NLRP7 or KHDC3L genes and the etiology of molar pregnancies and recurrent miscarriage-Reference-Cited by-同舟云学术

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

Published:2013-08-19 Issue:11 Volume:19 Page:773-781
ISSN:1460-2407
Container-title:MHR: Basic science of reproductive medicine
language:en
Short-container-title:

Author:

Andreasen L.,Christiansen O.B.,Niemann I.,Bolund L.,Sunde L.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Obstetrics and Gynecology,Genetics,Molecular Biology,Embryology,Reproductive Medicine

Link

http://academic.oup.com/molehr/article-pdf/19/11/773/13816056/gat056.pdf

Reference40 articles.

1. Mosaic moles and non-familial biparental moles are not caused by mutations in NLRP7, NLRP2 or C6orf221;Andreasen;Mol Hum Reprod,2012

2. Recurrent pregnancy loss: the key potential mechanisms;Baek;Trends Mol Med,2007

3. Gestational trophoblastic disease. Subsequent pregnancy outcome, including repeat molar pregnancy;Berkowitz;J Reprod Med,1998

4. NLRP7 Mutations in women with diploid androgenetic and triploid moles: a proposed mechanism for mole formation;Deveault;Hum Mol Genet,2009

5. Mutations in NLRP7 are associated with diploid biparental hydatidiform moles, but not androgenetic complete moles;Dixon;J Med Genet,2012

Cited by 26 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Clinical Significance of Monogenic Mutations in the Euploid Embryo Genome Associated with Miscarriage;Annals of the Russian academy of medical sciences;2024-06-11

2. Hydatidiform Mole—Between Chromosomal Abnormality, Uniparental Disomy and Monogenic Variants: A Narrative Review;Life;2023-12-10

3. Gestational trophoblastic disease;DiSaia and Creasman Clinical Gynecologic Oncology;2023

4. NLRP7 Mutation in Recurrent Non-familial Molar Pregnancies: A Case Series;Indian Journal of Gynecologic Oncology;2022-11-01

5. Losing the maternal effect gene Nlrp2 alters the ovulated mouse oocytes transcriptome and impacts histone demethylase KDM1B expression;2022-09-16

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