Publications by authors named "Jill Finlayson"

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ABO serology in a case of persistent weak A in a recipient following a group O-matched unrelated bone marrow transplant.
Dianne E Grey, Elizabeth A Fong, Catherine Cole, Jesper Jensen, Jill Finlayson

Immunohematology· September 2017

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Cell cycle, proliferation and apoptosis in erythroblasts cultured from patients with β-thalassaemia major.
Luke Forster, Scott Cornwall, Jill Finlayson, Reza Ghassemifar

Br J Haematol· November 2016

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RNF187 is Downregulated Following NF-κB Inhibition in Late Erythroblasts.
Luke Forster, Jill Finlayson, Reza Ghassemifar

Biochem Genet· October 2016

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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.
Talal Qadah, Jill Finlayson, Maxine Dennis, Christopher Newbound, Reza Ghassemifar

Hemoglobin· June 2016

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The Effect of Nonsense Mediated Decay on Transcriptional Activity Within the Novel β-Thalassemia Mutation HBB: c.129delT.
Luke Forster, Rasha Mesbah Ardakani, Talal Qadah, Jill Finlayson, Reza Ghassemifar

Hemoglobin· June 2016

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Molecular characterization of Hb Hamilton Hill (HBA2: c.388delC), a novel HBA2 variant generating a premature termination codon and truncated HBA2 chain.
Talal Qadah, Jill Finlayson, Emma North, Reza Ghassemifar

Hemoglobin· January 2016

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Differential gene expression analysis in early and late erythroid progenitor cells in β-thalassaemia.
Luke Forster, John McCooke, Matthew Bellgard, David Joske, Jill Finlayson

Br J Haematol· July 2015

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Validation of the immunochromatographic strip for α-thalassemia screening: a multicenter study.
Pranee Winichagoon, Pornnapa Kumpan, Paula Holmes, Jill Finlayson, Christopher Newbound

Transl Res· June 2015

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BRAF mutation detection in hairy cell leukaemia from archival haematolymphoid specimens.
Carla Thomas, Benhur Amanuel, Jill Finlayson, Fabienne Grieu-Iacopetta, Dominic V Spagnolo

Pathology· June 2015

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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.
Talal Qadah, Jill Finlayson, Philippe Joly, Reza Ghassemifar

Hemoglobin· September 2014

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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.
Talal Qadah, Jill Finlayson, Maxine Dennis, Reza Ghassemifar

Pathology· January 2014

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Alpha thalassaemia due to non-deletional mutations on the -3.7 alpha globin fusion gene: laboratory diagnosis and clinical importance.
Annie Chow, Reza Ghassemifar, Jill Finlayson

Pathology· October 2013

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Identification and characterization of two novel and differentially expressed isoforms of human α2- and α1-globin genes.
Reza Ghassemifar, Luke Forster, Talal Qadah, Jill Finlayson

Hemoglobin· January 2013

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α-thalassemia trait caused by frameshift mutations in exon 2 of the α2-globin gene: HBA2:c.131delT and HBA2:c.143delA.
Jill Finlayson, Reza Ghassemifar, Paula Holmes, Dianne Grey, Christopher Newbound

Hemoglobin· January 2013

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Differential expression of the Bcl-2 and Bax isoforms in CD19 positive B-lymphocytes isolated from patients diagnosed with chronic lymphocytic leukaemia.
Reza Ghassemifar, Luke Forster, Jill Finlayson, Tony Calogero, Brad Augustson

Pathology· December 2012

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Molecular and cellular characterization of a new α-thalassemia mutation (HBA2:c.94A>C) generating an alternative splice site and a premature stop codon.
Talal Qadah, Jill Finlayson, Christopher Newbound, Nicole Pell, Michelle Pascoe

Hemoglobin· October 2012

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In vitro characterization of the α-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1(G>A) (α2)].
Talal Qadah, Jill Finlayson, Reza Ghassemifar

Hemoglobin· June 2012

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A molecular tool to assess the pathological relevance of alpha-globin DNA variants.
Talal Qadah, Jill Finlayson, Christopher Newbound, Nicole Pell, Michelle Jennens

Pathology· June 2012

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Hematologic features of hepatosplenic T-cell lymphoma.
Wendy N Erber, Jill Finlayson

Am J Clin Pathol· February 2012

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Hb Lynwood [α107(G14) (-T) (α2) HBA2:c.323delT)] in conjunction with the α(3.7) deletion produces a moderately severe α-thalassemia phenotype.
Jill Finlayson, Reza Ghassemifar, Paula Holmes, Dianne Grey, Christopher Newbound

Hemoglobin· August 2011

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Hb East Timor [β80(EF4)Asn→His, AAC>CAC (HBB c.241A>C)], a variant hemoglobin associated with normal hematology.
Jill Finlayson, Reza Ghassemifar, Paula Holmes, Dianne Grey, Lisa Figliomeni

Hemoglobin· April 2011

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Incidence of c-Cbl mutations in human acute myeloid leukaemias in an Australian patient cohort.
Reza Ghassemifar, Christine B F Thien, Jill Finlayson, David Joske, Gavin M Cull

Pathology· April 2011

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Thalassemia in Western Australia: 11 novel deletions characterized by Multiplex Ligation-dependent Probe Amplification.
Marion Phylipsen, John F Prior, Erna Lim, Neela Lingam, Ingrid P Vogelaar, Jill Finlayson

Blood Cells Mol Dis· March 2010

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Two new alpha1-globin gene point mutations: Hb Nedlands (HBA1:c.86C>T) [alpha28(B9)Ala-->Val] and Hb Queens Park (HBA1:c.98T>A) [alpha32(B13)Met-->Lys].
Marion Phylipsen, John F Prior, Erna Lim, Neela Lingam, Jill Finlayson

Hemoglobin· January 2010

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A moderately severe alpha-thalassemia condition resulting from a combination of the alpha2 polyadenylation signal (AATAAA-->AATA- -) mutation and a 3.7 Kb alpha gene deletion in an Australian family.
John F Prior, Erna Lim, Neela Lingam, John L Raven, Jill Finlayson

Hemoglobin· July 2007

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