Associated Papers
Genetic screening of Chinese patients with hydatidiform mole by whole-exome sequencing and comprehensive analysis.
Yang J et al.
Journal of Assisted Reproduction and Genetics, 2022
DNA Methylation Dynamics in the Female Germline and Maternal-Effect Mutations That Disrupt Genomic Imprinting.
Anvar Z et al.
Genes, 2021
NLRP7: From inflammasome regulation to human disease.
Carriere J et al.
Immunology, 2021
Abnormal processing of IL-1β in NLRP7-mutated monocytes in hydatidiform mole patients.
Zhang P et al.
Clinical and Experimental Immunology, 2020
No evidence for mutations in NLRP7, NLRP2 or KHDC3L in women with unexplained recurrent pregnancy loss or infertility.
Aghajanova L et al.
Human Reproduction (oxford, England), 2015
No evidence for mutations in NLRP7 and KHDC3L in women with androgenetic hydatidiform moles.
Mahadevan S et al.
Prenatal Diagnosis, 2013
NLRP7 mutation analysis in sporadic hydatidiform moles in Tunisian patients: NLRP7 and sporadic mole.
Landolsi H et al.
Archives of Pathology & Laboratory Medicine, 2012
The genetics of recurrent hydatidiform moles in China: correlations between NLRP7 mutations, molar genotypes and reproductive outcomes.
Qian J et al.
Molecular Human Reproduction, 2011
NLRP7 in the spectrum of reproductive wastage: rare non-synonymous variants confer genetic susceptibility to recurrent reproductive wastage.
Messaed C et al.
Journal of Medical Genetics, 2011
[Family pedigree analysis in family member with history of hydatidiform mole and the NLRP7 gene expression].
Li Y et al.
Zhonghua Fu Chan Ke Za Zhi, 2011
NLRP7 mutations in women with diploid androgenetic and triploid moles: a proposed mechanism for mole formation.
Deveault C et al.
Human Molecular Genetics, 2009
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