diagn Ther; 2016 Apr; 20(2):161-73. PubMed ID: 26897028
    [TBL] [Abstract][Full Text] [Related]  

  • 2. An Aγ-globin G->A gene polymorphism associated with β
    Breveglieri G; Bianchi N; Cosenza LC; Gamberini MR; Chiavilli F; Zuccato C; Montagner G; Borgatti M; Lampronti I; Finotti A; Gambari R
    BMC Med Genet; 2017 Aug; 18(1):93. PubMed ID: 28851297
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Surface plasmon resonance based analysis of the binding of LYAR protein to the rs368698783 (G>A) polymorphic Aγ-globin gene sequences mutated in β-thalassemia.
    Gemmo C; Breveglieri G; Marzaro G; Lampronti I; Cosenza LC; Gasparello J; Zuccato C; Fabbri E; Borgatti M; Chilin A; Finotti A; Gambari R
    Anal Bioanal Chem; 2019 Nov; 411(29):7699-7707. PubMed ID: 31300855
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The rs368698783 (G>A) Polymorphism Affecting LYAR Binding to the Aγ-Globin Gene Is Associated with High Fetal Hemoglobin (HbF) in β-Thalassemia Erythroid Precursor Cells Treated with HbF Inducers.
    Zuccato C; Cosenza LC; Zurlo M; Breveglieri G; Bianchi N; Lampronti I; Gasparello J; Scapoli C; Borgatti M; Finotti A; Gambari R
    Int J Mol Sci; 2023 Jan; 24(1):. PubMed ID: 36614221
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Interpreting elevated fetal hemoglobin in pathology and health at the basic laboratory level: new and known γ- gene mutations associated with hereditary persistence of fetal hemoglobin.
    Amato A; Cappabianca MP; Perri M; Zaghis I; Grisanti P; Ponzini D; Di Biagio P
    Int J Lab Hematol; 2014 Feb; 36(1):13-9. PubMed ID: 23621512
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synergistic effect of two β globin gene cluster mutations leading to the hereditary persistence of fetal hemoglobin (HPFH) phenotype.
    Hariharan P; Sawant M; Gorivale M; Manchanda R; Colah R; Ghosh K; Nadkarni A
    Mol Biol Rep; 2017 Oct; 44(5):413-417. PubMed ID: 28879539
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular understanding of unusual HbE-β
    Jomoui W; Satthakarn S; Panyasai S
    Ann Med; 2023; 55(2):2267054. PubMed ID: 37816374
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Epigenetic inactivation of ERF reactivates γ-globin expression in β-thalassemia.
    Bao X; Zhang X; Wang L; Wang Z; Huang J; Zhang Q; Ye Y; Liu Y; Chen D; Zuo Y; Liu Q; Xu P; Huang B; Fang J; Lao J; Feng X; Li Y; Kurita R; Nakamura Y; Yu W; Ju C; Huang C; Mohandas N; Li D; Zhao C; Xu X
    Am J Hum Genet; 2021 Apr; 108(4):709-721. PubMed ID: 33735615
    [TBL] [Abstract][Full Text] [Related]  

  • 9. HbF production in beta thalassaemia heterozygotes for the IVS-II-1 G-->A beta(0)-globin mutation. Implication of the haplotype and the (G)gamma-158 C-->T mutation on the HbF level.
    Dedoussis GV; Mandilara GD; Boussiu M; Loutradis A
    Am J Hematol; 2000 Jul; 64(3):151-5. PubMed ID: 10861808
    [TBL] [Abstract][Full Text] [Related]  

  • 10. DNA methylation patterns of β-globin cluster in β-thalassemia patients.
    Bao X; Zuo Y; Chen D; Zhao C
    Clin Epigenetics; 2020 Dec; 12(1):187. PubMed ID: 33272312
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Xmn I polymorphism associated with concomitant activation of Gγ and Aγ globin gene transcription on a β0-thalassemia chromosome.
    Haj Khelil A; Morinière M; Laradi S; Khelif A; Perrin P; Ben Chibani J; Baklouti F
    Blood Cells Mol Dis; 2011 Feb; 46(2):133-8. PubMed ID: 21144779
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Combined effect of two different polymorphic sequences within the beta globin gene cluster on the level of HbF.
    Gonçalves I; Ducrocq R; Lavinha J; Nogueira PJ; Peres MJ; Picanço I; Correia E; Reis AB; Silva C; Krishnamoorthy R; Almeida LO
    Am J Hematol; 1998 Apr; 57(4):269-76. PubMed ID: 9544969
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genotypic heterogeneity and correlation to intergenic haplotype within high HbF beta-thalassemia intermedia.
    Papachatzopoulou A; Kourakli A; Makropoulou P; Kakagianne T; Sgourou A; Papadakis M; Athanassiadou A
    Eur J Haematol; 2006 Apr; 76(4):322-30. PubMed ID: 16519704
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Featured Article: Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting microRNAs.
    Fornari TA; Lanaro C; Albuquerque DM; Ferreira R; Costa FF
    Exp Biol Med (Maywood); 2017 Feb; 242(3):267-274. PubMed ID: 27591578
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Plastrum testudinis induces γ-globin gene expression through epigenetic histone modifications within the γ-globin gene promoter via activation of the p38 MAPK signaling pathway.
    Qian X; Chen J; Zhao D; Guo L; Qian X
    Int J Mol Med; 2013 Jun; 31(6):1418-28. PubMed ID: 23588991
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Trienone analogs of curcuminoids induce fetal hemoglobin synthesis via demethylation at
    Nuamsee K; Chuprajob T; Pabuprapap W; Jintaridth P; Munkongdee T; Phannasil P; Vadolas J; Chaichompoo P; Suksamrarn A; Svasti S
    Sci Rep; 2021 Apr; 11(1):8552. PubMed ID: 33879818
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A Genetic Variant Ameliorates β-Thalassemia Severity by Epigenetic-Mediated Elevation of Human Fetal Hemoglobin Expression.
    Chen D; Zuo Y; Zhang X; Ye Y; Bao X; Huang H; Tepakhan W; Wang L; Ju J; Chen G; Zheng M; Liu D; Huang S; Zong L; Li C; Chen Y; Zheng C; Shi L; Zhao Q; Wu Q; Fucharoen S; Zhao C; Xu X
    Am J Hum Genet; 2017 Jul; 101(1):130-138. PubMed ID: 28669403
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Effect of a group of genetic markers around the 5' regulatory regions of the β globin gene cluster linked to high HbF on the clinical severity of β thalassemia.
    Dabke P; Colah RB; Ghosh K; Nadkarni A
    Blood Cells Mol Dis; 2013 Mar; 50(3):156-60. PubMed ID: 23211376
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Fetal hemoglobin expression in the compound heterozygous state for -117 (G-->A) Agamma HPFH and IVSII-745 (C-->G) beta+ thalassemia: a case study.
    Dedoussis GV; Sinopoulou K; Gyparaki M; Loutradis A
    Am J Hematol; 1999 Jun; 61(2):139-43. PubMed ID: 10367795
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 28.