日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Multi-omics analysis of patient-derived organoids reveals that E3 ligase COP1 promotes liver metastasis and oxaliplatin resistance in colorectal cancer through LUZP1 degradation and MYL9 phosphorylation

对患者来源类器官的多组学分析表明,E3连接酶COP1通过LUZP1降解和MYL9磷酸化促进结直肠癌的肝转移和奥沙利铂耐药性。

Zhang, Ruijia; Luo, Wenqin; Zhou, Qikai; Liang, Dongguo; Hao, Yuankai; Chen, Fan; Qiu, Yulin; Cao, Yixian; Shan, Zezhi; Zhang, Yu; Li, Qingguo; Cai, Sanjun; Luo, Dakui; Mo, Shaobo; Ma, Bin; Li, Xinxiang

NF‑κB‑driven LUZP1 promotes metastasis and chemoresistance in head and neck squamous cell carcinoma

NF-κB驱动的LUZP1促进头颈部鳞状细胞癌的转移和化疗耐药性

Lin, Chen-Yuan; Hsieh, Ching-Yun; Lan, Hsin-Chi; Lin, Ching-Chan; Chen, Tzu-Ting; Tseng, Wei-Chi; Tsou, Yung-An; Chang, Wei-Chao

Abnormal zona pellucida and follicular development in ZP1-mutant macaques

ZP1 突变猕猴的透明带和卵泡发育异常

Wei Meng,Bao-Zhen Liu,Dan Huang,Yu-Tao Fan,Cheng-Gang Xiong,Ying-Ting Zhang,Lei-Lei Zhao,Yong-Long Guo,Mu-Hua Lai,Xin-Yuan Zhao,Ya-Qing Li,Shi-Kun Zhao,Jing-Tao Zeng,Chuan-He Liu,Ji-Long Liu,Chen-Hui Ding,Shi-Hua Yang

LUZP1 regulates the maturation of contractile actomyosin bundles

LUZP1 调控收缩性肌动蛋白束的成熟

Liang Wang,Hoi Ying Tsang,Ziyi Yan,Sari Tojkander,Katarzyna Ciuba,Konstantin Kogan,Xiaonan Liu,Hongxia Zhao

ZP1-Y262C mutation causes abnormal zona pellucida formation and female infertility in humans

ZP1-Y262C 突变导致人类透明带形成异常和女性不孕

Guangyi Cao #, Lina Yu #, Junshun Fang #, Ruixin Shi, Huijun Li, Feifei Lu, Xiaoyue Shen, Xiangyu Zhu, Shanshan Wang, Na Kong

A new negative link in flower development: Repression of ABC genes by Z factors-ZP1/ZFP8

花发育中一个新的负调控环节:Z因子-ZP1/ZFP8对ABC基因的抑制作用

Riechmann, José Luis

A recurrent ZP1 variant is responsible for oocyte maturation defect with degenerated oocytes in infertile females

一种反复出现的ZP1变异是导致卵母细胞成熟缺陷和不孕女性卵母细胞退化的原因。

Loeuillet, Corinne; Dhellemmes, Magali; Cazin, Caroline; Kherraf, Zine-Eddine; Fourati Ben Mustapha, Selima; Zouari, Raoudha; Thierry-Mieg, Nicolas; Arnoult, Christophe; Ray, Pierre F

A novel homozygous nonsense mutation in zona pellucida 1 (ZP1) causes human female empty follicle syndrome

透明带 1 (ZP1) 的新型纯合无义突变导致人类女性空卵泡综合征

Jing Wang #, Xiaoyu Yang #, Xueping Sun, Long Ma, Yaoxue Yin, Guoxiang He, Yuan Zhang, Jie Zhou, Lingbo Cai, Jiayin Liu, Xiang Ma

Homozygous Splice Site Mutation in ZP1 Causes Familial Oocyte Maturation Defect

ZP1基因纯合剪接位点突变导致家族性卵母细胞成熟缺陷

Okutman, Özlem; Demirel, Cem; Tülek, Firat; Pfister, Veronique; Büyük, Umut; Muller, Jean; Charlet-Berguerand, Nicolas; Viville, Stéphane

Novel biallelic loss-of-function variants in ZP1 identified in an infertile female with empty follicle syndrome

在一名患有空卵泡综合征的不孕女性中发现了ZP1基因中新的双等位基因功能缺失变异。

Liu, Mohan; Shen, Ying; Zhang, Xueguang; Wang, Xiang; Li, Dan; Wang, Yan