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shRNA knockdown of ZMIZ1 in human T-cell Acute Lymphoblastic Leukemia cell line CEM

ChEBI2012-12-13 更新2026-07-21 收录

肾病与白血病基因功能研究

shRNA基因敲降实验

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-32523 数据链接链接失效反馈

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资源简介：

shRNA knockdown of ZMIZ1 in human T-cell Acute Lymphoblastic Leukemia cell line CEM

应用场景：

创建时间：

2012-12-13

肾病与白血病基因功能研究

CRISPR-Cas9基因编辑

We evaluated the function of Meningioma 1 (MN1), a cofactor of HOXA9 and MEIS1, in murine MLL-r leukemia by CRISPR-Cas9 mediated deletion of MN1. MN1 was required for in vivo leukemogenicity of MLL-r

NIAID Data Ecosystem40

Effect of knocking out SLAMF6 in the cell line HNT-34

肾病与白血病基因功能研究

CRISPR基因敲除

This dataset includes RNA sequencing (RNA-seq) data from the HNT-34 AML (acute myeloid leukemia) cell line after knockout of the SLAMF6 gene by CRISPR/Cas9 (S3/S4) or mock-knockout with a construct ta

NIAID Data Ecosystem30

Mus musculus Transcriptome or Gene expression. Mus musculus

肾病与白血病基因功能研究

RNA测序分析

RNA sequencing was performed from WT and FGFR3-KO leukemia cells

NIAID Data Ecosystem20

A sub-genomic CRISPR/Cas9 screen of essential RNA binding protein in B-cell acute lymphoblastic leukemia.

肾病与白血病基因功能研究

CRISPR-Cas9

B-cell acute lymphoblastic leukemia (B-ALL) is one of most common type of leukemia in the pediatric population.Compared to different types of genetic translocations, MLL- AF4 translocation gives rise

NIAID Data Ecosystem40

TALENs-mediated gene disruption of FLT3 in leukemia cells: Using genome-editing approach for exploring the molecular basis of gene abnormality

肾病与白血病基因功能研究

基因组编辑表型分析

Novel analytic tools are needed to elucidate the molecular basis of leukemia-relevant gene mutations in the post-genome era. We generated isogenic leukemia cell clones in which the FLT3 gene was disru

NIAID Data Ecosystem20

shRNA knockdown of ZMIZ1 in human T-cell Acute Lymphoblastic Leukemia cell line CEM

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