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靶向 SARM1 可改善自噬应激诱导的轴突神经病。

Targeting SARM1 improves autophagic stress-induced axonal neuropathy.

机构信息

Peripheral Neuropathy Research Center (PNRC), Department of Molecular Neuroscience and Translational Biomedical Sciences, Dong-A University College of Medicine, Busan, Republic of Korea.

Department of Life Sciences, Division of Life Sciences and Biotechnology, Korea University, Seoul, Republic of Korea.

出版信息

Autophagy. 2024 Jan;20(1):29-44. doi: 10.1080/15548627.2023.2244861. Epub 2023 Aug 18.

Abstract

AAV

adeno-associated virus; ATF3: activating transcription factor 3; ATG7: autophagy related 7; AVIL: advillin; cADPR: cyclic ADP ribose; CALC: calcitonin/calcitonin-related polypeptide; CMT: Charcot-Marie-Tooth disease; cKO: conditional knockout; DEG: differentially expressed gene; DRG: dorsal root ganglion; FE-SEM: field emission scanning electron microscopy; IF: immunofluorescence; NCV: nerve conduction velocity; PVALB: parvalbumin; RAG: regeneration-associated gene; ROS: reactive oxygen species; SARM1: sterile alpha and HEAT/Armadillo motif containing 1; : synapsin I.

摘要

AAV

腺相关病毒;ATF3:激活转录因子 3;ATG7:自噬相关 7;AVIL:advillin;cADPR:环 ADP 核糖;CALC:降钙素/降钙素相关多肽;CMT:Charcot-Marie-Tooth 病;cKO:条件性敲除;DEG:差异表达基因;DRG:背根神经节;FE-SEM:场发射扫描电子显微镜;IF:免疫荧光;NCV:神经传导速度;PVALB:parvalbumin;RAG:再生相关基因;ROS:活性氧;SARM1:无菌α和 HEAT/Armadillo 结构域包含 1;synapsin I:突触结合蛋白 I。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb9/10761069/96f22025257c/KAUP_A_2244861_F0001_C.jpg

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