相关实验视频

Updated: Jul 17, 2026

Assessing Cardiomyocyte Subtypes Following Transcription Factor-mediated Reprogramming of Mouse Embryonic Fibroblasts
09:29

Assessing Cardiomyocyte Subtypes Following Transcription Factor-mediated Reprogramming of Mouse Embryonic Fibroblasts

Published on: March 22, 2017

7.4K

转录组学数据整合和分析,以揭示高性心肌病的标志性基因

Peng Chen1, Warda Yawar2, Ayesha Rida Farooqui3

  • 1Department of Cardiovascular Medicine, Taiyuan Central Hospital Taiyuan 030000, Shanxi, China.

American journal of translational research
|March 11, 2024
PubMed
概括

这项研究通过分析基因表达数据,确定了高性心肌病 (HCM) 中的8个关键枢纽基因. 这些发现提供了对HCM机制和潜在治疗点的见解.

关键词:
DEGs 是一个DEG.过度缩性心肌病变性是一种心脏病变.基因中心 基因枢纽这是一个小RNARNA.

更多相关视频

An Approach to Study Shape-Dependent Transcriptomics at a Single Cell Level06:02

An Approach to Study Shape-Dependent Transcriptomics at a Single Cell Level

Published on: November 2, 2020

5.7K
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model03:45

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

Published on: August 8, 2022

3.1K

相关概念视频

Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...