C
Chao Zhang
Researcher at Beihang University
Publications - 4347
Citations - 118320
Chao Zhang is an academic researcher from Beihang University. The author has contributed to research in topics: Medicine & Computer science. The author has an hindex of 127, co-authored 3119 publications receiving 84711 citations. Previous affiliations of Chao Zhang include West Virginia University & University of Oklahoma.
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Journal ArticleDOI
Pathological findings of COVID-19 associated with acute respiratory distress syndrome.
Zhe Xu,Lei Shi,Yijin Wang,Ji-Yuan Zhang,Lei Huang,Chao Zhang,Shuhong Liu,Peng Zhao,Hongxia Liu,Li Zhu,Yanhong Tai,Changqing Bai,Tingting Gao,Jin-Wen Song,Peng Xia,Jing-Hui Dong,Jingmin Zhao,Fu-Sheng Wang +17 more
TL;DR: O surto do novo coronavÃrus (COVID-19) em Wuhan, China, iniciado em dezembro de 2019, evoluiu para se tornar uma pandemia global A.
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Clinical efficacy of a RAF inhibitor needs broad target blockade in BRAF -mutant melanoma
Gideon Bollag,Peter Hirth,James Tsai,Jiazhong Zhang,Prabha N. Ibrahim,Hanna Cho,Wayne Spevak,Chao Zhang,Ying Zhang,Gaston Habets,Elizabeth A. Burton,Bernice Wong,Garson Tsang,Brian L. West,Ben Powell,Rafe Shellooe,Adhirai Marimuthu,Hoa Nguyen,Kam Y. J. Zhang,Dean R. Artis,Joseph Schlessinger,Fei Su,Brian Higgins,Raman Mahadevan Iyer,Kurt D'Andrea,Astrid Koehler,Michael Stumm,Paul S. Lin,Richard J. Lee,Joseph F. Grippo,Igor Puzanov,Kevin B. Kim,Antoni Ribas,Grant A. McArthur,Jeffrey A. Sosman,Paul B. Chapman,Keith T. Flaherty,Xiaowei Xu,Katherine L. Nathanson,K. B. Nolop +39 more
TL;DR: The structure-guided discovery of PLX4032 (RG7204), a potent inhibitor of oncogenic B-RAF kinase activity, and a remarkably high 81% response rate in metastatic melanoma patients treated at an oral dose of 960 mg twice daily are described, demonstrating that BRAF-mutant melanomas are highly dependent on B- RAF kinases activity.
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RAF inhibitors transactivate RAF dimers and ERK signalling in cells with wild-type BRAF
TL;DR: Because RAF inhibitors do not inhibit ERK signalling in other cells, the model predicts that they would have a higher therapeutic index and greater antitumour activity than mitogen-activated protein kinase (MEK) inhibitors, but could also cause toxicity due to MEK/ERK activation.
Journal ArticleDOI
Liver injury in COVID-19: management and challenges.
Chao Zhang,Lei Shi,Fu-Sheng Wang +2 more
Journal ArticleDOI
Discovery of a selective inhibitor of oncogenic B-Raf kinase with potent antimelanoma activity
James Tsai,John T. Lee,Weiru Wang,Jiazhong Zhang,Hanna Cho,Shumeye Mamo,Ryan Bremer,Sam Gillette,Jun Kong,Nikolas K. Haass,Katrin Sproesser,Ling Li,Keiran S.M. Smalley,D. Fong,Yong-Liang Zhu,Adhirai Marimuthu,Hoa Nguyen,Billy Lam,Jennifer S. Liu,Ivana Cheung,Julie Rice,Yoshihisa Suzuki,Catherine Luu,Calvin Settachatgul,Rafe Shellooe,John Cantwell,Sung-Hou Kim,Joseph Schlessinger,Kam Y. J. Zhang,Brian L. West,Ben Powell,Gaston Habets,Chao Zhang,Prabha N. Ibrahim,Peter Hirth,Dean R. Artis,Meenhard Herlyn,Gideon Bollag +37 more
TL;DR: PLX4720, a 7-azaindole derivative that inhibits B-RafV600E with an IC50 of 13 nM, defines a class of kinase inhibitor with marked selectivity in both biochemical and cellular assays and represents the entire discovery process from initial identification through structural and biological studies in animal models to a promising therapeutic for testing in cancer patients bearing B- RafV 600E-driven tumors.