登录后查看消息通知
搜索
常见问题
消息
登录
首页
/
数据集
/
In silico analyses of the GARS variants identified in this study.
In silico analyses of the GARS variants identified in this study.
收藏
Figshare
2017-06-09 更新
2026-04-29 收录
基因变异功能预测
遗传性神经病变
数据链接:
https://figshare.com/articles/dataset/_i_In_silico_i_analyses_of_the_GARS_variants_identified_in_this_study_/5093440
数据链接
链接失效反馈
官方服务:
问题咨询
购买咨询
在线客服
NEW
资源简介:
In silico analyses of the GARS variants identified in this study.
应用场景:
创建时间:
2017-06-09
相关数据集
Supplemental Table 1. In silico analyses of 13 novel missense variants.
基因变异功能预测
错义变体分析
Supplemental Table 1
NIAID Data Ecosystem
6
0
Variant frequencies and deleterious score predictions of carnitine acyltransferase genes.
基因变异功能预测
遗传病关联分析
Variant frequencies and deleterious score predictions of carnitine acyltransferase genes.
Figshare
2016-10-31 更新
3
0
Modeling CMT1A with human induced pluripotent stem cell derived Schwann cells. Homo sapiens
遗传性神经病变
干细胞分化模型
We obtained skin fibroblasts from CMT1A and control patients, and generated hiPSCs which were subsequently differentiated into cd49d+ human Schwann cells. We utilized microarray technology to explore
NIAID Data Ecosystem
2
0
Electrophysiologic findings of the three patients with PMP2 p.I43N mutation.
遗传性神经病变
神经电生理表型
Electrophysiologic findings of the three patients with PMP2 p.I43N mutation.
NIAID Data Ecosystem
4
0
Predicted and observed functional effects of missense variants in GABR genes in patients with genetic epilepsy and in the general population.
癫痫遗传学
基因变异功能预测
GECs = genetic epilepsy cases. ESP = Exome Sequencing Project. SP = signal peptide. CL = M3/M4 cytoplasmic loop. TM = transmembrane. NT = N-terminal.
Figshare
2016-09-14 更新
3
0
© 2023-2026 上海数据发展科技有限责任公司 版权所有
沪ICP备17003045号-15
沪公网安备31010402336585号
热门搜索
社区交流群
科研交流群
商业服务
数据资源
寻源服务
数据采集
标注服务
数据产品
代理销售
数据领域
凭证登记
数据产品
介绍推广