首页/数据集/A germline variant in the BET1L 3?-UTR confers colorectal cancer susceptibility by reducing miRNA binding and m6A modification

A germline variant in the BET1L 3?-UTR confers colorectal cancer susceptibility by reducing miRNA binding and m6A modification

NIAID Data Ecosystem2026-05-01 收录

肿瘤遗传学

结直肠癌易感性

数据链接：

https://www.omicsdi.org/dataset/eva/PRJEB61209 数据链接链接失效反馈

官方服务：

资源简介：

An investigation of genetic variants in BET1L

应用场景：

创建时间：

2023-04-11

转录组测序

肿瘤遗传学

The goal of this study was to identify important genetic pathways that are altered in mammary tumor cells upon over-expression of the tumor suppressor gene Arid1a. The results of this experiment revea

NIAID Data Ecosystem120

Germline mutations identified in patients with AML and MPN.

肿瘤遗传学

种系突变分析

Germline mutations identified in patients with AML and MPN.

Figshare2019-03-06 更新40

Affymetrix SNP array data for acute myeloid leukemia (AML) samples with complex karyotype. Homo sapiens

癌症基因组数据

肿瘤遗传学

AML with complex karyotype (CK-AML) is characterized by a high frequency of TP53 alteration (loss and/or mutation). TP53-altered CK-AML were characterized by a higher degree of genomic complexity (abe

NIAID Data Ecosystem30

Inherited KDM6AA649T facilitates tumor-immune escape and exacerbates colorectal signet-ring cell carcinoma outcomes

肿瘤遗传学

肿瘤免疫微环境

Childhood onset of colorectal signet ring cell carcinoma (CR-SRCC) is extremely rare and featured as highly malignant with poor prognosis. Here we reported a CR-SRCC case of 11-year-old boy with a nov

NIAID Data Ecosystem50

Predisposition to hematopoietic malignancies by deleterious germline CHEK2 variants

肿瘤遗传学

基因变异功能验证

The role of germline CHEK2 variants in hematopoietic malignancies (HMs) is poorly understood. We examined pathogenic/likely pathogenic (P/LP) CHEK2 variants in a hereditary hematopoietic malignancy (H

NIAID Data Ecosystem30

A germline variant in the BET1L 3?-UTR confers colorectal cancer susceptibility by reducing miRNA binding and m6A modification

资源简介：

相关数据集