about
Genomic imprinting in mammals: emerging themes and established theoriesPaternal age and reproductionParthenogenesis and Human Assisted ReproductionImprinted and X-linked non-coding RNAs as potential regulators of human placental functionA concise review on epigenetic regulation: insight into molecular mechanismsAltered gene expression in human placentas after IVF/ICSIThe opossum genome: insights and opportunities from an alternative mammalSex- and diet-specific changes of imprinted gene expression and DNA methylation in mouse placenta under a high-fat dietChild health, developmental plasticity, and epigenetic programmingA maternal-offspring coadaptation theory for the evolution of genomic imprintingComputational selection and prioritization of candidate genes for fetal alcohol syndrome.Expression and protein localisation of IGF2 in the marsupial placenta.Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome.Random X inactivation and extensive mosaicism in human placenta revealed by analysis of allele-specific gene expression along the X chromosome.DNA methylation-mediated down-regulation of DNA methyltransferase-1 (DNMT1) is coincident with, but not essential for, global hypomethylation in human placenta.The function of non-coding RNAs in genomic imprinting.Non-conflict theories for the evolution of genomic imprinting.Gene interactions in the evolution of genomic imprinting.Mammalian viviparity: a complex niche in the evolution of genomic imprinting.Genomic imprinting and parent-of-origin effects on complex traits.Extra-embryonic-specific imprinted expression is restricted to defined lineages in the post-implantation embryo.Loss of DNMT1o disrupts imprinted X chromosome inactivation and accentuates placental defects in females.A survey for novel imprinted genes in the mouse placenta by mRNA-seqImpact of DNA methylation on trophoblast function.Imprinted gene expression in fetal growth and developmentObstetric outcome in donor oocyte pregnancies: a matched-pair analysis.Selected imprinting of INS in the marsupial.The PcG gene Sfmbt2 is paternally expressed in extraembryonic tissues.G9a histone methyltransferase contributes to imprinting in the mouse placenta.Genomic imprinting leads to less selectively maintained polymorphism on X chromosomes.Systems genetics implicates cytoskeletal genes in oocyte control of cloned embryo quality.Nuclear reprogramming of cloned embryos and its implications for therapeutic cloning.Empirical testing of hypotheses about the evolution of genomic imprinting in mammalsComparative 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.Placental dysfunction and fetal programming: the importance of placental size, shape, histopathology, and molecular composition.Syngeneic immune-dependent abortions in mice suggest paternal alloantigen-independent mechanismsHsp90 affecting chromatin remodeling might explain transgenerational epigenetic inheritance in Drosophila.DNA methylation analysis of the mammalian PEG3 imprinted domainApplications of the site-specific recombinase Cre to the study of genomic imprintingMassive deregulation of miRNAs from nuclear reprogramming errors during trophoblast differentiation for placentogenesis in cloned pregnancy.
P2860
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P2860
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
Genomic imprinting in the placenta.
@ast
Genomic imprinting in the placenta.
@en
type
label
Genomic imprinting in the placenta.
@ast
Genomic imprinting in the placenta.
@en
prefLabel
Genomic imprinting in the placenta.
@ast
Genomic imprinting in the placenta.
@en
P2860
P356
P1476
Genomic imprinting in the placenta.
@en
P2093
Wagschal A
P2860
P356
10.1159/000090819
P50
P577
2006-01-01T00:00:00Z