A disease-driver population within interstitial cells of human calcific aortic valves identified via single-cell and proteomic profiling (Cell Reports IF=9.4)
'single-cell RNA seq','干细胞与转分化'。参与CAVD疾病驱动VICs亚群DDP-VICs(CD44^high^CD29^+^CD59^+^CD73^+^CD45^low^) 总结 作者通过高通量流式检测鉴定出一个参与CAVD疾病驱动VICs...
Giving Calcification Its Due: Recognition of a Diverse Disease: A First Attempt to Standardize the Field
Giving Calcification Its Due: Recognition of a Diverse Disease: A First Attempt to Standardize the Field Article type: Review Files: CIRCRESAHA.116.310060.pdf Publication Year: 201...
CV Weekly Digest | 2026-03-16
Source Agent: research 1. PRMT3-Mediated Arginine Methylation Stabilizes PCSK9 to Promote Aortic Valve Calcification Summary: 背景:CAVD 仍缺乏明确可药物化靶点。方法:研究结合患者...
CV Weekly Digest | 2026-03-09
本周最强的共通信号不是某一条孤立通路,而是代谢重编程、细胞状态转换、炎症/NETosis 与组织稳态失衡这四类机制正在不同心血管病中反复汇聚。对 CAVD 研究来说,这意味着下阶段最值得盯的是把 ...
CV Weekly Digest | 2026-03-03
本周高价值论文共同指向“细胞命运决定+微环境重塑”作为心血管疾病可干预主轴;对CAVD而言,优先把VIC表型转换与炎症/代谢/细胞器通讯做因果串联,将更容易产出可转化机制。 Source Agent: res...










