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

f-Block Element-Based MOF Thin Films: A Platform for Luminescence, Sensing, and Energy Applications

基于f区元素的MOF薄膜:用于发光、传感和能源应用的平台

Chen, Dong-Hui; Wöll, Christof

Single-cell sequencing elucidates the mechanism of NUSAP1 in glioma and its diagnostic and prognostic significance.

单细胞测序阐明了 NUSAP1 在胶质瘤中的作用机制及其诊断和预后意义

Zhao Meng-Yu, Shen Zhao-Lei, Dai Hongzhen, Xu Wan-Yan, Wang Li-Na, Gu Yu-, Zhao Jie-Hui, Yu Tian-Hang, Wang Cun-Zhi, Xu Jia-Feng, Chen Guan-Jun, Chen Dong-Hui, Hong Wen-Ming, Zhang Fang

Single-cell sequencing uncovers the mechanistic role of DAPK1 in glioma and its diagnostic and prognostic implications

单细胞测序揭示了DAPK1在胶质瘤中的机制作用及其诊断和预后意义

Yu, Tian-Hang; Ding, Yan-Yu; Zhao, Si-Guo; Zhao, Jie-Hui; Gu, Yu; Chen, Dong-Hui; Zhang, Fang; Hong, Wen-Ming

Vof16-miR-185-5p-GAP43 network improves the outcomes following spinal cord injury via enhancing self-repair and promoting axonal growth

Vof16-miR-185-5p-GAP43 网络通过增强自我修复和促进轴突生长改善脊髓损伤后的结果

Yue Hu, Yi-Fei Sun, Hao Yuan, Jia Liu, Li Chen, Dong-Hui Liu, Yang Xu, Xin-Fu Zhou, Li Ding, Ze-Tao Zhang, Liu-Lin Xiong, Lu-Lu Xue, Ting-Hua Wang

Transcription factor Dmrt1 triggers the SPRY1-NF-κB pathway to maintain testicular immune homeostasis and male fertility

转录因子 Dmrt1 触发 SPRY1-NF-κB 通路维持睾丸免疫稳态和男性生育能力

Meng-Fei Zhang, Shi-Cheng Wan, Wen-Bo Chen, Dong-Hui Yang, Wen-Qing Liu, Ba-Lun Li, Aili Aierken, Xiao-Min Du, Yun-Xiang Li, Wen-Ping Wu, Xin-Chun Yang, Yu-Dong Wei, Na Li, Sha Peng, Xue-Ling Li, Guang-Peng Li, Jin-Lian Hua

Solution Atomic Layer Deposition of Smooth, Continuous, Crystalline Metal-Organic Framework Thin Films

溶液原子层沉积法制备光滑、连续、结晶的金属有机框架薄膜

Barr, Maïssa K S; Nadiri, Soheila; Chen, Dong-Hui; Weidler, Peter G; Bochmann, Sebastian; Baumgart, Helmut; Bachmann, Julien; Redel, Engelbert

Familial Idiopathic Basal Ganglia Calcification: A Father-Son Dyad Demonstrate Heterogeneity of Presentation and Disease Progression

家族性特发性基底节钙化:父子病例显示临床表现和疾病进展的异质性

Zahniser, Evan; Bird, Thomas D; Chen, Dong-Hui; Hu, Shu-Ching; Raskind, Wendy H; Trittschuh, Emily H

Heterozygous STUB1 missense variants cause ataxia, cognitive decline, and STUB1 mislocalization

STUB1 杂合错义变异会导致共济失调、认知能力下降和 STUB1 定位异常。

Chen, Dong-Hui; Latimer, Caitlin; Yagi, Mayumi; Ndugga-Kabuye, Mesaki Kenneth; Heigham, Elyana; Jayadev, Suman; Meabon, James S; Gomez, Christopher M; Keene, C Dirk; Cook, David G; Raskind, Wendy H; Bird, Thomas D

Mutations in the SIGMAR1 gene cause a distal hereditary motor neuropathy phenotype mimicking ALS: Report of two novel variants

SIGMAR1基因突变导致远端遗传性运动神经病表型,类似肌萎缩侧索硬化症(ALS):两种新变异的报告

Ma, Maxwell T; Chen, Dong-Hui; Raskind, Wendy H; Bird, Thomas D

Hyperphosphorylated Tau, Increased Adenylate Cyclase 5 (ADCY5) Immunoreactivity, but No Neuronal Loss in ADCY5-Dyskinesia

ADCY5相关运动障碍中,Tau蛋白过度磷酸化,腺苷酸环化酶5 (ADCY5) 免疫反应性增强,但无神经元丢失。

Chen, Dong-Hui; Latimer, Caitlin S; Spencer, Min; Karna, Prasanthi; Gonzalez-Cuyar, Luis F; Davis, Marie Y; Keene, C Dirk; Bird, Thomas D; Raskind, Wendy H