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

Mechanism of Non-Small Cell Lung Cancer-Derived Extracellular Vesicle miRNA hsa-let-7b-5p Targeting AP1S1 to Regulate M2 Macrophage Polarization

非小细胞肺癌来源的细胞外囊泡 miRNA hsa-let-7b-5p 靶向 AP1S1 调控 M2 巨噬细胞极化的机制

Liu, Lijuan; Kou, Zixing; Wang, Tianhua; Shang, Qihang; Zhang, Qinxiang; Liu, Guanghui; Ai, Jing; Zhao, Yanwen; Sun, Changgang

Ap1s1 reduction in the aging brain heightens neuronal vulnerability to amyloid-β and oxidative stress in Alzheimer's pathogenesis.

衰老大脑中 Ap1s1 的减少会加剧阿尔茨海默病发病机制中神经元对淀粉样蛋白-β 和氧化应激的脆弱性。

Yang Xuehan, Geng Xinru, Xu Zhuoyan, Xu Yang, Han Hao, Zhang Qiang, Jin Honglian, Wang Yuxin, Sun Bin, Zhang Ming, Zhang Siwei, Chen Li

Feeding-Triggered Seizures in a Newborn with AP1S1-Related MEDNIK Syndrome: Expanding the Phenotype of a Hyper-Rare Disease

AP1S1相关MEDNIK综合征新生儿喂养诱发性癫痫:拓展一种超罕见疾病的表型

Cavalli, Anna; Peluso, Francesca; Frattini, Daniele; Cesaroni, Carlo Alberto; Bondi, Carolina; Malmusi, Giovanni; Peruzzi, Adelaide; Rizzi, Susanna; Pantani, Agnese; Trimarchi, Gabriele; Melli, Nives; Novelli, Antonio; Zuntini, Roberta; Gargano, Giancarlo; Garavelli, Livia; Fusco, Carlo

IDEDNIK syndrome: a newly recognized rare genetic disorder caused by AP1S1 and AP1B1 mutations

IDEDNIK综合征:一种新近发现的罕见遗传性疾病,由AP1S1和AP1B1基因突变引起

Wu, Rong; Luo, Xingguang; Wang, Xiao-Ping

Clinical and Genetic Functional Validation of a Novel AP1S1 Mutation Causing MEDNIK Syndrome

对导致MEDNIK综合征的新型AP1S1突变进行临床和遗传功能验证

Duan, Lifen; Shen, Ru; Yin, Guoyan; Tao, Ruixi; Zhang, Yi; Yu, Wei; Bao, Lishimeng; Ye, Weitao; Yin, Runxiu; Tian, Xin

Revising pathogenesis of AP1S1-related MEDNIK syndrome: a missense variant in the AP1S1 gene as a causal genetic lesion

修正AP1S1相关MEDNIK综合征的发病机制:AP1S1基因中的错义变异是致病基因病变

Rackova, Marketa; Mattera, Rafael; Svaton, Michael; Fencl, Filip; Kanderova, Veronika; Spicakova, Karolina; Park, Sang Yoon; Fabian, Ondrej; Koblizek, Miroslav; Fronkova, Eva; Bonifacino, Juan S; Skvarova Kramarzova, Karolina

Oligomer-to-monomer transition underlies the chaperone function of AAGAB in AP1/AP2 assembly

低聚物到单体的转变是 AAGAB 在 AP1/AP2 组装中发挥伴侣作用的基础

Yuan Tian, Ishara Datta, Rui Yang, Chun Wan, Bing Wang, Lauren Crisman, Huan He, Chad A Brautigam, Suzhao Li, Jingshi Shen, Qian Yin

The Overexpression and Clinical Significance of AP1S1 in Breast Cancer

AP1S1在乳腺癌中的过表达及其临床意义

Zheng, Danni; Fu, Weida; Jin, Lingli; Jiang, Xiaofang; Jiang, Wenjie; Guan, Yaoyao; Hao, Rutian

The Single Nucleotide Polymorphisms of AP1S1 are Associated with Risk of Esophageal Squamous Cell Carcinoma in Chinese Population

AP1S1单核苷酸多态性与中国人群食管鳞状细胞癌风险相关

Su, Feng; Fang, Yong; Yu, Jinjie; Jiang, Tian; Lin, Siyun; Zhang, Shaoyuan; Lv, Lu; Long, Tao; Pan, Huiwen; Qi, Junqing; Zhou, Qiang; Tang, Weifeng; Ding, Guowen; Wang, Liming; Tan, Lijie; Yin, Jun