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6. Preclinical evaluation of the WEE1 inhibitor MK-1775 as single-agent anticancer therapy. Guertin AD; Li J; Liu Y; Hurd MS; Schuller AG; Long B; Hirsch HA; Feldman I; Benita Y; Toniatti C; Zawel L; Fawell SE; Gilliland DG; Shumway SD Mol Cancer Ther; 2013 Aug; 12(8):1442-52. PubMed ID: 23699655 [TBL] [Abstract][Full Text] [Related]
7. Chk1 inhibition and Wee1 inhibition combine synergistically to impede cellular proliferation. Davies KD; Cable PL; Garrus JE; Sullivan FX; von Carlowitz I; Huerou YL; Wallace E; Woessner RD; Gross S Cancer Biol Ther; 2011 Nov; 12(9):788-96. PubMed ID: 21892012 [TBL] [Abstract][Full Text] [Related]
8. Combined inhibition of the cell cycle related proteins Wee1 and Chk1/2 induces synergistic anti-cancer effect in melanoma. Magnussen GI; Emilsen E; Giller Fleten K; Engesæter B; Nähse-Kumpf V; Fjær R; Slipicevic A; Flørenes VA BMC Cancer; 2015 Jun; 15():462. PubMed ID: 26054341 [TBL] [Abstract][Full Text] [Related]
9. Differential Activity of ATR and WEE1 Inhibitors in a Highly Sensitive Subpopulation of DLBCL Linked to Replication Stress. Young LA; O'Connor LO; de Renty C; Veldman-Jones MH; Dorval T; Wilson Z; Jones DR; Lawson D; Odedra R; Maya-Mendoza A; Reimer C; Bartek J; Lau A; O'Connor MJ Cancer Res; 2019 Jul; 79(14):3762-3775. PubMed ID: 31123088 [TBL] [Abstract][Full Text] [Related]
11. Targeting histone deacetylases (HDACs) and Wee1 for treating high-risk neuroblastoma. Hanmod SS; Wang G; Edwards H; Buck SA; Ge Y; Taub JW; Wang Z Pediatr Blood Cancer; 2015 Jan; 62(1):52-9. PubMed ID: 25308916 [TBL] [Abstract][Full Text] [Related]
12. MK-1775, a potent Wee1 inhibitor, synergizes with gemcitabine to achieve tumor regressions, selectively in p53-deficient pancreatic cancer xenografts. Rajeshkumar NV; De Oliveira E; Ottenhof N; Watters J; Brooks D; Demuth T; Shumway SD; Mizuarai S; Hirai H; Maitra A; Hidalgo M Clin Cancer Res; 2011 May; 17(9):2799-806. PubMed ID: 21389100 [TBL] [Abstract][Full Text] [Related]
13. Combined inhibition of Wee1 and Chk1 gives synergistic DNA damage in S-phase due to distinct regulation of CDK activity and CDC45 loading. Hauge S; Naucke C; Hasvold G; Joel M; Rødland GE; Juzenas P; Stokke T; Syljuåsen RG Oncotarget; 2017 Feb; 8(7):10966-10979. PubMed ID: 28030798 [TBL] [Abstract][Full Text] [Related]
14. Pharmacological targeting the ATR-CHK1-WEE1 axis involves balancing cell growth stimulation and apoptosis. Mak JP; Man WY; Ma HT; Poon RY Oncotarget; 2014 Nov; 5(21):10546-57. PubMed ID: 25301733 [TBL] [Abstract][Full Text] [Related]
15. Targeting AXL and mTOR Pathway Overcomes Primary and Acquired Resistance to WEE1 Inhibition in Small-Cell Lung Cancer. Sen T; Tong P; Diao L; Li L; Fan Y; Hoff J; Heymach JV; Wang J; Byers LA Clin Cancer Res; 2017 Oct; 23(20):6239-6253. PubMed ID: 28698200 [No Abstract] [Full Text] [Related]
16. Wee1 is required to sustain ATR/Chk1 signaling upon replicative stress. Saini P; Li Y; Dobbelstein M Oncotarget; 2015 May; 6(15):13072-87. PubMed ID: 25965828 [TBL] [Abstract][Full Text] [Related]
17. Antitumor effect of WEE1 blockade as monotherapy or in combination with cisplatin in urothelial cancer. Murakami K; Kita Y; Sakatani T; Hamada A; Mizuno K; Nakamura K; Takada H; Matsumoto K; Sano T; Goto T; Akamatsu S; Saito R; Tsuruyama T; Ogawa O; Kobayashi T Cancer Sci; 2021 Sep; 112(9):3669-3681. PubMed ID: 34212455 [TBL] [Abstract][Full Text] [Related]
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19. CHK1 plays a critical role in the anti-leukemic activity of the wee1 inhibitor MK-1775 in acute myeloid leukemia cells. Qi W; Xie C; Li C; Caldwell JT; Edwards H; Taub JW; Wang Y; Lin H; Ge Y J Hematol Oncol; 2014 Aug; 7():53. PubMed ID: 25084614 [TBL] [Abstract][Full Text] [Related]
20. MK-1775, a novel Wee1 kinase inhibitor, radiosensitizes p53-defective human tumor cells. Bridges KA; Hirai H; Buser CA; Brooks C; Liu H; Buchholz TA; Molkentine JM; Mason KA; Meyn RE Clin Cancer Res; 2011 Sep; 17(17):5638-48. PubMed ID: 21799033 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]