Ruth N. Mackinnon

St. Vincent's Hospital Melbourne
Fitzroy, VIC, Australia

Last Updated: 09/26/2026

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Found 22 publications

Detailed molecular cytogenetic characterisation of the myeloid cell line U937 reveals the fate of homologous chromosomes and shows that centromere capture is a feature of genome instability.

Detailed molecular cytogenetic characterisation of the myeloid cell line U937 reveals the fate of homologous chromosomes and shows that centromere capture is a feature of genome instability.

Journal: Molecular cytogenetics
Published: October 15, 2020

BCL-XL inhibition by BH3-mimetic drugs induces apoptosis in models of Epstein-Barr virus-associated T/NK-cell lymphoma.

BCL-XL inhibition by BH3-mimetic drugs induces apoptosis in models of Epstein-Barr virus-associated T/NK-cell lymphoma.

Journal: Blood advances
Published: May 26, 2020

Hemopoietic Cell Kinase amplification with Protein Tyrosine Phosphatase Receptor T depletion leads to polycythemia, aberrant marrow erythoid maturation, and splenomegaly.

Hemopoietic Cell Kinase amplification with Protein Tyrosine Phosphatase Receptor T depletion leads to polycythemia, aberrant marrow erythoid maturation, and splenomegaly.

Journal: Scientific reports
Published: February 06, 2019

Analysis of Chromothripsis by Combined FISH and Microarray Analysis.

Analysis of Chromothripsis by Combined FISH and Microarray Analysis.

Journal: Methods in molecular biology (Clifton, N.J.)
Published: March 23, 2018

MACROD2 Haploinsufficiency Impairs Catalytic Activity of PARP1 and Promotes Chromosome Instability and Growth of Intestinal Tumors.

MACROD2 Haploinsufficiency Impairs Catalytic Activity of PARP1 and Promotes Chromosome Instability and Growth of Intestinal Tumors.

Journal: Cancer discovery
Published: August 11, 2017

The Dicentric Chromosome dic(20;22) Is a Recurrent Abnormality in Myelodysplastic Syndromes and Is a Product of Telomere Fusion.

The Dicentric Chromosome dic(20;22) Is a Recurrent Abnormality in Myelodysplastic Syndromes and Is a Product of Telomere Fusion.

Journal: Cytogenetic and genome research
Published: March 06, 2017

Active centromere and chromosome identification in fixed cell lines.

Active centromere and chromosome identification in fixed cell lines.

Journal: Molecular cytogenetics
Published: February 06, 2016

Src family kinases and their role in hematological malignancies.

Src family kinases and their role in hematological malignancies.

Journal: Leukemia & lymphoma
Published: June 06, 2014

Genome organization and the role of centromeres in evolution of the erythroleukaemia cell line HEL.

Genome organization and the role of centromeres in evolution of the erythroleukaemia cell line HEL.

Journal: Evolution, medicine, and public health
Published: February 01, 2014

Chromothripsis under the microscope: a cytogenetic perspective of two cases of AML with catastrophic chromosome rearrangement.

Chromothripsis under the microscope: a cytogenetic perspective of two cases of AML with catastrophic chromosome rearrangement.

Journal: Cancer genetics
Published: February 07, 2013

ETV6 deletion is a common additional abnormality in patients with myelodysplastic syndromes or acute myeloid leukemia and monosomy 7.

ETV6 deletion is a common additional abnormality in patients with myelodysplastic syndromes or acute myeloid leukemia and monosomy 7.

Journal: Haematologica
Published: August 10, 2012

11q23 rearrangement and duplication of MLLT1-MLL gene fusion in therapy-related acute myeloid leukemia.

11q23 rearrangement and duplication of MLLT1-MLL gene fusion in therapy-related acute myeloid leukemia.

Journal: Leukemia & lymphoma
Published: February 17, 2012
Showing 1-12 of 22

Last Updated: 09/26/2026