No evidence for mutations in NLRP7, NLRP2 or KHDC3L in women with unexplained recurrent pregnancy loss or infertility

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

(2013) Sangeetha Mahadevan et al.   HUMAN MOLECULAR GENETICS

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

(2013) Jyun-Yuan Huang et al.   HUMAN REPRODUCTION

NLRP7 and related inflammasome activating pattern recognition receptors and their function in host defense and disease

(2013) Alexander D. Radian et al.   MICROBES AND INFECTION

Maternal NLRP7 and C6orf221 variants are not a common risk factor for androgenetic moles, triploidy and recurrent miscarriage

(2013) I. Manokhina et al.   MOLECULAR HUMAN REPRODUCTION

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

(2013) L. Andreasen et al.   MOLECULAR HUMAN REPRODUCTION

The p.L750V mutation in theNLRP7gene is frequent in Mexican patients with recurrent molar pregnancies and is not associated with recurrent pregnancy loss

(2013) Higinio Estrada et al.   PRENATAL DIAGNOSIS

No evidence for mutations inNLRP7andKHDC3Lin women with androgenetic hydatidiform moles

(2013) Sangeetha Mahadevan et al.   PRENATAL DIAGNOSIS

Genetic Polymorphisms and Recurrent Spontaneous Abortions: An Overview of Current Knowledge

(2012) Silvia Daher et al.   AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY

NLRP7Mutation Analysis in Sporadic Hydatidiform Moles in Tunisian Patients:NLRP7and Sporadic Mole

(2012) Hanène Landolsi et al.   ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE

Genetic Factors as a Cause of Miscarriage

(2012) N. Suzumori et al.   CURRENT MEDICINAL CHEMISTRY

Mutations inNLRP7are associated with diploid biparental hydatidiform moles, but not androgenetic complete moles

(2012) Peter H Dixon et al.   JOURNAL OF MEDICAL GENETICS

Mosaic moles and non-familial biparental moles are not caused by mutations in NLRP7, NLRP2 or C6orf221

(2012) L. Andreasen et al.   MOLECULAR HUMAN REPRODUCTION

Genetics of Recurrent Miscarriage: Challenges, Current Knowledge, Future Directions

(2012) Kristiina Rull et al.   Frontiers in Genetics

Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte

(2011) David A. Parry et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The spectrum of NLRP7 mutations in French patients with recurrent hydatidiform mole

(2011) Joël Muhlstein et al.   European Journal of Obstetrics & Gynecology and Reproductive Biology

Genetic association studies of angiogenesis- and vasoconstriction-related genes in women with recurrent pregnancy loss: a systematic review and meta-analysis

(2011) Mei-Tsz Su et al.   HUMAN REPRODUCTION UPDATE

NLRP7 in the spectrum of reproductive wastage: rare non-synonymous variants confer genetic susceptibility to recurrent reproductive wastage

(2011) C. Messaed et al.   JOURNAL OF MEDICAL GENETICS

The genetics of recurrent hydatidiform moles in China: correlations between NLRP7 mutations, molar genotypes and reproductive outcomes

(2011) JianHua Qian et al.   MOLECULAR HUMAN REPRODUCTION

NLR functions beyond pathogen recognition

(2011) Thomas A Kufer et al.   NATURE IMMUNOLOGY

Recurrent triploid and dispermic conceptions in patients with NLRP7 mutations

(2011) R. Slim et al.   PLACENTA

Tissue Factor and Tissue Factor Pathway Inhibitors TFPI and TFPI2 in Human Secretory Endometrium—Possible Link to Female Infertility

(2011) Signe Altmäe et al.   Reproductive Sciences

Recurrent first trimester pregnancy loss: revised definitions and novel causes

(2011) Jana L Allison et al.   Current Opinion in Endocrinology Diabetes and Obesity

Fertility treatments and outcomes among couples seeking fertility care: data from a prospective fertility cohort in the United States

(2010) James F. Smith et al.   FERTILITY AND STERILITY

Maternal-effect gene Ces5/Ooep/Moep19/Floped is essential for oocyte cytoplasmic lattice formation and embryonic development at the maternal-zygotic stage transition

(2010) Fumi Tashiro et al.   GENES TO CELLS

Aromatase gene (CYP19A1) variants, female infertility and ovarian stimulation outcome: a preliminary report

(2010) Signe Altmäe et al.   REPRODUCTIVE BIOMEDICINE ONLINE

Variation in Hyaluronan-Binding Protein 2 (HABP2) Promoter Region is Associated With Unexplained Female Infertility

(2010) Signe Altmäe et al.   Reproductive Sciences

Gene Birth, Death, and Divergence: The Different Scenarios of Reproduction-Related Gene Evolution1

(2009) Xin Tian et al.   BIOLOGY OF REPRODUCTION

Evolution and functional divergence of NLRP genes in mammalian reproductive systems

(2009) Xin Tian et al.   BMC EVOLUTIONARY BIOLOGY

Association study of AMH and AMHRII polymorphisms with unexplained infertility

(2009) Chiara Rigon et al.   FERTILITY AND STERILITY

Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region

(2009) C M Wang et al.   JOURNAL OF MEDICAL GENETICS

Endometrial gene expression analysis at the time of embryo implantation in women with unexplained infertility

(2009) S. Altmae et al.   MOLECULAR HUMAN REPRODUCTION

Germline Mutation in NLRP2 (NALP2) in a Familial Imprinting Disorder (Beckwith-Wiedemann Syndrome)

(2009) Esther Meyer et al.   PLoS Genetics

Expression Analysis of the NLRP Gene Family Suggests a Role in Human Preimplantation Development

(2008) Pu Zhang et al.   PLoS One

Uterine receptivity to human embryonic implantation: Histology, biomarkers, and transcriptomics

(2007) L. Aghajanova et al.   SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY