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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

57 related articles for article (PubMed ID: 24300714)

  • 1. Molecular and cellular analysis of three novel alpha2-globin gene promoter mutations [HBA2: c.-59C>T], [HBA2: c.-81C>A] and [HBA2: c.-91G>A] reveal varying patterns of transcriptional and translational activities.
    Qadah T; Finlayson J; Dennis M; Ghassemifar R
    Pathology; 2014 Jan; 46(1):46-52. PubMed ID: 24300714
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular characterization of Hb Hamilton Hill (HBA2: c.388delC), a novel HBA2 variant generating a premature termination codon and truncated HBA2 chain.
    Qadah T; Finlayson J; North E; Ghassemifar R
    Hemoglobin; 2015; 39(2):88-94. PubMed ID: 25791745
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Experimental Characterization of Hb Flurlingen (HBA2: c.177 C > G, p.His > Gln) and Hb Boghé (HBA2: c.177 C > A, p.His > Gln) Reveals Contradictory HBA2 Expression and Translation Patterns Despite Identical Amino Acid Substitutions.
    Qadah T; Finlayson J; Dennis M; Newbound C; Ghassemifar R
    Hemoglobin; 2015; 39(5):340-5. PubMed ID: 26193975
    [TBL] [Abstract][Full Text] [Related]  

  • 4. In vitro characterization of the α-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1(G>A) (α2)].
    Qadah T; Finlayson J; Ghassemifar R
    Hemoglobin; 2012; 36(1):38-46. PubMed ID: 21967524
    [TBL] [Abstract][Full Text] [Related]  

  • 5. α-thalassemia trait caused by frameshift mutations in exon 2 of the α2-globin gene: HBA2:c.131delT and HBA2:c.143delA.
    Finlayson J; Ghassemifar R; Holmes P; Grey D; Newbound C; Pell N; Jennens M; Greenwood L; Beilby J
    Hemoglobin; 2012; 36(5):511-5. PubMed ID: 22943743
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Comparative studies of nondeletional HPFH gamma-globin gene promoters.
    Motum PI; Lindeman R; Harvey MP; Trent RJ
    Exp Hematol; 1993 Jul; 21(7):852-8. PubMed ID: 7686501
    [TBL] [Abstract][Full Text] [Related]  

  • 7. delta-Thalassemic phenotype due to two "novel" delta-globin gene mutations: CD11[GTC-->GGC (A8)-HbA2-Pylos] and CD 85[TTT-->TCT(F1)-HbA2-Etolia].
    Drakoulakou O; Papapanagiotou E; Loutradi-Anagnostou A; Papadakis M
    Hum Mutat; 1997; 9(4):344-7. PubMed ID: 9101295
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutational spectrum of delta-globin gene in the Portuguese population.
    Morgado A; Picanço I; Gomes S; Miranda A; Coucelo M; Seuanes F; Seixas MT; Romão L; Faustino P
    Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Increased promoter activity of human delta-globin gene with point mutation of C-T at site-64].
    Zhang J; Kou H; Di X; Chen S; Liang Z
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1996 Dec; 18(6):429-34. PubMed ID: 9388948
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel alpha-thalassemia nonsense mutation in HBA2: C.382 A > T globin gene.
    Hamid M; Bokharaei Merci H; Galehdari H; Saberi AH; Kaikhaei B; Mohammadi-Anaei M; Ahmadzadeh A; Shariati G
    Arch Iran Med; 2014 Jul; 17(7):475-6. PubMed ID: 24979558
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Restoration of the CCAAT box or insertion of the CACCC motif activates [corrected] delta-globin gene expression.
    Tang DC; Ebb D; Hardison RC; Rodgers GP
    Blood; 1997 Jul; 90(1):421-7. PubMed ID: 9207479
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hb AHVAZ [α83(F4)Leu→Arg, CTG>CGG (α2); HBA2: c.251T>G],a new hemoglobin variant of the α2-globin gene.
    Hamid M; Shariati G; Saberi A; Galehdari H; Kaikhaei B; Mohammadi-Anaei M
    Hemoglobin; 2013; 37(5):477-80. PubMed ID: 23672273
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A point mutation affecting an SP1 binding site in the promoter of the ferrochelatase gene impairs gene transcription and causes erythropoietic protoporphyria.
    Di Pierro E; Cappellini MD; Mazzucchelli R; Moriondo V; Mologni D; Zanone Poma B; Riva A
    Exp Hematol; 2005 May; 33(5):584-91. PubMed ID: 15850836
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Known and new delta globin gene mutations and their diagnostic significance.
    Bouva MJ; Harteveld CL; van Delft P; Giordano PC
    Haematologica; 2006 Jan; 91(1):129-32. PubMed ID: 16434382
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular and cellular characterization of a new α-thalassemia mutation (HBA2:c.94A>C) generating an alternative splice site and a premature stop codon.
    Qadah T; Finlayson J; Newbound C; Pell N; Pascoe M; Greenwood L; Holmes P; Grey D; Beilby J; Ghassemifar R
    Hemoglobin; 2012; 36(3):244-52. PubMed ID: 22524210
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Regulation of the human leukemia inhibitory factor gene by ETS transcription factors.
    Bamberger AM; Jenatschke S; Schulte HM; Ellebrecht I; Beil FU; Bamberger CM
    Neuroimmunomodulation; 2004; 11(1):10-9. PubMed ID: 14557674
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical presentation and molecular identification of four uncommon alpha globin variants in Thailand. Initiation codon mutation of α2-globin Gene (HBA2:c.1delA), donor splice site mutation of α1-globin gene (IVSI-1, HBA1:c.95 + 1G>A), hemoglobin Queens Park/Chao Pra Ya (HBA1:c.98T>A) and hemoglobin Westmead (HBA2:c.369C>G).
    Viprakasit V; Ekwattanakit S; Chalaow N; Riolueang S; Wijit S; Tanyut P; Chat-Uthai N; Tachavanich K
    Acta Haematol; 2014; 131(2):88-94. PubMed ID: 24081251
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular and cellular analysis of a novel HBA2 mutation (HBA2: c.94A > G) shows activation of a cryptic splice site and generation of a premature termination codon.
    Qadah T; Finlayson J; Joly P; Ghassemifar R
    Hemoglobin; 2014; 38(1):13-8. PubMed ID: 24274170
    [TBL] [Abstract][Full Text] [Related]  

  • 19. First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia with delta globin CD12 {Asn-->Lys (AAT-->AAA)}HbA₂-NYU in Iran.
    Amirian A; Karimipoor M; Jafarinejad M; Taghavi M; Kordafshari A; Fathi Azar S; Mohammadi MS; Zeinali S
    Arch Iran Med; 2011 Jan; 14(1):8-11. PubMed ID: 21194254
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [The transcriptional regulation study on human delta globin gene with CAAT box C-->T point mutation in its promoter].
    Yao J; Chen SS; Yang KG; Di X; Xiong AQ; Zhang YH
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2002 Apr; 24(2):140-3. PubMed ID: 12905790
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.