Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.
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Evolution and functional divergence of NLRP genes in mammalian reproductive systemsMutations in NALP12 cause hereditary periodic fever syndromesHorror autoinflammaticus: the molecular pathophysiology of autoinflammatory disease (*)Mapping and identification of candidate loci responsible for Peromyscus hybrid overgrowthMolecular genetic studies of complete hydatidiform molesNOD-Like Receptors in Infection, Immunity, and DiseasesGestational Trophoblastic Disorders: An Update in 2015New insights into establishment and maintenance of DNA methylation imprints in mammalsThe specification of imprints in mammalsImprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted lociA clear and present danger: inflammasomes DAMPing down disorders of pregnancyChromatin regulators of genomic imprintingGenetics and Epigenetics of Recurrent Hydatidiform Moles: Basic Science and Genetic CounsellingThree-dimensional Structure of the NLRP7 Pyrin Domain: INSIGHT INTO PYRIN-PYRIN-MEDIATED EFFECTOR DOMAIN SIGNALING IN INNATE IMMUNITYStructures of the NLRP14 pyrin domain reveal a conformational switch mechanism regulating its molecular interactionsATP binding by NLRP7 is required for inflammasome activation in response to bacterial lipopeptidesNod-like receptors: cytosolic watchdogs for immunity against pathogens.Expression analysis of the NLRP gene family suggests a role in human preimplantation development.Patterns of hybrid loss of imprinting reveal tissue- and cluster-specific regulationGermline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome).Understanding diversity of human innate immunity receptors: analysis of surface features of leucine-rich repeat domains in NLRs and TLRs.Recent evolution of the NF-κB and inflammasome regulating protein POP2 in primatesCharacterisation of marsupial PHLDA2 reveals eutherian specific acquisition of imprinting.Mammalian genomic imprinting.Histopathological diagnosis of hydatidiform mole: contemporary features and clinical implications.Nlrp2, a maternal effect gene required for early embryonic development in the mouseGenetics of gestational trophoblastic neoplasia: an update for the clinician.NLRP7 inter-domain interactions: the NACHT-associated domain is the physical mediator for oligomeric assemblyPre- and postovulatory aging of murine oocytes affect the transcript level and poly(A) tail length of maternal effect genes.A definitive haplotype map as determined by genotyping duplicated haploid genomes finds a predominant haplotype preference at copy-number variation eventsA 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 infertilityInflammasomes and their activation.Deep bisulfite sequencing of aberrantly methylated loci in a patient with multiple methylation defectsDppa3 expression is critical for generation of fully reprogrammed iPS cells and maintenance of Dlk1-Dio3 imprinting.Congenital imprinting disorders: EUCID.net - a network to decipher their aetiology and to improve the diagnostic and clinical careMutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte.Recurrent triploidy due to a failure to complete maternal meiosis II: whole-exome sequencing reveals candidate variantsGenes and Conditions Controlling Mammalian Pre- and Post-implantation Embryo Development.No evidence for pathogenic variants or maternal effect of ZFP57 as the cause of Beckwith-Wiedemann Syndrome
P2860
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P2860
Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.
description
2006 nî lūn-bûn
@nan
2006 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.
@ast
Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.
@en
Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.
@nl
type
label
Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.
@ast
Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.
@en
Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.
@nl
prefLabel
Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.
@ast
Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.
@en
Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.
@nl
P2093
P2860
P356
P1433
P1476
Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.
@en
P2093
Asangla Ao
Batool Mazhar
Bhawna Ratti
Muheiddine Seoud
Rabia Khan
Rashmi Bagga
Renate Kircheisen
Rork Kuick
Samir Hanash
P2860
P2888
P304
P356
10.1038/NG1740
P407
P577
2006-02-05T00:00:00Z
P5875
P6179
1033608183