增殖性玻璃体视网膜病变
血小板源性生长因子受体
免疫印迹
玻璃体切除术
基因亚型
血小板衍生生长因子
视网膜
化学
细胞生物学
受体
生长因子
癌症研究
生物
医学
分子生物学
眼科
视网膜脱离
内科学
生物化学
视力
基因
作者
Hetian Lei,Peter Hovland,Gisela Velez,Aaron C. Haran,Debra G. Gilbertson,Tatsuo Hirose,Andrius Kazlauskas
摘要
The predominance of PDGF isoforms that activate PDGFRalpha support the ligand hypothesis as an explanation of why PDGFRalpha is more capable of inducing PVR than is PDGFRbeta. Furthermore, the profile of PDGF isoforms observed in the rabbit model accurately reflected the clinical specimens from patients with PVR. Finally, these findings implicate one of the new PDGF family members as an important contributor to experimental and clinical PVR.
科研通智能强力驱动
Strongly Powered by AbleSci AI