Joshua M. Korn, Ph.D.
Affiliations: | 2010 | Harvard University, Cambridge, MA, United States |
Area:
structural biologyGoogle:
"Joshua Korn"Mean distance: 9.52 | S | N | B | C | P |
Parents
Sign in to add mentorJames M. Hogle | grad student | 2010 | Harvard | |
(Copy Number Variation in the Human Genome: Tools, Methods, and Applications to Disease.) |
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Publications
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Palmer AC, Plana D, Gao H, et al. (2020) A proof of concept for biomarker-guided targeted therapy against ovarian cancer based on patient-derived tumor xenografts. Cancer Research |
Ye LF, Reznik E, Korn JM, et al. (2020) Patient-derived glioblastoma cultures as a tool for small-molecule drug discovery. Oncotarget. 11: 443-451 |
Raoof S, Mulford IJ, Frisco-Cabanos H, et al. (2019) Targeting FGFR overcomes EMT-mediated resistance in EGFR mutant non-small cell lung cancer. Oncogene |
Ghandi M, Huang FW, Jané-Valbuena J, et al. (2019) Next-generation characterization of the Cancer Cell Line Encyclopedia. Nature |
Bhang HC, DiMare MT, Kodack DP, et al. (2019) Abstract 394: In vivo shRNA screens under treatment pressure by BRAF and MEK inhibitors to identify novel combination treatment strategies for BRAF-mutant colorectal cancer Cancer Research. 79: 394-394 |
Cotton JL, KrishnamurthyRadhakrishna V, Chen J, et al. (2019) Abstract A122: Molecular barcoding and single cell approaches to investigate drug tolerance in EGFRmut NSCLC Molecular Cancer Therapeutics. 18 |
Liu H, Golji J, Brodeur LK, et al. (2018) Tumor-derived IFN triggers chronic pathway agonism and sensitivity to ADAR loss. Nature Medicine |
de Weck A, Golji J, Jones MD, et al. (2018) Correction of copy number induced false positives in CRISPR screens. Plos Computational Biology. 14: e1006279 |
Shao W, Mishina Y, Feng Y, et al. (2018) Antitumor properties of RAF709, a highly selective and potent inhibitor of RAF kinase dimers, in tumors driven by mutant RAS or BRAF. Cancer Research |
Stuart DD, Shao W, Mishina Y, et al. (2018) Abstract DDT01-04: Pharmacological profile and anti-tumor properties of LXH254, a highly selective RAF kinase inhibitor Cancer Research. 78 |