Search Results - Ghassemifar, Reza

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  1. 1
    Advancing towards a tissue-engineered tympanic membrane: Silk fibroin as a substratum for growing human eardrum keratinocytes

    Advancing towards a tissue-engineered tympanic membrane: Silk fibroin as a substratum for growing human eardrum keratinocytes by Ghassemifar, Reza, Redmond, S., Zainuddin, Chirila, T.

    Published 2010
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  2. 2
    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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  3. 3
    Alpha thalassaemia due to non-deletional mutations on the -3.7 alpha globin fusion gene: Laboratory diagnosis and clinical importance

    Alpha thalassaemia due to non-deletional mutations on the -3.7 alpha globin fusion gene: Laboratory diagnosis and clinical importance by Chow, A., Ghassemifar, Reza, Finlayson, J.

    Published 2013
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  4. 4
    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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  5. 5
    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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  6. 6
    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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  7. 7
    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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  8. 8
    Histology of the healing tympanic membrane following perforation in rats

    Histology of the healing tympanic membrane following perforation in rats by Maria, P., Redmond, S., Atlas, M., Ghassemifar, Reza

    Published 2010
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  9. 9
    Keratinocyte growth factor 1, fibroblast growth factor 2 and 10 in the healing tympanic membrane following perforation in rats

    Keratinocyte growth factor 1, fibroblast growth factor 2 and 10 in the healing tympanic membrane following perforation in rats by Santa Maria, P., Redmond, S., Atlas, M., Ghassemifar, Reza

    Published 2011
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  10. 10
    The role of epidermal growth factor in the healing tympanic membrane following perforation in rats

    The role of epidermal growth factor in the healing tympanic membrane following perforation in rats by Santa Maria, P., Redmond, S., Atlas, M., Ghassemifar, Reza

    Published 2010
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  11. 11
    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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  12. 12
    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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  13. 13
    Tympanic membrane wound healing in rats assessed by transcriptome profiling

    Tympanic membrane wound healing in rats assessed by transcriptome profiling by Santa Maria, P., Redmond, S., McInnes, R., Atlas, M., Ghassemifar, Reza

    Published 2011
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  14. 14
    Differential gene expression analysis in early and late erythroid progenitor cells in ß-thalassaemia

    Differential gene expression analysis in early and late erythroid progenitor cells in ß-thalassaemia by Forster, L., McCooke, J., Bellgard, M., Joske, D., Finlayson, J., Ghassemifar, Reza

    Published 2015
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  15. 15
    Differential expression of the Bcl-2 and Bax isoforms in CD19 positive B-lymphocytes isolated from patients diagnosed with chronic lymphocytic leukaemia

    Differential expression of the Bcl-2 and Bax isoforms in CD19 positive B-lymphocytes isolated from patients diagnosed with chronic lymphocytic leukaemia by Ghassemifar, Reza, Forster, L., Finlayson, J., Calogero, T., Augustson, B., Joske, D., Cull, G.

    Published 2012
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  16. 16
    Incidence of c-Cbl mutations in human acute myeloid leukaemias in an Australian patient cohort

    Incidence of c-Cbl mutations in human acute myeloid leukaemias in an Australian patient cohort by Ghassemifar, Reza, Thien, C., Finlayson, J., Joske, D., Cull, G., Augustson, B., Langdon, W.

    Published 2011
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  17. 17
    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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  18. 18
    a-Thalassemia trait caused by frameshift mutations in exon 2 of the a2-globin gene: HBA2:c.131delT and HBA2:c.143delA

    a-Thalassemia trait caused by frameshift mutations in exon 2 of the a2-globin gene: HBA2:c.131delT and HBA2:c.143delA by Finlayson, J., Ghassemifar, Reza, Holmes, P., Grey, D., Newbound, C., Pell, N., Jennens, M., Greenwood, L., Beilby, J.

    Published 2012
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  19. 19
    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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  20. 20
    Hb lynwood [a107(G14) (-T) (a2) HBA2:c.323delT)] in conjunction with the a3.7 deletion produces a moderately severe a-thalassemia phenotype

    Hb lynwood [a107(G14) (-T) (a2) HBA2:c.323delT)] in conjunction with the a3.7 deletion produces a moderately severe a-thalassemia phenotype by Finlayson, J., Ghassemifar, Reza, Holmes, P., Grey, D., Newbound, C., Pell, N., Jennens, M., MacAulay, C., Greenwood, L., Beilby, J.

    Published 2011
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