A global disorder of imprinting in the human female germ line.
about
The DNA methyltransferase-like protein DNMT3L stimulates de novo methylation by Dnmt3aMapping and identification of candidate loci responsible for Peromyscus hybrid overgrowthLack of involvement of known DNA methyltransferases in familial hydatidiform mole implies the involvement of other factors in establishment of imprinting in the human female germlineGestational Trophoblastic Disorders: An Update in 2015Bisphenol A Effects on Mammalian Oogenesis and Epigenetic Integrity of Oocytes: A Case Study Exploring Risks of Endocrine Disrupting ChemicalsGenetics and Epigenetics of Recurrent Hydatidiform Moles: Basic Science and Genetic CounsellingGenomic imprinting and epigenetic reprogramming: unearthing the garden of forking pathsIdentification of the control region for tissue-specific imprinting of the stimulatory G protein alpha-subunitEssential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprintingMammalian-specific genomic functions: Newly acquired traits generated by genomic imprinting and LTR retrotransposon-derived genes in mammalsGenome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genesMaternally expressed NLRP2 links the subcortical maternal complex (SCMC) to fertility, embryogenesis and epigenetic reprogramming.Patterns of hybrid loss of imprinting reveal tissue- and cluster-specific regulationPathogenic variant in NLRP7 (19q13.42) associated with recurrent gestational trophoblastic disease: Data from early embryo development observed during in vitro fertilizationCharacterisation of marsupial PHLDA2 reveals eutherian specific acquisition of imprinting.Histopathological diagnosis of hydatidiform mole: contemporary features and clinical implications.Genetics of gestational trophoblastic neoplasia: an update for the clinician.The imprinted brain: how genes set the balance between autism and psychosis.Aberrant growth and pattern formation in Peromyscus hybrid placental development.Future potential of the Human Epigenome Project.A novel approach identifies new differentially methylated regions (DMRs) associated with imprinted genesNo evidence for mutations in NLRP7, NLRP2 or KHDC3L in women with unexplained recurrent pregnancy loss or infertilityDeep bisulfite sequencing of aberrantly methylated loci in a patient with multiple methylation defectsRegulation of imprinting: A multi-tiered process.Epigenetic properties and identification of an imprint mark in the Nesp-Gnasxl domain of the mouse Gnas imprinted locus.Derivation of primordial germ cells from human embryonic and induced pluripotent stem cells is significantly improved by coculture with human fetal gonadal cells.Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte.Mosaics and moles.Loss of non-coding RNA expression from the DLK1-DIO3 imprinted locus correlates with reduced neural differentiation potential in human embryonic stem cell lines.Clinical aspects of gestational trophoblastic disease: a review based partly on 25-year experience of a statewide registry.Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans.Gametes and embryo epigenetic reprogramming affect developmental outcome: implication for assisted reproductive technologies.Absence of Maternal Methylation in Biparental Hydatidiform Moles from Women with NLRP7 Maternal-Effect Mutations Reveals Widespread Placenta-Specific Imprinting.Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS.The PcG gene Sfmbt2 is paternally expressed in extraembryonic tissues.Complementation hypothesis: the necessity of a monoallelic gene expression mechanism in mammalian development.Intracytoplasmic sperm injection--an assisted reproduction technique that should make us cautious about imprinting deregulation.The hydatidiform mole.Paternal Hemizygosity in 11p15 in Mole-like Conceptuses: Two Case Reports.Report of four new patients with protein-truncating mutations in C6orf221/KHDC3L and colocalization with NLRP7
P2860
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P2860
A global disorder of imprinting in the human female germ line.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh
2002年學術文章
@zh-hant
name
A global disorder of imprinting in the human female germ line.
@en
A global disorder of imprinting in the human female germ line.
@en-gb
A global disorder of imprinting in the human female germ line.
@nl
type
label
A global disorder of imprinting in the human female germ line.
@en
A global disorder of imprinting in the human female germ line.
@en-gb
A global disorder of imprinting in the human female germ line.
@nl
prefLabel
A global disorder of imprinting in the human female germ line.
@en
A global disorder of imprinting in the human female germ line.
@en-gb
A global disorder of imprinting in the human female germ line.
@nl
P2093
P2860
P356
P1433
P1476
A global disorder of imprinting in the human female germ line.
@en
P2093
Bruce E Hayward
Eamonn Sheridan
Hannah Judson
P2860
P2888
P304
P356
10.1038/416539A
P407
P5530
P577
2002-04-01T00:00:00Z
P5875
P6179
1051945129