PRION

作品数：175被引量：154H指数：5
导出分析报告
相关领域：医药卫生生物学更多>>
相关作者：朱钦士赵德明周筠梅练富林柯莎更多>>
相关机构：中国农业大学中国科学院南加州大学厦门大学更多>>
相关期刊：更多>>
相关基金：国家自然科学基金国家重点基础研究发展计划国家高技术研究发展计划中国科学院知识创新工程重要方向项目更多>>
-
在结果中检索

检索结果分析

结果分析中...
选择条件：
  • 期刊=Neuroscience Bulletinx
共 条 记 录，以下是1-3
全选清除导出
参考文献引证文献引用追踪
视图：
排序：
NG2 Glia:The Guardians Against Prion‑induced Neurotoxicity Through Prostaglandin E2 Blockade
《Neuroscience Bulletin》2025年第3期539-542,共4页Shu Feng Emily Parker Timon Cheng‑Yi Liu Luodan Yang 
supported by the National Natural Science Foundation of China(32300959);a Guangzhou Scientific Research Grant(SL2024A04J00578);the SCNU Young Faculty Development Program(22KJ04).
Neuron glia antigen-2(NG2)glia,also known as oligodendrocyte precursor cells(OPCs),are essential for maintaining the normal function and structure of the central nervous system(CNS)due to their supportive role[1].Unde...
关键词：maintaining normal function structure myelin sheath axons oligodendrocyte precursor cells opcs receiving synaptic input neurons NEUROTOXICITY PRION central nervous system cns due ng glia 
Decoding the Cellular Trafficking of Prion-like Proteins in Neurodegenerative Diseases
《Neuroscience Bulletin》2024年第2期241-254,共14页Chenjun Hu Yiqun Yan Yanhong Jin Jun Yang Yongmei Xi Zhen Zhong 
supported by the National Natural Science Foundation of China(82071424);the Zhejiang University Education Foundation Global Partnership Fund(188170+194452115/011).
The accumulation and spread of prion-like proteins is a key feature of neurodegenerative diseases(NDs)such as Alzheimer’s disease,Parkinson's disease,or Amyotrophic Lateral Sclerosis.In a process known as‘seeding’,...
关键词：Neurodegenerative diseases Prion-like propagation SEEDING ENDOCYTOSIS Endolyosomal leaking Degradation 
T188K-Familial Creutzfeldt–Jacob Disease, Predominant Among Chinese, has a Reactive Pattern in CSF RT-QuIC Different from D178N-Fatal Familial Insomnia and E200K-Familial CJD被引量：6
《Neuroscience Bulletin》2019年第3期519-521,共3页Kang Xiao Qi Shi Wei Zhou Bao-Yun Zhang Yuan Wang Cao Chen Yue Ma Chen Gao Xiao-Ping Dong 
supported by National Science and Technology Major Project of China(2017ZX10104001002005);the National Natural Science Foundation of China(81630062,81301429,and 81572048);National Key R&D Program(2016YFC1202700);State Key Laboratory of Infectious Disease Prevention and Control(SKLID)Program of China(2012SKLID102and 2015SKLID503)
Dear Editor,Human prion diseases consist of sporadic, genetic/familial, and acquired forms. The familial form accounts for 5%-15% of all human prion diseases, including familial Creutzfeldt- Jacob disease (fCJD), Gers...
关键词：Human PRION diseases sporadic ethnicity-associated features 
全选清除导出
共1页<1>
检索报告 对象比较 聚类工具 使用帮助 返回顶部