Loss of DNMT1o disrupts imprinted X chromosome inactivation and accentuates placental defects in females.
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Epigenetics: A key paradigm in reproductive healthYou are what you eat: O-linked N-acetylglucosamine in disease, development and epigeneticsEmbryonic loss of human females with partial trisomy 19 identifies region critical for the single active X.Protective Effect of Icariin on the Development of Preimplantation Mouse Embryos against Hydrogen Peroxide-Induced Oxidative Injury.Epigenetic mechanisms underlying learning and the inheritance of learned behaviorsTransient DNMT1 suppression reveals hidden heritable marks in the genomeCOLD-PCR amplification of bisulfite-converted DNA allows the enrichment and sequencing of rare un-methylated genomic regionsA novel role for DNA methyltransferase 1 in regulating oocyte cytoplasmic maturation in pigsNon-germ Line Restoration of Genomic Imprinting for a Small Subset of Imprinted Genes in Ubiquitin-like PHD and RING Finger Domain-Containing 1 (Uhrf1) Null Mouse Embryonic Stem CellsPartial Loss of Genomic Imprinting Reveals Important Roles for Kcnq1 and Peg10 Imprinted Domains in Placental Development.Early Developmental and Evolutionary Origins of Gene Body DNA Methylation Patterns in Mammalian Placentas.Cigarette smoke induces proteasomal-mediated degradation of DNA methyltransferases and methyl CpG-/CpG domain-binding proteins in embryonic orofacial cells.Antagonist Xist and Tsix co-transcription during mouse oogenesis and maternal Xist expression during pre-implantation development calls into question the nature of the maternal imprint on the X chromosome.Global assessment of imprinted gene expression in the bovine conceptus by next generation sequencing.The Role of Maternal-Effect Genes in Mammalian Development: Are Mammalian Embryos Really an Exception?On the potential role of DNMT1 in acute myeloid leukemia and myelodysplastic syndromes: not another mutated epigenetic driver.The loss of imprinted DNA methylation in mouse blastocysts is inflicted to a similar extent by in vitro follicle culture and ovulation induction.Genetic Studies on Mammalian DNA Methyltransferases.Dynamic epigenomic landscapes during early lineage specification in mouse embryos.Aneuploidy: an important model system to understand salient aspects of functional genomics.Compromised oocyte quality and assisted reproduction contribute to sex-specific effects on offspring outcomes and epigenetic patterning.Preimplantation alcohol exposure and developmental programming of FASD: An epigenetic perspective.Genome-Wide Screening of Aberrant Methylation Loci for Nonsyndromic Cleft Lip
P2860
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P2860
Loss of DNMT1o disrupts imprinted X chromosome inactivation and accentuates placental defects in females.
description
2013 nî lūn-bûn
@nan
2013 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Loss of DNMT1o disrupts imprin ...... placental defects in females.
@ast
Loss of DNMT1o disrupts imprin ...... placental defects in females.
@en
type
label
Loss of DNMT1o disrupts imprin ...... placental defects in females.
@ast
Loss of DNMT1o disrupts imprin ...... placental defects in females.
@en
prefLabel
Loss of DNMT1o disrupts imprin ...... placental defects in females.
@ast
Loss of DNMT1o disrupts imprin ...... placental defects in females.
@en
P2093
P2860
P1433
P1476
Loss of DNMT1o disrupts imprin ...... placental defects in females.
@en
P2093
Christoph Plass
Christopher C Oakes
J Richard Chaillet
Jacquetta M Trasler
Josée Martel
M Cecilia Cirio
Pauline de Zeeuw
Winifred Mak
P2860
P304
P356
10.1371/JOURNAL.PGEN.1003873
P577
2013-11-21T00:00:00Z