Search Results - Qadah, T.

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  1. 1
    In vitro characterization of the a-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1(G>A) (a2)]

    In vitro characterization of the a-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1(G>A) (a2)] by Qadah, T., Finlayson, J., Ghassemifar, Reza

    Published 2012
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  2. 2
    Identification and characterization of two novel and differentially expressed isoforms of human a2-and a1-globin genes

    Identification and characterization of two novel and differentially expressed isoforms of human a2-and a1-globin genes by Ghassemifar, Reza, Forster, L., Qadah, T., Finlayson, J.

    Published 2012
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  3. 3
    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

    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 by Qadah, T., Finlayson, J., Joly, P., Ghassemifar, Reza

    Published 2014
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  4. 4
    Molecular characterization of Hb hamilton hill (HBA2: c.388delC), a novel HBA2 variant generating a premature termination codon and truncated HBA2 chain

    Molecular characterization of Hb hamilton hill (HBA2: c.388delC), a novel HBA2 variant generating a premature termination codon and truncated HBA2 chain by Qadah, T., Finlayson, J., North, E., Ghassemifar, Reza

    Published 2015
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  5. 5
    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

    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 transcriptio... by Qadah, T., Finlayson, J., Dennis, M., Ghassemifar, Reza

    Published 2014
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  6. 6
    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

    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... by Qadah, T., Finlayson, J., Dennis, M., Newbound, C., Ghassemifar, Reza

    Published 2015
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  7. 7
    The Effect of Nonsense Mediated Decay on Transcriptional Activity Within the Novel ß-Thalassemia Mutation HBB: c.129delT

    The Effect of Nonsense Mediated Decay on Transcriptional Activity Within the Novel ß-Thalassemia Mutation HBB: c.129delT by Forster, L., Ardakani, R., Qadah, T., Finlayson, J., Ghassemifar, Reza

    Published 2015
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  8. 8
    A molecular tool to assess the pathological relevance of alpha-globin DNA variants

    A molecular tool to assess the pathological relevance of alpha-globin DNA variants by Qadah, T., Finlayson, J., Newbound, C., Pell, N., Jennens, M., Holmes, P., Grey, D., Beilby, J., Ghassemifar, Reza

    Published 2012
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  9. 9
    Molecular and cellular characterization of a new a-Thalassemia mutation (HBA2:c.94A>C) generating an alternative splice site and a premature stop codon

    Molecular and cellular characterization of a new a-Thalassemia mutation (HBA2:c.94A>C) generating an alternative splice site and a premature stop codon by Qadah, T., Finlayson, J., Newbound, C., Pell, N., Pascoe, M., Greenwood, L., Holmes, P., Grey, D., Beilby, J., Ghassemifar, Reza

    Published 2012
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