SciHub
文献互助
期刊查询
一搜即达
科研导航
即时热点
交流社区
登录
注册
发布
文献
求助
首页
我的求助
捐赠本站
已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整的填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!
MMMM
Lv3
266 积分
2023-01-07 加入
最近求助
最近应助
互助留言
Atlas of the plasma proteome in health and disease in 53,026 adults
2小时前
待确认
TAF15 Overexpression Impairs Memory in Mice by Inhibiting the Transcription of Npas4
14天前
已完结
Bidirectional interaction between IL and 17A/IL-17RA pathway dysregulation and α-synuclein in the pathogenesis of Parkinson’s disease
16天前
已完结
Impact of ABO Blood Type on Outcomes in Patients with Primary Nonmuscle Invasive Bladder Cancer
20天前
已关闭
Spinocerebellar ataxia type 11 (SCA11): An update
26天前
已完结
Restoring hippocampal glucose metabolism rescues cognition across Alzheimer's disease pathologies
29天前
已完结
What Is the Role of Glucagon-Like Peptide 1 Signaling in the Nervous System and Its Potential Neuroprotective Effects?
1个月前
已完结
Human iPSC 4R tauopathy model uncovers modifiers of tau propagation
1个月前
已完结
Serum Ammonia Level for the Evaluation of Hepatic Encephalopathy
2个月前
已完结
Association between trichlorophenols and neurodegenerative diseases: A cross-sectional study from NHANES 2003–2010
3个月前
已完结
High-Speed Rail and Energy Productivity: Evidence from China
1年前
已驳回
标题错误,我的标题是Autosomal dominant Parkinson's disease caused by the recently identified LRRK2 N1437D mutation in a Chinese family: Clinical features, imaging findings, and functional impact.
1年前
最近帖子
最近评论
没有发布任何帖子
没有发布任何评论