Research Topics
| Ruth N MacKinnonSummaryAffiliation: St Vincent's Hospital Country: Australia Publications
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Publications
CGH and SNP array using DNA extracted from fixed cytogenetic preparations and long-term refrigerated bone marrow specimensRuth N MacKinnon
Victorian Cancer Cytogenetics Service, St Vincent s Hospital Melbourne, Fitzroy, Vic, Australia
Mol Cytogenet 5:10. 2012..abstract:..
Recurrent duplication of Xq27-qter in hematological malignancies revealed by multicolor fluorescence in situ hybridization and multicolor bandingRuth N MacKinnon
University of Melbourne Department of Medicine, St Vincent s Hospital, Melbourne, Victoria, Australia
Cancer Genet Cytogenet 161:125-9. 2005..e., in one third of male cases and one fifth of all cases). These preliminary results may point to the existence of a recurrent chromosome abnormality, either translocation at a specific Xq27 locus or duplication of Xq27-qter...
A comparison of two contrasting recurrent isochromosomes 20 found in myelodysplastic syndromes suggests that retention of proximal 20q is a significant factor in myeloid malignanciesRuth N MacKinnon
Victorian Cancer Cytogenetics Service, Department of Medicine, St Vincent s Hospital Melbourne and University of Melbourne, Fitzroy Vic, Australia
Cancer Genet Cytogenet 163:176-9. 2005..We speculate that a region of proximal 20q is preferentially retained during deletions of the critical region in MDS and acute myeloid leukemia...
A FISH comparison of variant derivatives of the recurrent dic(17;20) of myelodysplastic syndromes and acute myeloid leukemia: Obligatory retention of genes on 17p and 20q may explain the formation of dicentric chromosomesRuth N MacKinnon
Victorian Cancer Cytogenetics Service, St Vincent s Hospital Melbourne, Australia
Genes Chromosomes Cancer 46:27-36. 2007..This would explain the excess of dicentric chromosomes resulting from 17;20 translocation, and the apparent stabilization of the unstable derivatives by further rearrangements which preserve 17p and 20q material...
Dicentric chromosomes and 20q11.2 amplification in MDS/AML with apparent monosomy 20R N MacKinnon
Victorian Cancer Cytogenetics Service, St Vincent s Hospital, University of Melbourne, Melbourne, Australia
Cytogenet Genome Res 119:211-20. 2007..The reported incidence of dicentric chromosomes is clearly an under-estimate but is increasing in myeloid disorders as more cases are studied with methods allowing their detection...
The paradox of 20q11.21 amplification in a subset of cases of myeloid malignancy with chromosome 20 deletionRuth N MacKinnon
Victorian Cancer Cytogenetics Service, St Vincent s Hospital, Melbourne, Australia
Genes Chromosomes Cancer 49:998-1013. 2010..Chromosome sub-band 20q11.21 amplification may therefore prove to be a marker of a specific subset of AML/MDS with a significant erythroid component...
The use of M-FISH and M-BAND to define chromosome abnormalitiesRuth N MacKinnon
Victorian Cancer Cytogenetics Service, St Vincent s Hospital Melbourne, Fitzroy, Vic, Australia
Methods Mol Biol 730:203-18. 2011..The single colour galleries - which show the hybridisation patterns of the individual fluorochromes - are useful to help interpret and confirm the false colour images produced by the software, including ambiguous signals...
Unbalanced translocations of 20q in AML and MDS often involve interstitial rather than terminal deletions of 20qRuth N MacKinnon
Victorian Cancer Cytogenetics Service, St Vincent s Hospital, Melbourne, Victoria, Australia
Cancer Genet 204:153-61. 2011..This points to a more complex mechanism of translocation involving at least three breakpoints and two separate events, and raises questions about the order of these events and the significance of these abnormalities...
A cryptic deletion in 5q31.2 provides further evidence for a minimally deleted region in myelodysplastic syndromesRuth N MacKinnon
Victorian Cancer Cytogenetics Service, St Vincent s Hospital Melbourne, Fitzroy, Vic, Australia
Cancer Genet 204:187-94. 2011..This case, together with previously published studies, suggests that the proximal boundary of the common deleted region may lie within the KDM3B gene...
