Van den Veyver IB

No ORCID on file · 3 papers in corpus · active 2015-2021

Condition tags

  • infertility 1
2021
Reproductive Outcomes from Maternal Loss of Nlrp2 Are Not Improved by IVF or Embryo Transfer Consistent with Oocyte-Specific Defect.
Reproductive sciences (Thousand Oaks, Calif.) ·doi:10.1007/s43032-020-00360-x

Nlrp2 encodes a protein of the oocyte subcortical maternal complex (SCMC), required for embryo development. We previously showed that loss of maternal Nlrp2 in mice causes subfertility, smaller litters with birth defects, and growth abnorma…

2015
A genome-wide screen for copy number alterations in an adolescent pilot cohort with müllerian anomalies.
Fertility and sterility ·doi:10.1016/j.fertnstert.2014.10.044

ObjectiveTo examine whether pathogenic copy number changes (CNCs) can be identified in deoxyribonucleic acid from females with different classes of müllerian anomalies.DesignWe conducted array-based copy number variant (CNV) analysis using …

2015
No evidence for mutations in NLRP7, NLRP2 or KHDC3L in women with unexplained recurrent pregnancy loss or infertility.
Human reproduction (Oxford, England) ·doi:10.1093/humrep/deu296

Study questionAre mutations in NLRP2/7 (NACHT, LRR and PYD domains-containing protein 2/7) or KHDC3L (KH Domain Containing 3 Like) associated with recurrent pregnancy loss (RPL) or infertility?Summary answerWe found no evidence for mutation…