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

Linking kinetochore attachment to checkpoint control: the role of Aurora B in BubR1 acetylation.

将动粒附着与检查点控制联系起来:Aurora B 在 BubR1 乙酰化中的作用。

The BUB1 and BUBR1 paralogs scaffold the kinetochore fibrous corona

BUB1 和 BUBR1 旁系同源基因构成着丝粒纤维冠的支架。

Cmentowski, Verena; Musacchio, Andrea

UBR1 Promotes Sex-Dependent ACE2 Ubiquitination in Hypertension

UBR1促进高血压中性别依赖性的ACE2泛素化

Elgazzaz, Mona; Lakkappa, Navya; Berdasco, Clara; Mohan, Uma Priya; Nuzzo, Anna; Restivo, Luke; Martinez, Alexa; Scarborough, Amy; Guidry, Jessie J; Sriramula, Srinivas; Xu, Jiaxi; Daoud, Hisham; Mendiola Plá, Michelle A; Bowles, Dawn E; Beyer, Andreas M; Mauvais-Jarvis, Franck; Yue, Xinping; Filipeanu, Catalin M; Lazartigues, Eric

An alternative pocket for binding the N-degrons by the UBR1 and UBR2 ubiquitin E3 ligases

UBR1和UBR2泛素E3连接酶结合N-降解子的另一种口袋

Huang, Shih-Ting; Chen, Dai-Hua; Ren, Tianchen; Thomas, Nicole; Wu, Jian; Sankaran, Banumathi; Jones, Renee; Taylor, Susan; Chen, Yuan

Sod1 deficiency in mouse oocytes during in vitro maturation increases chromosome segregation errors with a reduced BUBR1 at kinetochore

小鼠卵母细胞体外成熟过程中Sod1缺陷会导致染色体分离错误增加,并伴有着丝粒处BUBR1减少。

Nago, Mitsuru; Yanai, Masumi; Ishii, Mika; Sato, Yasuko; Odajima, Kazuharu; Kimura, Naoko

Pathogenic variants of BUB1 and BUBR1 genes are not prioritized in screening tests of couples with aborted aneuploid fetuses

在对流产的非整倍体胎儿夫妇进行筛查时,BUB1 和 BUBR1 基因的致病性变异并非优先检测项目。

Gorji, Raziyeh; Borjian-Boroujeni, Parnaz; Bazrgar, Masood

A conserved CENP-E region mediates BubR1-independent recruitment to the outer corona at mitotic onset

保守的CENP-E区域介导有丝分裂开始时BubR1非依赖性的蛋白募集至外冠状层。

Jeraldine Weber ,Thibault Legal ,Alicia Perez Lezcano ,Agata Gluszek-Kustusz ,Calum Paterson ,Susana Eibes ,Marin Barisic ,Owen R Davies ,Julie P I Welburn

UBR1 promotes anaplastic thyroid carcinoma progression via stabilizing YAP through monoubiquitylation

UBR1 通过单泛素化稳定 YAP 促进未分化甲状腺癌进展

Min Xia #, Chen Liang #, Yu Yuan, Jiang Luo, Yuxin Zeng, Mini Zhang, Jiawen Tang, Ziyu Jiang, Yan Gong, Conghua Xie

Johanson-Blizzard syndrome caused by novel UBR1 mutation in four Saudi patients

四名沙特阿拉伯患者因UBR1基因新突变而患上约翰逊-布利扎德综合征

Noli, Khalid; Aleysae, Nabil; Alzahrani, Ismail; Al-Ghamdi, Ahmed; Alkazmi, Mohammed; Almasoudi, Ahmed

E3-ubiquitin ligase, FBXW7 regulates mitotic progression by targeting BubR1 for ubiquitin-mediated degradation

E3泛素连接酶FBXW7通过靶向BubR1进行泛素介导的降解来调控有丝分裂进程。

Vishnu M Nair ,Amit Santhu Sabu ,Ahmed Hussain ,Delvin P Kombarakkaran ,R Bhagya Lakshmi ,Tapas K Manna