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

Epilepsy-associated FOXJ3 variants link a transcriptional program of the PTEN-mTOR pathway to neuronal specification and cortical lamination.

与癫痫相关的 FOXJ3 变异将 PTEN-mTOR 通路的转录程序与神经元分化和皮质分层联系起来。

Cheng Haw-Yuan, Liu Chen, Nien Chiao-Wen, Huang Hui-Chin, Zhao Hong-Jun, Nian Fang-Shin, Chen Chien, Custodio Helena Martins, Sisodiya Sanjay M, Lu Chien, Chen Hsin-Hung, Hsu Chih-Sin, Pi Wen-Chieh, Chu Chia-Chi, Hsu Jacob Shu-Jui, Chen Pei-Lung, Chang Fu-Pang, Tung Chien-Yi, Chou Shen-Ju, Alavi Shahryar, Houlden Henry, Chen Wei-Yi, Liu Yo-Tsen, Hou Pei-Shan, Tsai Jin-Wu

Recessive TMEM167A variants cause neonatal diabetes, microcephaly, and epilepsy syndrome

TMEM167A隐性变异会导致新生儿糖尿病、小头畸形和癫痫综合征。

Virgilio, Enrico; Tielens, Sylvia; Bonfield, Georgia; Nian, Fang-Shin; Sawatani, Toshiaki; Vinci, Chiara; Govier, Molly; Montaser, Hossam; Lartigue, Romane; Arunagiri, Anoop; Liboz, Alexandrine; Da Silva, Flavia Natividade; Lytrivi, Maria; Papadopoulou, Theodora; Wakeling, Matthew N; Russ-Silsby, James; Bowman, Pamela; Johnson, Matthew B; Laver, Thomas W; Piron, Anthony; Yi, Xiaoyan; Fantuzzi, Federica; Hendrickx, Sirine; Igoillo-Esteve, Mariana; Santacreu, Bruno J; Suntharesan, Jananie; Ghildiyal, Radha; Hegde, Darshan; Shah, Nikhil; Acar, Sezer; Dönmez, Beyhan Özkaya; Özkan, Behzat; Mohsin, Fauzia; Talaat, Iman M; Abbas, Mohamed Tarek; Abbas, Omar Tarek; Alghamdi, Hamed Ali; Kandemir, Nurgun; Flanagan, Sarah E; Scharfmann, Raphael; Arvan, Peter; Raoux, Matthieu; Nguyen, Laurent; Hattersley, Andrew T; Cnop, Miriam; De Franco, Elisa

How hunger guides new brain cells to their destination

饥饿如何引导新生脑细胞到达目的地

Nian, Fang-Shin; Nguyen, Laurent

Oscillatory DeltaC Expression in Neural Progenitors Primes the Prototype of Forebrain Development

神经祖细胞中振荡性δC表达启动前脑发育原型

Nian, Fang-Shin; Liao, Bo-Kai; Su, Yen-Lin; Wu, Pei-Rong; Tsai, Jin-Wu; Hou, Pei-Shan

Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations

新型无脑畸形相关 NDEL1 变体揭示了 NDE1 和 NDEL1 在核运动和人类皮质畸形中的不同作用

Meng-Han Tsai #, Hao-Chen Ke #, Wan-Cian Lin, Fang-Shin Nian, Chia-Wei Huang, Haw-Yuan Cheng, Chi-Sin Hsu, Tiziana Granata, Chien-Hui Chang, Barbara Castellotti, Shin-Yi Lin, Fabio M Doniselli, Cheng-Ju Lu, Silvana Franceschetti, Francesca Ragona, Pei-Shan Hou, Laura Canafoglia, Chien-Yi Tung, Mei-H

Impairment in dynein-mediated nuclear translocation by BICD2 C-terminal truncation leads to neuronal migration defect and human brain malformation

BICD2 C 端截短导致动力蛋白介导的核转位受损,进而引起神经元迁移缺陷和人脑畸形。

Meng-Han Tsai ,Haw-Yuan Cheng ,Fang-Shin Nian ,Chen Liu ,Nian-Hsin Chao ,Kuo-Liang Chiang ,Shu-Fang Chen ,Jin-Wu Tsai

Rab18 Collaborates with Rab7 to Modulate Lysosomal and Autophagy Activities in the Nervous System: an Overlapping Mechanism for Warburg Micro Syndrome and Charcot-Marie-Tooth Neuropathy Type 2B

Rab18 与 Rab7 协同调节神经系统中的溶酶体和自噬活动:瓦尔堡微综合征和 2B 型夏科-马里-图斯神经病的重叠机制

Fang-Shin Nian, Lei-Li Li, Chih-Ya Cheng, Pei-Chun Wu, You-Tai Lin, Cheng-Yung Tang, Bo-Shiun Ren, Chin-Yin Tai, Ming-Ji Fann, Lung-Sen Kao, Chen-Jee Hong, Jin-Wu Tsai

The clinical value and safety of ECG-gated dipyridamole myocardial perfusion imaging in patients with aortic stenosis

心电门控双嘧达莫心肌灌注显像在主动脉瓣狭窄患者中的临床价值和安全性

Liu, Fang-Shin; Wang, Shan-Ying; Shiau, Yu-Chien; Wu, Yen-Wen

Genes involved in angiogenesis and mTOR pathways are frequently mutated in Asian patients with pancreatic neuroendocrine tumors

在患有胰腺神经内分泌肿瘤的亚洲患者中,参与血管生成和mTOR通路的相关基因经常发生突变。

Wen-Chi Chou ,Po-Han Lin ,Yi-Chen Yeh ,Yi-Ming Shyr ,Wen-Liang Fang ,Shin-E Wang ,Chun-Yu Liu ,Peter Mu-Hsin Chang ,Ming-Han Chen ,Yi-Ping Hung ,Chung-Pin Li ,Yee Chao ,Ming-Huang Chen

Dexamethasone Drug Eluting Nanowafers Control Inflammation in Alkali-Burned Corneas Associated With Dry Eye

地塞米松药物洗脱纳米晶片可控制碱烧伤角膜引起的干眼症炎症

Bian, Fang; Shin, Crystal S; Wang, Changjun; Pflugfelder, Stephen C; Acharya, Ghanashyam; De Paiva, Cintia S