Lista de obras - Wendy Dean - Dominio Público Uruguay

5-Formylcytosine organizes nucleosomes and forms Schiff base interactions with histones in mouse embryonic stem cells

artículo científico publicado en 2018

A non-catalytic role of TET3 promotes open chromatin and enhances global transcription

Activation-induced cytidine deaminase deaminates 5-methylcytosine in DNA and is expressed in pluripotent tissues: implications for epigenetic reprogramming

artículo científico publicado en 2004

Altered imprinted gene methylation and expression in completely ES cell-derived mouse fetuses: association with aberrant phenotypes.

artículo científico publicado en 1998

An endosiRNA-Based Repression Mechanism Counteracts Transposon Activation during Global DNA Demethylation in Embryonic Stem Cells

artículo científico publicado en 2017

An intragenic methylated region in the imprinted Igf2 gene augments transcription.

artículo científico publicado en 2001

Cellular Reprogramming in Basic and Applied Biomedicine: The Dawn of Regenerative Medicine.

artículo científico publicado en 2015

Chromosome loops, insulators, and histone methylation: new insights into regulation of imprinting in clusters.

artículo científico publicado en 2004

Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark ⬇️

artículo científico publicado el 1 de mayo de 2003

Culture of preimplantation embryos and its long-term effects on gene expression and phenotype.

artículo científico publicado en 2001

Culture of preimplantation mouse embryos affects fetal development and the expression of imprinted genes

scientific article published on 01 March 2001

DNA methylation and demethylation: a pathway to gametogenesis and development.

artículo científico publicado en 2013

DNA methylation in mammalian development and disease.

artículo científico publicado en 2005

Dynamic chromatin modifications characterise the first cell cycle in mouse embryos.

artículo científico publicado en 2005

Dynamic reprogramming of DNA methylation in the early mouse embryo.

artículo científico publicado en 2002

Environmental effects on genomic imprinting in mammals.

artículo científico publicado en 2001

Epigenetic arbitration of cell fate decisions: tipping the bias

artículo científico publicado en 2007

Epigenetic asymmetry in the mammalian zygote and early embryo: relationship to lineage commitment?

artículo científico publicado en 2003

Epigenetic marking correlates with developmental potential in cloned bovine preimplantation embryos.

artículo científico publicado en 2003

Epigenetic memory of the first cell fate decision prevents complete ES cell reprogramming into trophoblast.

artículo científico publicado en 2014

Epigenetic properties and identification of an imprint mark in the Nesp-Gnasxl domain of the mouse Gnas imprinted locus.

artículo científico publicado en 2003

Epigenetic reprogramming during early development in mammals.

artículo científico publicado en 2004

Epigenetic reprogramming in early mammalian development and following somatic nuclear transfer.

artículo científico publicado en 2003

Evaluation of epigenetic marks in human embryos derived from IVF and ICSI.

artículo científico publicado en 2010

Evidence that Hoxa expression domains are evolutionarily transposed in spinal ganglia, and are established by forward spreading in paraxial mesoderm.

artículo científico publicado en 1999

Gender Differences in Global but Not Targeted Demethylation in iPSC Reprogramming.

artículo científico publicado en 2017

Generation of monoparental embryos for investigation into genomic imprinting.

artículo científico publicado en 2001

Genome-Scale Oscillations in DNA Methylation during Exit from Pluripotency

scientific article published on 01 July 2018

Genome-wide bisulfite sequencing in zygotes identifies demethylation targets and maps the contribution of TET3 oxidation.

artículo científico publicado en 2014

Genome-wide erasure of DNA methylation in mouse primordial germ cells is affected by AID deficiency.

artículo científico publicado en 2010

Identification of novel imprinted genes in a genome-wide screen for maternal methylation.

artículo científico publicado en 2003

Igf2 imprinting in development and disease.

artículo científico publicado en 2000

Impaired glucose homeostasis in transgenic mice expressing the human transient neonatal diabetes mellitus locus, TNDM

artículo científico publicado en 2004

Imprinted Nesp55 influences behavioral reactivity to novel environments

artículo científico publicado en 2005

Imprinted genes and the coordination of fetal and postnatal growth in mammals.

artículo científico publicado en 2001

Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation.

artículo científico publicado en 2004

Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans

scientific journal article

MLL2 conveys transcription-independent H3K4 trimethylation in oocytes.

artículo científico publicado en 2018

Maintenance of silent chromatin through replication requires SWI/SNF-like chromatin remodeler SMARCAD1

artículo científico publicado en 2011

Mammalian epigenomics: reprogramming the genome for development and therapy.

artículo científico publicado en 2003

Mechanisms of early placental development in mouse and humans

scientific article published on 18 September 2019

Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA.

artículo científico publicado en 2003

Pathways of DNA Demethylation

artículo científico publicado en 2016

Placental-specific IGF-II is a major modulator of placental and fetal growth.

artículo científico publicado en 2002

Processive DNA demethylation via DNA deaminase-induced lesion resolution

artículo científico publicado en 2014

Regulation of Igf2 imprinting in development and disease.

artículo científico publicado en 1996

Regulation of lineage specific DNA hypomethylation in mouse trophectoderm

artículo científico publicado en 2013

Regulation of supply and demand for maternal nutrients in mammals by imprinted genes.

artículo científico publicado en 2003

Reprogramming DNA methylation in the mammalian life cycle: building and breaking epigenetic barriers

artículo científico publicado en 2013

Resistance of IAPs to methylation reprogramming may provide a mechanism for epigenetic inheritance in the mouse

artículo científico publicado en 2003

Single-cell Hi-C for genome-wide detection of chromatin interactions that occur simultaneously in a single cell.

artículo científico publicado en 2015

Single-cell Hi-C reveals cell-to-cell variability in chromosome structure

artículo científico publicado en 2013

Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.

artículo científico publicado en 1998

The imprinted signaling protein XL alpha s is required for postnatal adaptation to feeding.

artículo científico publicado en 2004

The mouse Zac1 locus: basis for imprinting and comparison with human ZAC.

artículo científico publicado en 2002

Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.

artículo científico publicado en 1997

Lista de obras de Wendy Dean

5-Formylcytosine organizes nucleosomes and forms Schiff base interactions with histones in mouse embryonic stem cells

A non-catalytic role of TET3 promotes open chromatin and enhances global transcription

Activation-induced cytidine deaminase deaminates 5-methylcytosine in DNA and is expressed in pluripotent tissues: implications for epigenetic reprogramming

Altered imprinted gene methylation and expression in completely ES cell-derived mouse fetuses: association with aberrant phenotypes.

An endosiRNA-Based Repression Mechanism Counteracts Transposon Activation during Global DNA Demethylation in Embryonic Stem Cells

An intragenic methylated region in the imprinted Igf2 gene augments transcription.

Cellular Reprogramming in Basic and Applied Biomedicine: The Dawn of Regenerative Medicine.

Chromosome loops, insulators, and histone methylation: new insights into regulation of imprinting in clusters.

Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark ⬇️

Culture of preimplantation embryos and its long-term effects on gene expression and phenotype.

Culture of preimplantation mouse embryos affects fetal development and the expression of imprinted genes

DNA methylation and demethylation: a pathway to gametogenesis and development.

DNA methylation in mammalian development and disease.

Dynamic chromatin modifications characterise the first cell cycle in mouse embryos.

Dynamic reprogramming of DNA methylation in the early mouse embryo.

Environmental effects on genomic imprinting in mammals.

Epigenetic arbitration of cell fate decisions: tipping the bias

Epigenetic asymmetry in the mammalian zygote and early embryo: relationship to lineage commitment?

Epigenetic marking correlates with developmental potential in cloned bovine preimplantation embryos.

Epigenetic memory of the first cell fate decision prevents complete ES cell reprogramming into trophoblast.

Epigenetic properties and identification of an imprint mark in the Nesp-Gnasxl domain of the mouse Gnas imprinted locus.

Epigenetic reprogramming during early development in mammals.

Epigenetic reprogramming in early mammalian development and following somatic nuclear transfer.

Evaluation of epigenetic marks in human embryos derived from IVF and ICSI.

Evidence that Hoxa expression domains are evolutionarily transposed in spinal ganglia, and are established by forward spreading in paraxial mesoderm.

Gender Differences in Global but Not Targeted Demethylation in iPSC Reprogramming.

Generation of monoparental embryos for investigation into genomic imprinting.

Genome-Scale Oscillations in DNA Methylation during Exit from Pluripotency

Genome-wide bisulfite sequencing in zygotes identifies demethylation targets and maps the contribution of TET3 oxidation.

Genome-wide erasure of DNA methylation in mouse primordial germ cells is affected by AID deficiency.

Identification of novel imprinted genes in a genome-wide screen for maternal methylation.

Igf2 imprinting in development and disease.

Impaired glucose homeostasis in transgenic mice expressing the human transient neonatal diabetes mellitus locus, TNDM

Imprinted Nesp55 influences behavioral reactivity to novel environments

Imprinted genes and the coordination of fetal and postnatal growth in mammals.

Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation.

Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans

MLL2 conveys transcription-independent H3K4 trimethylation in oocytes.

Maintenance of silent chromatin through replication requires SWI/SNF-like chromatin remodeler SMARCAD1

Mammalian epigenomics: reprogramming the genome for development and therapy.

Mechanisms of early placental development in mouse and humans

Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA.

Pathways of DNA Demethylation

Placental-specific IGF-II is a major modulator of placental and fetal growth.

Processive DNA demethylation via DNA deaminase-induced lesion resolution

Regulation of Igf2 imprinting in development and disease.

Regulation of lineage specific DNA hypomethylation in mouse trophectoderm

Regulation of supply and demand for maternal nutrients in mammals by imprinted genes.

Reprogramming DNA methylation in the mammalian life cycle: building and breaking epigenetic barriers

Resistance of IAPs to methylation reprogramming may provide a mechanism for epigenetic inheritance in the mouse

Single-cell Hi-C for genome-wide detection of chromatin interactions that occur simultaneously in a single cell.

Single-cell Hi-C reveals cell-to-cell variability in chromosome structure

Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.

The imprinted signaling protein XL alpha s is required for postnatal adaptation to feeding.

The mouse Zac1 locus: basis for imprinting and comparison with human ZAC.

Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.