Talal Qadah
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ORCID
Published in 2015
- 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.
- Authors: -
- Journal: Hemoglobin
ORCID
Published in 2015
- Molecular characterization of Hb Hamilton Hill (HBA2: c.388delC), a novel HBA2 variant generating a premature termination codon and truncated HBA2 chain.
- Authors: Talal Qadah, Jill Finlayson, Emma North, Reza Ghassemifar
- Journal: Hemoglobin
ORCID
Published in 2014
- 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.
- Authors: Talal Qadah, Jill Finlayson, Maxine Dennis, Reza Ghassemifar
- Journal: Pathology
ORCID
Published in 2013
- 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.
- Authors: Talal Qadah, Jill Finlayson, Philippe Joly, Reza Ghassemifar
- Journal: Hemoglobin
ORCID
Published in 2012
- A molecular tool to assess the pathological relevance of alpha-globin DNA variants.
- Authors: Talal Qadah, Jill Finlayson, Christopher Newbound, Nicole Pell, Michelle Jennens, Paula Holmes, Dianne Grey, John Beilby, Reza Ghassemifar
- Journal: Pathology
ORCID
Published in 2012
- Molecular and cellular characterization of a new α-thalassemia mutation (HBA2:c.94A>C) generating an alternative splice site and a premature stop codon.
- Authors: Talal Qadah, Jill Finlayson, Christopher Newbound, Nicole Pell, Michelle Pascoe, Laura Greenwood, Paula Holmes, Dianne Grey, John Beilby, Reza Ghassemifar
- Journal: Hemoglobin
ORCID
Published in 2012
- Identification and characterization of two novel and differentially expressed isoforms of human α2- and α1-globin genes.
- Authors: Reza Ghassemifar, Luke Forster, Talal Qadah, Jill Finlayson
- Journal: Hemoglobin
ORCID
Published in 2011
- In vitro characterization of the α-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1(G>A) (α2)].
- Authors: Talal Qadah, Jill Finlayson, Reza Ghassemifar
- Journal: Hemoglobin