Absence of Maternal Methylation in Biparental Hydatidiform Moles from Women with NLRP7 Maternal-Effect Mutations Reveals Widespread Placenta-Specific Imprinting. (Q36257278)

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English	Absence of Maternal Methylation in Biparental Hydatidiform Moles from Women with NLRP7 Maternal-Effect Mutations Reveals Widespread Placenta-Specific Imprinting.	scientific article

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29 February 2020

Absence of Maternal Methylation in Biparental Hydatidiform Moles from Women with NLRP7 Maternal-Effect Mutations Reveals Widespread Placenta-Specific Imprinting (English)

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29 February 2020

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29 February 2020

Marta Sanchez-Delgado

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29 February 2020

Isabel Iglesias-Platas

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29 February 2020

Rosemary A Fisher

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29 February 2020

author name string

Alejandro Martin-Trujillo

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Chiharu Tayama

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29 February 2020

Enrique Vidal

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29 February 2020

Nandita Deo

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Olivia Barney

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Ken Maclean

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29 February 2020

Kenichiro Hata

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29 February 2020

Kazuhiko Nakabayashi

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29 February 2020

David Monk

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publication date

6 November 2015

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29 February 2020

e1005644

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29 February 2020

copyright license

Creative Commons Attribution 4.0 International

6 November 2015

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April 2022 Public Data File from Crossref

copyright status

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NLRP7, Involved in Hydatidiform Molar Pregnancy (HYDM1), Interacts with the Transcriptional Repressor ZBTB16.

1 reference

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Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta

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C19MC microRNAs regulate the migration of human trophoblasts

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The Gpr1/Zdbf2 locus provides new paradigms for transient and dynamic genomic imprinting in mammals

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Genetics and Epigenetics of Recurrent Hydatidiform Moles: Basic Science and Genetic Counselling

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Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment

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NLRP7 affects trophoblast lineage differentiation, binds to overexpressed YY1 and alters CpG methylation

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Epigenetic and transcriptional features of the novel human imprinted lncRNA GPR1AS suggest it is a functional ortholog to mouse Zdbf2linc

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The ontogeny of cKIT+ human primordial germ cells proves to be a resource for human germ line reprogramming, imprint erasure and in vitro differentiation.

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Report of four new patients with protein-truncating mutations in C6orf221/KHDC3L and colocalization with NLRP7

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Cytochrome P450 subfamily 2J polypeptide 2 expression and circulating epoxyeicosatrienoic metabolites in preeclampsia

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The genetics of gestational trophoblastic disease: a rare complication of pregnancy

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Soluble THSD7A is an N-glycoprotein that promotes endothelial cell migration and tube formation in angiogenesis

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NLRP7, a nucleotide oligomerization domain-like receptor protein, is required for normal cytokine secretion and co-localizes with Golgi and the microtubule-organizing center

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Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte

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Genome-wide mapping of imprinted differentially methylated regions by DNA methylation profiling of human placentas from triploidies

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5-Hydroxymethylcytosine in the mammalian zygote is linked with epigenetic reprogramming

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The primate-specific microRNA gene cluster (C19MC) is imprinted in the placenta

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A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints

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Expression analysis of the NLRP gene family suggests a role in human preimplantation development

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A recurrent intragenic genomic duplication, other novel mutations in NLRP7 and imprinting defects in recurrent biparental hydatidiform moles

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30 September 2017

NLRP7 and KHDC3L, the two maternal-effect proteins responsible for recurrent hydatidiform moles, co-localize to the oocyte cytoskeleton

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Mutations in NLRP7 are associated with diploid biparental hydatidiform moles, but not androgenetic complete moles.

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Methylation screening of reciprocal genome-wide UPDs identifies novel human-specific imprinted genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/26544189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide allelic methylation analysis reveals disease-specific susceptibility to multiple methylation defects in imprinting syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/26544189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1371/JOURNAL.PGEN.1005644

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29 February 2020

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29 February 2020

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29 February 2020

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