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Over-expression of truncated FMRP with 295 amino acid residues: HEK293T cells

ChEBI2015-05-08 更新2026-07-21 收录

脆性X综合征

蛋白质功能细胞实验

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-68668 数据链接链接失效反馈

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资源简介：

Over-expression of truncated FMRP with 295 amino acid residues: HEK293T cells

应用场景：

创建时间：

2015-05-08

脆性X综合征

AMPA受体

Fragile X syndrome (FXS) is the most common monogenetic cause of inherited intellectual disability and autism in humans. One of the well-characterized molecular phenotypes of Fmr1 KO mice, a model of

figshare.com2023-11-09 更新120

Additional file 10 of Altered brain-wide auditory networks in a zebrafish model of fragile X syndrome

神经科学

脆性X综合征

Additional file 10. Summary of segmentation for multisensory dataset. Total number of ROIs detected per fish for the multisensory dataset in WT (n = 7) and fmr1−/− (n = 5) larvae. WB, whole brain; Tel

NIAID Data Ecosystem80

Excessive Astrocyte-Derived Neurotrophin-3 Contributes to the Abnormal Neuronal Dendritic Development in a Mouse Model of Fragile X Syndrome

神经科学

脆性X综合征

Fragile X syndrome (FXS) is a form of inherited mental retardation in humans that results from expansion of a CGG repeat in the Fmr1 gene. Recent studies suggest a role of astrocytes in neuronal devel

NIAID Data Ecosystem70

Data_Cluster_Fragile_X_Stasolla_et_al_2018_JODD.xlsx

脆性X综合征

辅助技术

An assistive technology-based intervention and microswitch-cluster technology for promoting occupation and reducing hand biting of 6 adolescents with fragile X sydrome

DataCite Commons2020-08-28 更新120

Novel FMR1 sequence variants identified in FXS-like males.

FMR1基因表达

脆性X综合征

Novel FMR1 sequence variants identified in FXS-like males.

NIAID Data Ecosystem70