Lista de obras - Déborah Bourc'his - Dominio Público Uruguay

A piRNA pathway primed by individual transposons is linked to de novo DNA methylation in mice

scientific journal article

A small-RNA perspective on gametogenesis, fertilization, and early zygotic development.

artículo científico publicado en 2010

Abnormal methylation does not prevent X inactivation in ICF patients.

artículo científico publicado en 1999

Allele-specific demethylation at an imprinted mammalian promoter

artículo científico publicado en 2007

An epigenetic switch ensures transposon repression upon dynamic loss of DNA methylation in embryonic stem cells

artículo científico publicado en 2016

Characterization of novel paternal ncRNAs at the Plagl1 locus, including Hymai, predicted to interact with regulators of active chromatin

artículo científico publicado en 2012

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

artículo científico publicado en 1999

Chromosome methylation patterns during mammalian preimplantation development

artículo científico publicado en 1998

Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing

artículo científico publicado en 2008

Cultural relativism: maintenance of genomic imprints in pluripotent stem cell culture systems

artículo científico

DNA methylation restrains transposons from adopting a chromatin signature permissive for meiotic recombination

artículo científico publicado en 2015

DNMT3B mutations and DNA methylation defect define two types of ICF syndrome.

artículo científico publicado en 2005

Direct analysis of chromosome methylation

scientific article published on 01 January 2001

Dnmt3l-knockout donor cells improve somatic cell nuclear transfer reprogramming efficiency

artículo científico publicado en 2015

Dynamic enhancer partitioning instructs activation of a growth-related gene during exit from naïve pluripotency

article

Dynamic evolution of de novo DNA methyltransferases in rodent and primate genomes

artículo científico publicado en 2020

Epigenetic decisions in mammalian germ cells.

artículo científico publicado en 2007

Evolution of genomic imprinting in mammals: what a zoo!

artículo científico publicado en 2010

Extensive meiotic asynapsis in mice antagonises meiotic silencing of unsynapsed chromatin and consequently disrupts meiotic sex chromosome inactivation

artículo científico publicado en 2008

Fundamentals of epigenetics ⬇️

artículo científico publicado el 1 de febrero de 2010

Genetics and epigenetics of hydatidiform moles.

artículo científico publicado en 2006

Germline correction of an epimutation related to Silver-Russell syndrome

artículo científico publicado en 2015

Helicase homologues maintain cytosine methylation in plants and mammals.

artículo científico publicado en 2002

Human imprinted retrogenes exhibit non-canonical imprint chromatin signatures and reside in non-imprinted host genes ⬇️

artículo científico publicado en 2011

Identification and resolution of artifacts in the interpretation of imprinted gene expression

artículo científico publicado en 2010

Identification of the control region for tissue-specific imprinting of the stimulatory G protein alpha-subunit ⬇️

scientific journal article

Loss of spermatogonia and wide-spread DNA methylation defects in newborn male mice deficient in DNMT3L.

artículo científico publicado en 2007

MIWI2 is essential for spermatogenesis and repression of transposons in the mouse male germline

scientific journal article

MORC1 represses transposable elements in the mouse male germline

scientific journal article

Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L

scientific journal article

Origins of extreme sexual dimorphism in genomic imprinting.

artículo científico publicado en 2006

Plasticity in Dnmt3L-dependent and -independent modes of de novo methylation in the developing mouse embryo.

artículo científico publicado en 2013

Protection against de novo methylation is instrumental in maintaining parent-of-origin methylation inherited from the gametes

scientific article published on 16 August 2012

Regulation of alternative polyadenylation by genomic imprinting

artículo científico publicado en 2008

Sex-specific promoters regulate Dnmt3L expression in mouse germ cells

artículo científico publicado en 2006

Sexual dimorphism in parental imprint ontogeny and contribution to embryonic development.

artículo científico publicado en 2007

The DNA methyltransferase DNMT3C protects male germ cells from transposon activity

artículo científico publicado en 2016

The Gpr1/Zdbf2 locus provides new paradigms for transient and dynamic genomic imprinting in mammals

artículo científico publicado en 2014

The discovery and importance of genomic imprinting

scientific article published on 22 October 2018

The mammalian-specific Tex19.1 gene plays an essential role in spermatogenesis and placenta-supported development

artículo científico publicado en 2013

The parental non-equivalence of imprinting control regions during mammalian development and evolution

artículo científico publicado en 2010

Tools and best practices for retrotransposon analysis using high-throughput sequencing data

artículo científico publicado en 2019

Transient transcription in the early embryo sets an epigenetic state that programs postnatal growth.

artículo científico publicado en 2016

Undermethylation of Alu sequences in ICF syndrome: molecular and in situ analysis

scientific article published on 01 January 1997

WAMIDEX: a web atlas of murine genomic imprinting and differential expression

artículo científico publicado en 2008

Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2.

artículo científico publicado en 2000

[Heritable epimutations: a case study in humans]

artículo científico publicado en 2008

[In vitro methods of male germ cell specification and differentiation]

artículo científico publicado en 2007

alpha-satellite DNA methylation in normal individuals and in ICF patients: heterogeneous methylation of constitutive heterochromatin in adult and fetal tissues

scientific article published on 01 June 1997

Lista de obras de Déborah Bourc'his

A piRNA pathway primed by individual transposons is linked to de novo DNA methylation in mice

A small-RNA perspective on gametogenesis, fertilization, and early zygotic development.

Abnormal methylation does not prevent X inactivation in ICF patients.

Allele-specific demethylation at an imprinted mammalian promoter

An epigenetic switch ensures transposon repression upon dynamic loss of DNA methylation in embryonic stem cells

Characterization of novel paternal ncRNAs at the Plagl1 locus, including Hymai, predicted to interact with regulators of active chromatin

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

Chromosome methylation patterns during mammalian preimplantation development

Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing

Cultural relativism: maintenance of genomic imprints in pluripotent stem cell culture systems

DNA methylation restrains transposons from adopting a chromatin signature permissive for meiotic recombination

DNMT3B mutations and DNA methylation defect define two types of ICF syndrome.

Direct analysis of chromosome methylation

Dnmt3l-knockout donor cells improve somatic cell nuclear transfer reprogramming efficiency

Dynamic enhancer partitioning instructs activation of a growth-related gene during exit from naïve pluripotency

Dynamic evolution of de novo DNA methyltransferases in rodent and primate genomes

Epigenetic decisions in mammalian germ cells.

Evolution of genomic imprinting in mammals: what a zoo!

Extensive meiotic asynapsis in mice antagonises meiotic silencing of unsynapsed chromatin and consequently disrupts meiotic sex chromosome inactivation

Fundamentals of epigenetics ⬇️

Genetics and epigenetics of hydatidiform moles.

Germline correction of an epimutation related to Silver-Russell syndrome

Helicase homologues maintain cytosine methylation in plants and mammals.

Human imprinted retrogenes exhibit non-canonical imprint chromatin signatures and reside in non-imprinted host genes ⬇️

Identification and resolution of artifacts in the interpretation of imprinted gene expression

Identification of the control region for tissue-specific imprinting of the stimulatory G protein alpha-subunit ⬇️

Loss of spermatogonia and wide-spread DNA methylation defects in newborn male mice deficient in DNMT3L.

MIWI2 is essential for spermatogenesis and repression of transposons in the mouse male germline

MORC1 represses transposable elements in the mouse male germline

Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L

Origins of extreme sexual dimorphism in genomic imprinting.

Plasticity in Dnmt3L-dependent and -independent modes of de novo methylation in the developing mouse embryo.

Protection against de novo methylation is instrumental in maintaining parent-of-origin methylation inherited from the gametes

Regulation of alternative polyadenylation by genomic imprinting

Sex-specific promoters regulate Dnmt3L expression in mouse germ cells

Sexual dimorphism in parental imprint ontogeny and contribution to embryonic development.

The DNA methyltransferase DNMT3C protects male germ cells from transposon activity

The Gpr1/Zdbf2 locus provides new paradigms for transient and dynamic genomic imprinting in mammals

The discovery and importance of genomic imprinting

The mammalian-specific Tex19.1 gene plays an essential role in spermatogenesis and placenta-supported development

The parental non-equivalence of imprinting control regions during mammalian development and evolution

Tools and best practices for retrotransposon analysis using high-throughput sequencing data

Transient transcription in the early embryo sets an epigenetic state that programs postnatal growth.

Undermethylation of Alu sequences in ICF syndrome: molecular and in situ analysis

WAMIDEX: a web atlas of murine genomic imprinting and differential expression

Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2.

[Heritable epimutations: a case study in humans]

[In vitro methods of male germ cell specification and differentiation]

alpha-satellite DNA methylation in normal individuals and in ICF patients: heterogeneous methylation of constitutive heterochromatin in adult and fetal tissues