作者: Koh Miura , Masayuki Satoh , Makoto Kinouchi , Kuniharu Yamamoto , Yasuhiro Hasegawa
DOI: 10.1517/17460441.2014.924923
关键词:
摘要: … as a RAF1 (CRAF) kinase inhibitor, and consequent studies revealed regorafenib to be a … in VEGFR3 and wild-type BRAF, and regorafenib seemed more potent in RAF1, BRAF(V600E), …