登录后查看消息通知
搜索
常见问题
消息
登录
首页
/
数据集
/
Additional file 3 of Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme
Additional file 3 of Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme
收藏
Figshare
2024-03-01 更新
2026-04-08 收录
遗传性耳聋
基因敲除表型分析
数据链接:
https://springernature.figshare.com/articles/dataset/Additional_file_3_of_Identification_and_characterisation_of_spontaneous_mutations_causing_deafness_from_a_targeted_knockout_programme/19373364/1
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:
Additional file 3.
应用场景:
提供机构:
Ingham, Neil J.; Pearson, Selina; Allen, Rochelle; Tucker, Abigail S.; Chen, Jing; Steel, Karen P.; Willaert, Annelore; Keane, Thomas; Rekhi, Sohinder; Drake, Matthew; Rook, Victoria; Pass, Johanna; Di Domenico, Francesca; Lewis, Morag A.; White, Jacqueline K.; Adams, David J.
创建时间:
2022-03-17
相关数据集
Fmo5(-/-) mouse: liver transcriptomics
肝脏转录组
基因敲除表型分析
We report the consequences of the disruption of the Fmo5 gene on transcription of genes in liver. Comparison of liver gene expression in wild-type and Fmo5(-/-) mice
NIAID Data Ecosystem
7
0
GJB2 mutations and their allele frequencies.
遗传性耳聋
等位基因频率
GJB2 mutations and their allele frequencies.
NIAID Data Ecosystem
5
0
Summary of phenotypes observed in global AHR-KO mice.
基因敲除表型分析
芳烃受体
Summary of phenotypes observed in global AHR-KO mice.
NIAID Data Ecosystem
4
0
A9-FibrinGel-TNC-KO project
组织工程生物材料
基因敲除表型分析
Each folder contains the distinct experiments for the corresponding condition, along with Excel files and statistical analysis files of the data.
Zenodo
2024-08-05 更新
6
0
KDM6B KO Embryonic spine scRNAseq
单细胞系统发育学
基因敲除表型分析
Preprocessed and annotated scRNA-seq Seurat object of Kdm6b KO dataset from mouse embryonic spine neurons [GSE156609].
Figshare
2024-11-13 更新
5
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