Search Results - Newbound, C.

  • Showing 1 - 6 results of 6
Refine Results
  1. 1
    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
    Get full text
  2. 2
    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
    Get full text
  3. 3
    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
    Get full text
  4. 4
    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
    Get full text
  5. 5
    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
    Get full text
  6. 6
    Hb East Timor [ß80(EF4)Asn?His, AAC>CAC (HBB c.241A>C)], a variant hemoglobin associated with normal hematology

    Hb East Timor [ß80(EF4)Asn?His, AAC>CAC (HBB c.241A>C)], a variant hemoglobin associated with normal hematology by Finlayson, J., Ghassemifar, Reza, Holmes, P., Grey, D., Figliomeni, L., Newbound, C., Pell, N., Kersten, M., Jennens, M., Macaulay, C., Greenwood, L., Beilby, J.

    Published 2010
    Get full text

Search Tools: