Lv4
600 积分 2022-09-23 加入
Mini-CEX联合病例分析评估在儿科住院医师规范化培训中的应用
7天前
已完结
The PLAAT family as phospholipid-related enzymes
1个月前
已完结
Hereditary spastic paraplegia HSP26: clinical and electrophysiological characteristics
1个月前
已完结
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1
1个月前
已完结
Single-cell transcriptomic and proteomic analysis of Parkinson’s disease Brains
1个月前
已完结
Neuronal FAM171A2 mediates α-synuclein fibril uptake and drives Parkinson’s disease
1个月前
已完结
The FAM171A2 gene is a key regulator of progranulin expression and modifies the risk of multiple neurodegenerative diseases
2个月前
已完结
The lysosomal function of progranulin, a guardian against neurodegeneration
2个月前
已完结
Tau gene mutations: dissecting the pathogenesis of FTDP-17
2个月前
已完结
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
2个月前
已完结
皖公网安备34019202002308
