Bourc'his, Déborah, 19..-....
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
Déborah Bourc'his chercheuse française
Bourc'his, Déborah
VIAF ID: 215223029 (Personal)
Permalink: http://viaf.org/viaf/215223029
Preferred Forms
4xx's: Alternate Name Forms (3)
Works
| Title | Sources |
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| Abnormal methylation does not prevent X inactivation in ICF patients. |
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| Activité du rétrotransposon L1 dans les cellules musculaires |
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| alpha-satellite DNA methylation in normal individuals and in ICF patients: heterogeneous methylation of constitutive heterochromatin in adult and fetal tissues |
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| Atypical forms of genomic imprinting : transient, tissue-specific and strain-specific. |
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| Bioinformatics analysis of transposable elements regulation in mammals. |
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| Caractérisation fonctionnelle du locus Liz/Zdbf2 soumis à empreinte chez la souris : de l'embryon précoce à la physiologie adulte. |
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| Caractérisation génomique et fonctionnelle de l'empreinte parentale par le modèle murin mutant pour Dnmt3L |
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| Characterization of novel paternal ncRNAs at the Plagl1 locus, including Hymai, predicted to interact with regulators of active chromatin |
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| Chromatin mark interplays in the mammalian oocyte |
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| Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene |
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| Chromosome methylation patterns during mammalian preimplantation development |
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| 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 |
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| Un coup de ciseaux dans la création : CRISPR-Cas9 : le redoutable pouvoir de contrôler l'évolution |
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| Cultural relativism: maintenance of genomic imprints in pluripotent stem cell culture systems |
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| Deciphering the role of DNA methylation in early cellular transitions |
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| The discovery and importance of genomic imprinting |
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| DNA methylation and cellular identity : function of DNA methylation in gametic and hematopoietic lineages in mouse. |
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| DNA methylation : functions and recruitment during mouse development.. |
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| DNA methylation restrains transposons from adopting a chromatin signature permissive for meiotic recombination |
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| The DNA methyltransferase DNMT3C protects male germ cells from transposon activity |
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| DNMT3B mutations and DNA methylation defect define two types of ICF syndrome. |
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| Dnmt3l-knockout donor cells improve somatic cell nuclear transfer reprogramming efficiency |
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| Dynamic enhancer partitioning instructs activation of a growth-related gene during exit from naïve pluripotency |
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| Dynamic evolution of de novo DNA methyltransferases in rodent and primate genomes |
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| Effet du remodelage de l'hétérochromatine sur le destin cellulaire et le développement préimplantatoire chez la souris. |
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| Epigenetic decisions in mammalian germ cells. |
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| Epigenetic inheritance from the oocyte |
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| Évolution du réseau de régulation de l’inactivation du chromosome X chez l’homme et la souris. |
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| Evolution of genomic imprinting in mammals: what a zoo! |
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| Exploration pangénomique des effets épigénétiques et transcriptomiques liés aux techniques d'assistance médicale à la procréation |
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| Extensive meiotic asynapsis in mice antagonises meiotic silencing of unsynapsed chromatin and consequently disrupts meiotic sex chromosome inactivation |
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| Formes atypiques d'empreinte génomique : transitoire, tissu-spécifique et lignée-spécifique |
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| Functional characterization of the imprinted Liz/Zdbf2 locus in mice : from the early embryo to adult physiology |
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| Fundamentals of epigenetics |
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| Genetics and epigenetics of hydatidiform moles. |
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| A genome-wide CRISPR screen to uncover novel epigenetic regulators in mouse embryonic stem cells. |
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| Genomic and functional characterisation of genomic imprinting using the DNMT3L mutant mouse. |
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| Germline correction of an epimutation related to Silver-Russell syndrome |
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| The Gpr1/Zdbf2 locus provides new paradigms for transient and dynamic genomic imprinting in mammals |
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| [Heritable epimutations: a case study in humans] |
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| Héritage épigénétique de l'ovocyte. |
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| Human imprinted retrogenes exhibit non-canonical imprint chromatin signatures and reside in non-imprinted host genes |
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| The ICF syndrome and emergent players in DNA methylation and development : when studying a rare genetic disease sheds new light on an "old" field |
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| IDENTIFICATION DU GENE ET DE L'ORIGINE EMBRYONNAIRE DU DEFAUT DE METHYLATION DE L'AON DES PATIENST ICF |
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| Identification of the control region for tissue-specific imprinting of the stimulatory G protein alpha-subunit |
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| Identification systématique de nouveaux régulateurs épigénétiques par criblage CRISPR-Cas9 pangénomique |
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| Impact of supra physiological concentrations of bile acids on male reproductive functions and transgenerational inheritance. |
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| Impacts de concentrations supraphysiologiques d'acides biliaires sur la physiologie testiculaire et les fonctions de reproduction |
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| Importance of genetic and epigenetic interactions on the transcriptional response to environmental stimuli. |
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| [In vitro methods of male germ cell specification and differentiation] |
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| L'impact des variations génétiques et épigénétiques sur les réponses transcriptionnelles aux stimuli environnementaux |
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| Loss of spermatogonia and wide-spread DNA methylation defects in newborn male mice deficient in DNMT3L. |
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| The mammalian-specific Tex19.1 gene plays an essential role in spermatogenesis and placenta-supported development |
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| Mechanisms of cell fate and chromatin plasticity during early mouse embryogenesis |
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| Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L |
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| Méthylation de l'ADN et identité cellulaire : fonctions de la méthylation de l'ADN dans les lignages gamétiques et hématopoïétiques chez la souris |
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| MORC1 represses transposable elements in the mouse male germline |
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| Nouvelle voie de contrôle des transposons et implication pour la stabilité des génomes. |
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| Novel chromatin pathway controlling transposable elements and impact on genome stability |
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| Origins of extreme sexual dimorphism in genomic imprinting. |
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| A piRNA pathway primed by individual transposons is linked to de novo DNA methylation in mice |
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| Piwi function and piRNA cluster regulation : Drosophila melanogaster |
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| Plasticity in Dnmt3L-dependent and -independent modes of de novo methylation in the developing mouse embryo. |
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| Protection against de novo methylation is instrumental in maintaining parent-of-origin methylation inherited from the gametes |
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| Régulation de l'expression du gène Nodal lors de la différenciation des cellules souches embryonnaires |
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| Regulation of alternative polyadenylation by genomic imprinting |
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| Régulations épigénétiques des éléments transposables au cours de l'ovogenèse de Drosophila melanogaster |
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| Rôle de l'activité méthyltransférase de la protéine PRDM9 dans la recombinaison méiotique chez la souris |
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| The role of retinoic acid in the formation of gametes in mice. |
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| Sex-specific promoters regulate Dnmt3L expression in mouse germ cells |
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| A small-RNA perspective on gametogenesis, fertilization, and early zygotic development. |
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| Syndrome ICF et acteurs émergents dans la méthylation de l'ADN et le développement : l’étude d’une maladie génétique rare apporte un regard nouveau sur un « ancien » domaine. |
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| Tools and best practices for retrotransposon analysis using high-throughput sequencing data |
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| Toward the identification of factors involved into concerted regulation of imprinted genes in brain. |
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| Transient transcription in the early embryo sets an epigenetic state that programs postnatal growth. |
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| Transposon regulation upon dynamic loss of DNA methylation |
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| Undermethylation of Alu sequences in ICF syndrome: molecular and in situ analysis |
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| Vers l'identification des facteurs impliqués dans la régulation concertée des gènes soumis à empreinte dans le cerveau |
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| WAMIDEX: a web atlas of murine genomic imprinting and differential expression |
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| Whole genome exploration of epigenetic and transcriptomic effects of Assisted Reproductive Technologies. |
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| Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2. |
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