Lista de obras - Ian M. Morison - Dominio Público Uruguay

5-hydroxymethylcytosine: a potential therapeutic target in cancer

artículo científico

A census of mammalian imprinting.

artículo científico publicado en 2005

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

artículo científico publicado en 2008

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

artículo científico publicado en 2002

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

artículo científico publicado en 2017

Base-resolution DNA methylation landscape of zebrafish brain and liver

artículo científico publicado en 2014

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.

artículo científico publicado en 2017

Comparison of alignment software for genome-wide bisulphite sequence data

artículo científico publicado en 2012

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

artículo científico publicado en 2011

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

artículo científico publicado en 1993

Correct usage of "loss of imprinting"

scientific article published on 01 November 2005

DMAP: differential methylation analysis package for RRBS and WGBS data

artículo científico publicado en 2014

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

artículo científico publicado en 2018

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

artículo científico publicado en 2011

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

artículo científico publicado en 2006

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

artículo científico publicado en 2013

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

artículo científico publicado en 2014

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

artículo científico publicado en 1997

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

artículo científico publicado en 2004

Genome-scale DNA methylome and transcriptome profiling of human neutrophils

artículo científico publicado en 2016

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

artículo científico publicado en 2015

Germline mutations and somatic inactivation of TRIM28 in Wilms tumour.

artículo científico publicado en 2018

Global demethylation in loss of imprinting subtype of Wilms tumor.

artículo científico publicado en 2012

Green neutrophil and monocyte inclusions - time to acknowledge and report

artículo científico publicado en 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

artículo científico publicado en 2011

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

artículo científico publicado en 2015

Imprinting, expression, and localisation of DLK1 in Wilms tumours

artículo científico publicado en 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

artículo científico publicado en 1998

Insulin-like growth factor-II imprinting in cancer

artículo científico publicado en 2002

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

artículo científico publicado en 2010

Interspecies Variation in the Functional Consequences of Mutation of Cytochrome c

artículo científico publicado en 2015

Mapping the zebrafish brain methylome using reduced representation bisulfite sequencing

artículo científico publicado en 2013

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

artículo científico publicado en 2016

Monozygotic twins: genes are not the destiny? ⬇️

artículo científico publicado el 10 de diciembre de 2011

Myelodysplastic syndrome in New Zealand and Australia

artículo científico publicado en 2012

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

artículo científico publicado en 2004

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

artículo científico publicado en 2005

Physiological functions of imprinted genes.

artículo científico publicado en 2002

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

artículo científico publicado en 2016

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

artículo científico publicado en 2002

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

artículo científico publicado en 1997

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

artículo científico publicado en 2005

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

artículo científico publicado en 2000

Random monoallelic expression: making a choice.

artículo científico publicado en 2008

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

artículo científico publicado en 2003

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

artículo científico publicado en 2014

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

artículo científico publicado en 2018

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

artículo científico publicado en 2010

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

artículo científico publicado en 1996

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

artículo científico publicado en 2016

Targeting the apoptosome for cancer therapy

artículo científico publicado en 2009

Technical considerations for reduced representation bisulfite sequencing with multiplexed libraries

artículo científico publicado en 2012

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

artículo científico publicado en 2017

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

artículo científico publicado en 2017

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

artículo científico publicado en 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

artículo científico publicado en 2008

Lista de obras de Ian M. Morison

5-hydroxymethylcytosine: a potential therapeutic target in cancer

A census of mammalian imprinting.

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

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

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

Base-resolution DNA methylation landscape of zebrafish brain and liver

CYCS gene variants associated with thrombocytopenia

Canonical WNT signalling determines lineage specificity in Wilms tumour

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

Comparison of alignment software for genome-wide bisulphite sequence data

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

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

Correct usage of "loss of imprinting"

DMAP: differential methylation analysis package for RRBS and WGBS data

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

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

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

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

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

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

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

Genome-scale DNA methylome and transcriptome profiling of human neutrophils

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

Germline mutations and somatic inactivation of TRIM28 in Wilms tumour.

Global demethylation in loss of imprinting subtype of Wilms tumor.

Green neutrophil and monocyte inclusions - time to acknowledge and report

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

Hypomethylation of functional retrotransposon-derived genes in the human placenta

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

Imprinting, expression, and localisation of DLK1 in Wilms tumours

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

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

Insulin-like growth factor-II imprinting in cancer

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

Interspecies Variation in the Functional Consequences of Mutation of Cytochrome c

Mapping the zebrafish brain methylome using reduced representation bisulfite sequencing

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

Monozygotic twins: genes are not the destiny? ⬇️

Myelodysplastic syndrome in New Zealand and Australia

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

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

Physiological functions of imprinted genes.

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

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

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

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

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

Random monoallelic expression: making a choice.

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

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

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

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

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

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

Targeting the apoptosome for cancer therapy

Technical considerations for reduced representation bisulfite sequencing with multiplexed libraries

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

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

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

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

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