Search filters

List of works by Ian Morison

5-hydroxymethylcytosine: a potential therapeutic target in cancer

scientific article published on January 2014

A census of mammalian imprinting.

scientific article

A mutation of human cytochrome c enhances the intrinsic apoptotic pathway but causes only thrombocytopenia.

scientific article

A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362X

scientific article (publication date: April 2002)

A streamlined method for analysing genome-wide DNA methylation patterns from low amounts of FFPE DNA.

scientific article

Base-resolution DNA methylation landscape of zebrafish brain and liver

scientific article

CYCS gene variants associated with thrombocytopenia

scientific article published on 19 November 2018

Canonical WNT signalling determines lineage specificity in Wilms tumour

scientific article published on 12 January 2009

Comparative assessment of DNA methylation patterns between reduced representation bisulfite sequencing and Sequenom EpiTyper methylation analysis.

scientific article published on 19 May 2017

Comparison of alignment software for genome-wide bisulphite sequence data

scientific article

Congenital thrombocytopenia and cytochrome C mutation: a matter of birth and death

scientific article

Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumour and gigantism

scientific article

Correct usage of "loss of imprinting"

scientific article published on 01 November 2005

DMAP: differential methylation analysis package for RRBS and WGBS data

scientific article

DNA methylation of hepatic iron sensing genes and the regulation of hepcidin expression.

scientific article

Defects in imprinting and genome-wide DNA methylation are not common in the in vitro fertilization population.

scientific article

Detailed methylation analysis of CpG islands on human chromosome region 9p21

scientific article published on 01 April 2006

Disadvantaged pre-schoolers attending day care in Salvador, Northeast Brazil have a low prevalence of anaemia and micronutrient deficiencies

scientific article published on 5 September 2013

Enhancing the peroxidase activity of cytochromecby mutation of residue 41: implications for the peroxidase mechanism and cytochromecrelease

scientific article published on 01 March 2014

Epigenetic changes at the insulin-like growth factor II/H19 locus in developing kidney is an early event in Wilms tumorigenesis.

scientific article published on May 1997

Epigenetic differences between Wilms' tumours in white and east-Asian children

scientific article published in February 2004

Genome-scale DNA methylome and transcriptome profiling of human neutrophils

scientific article published on 15 March 2016

Genome-wide DNA methylation map of human neutrophils reveals widespread inter-individual epigenetic variation.

scientific article

Germline mutations and somatic inactivation of TRIM28 in Wilms tumour.

scientific article published on 18 June 2018

Global demethylation in loss of imprinting subtype of Wilms tumor.

scientific article

Green neutrophil and monocyte inclusions - time to acknowledge and report

scientific article published on 20 April 2015

Human insulin-like growth factor type I and type II receptors are not imprinted

scientific article published on 01 December 1993

Hypomethylation of functional retrotransposon-derived genes in the human placenta

scientific article published on 27 August 2011

Identification of X monosomy cells from a gonad of mixed gonadal dysgenesis with a 46,XY karyotype: case report.

scientific article

Imprinting, expression, and localisation of DLK1 in Wilms tumours

scientific article published on February 2005

Influence of the glutathione peroxidase 1 Pro200Leu polymorphism on the response of glutathione peroxidase activity to selenium supplementation: a randomized controlled trial

scholarly article

Insulin-like growth factor 2 and overgrowth: molecular biology and clinical implications

scientific article published on March 1998

Insulin-like growth factor-II imprinting in cancer

scientific article published on 01 June 2002

Integrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locus

scientific article

Interspecies Variation in the Functional Consequences of Mutation of Cytochrome c

scientific article

Mapping the zebrafish brain methylome using reduced representation bisulfite sequencing

scientific article

Megakaryocytes from CYCS mutation-associated thrombocytopenia release platelets by both proplatelet-dependent and -independent processes

scientific article

Monozygotic twins: genes are not the destiny?

scientific article published on December 10, 2011

Myelodysplastic syndrome in New Zealand and Australia

scientific article published in November 2012

Myogenesis in Wilms' tumors is associated with mutations of the WT1 gene and activation of Bcl-2 and the Wnt signaling pathway

scientific article published on 4 March 2004

No evidence for preferential maternal origin of duplicated chromosome 14 in hyperdiploid ALL

scientific article published on 01 February 2005

Physiological functions of imprinted genes.

scientific article

Placental Hypomethylation Is More Pronounced in Genomic Loci Devoid of Retroelements.

scientific article published on 29 April 2016

Preferential loss of maternal 9p alleles in childhood acute lymphoblastic leukemia

scientific article published on 01 January 2002

Progression of the culprit lesion in unstable coronary artery disease with warfarin and aspirin versus aspirin alone: preliminary study.

scientific article

Promoter haplotype of a new ABCA1 mutant influences expression of familial hypoalphalipoproteinemia

scientific article

Proportion of cells with paternal 11p15 uniparental disomy correlates with organ enlargement in Wiedemann-beckwith syndrome

scientific article published on 01 May 2000

Random monoallelic expression: making a choice.

scientific article published on 29 April 2008

Reassessment of loss of heterozygosity within MLL in childhood acute lymphoblastic leukemia.

scientific article

Retrotransposon hypomethylation in melanoma and expression of a placenta-specific gene

scientific article

Roxithromycin monotherapy inducing a partial response in a patient with myeloma: a case report.

scientific article published on 10 May 2018

Silencing of TESTIN by dense biallelic promoter methylation is the most common molecular event in childhood acute lymphoblastic leukaemia

scientific article

Somatic overgrowth associated with overexpression of insulin-like growth factor II.

scientific article published in March 1996

TESTIN Induces Rapid Death and Suppresses Proliferation in Childhood B Acute Lymphoblastic Leukaemia Cells.

scientific article

Targeting the apoptosome for cancer therapy

scientific article published on January 2009

Technical considerations for reduced representation bisulfite sequencing with multiplexed libraries

scientific article

The Genes of Life and Death: A Potential Role for Placental-Specific Genes in Cancer: Active retrotransposons in the placenta encode unique functional genes that may also be used by cancer cells to promote malignancy

scientific article published on 4 October 2017

The developmental programme for genesis of the entire kidney is recapitulated in Wilms tumour

scientific article published on 17 October 2017

Tools and Strategies for Analysis of Genome-Wide and Gene-Specific DNA Methylation Patterns

scientific article published on January 2017

Trends in myeloma incidence, mortality and survival in New Zealand (1985-2016)

scientific article published on 25 March 2019

Wilms tumour histology is determined by distinct types of precursor lesions and not epigenetic changes

scientific article