A novel gene mutation in ZP3 loop region identified in patients with empty follicle syndrome-Reference-Cited by-同舟云学术

A novel gene mutation in ZP3 loop region identified in patients with empty follicle syndrome

Published:2021-12-19 Issue:2 Volume:43 Page:180-188
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Zhang Zhiqiang¹^ORCID,Guo Qi¹,Jia Lei¹,Zhou Chuanchuan¹,He Shujing¹,Fang Cong¹,Zhang Minfang¹,Sun Peng¹,Zeng Zhi¹,Wang Meng¹,Wang Dandan¹,Liang Xiaoyan¹

Affiliation:

1. Department of Gynaecology and Obstetrics, Center of Reproductive Medicine, The Sixth Affiliated Hospital Sun Yat‐sen University Guangzhou China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.24297

Reference36 articles.

1. Structure and function of the zona pellucida: Identification and characterization of the proteins of the mouse oocyte's zona pellucida

2. Structure of Zona Pellucida Module Proteins

3. A large domain common to sperm receptors (Zp2 and Zp3) and TGF-β type III receptor

4. Heterozygous mutations in ZP1 and ZP3 cause formation disorder of ZP and female infertility in human

5. A Recurrent Missense Mutation in ZP3 Causes Empty Follicle Syndrome and Female Infertility

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1. ZP2 cleavage blocks polyspermy by modulating the architecture of the egg coat;Cell;2024-03

2. Case report: A novel homozygous variant in ZP3 is associated with human empty follicle syndrome;Frontiers in Genetics;2023-10-16

3. Architecture of the vertebrate egg coat and structural basis of the ZP2 block to polyspermy;2023-06-22

4. Novel variants in ZP1, ZP2 and ZP3 associated with empty follicle syndrome and abnormal zona pellucida;Reproductive BioMedicine Online;2023-05

5. Integrative analyses of the mRNA expression profile reveal the involvement of STC1 in chicken folliculogenesis;Journal of Animal Science;2023-01-01