Loss of GM130 does not impair oocyte meiosis and embryo development in mice-Reference-Cited by-同舟云学术

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Loss of GM130 does not impair oocyte meiosis and embryo development in mice

Published:2020-11 Issue:3 Volume:532 Page:336-340
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Jiang Yonghui^ORCID,Liu Yue,Han Feng,Zhou Jingjing,Zhang Xinze,Xu Junting,Yu Zhiheng,Zhao Shigang^ORCID,Gao Fei,Zhao Han

Funder

National Natural Science Foundation of China

Key Research and Development Program of Shandong Province

National Natural Science Foundation of Shandong Province

innovative research team of high-level local universities in Shanghai

The Fundamental Research Funds of Shandong University

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference31 articles.

1. The Golgi ribbon: mechanisms of maintenance and disassembly during the cell cycle;Ayala;Biochem. Soc. Trans.,2020

2. Golgi structure formation, function, and post-translational modifications in mammalian cells;Huang;F1000Res,2017

3. Golgi dynamics during meiosis are distinct from mitosis and are coupled to endoplasmic reticulum dynamics until fertilization;Payne;Dev. Biol.,2003

4. Dynamic changes of the Golgi apparatus during bovine in vitro oocyte maturation;Racedo;Reproduction,2012

5. Emerging new roles of GM130, a cis-Golgi matrix protein, in higher order cell functions;Nakamura;J. Pharmacol. Sci.,2010

Cited by 4 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. Aluminum exposure impairs oocyte quality via subcellular structure disruption and DNA damage-related apoptosis in mice;Journal of Environmental Sciences;2024-05

2. BCAS2 regulates oocyte meiotic prophase I by participating in mRNA alternative splicing;The FASEB Journal;2023-12-12

3. Bi‐allelic loss of function variants in GOLGA2 are associated with a complex neurological phenotype: Report of a second family;Clinical Genetics;2021-08-29

4. Molecular characterization of the Yp11.2 region deletion in the Chinese Han population;International Journal of Legal Medicine;2021-04-26

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