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

KCNB1 mutation impairs neuronal differentiation by disrupting gene expression temporal regulation and neuron-specific pathways.

KCNB1 突变会破坏基因表达的时间调控和神经元特异性通路,从而损害神经元分化。

Guo Yufan, Wu Lifang, Ye Danfeng, Lin Xueting, Jin Yuting, Zhang Chudi, Lou Yuting, Miao Pu, Wang Ye, Zhang Bijun, Feng Jianhua

Single-cell RNA sequencing reveals cell immune status and dysregulated monocytes in patients with myasthenia gravis

单细胞RNA测序揭示重症肌无力患者的细胞免疫状态和单核细胞失调

Guo, Yufan; Gu, Yu; Jin, Yuting; Wu, Xintao; Lou, Yuting; Miao, Pu; Wang, Ye; Zhang, Bijun; Lin, Xueting; Zhang, Chudi; Feng, Jianhua

Novel Loss of Function Variant in SOST From Chinese Family Results in Sclerosteosis 1.

来自中国家族的SOST基因新型功能丧失变异导致骨硬化症1型

Guo Yufan, Wu Xintao, Jin Yuting, Gu Yu, Lou Yuting, Miao Pu, Wang Ye, Zhang Bijun, Lin Xueting, Zhang Chudi, Feng Jianhua

Cell-free fat extract restores hair loss: a novel therapeutic strategy for androgenetic alopecia

无细胞脂肪提取物恢复脱发:雄激素性脱发的新型治疗策略

Yizuo Cai #, Zhuoxuan Jia #, Yichen Zhang, Bijun Kang, Chingyu Chen, Wei Liu, Wei Li, Wenjie Zhang

A novel variant in the FBP1 gene causes fructose-1,6-bisphosphatase deficiency through increased ubiquitination

FBP1 基因中的一种新变体通过增加泛素化导致果糖-1,6-双磷酸酶缺乏

Xiaoyan Liang, Xiaoliang Liu, Wenjing Li, Lu Zhang, Bijun Zhang, Guangrui Lai, Yanyan Zhao

Single-cell transcriptional regulation and genetic evolution of neuroendocrine prostate cancer

神经内分泌前列腺癌的单细胞转录调控和遗传进化

Ziwei Wang, Tao Wang, Danni Hong, Baijun Dong, Yan Wang, Huaqiang Huang, Wenhui Zhang, Bijun Lian, Boyao Ji, Haoqing Shi, Min Qu, Xu Gao, Daofeng Li, Colin Collins, Gonghong Wei, Chuanliang Xu, Hyung Joo Lee, Jialiang Huang, Jing Li

Genetic subtypes and phenotypic characteristics of 110 patients with Prader-Willi syndrome

110例普拉德-威利综合征患者的遗传亚型和表型特征

Zhang, Lu; Liu, Xiaoliang; Zhao, Yunjing; Wang, Qingyi; Zhang, Yuanyuan; Gao, Haiming; Zhang, Bijun; Cui, Wanting; Zhao, Yanyan

Knowledge structure and emerging trends in the application of deep learning in genetics research: A bibliometric analysis [2000-2021]

遗传学研究中深度学习应用的知识结构和新兴趋势:文献计量分析[2000-2021]

Zhang, Bijun; Fan, Ting

Nedd4-2 haploinsufficiency in mice causes increased seizure susceptibility and impaired Kir4.1 ubiquitination

小鼠中 Nedd4-2 单倍体不足导致癫痫易感性增加和 Kir4.1 泛素化受损

Xiaoliang Liu, Hebo Zhang, Bijun Zhang, Jianqiao Tu, Xiaoming Li, Yanyan Zhao

Prenatal diagnosis of auriculocondylar syndrome with a novel missense variant of GNAI3: a case report

GNAI3基因新型错义变异导致耳廓髁综合征的产前诊断:病例报告

Liu, Xiaoliang; Sun, Wei; Wang, Jun; Chu, Guoming; He, Rong; Zhang, Bijun; Zhao, Yanyan