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GENETIC CORRECTION OF HUNTINGTON'S DISEASE PHENOTYPES IN INDUCED PLURIPOTENT STEM CELLS

ChEBI2012-06-14 更新2026-07-21 收录

神经退行性疾病基因

诱导多能干细胞

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-37547 数据链接链接失效反馈

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资源简介：

GENETIC CORRECTION OF HUNTINGTON'S DISEASE PHENOTYPES IN INDUCED PLURIPOTENT STEM CELLS

应用场景：

创建时间：

2012-06-14

亨廷顿病下丘脑转录组

神经退行性疾病基因

We used microarrays to investigate whether transcriptional dysregulation in hypothalamus is caused by expression of the huntingtin (HTT) protein We used two different Huntington's disease mouse models

NIAID Data Ecosystem110

Targeted Correction of CFTR Gene in Cystic Fibrosis iPS Exome Seq. Homo sapiens

囊性纤维化基因

诱导多能干细胞

Exome sequencing for determination of novel mutations in CF fibroblast, reprogrammed iPS, and 2 zinc finger corrected CFTR iPS clones.

NIAID Data Ecosystem70

Coordination of engineered factors with TET1/2 promotes early stage epigenetic modification during somatic cell reprogramming

诱导多能干细胞

表观遗传修饰

Somatic cell reprogramming towards induced pluripotent stem cells (iPSCs) holds great promise in future regenerative medicine, however, the reprogramming process mediated by the traditional defined fa

NIAID Data Ecosystem50

EGAS00001006234-sc-2023-01-04T09:35:03Z - samples

脊髓小脑性共济失调

诱导多能干细胞

A collection of four induced pluripotent stem cell models (iPSC) derived from patients diagnosed with Spinocerebellar ataxia 15 (SCA15) . Spinocerebellar ataxia 15 (SCA15) is a neurological condition

NIAID Data Ecosystem90

Additional file 6: of Genome-wide transcriptome analysis using RNA-Seq reveals a large number of differentially expressed genes in a transient MCAO rat model

神经退行性疾病基因

细胞凋亡通路转录组学

Table S6. The RNA-Seq analysis of DEGs associated with the functional category â Apoptosisâ . (XLSX 23Â kb)

Figshare2018-09-06 更新60