nlrp7

Louise E Docherty Faisal I Rezwan Rebecca L Poole Claire L S Turner Emma Kivuva Eamonn R Maher Sarah F Smithson Julian P Hamilton-Shield Michal Patalan Maria Gizewska Jaroslaw Peregud-Pogorzelski Jasmin Beygo Karin Buiting Bernhard Horsthemke Lukas Soellner Matthias Begemann Thomas Eggermann Emma Baple Sahar Mansour I Karen Temple Deborah J G Mackay

Human-imprinting disorders are congenital disorders of growth, development and metabolism, associated with disturbance of parent of origin-specific DNA methylation at imprinted loci across the genome. Some imprinting disorders have higher than expected prevalence of monozygotic twinning, of assisted reproductive technology among parents, and of disturbance of multiple imprinted loci, for which ...

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A genetic association study of NLRP2 and NLRP7 genes in idiopathic recurrent miscarriage

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

Live births in women with recurrent hydatidiform mole and two NLRP7 mutations

NLRP7 and the Genetics of Hydatidiform Moles: Recent Advances and New Challenges

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

NLRP7 or KHDC3L genes and the etiology of molar pregnancies and recurrent miscarriage

Mutations in NLRP5 are associated with reproductive wastage and multi-locus imprinting disorders in humans

ATP binding by NLRP7 is required for inflammasome activation in response to bacterial lipopeptides

No evidence for mutations in NLRP7 and KHDC3L in women with androgenetic hydatidiform moles

NLRP7 inter-domain interactions: the NACHT-associated domain is the physical mediator for oligomeric assembly