Fig 4 Paired-Pulse Facilitation in TG and WT mice at 9 months

Dryad2017-01-01 更新2026-04-13 收录

突触可塑性电生理

神经退行性疾病模型

数据链接：

http://datadryad.org/resource/doi:10.5061/dryad.0008d/3 数据链接链接失效反馈

官方服务：

资源简介：

PPF in CA1 neurons of TG and WT mice 9 months post-irradiation. PPF ratios are shown at all tested inter-stimulus intervals (ISI) of 20-400 ms.

创建时间：

2017-01-01

Next Generation Sequencing of wild type N2 and pan-neuronal overexpression of α-syn C. elegans fed with K12 BW25113 and csgA(-) bacteria. Next Generation Sequencing of wild type N2 and pan-neuronal overexpression of α-syn C. elegans fed with K12 BW25113 and csgA(-) bacteria

神经退行性疾病模型

差异基因表达分析

The goal of this study is to extract differentially expressed genes between K12 BW25113 and csgA(-) fed N2 and PD C. elegans. Methods: mRNA profile of K12 BW25113 and csgA(-) fed N2 and UM10 strains w

NIAID Data Ecosystem100

OW940 zgIs128[P(dat-1)::alpha-Synuclein::YFP] | 2014-04-01T13:04:34+02:00

虫类行为分析

神经退行性疾病模型

This experiment is part of the C.elegans behavioural database. For more information and the complete collection of experiments visit http://movement.openworm.org preview link : https://www.youtub

NIAID Data Ecosystem60

Ow949 Zgis125[P(Dat-1)::Alpha-Synuclein::Yfp] | 2014-04-05T15:40:24+02:00

秀丽隐杆线虫行为

神经退行性疾病模型

This experiment is part of the C.elegans behavioural database . For more information and the complete collection of experiments visit http://movement.openworm.org preview link : http

Zenodo2020-09-20 更新20

E46K mutant α-synuclein is more degradation resistant and exhibits greater toxic effects than wild-type α-synuclein in Drosophila models of Parkinson's disease

神经退行性疾病模型

α-突触核蛋白毒性

Parkinson’s disease (PD) is one of the most common neurodegenerative diseases, which is characterized by progressive motor dysfunction as well as non-motor symptoms. Pathological and genetic studies h

NIAID Data Ecosystem80

Aberrant neurodevelopment in human iPS cell-derived models of Alexander disease

神经退行性疾病模型

细胞分化异常

Alexander disease (AxD) is a rare, severe neurodegenerative disorder caused by mutations in the glial fibrillary acidic protein (GFAP). While the exact disease mechanism remains unknown, existing stud

NIAID Data Ecosystem30

Fig 4 Paired-Pulse Facilitation in TG and WT mice at 9 months

资源简介：

相关数据集