Mechanistic aspects of genome-wide demethylation in the preimplantation mouse embryo.
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Evidence for conserved DNA and histone H3 methylation reprogramming in mouse, bovine and rabbit zygotesRegulation of X-chromosome inactivation in development in mice and humansDiet and the epigenetic (re)programming of phenotypic differences in behaviorDNA methylation: past, present and future directions.Site-specific methylation of the promoter alters deoxyribonucleic acid-protein interactions and prevents follicle-stimulating hormone receptor gene transcription.DNA demethylation.Embryonic germ cells induce epigenetic reprogramming of somatic nucleus in hybrid cellsAn embryonic demethylation mechanism involving binding of transcription factors to replicating DNAChromosome methylation patterns during mammalian preimplantation developmentTherapeutic implications of DNA methylation.Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern.Comparison of DNA methylation patterns among mouse cell lines by restriction landmark genomic scanningDNA methylation is a reversible biological signal.Diversity of two forms of DNA methylation in the brain.DNA methylation: an epigenetic risk factor in preterm birth.DNA methylation program during development.Genome-wide sperm DNA methylation changes after 3 months of exercise training in humans.5-Methylcytosine DNA glycosylase participates in the genome-wide loss of DNA methylation occurring during mouse myoblast differentiation.Evidence that protein binding specifies sites of DNA demethylation.A unique developmental pattern of Oct-3/4 DNA methylation is controlled by a cis-demodification element.TRIM28 Controls Genomic Imprinting through Distinct Mechanisms during and after Early Genome-wide Reprogramming.Aberrant methylation patterns at the two-cell stage as an indicator of early developmental failure.Impact of Lactational Exposure to Polychlorinated Biphenyl Causes Epigenetic Modification and Impairs Sertoli Cells Functional Regulators in F1 Progeny.Sequence-specific methylation of the mouse H19 gene in embryonic cells deficient in the Dnmt-1 gene.Mouse DNA methyltransferase (MTase) deletion mutants that retain the catalytic domain display neither de novo nor maintenance methylation activity in vivo.The imprinting box of the mouse Igf2r gene
P2860
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P2860
Mechanistic aspects of genome-wide demethylation in the preimplantation mouse embryo.
description
1993 nî lūn-bûn
@nan
1993 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Mechanistic aspects of genome-wide demethylation in the preimplantation mouse embryo.
@ast
Mechanistic aspects of genome-wide demethylation in the preimplantation mouse embryo.
@en
Mechanistic aspects of genome-wide demethylation in the preimplantation mouse embryo.
@nl
type
label
Mechanistic aspects of genome-wide demethylation in the preimplantation mouse embryo.
@ast
Mechanistic aspects of genome-wide demethylation in the preimplantation mouse embryo.
@en
Mechanistic aspects of genome-wide demethylation in the preimplantation mouse embryo.
@nl
prefLabel
Mechanistic aspects of genome-wide demethylation in the preimplantation mouse embryo.
@ast
Mechanistic aspects of genome-wide demethylation in the preimplantation mouse embryo.
@en
Mechanistic aspects of genome-wide demethylation in the preimplantation mouse embryo.
@nl
P2093
P2860
P356
P1476
Mechanistic aspects of genome-wide demethylation in the preimplantation mouse embryo.
@en
P2093
P2860
P304
10558-10562
P356
10.1073/PNAS.90.22.10558
P407
P577
1993-11-01T00:00:00Z