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

USP30-AS1 functions as a post-transcriptional amplifier of interferon signalling to drive autoimmune pathogenesis

USP30-AS1作为干扰素信号的转录后放大器,驱动自身免疫发病机制。

Pan, Jie; Feng, Min-Yi; Xia, Tian; Jiang, Shuai; Zhu, Peng-Peng; Yu, Xi-Ping; Su, Zhi-Hui; Liu, Yu; Wu, Jia-Qi; Zhao, Ming; Li, Tao; Xue, Wen; Yu, Yu; Chen, Liang; Cai, Hong

TNIP1 and autophagy receptors regulate STING signaling.

TNIP1 和自噬受体调节 STING 信号传导。

Bunker Eric N, Fischer Tara D, Zhu Peng-Peng, Le Guerroué François, Johnson Kory R, Youle Richard J

TNIP1 and Autophagy Receptors regulate STING Signaling.

TNIP1 和自噬受体调节 STING 信号传导

Bunker Eric N, Fischer Tara D, Zhu Peng-Peng, Le Guerroué François, Youle Richard J

Research hotspots and trends in transcranial magnetic stimulation for cognitive impairment: A bibliometric analysis from 2014 to 2023

经颅磁刺激治疗认知障碍的研究热点和趋势:2014年至2023年的文献计量分析

Zhang, Qi; Zhu, Peng-Peng; Yang, Lun; Guo, Ai-Song

STING induces HOIP-mediated synthesis of M1 ubiquitin chains to stimulate NFκB signaling.

STING 诱导 HOIP 介导的 M1 泛素链合成,从而刺激 NF-κB 信号传导

Fischer Tara D, Bunker Eric N, Zhu Peng-Peng, Guerroué François Le, Hadjian Mahan, Dominguez-Martin Eunice, Scavone Francesco, Cohen Robert, Yao Tingting, Wang Yan, Werner Achim, Youle Richard J

The application of del Nido cardioplegia for myocardial protection in adult coronary artery bypass grafting: a cohort study

del Nido心脏停搏液在成人冠状动脉旁路移植术中用于心肌保护的应用:一项队列研究

Lin, Xuefeng; Jiang, Yanping; Zhu, Peng; Peng, Qinbao; Meng, Weipeng; Zheng, Shaoyi

PML(NLS¯) protein: A novel marker for the early diagnosis of acute promyelocytic leukemia

PML(NLS¯)蛋白:急性早幼粒细胞白血病早期诊断的新标志物

Zhi-Ling Shan, Xin-Yu Zhu, Peng-Peng Ma, Hui Wang, Jianbin Chen, Jun Li, Liang Zhong, Bei-Zhong Liu

Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12

遗传性痉挛性截瘫43型(SPG43)是由C19orf12基因突变引起的。

Landouré, Guida; Zhu, Peng-Peng; Lourenço, Charles M; Johnson, Janel O; Toro, Camilo; Bricceno, Katherine V; Rinaldi, Carlo; Meilleur, Katherine G; Sangaré, Modibo; Diallo, Oumarou; Pierson, Tyler M; Ishiura, Hiroyuki; Tsuji, Shoji; Hein, Nichole; Fink, John K; Stoll, Marion; Nicholson, Garth; Gonzalez, Michael A; Speziani, Fiorella; Dürr, Alexandra; Stevanin, Giovanni; Biesecker, Leslie G; Accardi, John; Landis, Dennis M D; Gahl, William A; Traynor, Bryan J; Marques, Wilson Jr; Züchner, Stephan; Blackstone, Craig; Fischbeck, Kenneth H; Burnett, Barrington G

Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type I

靶向高通量测序鉴定出atlastin-1基因突变是I型遗传性感觉神经病的原因。

Guelly, Christian; Zhu, Peng-Peng; Leonardis, Lea; Papić, Lea; Zidar, Janez; Schabhüttl, Maria; Strohmaier, Heimo; Weis, Joachim; Strom, Tim M; Baets, Jonathan; Willems, Jan; De Jonghe, Peter; Reilly, Mary M; Fröhlich, Eleonore; Hatz, Martina; Trajanoski, Slave; Pieber, Thomas R; Janecke, Andreas R; Blackstone, Craig; Auer-Grumbach, Michaela

Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network

遗传性痉挛性截瘫蛋白 REEP1、spastin 和 atlastin-1 协调微管与管状内质网网络的相互作用。

Park, Seong H; Zhu, Peng-Peng; Parker, Rell L; Blackstone, Craig