脂肪生成
碱性成纤维细胞生长因子
血小板源性生长因子受体
内分泌学
内科学
生长因子
血小板衍生生长因子
脂肪细胞
化学
生物
细胞生物学
受体
脂肪组织
医学
作者
Benjamin Schrijver,Merel A. Kooiman,Esmee Kasteleijn,Conny van Holten-Neelen,Sita Virakul,Dion Paridaens,Robin P. Peeters,P. Martin van Hagen,Virgil A. S. H. Dalm,Willem A. Dik
出处
期刊:Thyroid
[Mary Ann Liebert, Inc.]
日期:2019-02-06
卷期号:29 (3): 395-404
被引量:21
标识
DOI:10.1089/thy.2018.0544
摘要
bFGF induces adipogenesis in orbital fibroblasts and as such may contribute to GO. The additive effect of bFGF and PDGF-BB on adipogenesis, along with the observed inhibitory effects of dasatinib and nintedanib, point at independent receptor-mediated effects. This supports the hypothesis that multi-target directed therapy might be more efficient in the treatment of GO.
科研通智能强力驱动
Strongly Powered by AbleSci AI