-
1
-
-
33846856967
-
CHIR-124, a novel potent inhibitor of Chk1, potentiates the cytotoxicity of topoisomerase I poisons in vitro and in vivo
-
PMID:17255282; DOI:10.1158/1078-0432.CCR-06-1424
-
Tse AN, Rendahl KG, Sheikh T, Cheema H, Aardalen K, Embry M, et al. CHIR-124, a novel potent inhibitor of Chk1, potentiates the cytotoxicity of topoisomerase I poisons in vitro and in vivo. Clin Cancer Res 2007; 13:591-602; PMID:17255282; DOI:10.1158/1078-0432.CCR-06-1424.
-
(2007)
Clin Cancer Res
, vol.13
, pp. 591-602
-
-
Tse, A.N.1
Rendahl, K.G.2
Sheikh, T.3
Cheema, H.4
Aardalen, K.5
Embry, M.6
-
2
-
-
33846567414
-
Pharmacological abrogation of S-phase checkpoint enhances the anti-tumor activity of gemcitabine in vivo
-
PMID:17245119; DOI:10.4161/cc.6.1.3699
-
Matthews DJ, Yakes FM, Chen J, Tadano M, Bornheim L, Clary DO, et al. Pharmacological abrogation of S-phase checkpoint enhances the anti-tumor activity of gemcitabine in vivo. Cell Cycle 2007; 6:104-10; PMID:17245119; DOI:10.4161/cc.6.1.3699.
-
(2007)
Cell Cycle
, vol.6
, pp. 104-110
-
-
Matthews, D.J.1
Yakes, F.M.2
Chen, J.3
Tadano, M.4
Bornheim, L.5
Clary, D.O.6
-
3
-
-
53349156857
-
Breaching the DNA damage checkpoint via PF-00477736, a novel small-molecule inhibitor of checkpoint kinase 1
-
PMID:18723486; DOI:10.1158/1535-7163.MCT-07-2391
-
Blasina A, Hallin J, Chen E, Arango ME, Kraynov E, Register J, et al. Breaching the DNA damage checkpoint via PF-00477736, a novel small-molecule inhibitor of checkpoint kinase 1. Mol Cancer Ther 2008; 7:2394-404; PMID:18723486; DOI:10.1158/1535-7163.MCT-07-2391.
-
(2008)
Mol Cancer Ther
, vol.7
, pp. 2394-2404
-
-
Blasina, A.1
Hallin, J.2
Chen, E.3
Arango, M.E.4
Kraynov, E.5
Register, J.6
-
4
-
-
58149500122
-
Gemcitabine sensitization by checkpoint kinase 1 inhibition correlates with inhibition of a Rad51 DNA damage response in pancreatic cancer cells
-
PMID:19139112; DOI:10.1158/1535-7163. MCT-08-0662
-
Parsels LA, Morgan MA, Tanska DM, Parsels JD, Palmer BD, Booth RJ, et al. Gemcitabine sensitization by checkpoint kinase 1 inhibition correlates with inhibition of a Rad51 DNA damage response in pancreatic cancer cells. Mol Cancer Ther 2009; 8:45-54; PMID:19139112; DOI:10.1158/1535-7163. MCT-08-0662.
-
(2009)
Mol Cancer Ther
, vol.8
, pp. 45-54
-
-
Parsels, L.A.1
Morgan, M.A.2
Tanska, D.M.3
Parsels, J.D.4
Palmer, B.D.5
Booth, R.J.6
-
5
-
-
68049107474
-
PF-00477736 mediates checkpoint kinase 1 signaling pathway and potentiates docetaxel-induced efficacy in xenografts
-
PMID:19584159; DOI:10.1158/1078-0432.CCR-08-3272
-
Zhang C, Yan Z, Painter CL, Zhang Q, Chen E, Arango ME, et al. PF-00477736 mediates checkpoint kinase 1 signaling pathway and potentiates docetaxel-induced efficacy in xenografts. Clin Cancer Res 2009; 15:4630-40; PMID:19584159; DOI:10.1158/1078-0432.CCR-08-3272.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 4630-4640
-
-
Zhang, C.1
Yan, Z.2
Painter, C.L.3
Zhang, Q.4
Chen, E.5
Arango, M.E.6
-
6
-
-
77953770987
-
Mechanism of radiosensitization by the Chk1/2 inhibitor AZD7762 involves abrogation of the G2 checkpoint and inhibition of homologous recombinational DNA repair
-
PMID:20501833; DOI:10.1158/0008-5472.CAN-09-3573
-
Morgan MA, Parsels LA, Zhao L, Parsels JD, Davis MA, Hassan MC, et al. Mechanism of radiosensitization by the Chk1/2 inhibitor AZD7762 involves abrogation of the G2 checkpoint and inhibition of homologous recombinational DNA repair. Cancer Res 2010; 70:4972-81; PMID:20501833; DOI:10.1158/0008-5472.CAN- 09-3573.
-
(2010)
Cancer Res
, vol.70
, pp. 4972-4981
-
-
Morgan, M.A.1
Parsels, L.A.2
Zhao, L.3
Parsels, J.D.4
Davis, M.A.5
Hassan, M.C.6
-
7
-
-
17644432403
-
Chk1 is an essential kinase that is regulated by Atr and required for the G(2)/M DNA damage checkpoint
-
PMID:10859164
-
Liu Q, Guntuku S, Cui XS, Matsuoka S, Cortez D, Tamai K, et al. Chk1 is an essential kinase that is regulated by Atr and required for the G(2)/M DNA damage checkpoint. Genes Dev 2000; 14:1448-59; PMID:10859164.
-
(2000)
Genes Dev
, vol.14
, pp. 1448-1459
-
-
Liu, Q.1
Guntuku, S.2
Cui, X.S.3
Matsuoka, S.4
Cortez, D.5
Tamai, K.6
-
8
-
-
0034659341
-
Aberrant cell cycle checkpoint function and early embryonic death in Chk1(-/-) mice
-
PMID:10859163
-
Takai H, Tominaga K, Motoyama N, Minamishima YA, Nagahama H, Tsukiyama T, et al. Aberrant cell cycle checkpoint function and early embryonic death in Chk1(-/-) mice. Genes Dev 2000; 14:1439-47; PMID:10859163.
-
(2000)
Genes Dev
, vol.14
, pp. 1439-1447
-
-
Takai, H.1
Tominaga, K.2
Motoyama, N.3
Minamishima, Y.A.4
Nagahama, H.5
Tsukiyama, T.6
-
9
-
-
20244388673
-
Inhibition of human Chk1 causes increased initiation of DNA replication, phosphorylation of ATR targets and DNA breakage
-
PMID:15831461; DOI:10.1128/MCB.25.9.3553-62.2005
-
Syljuåsen RG, Sorensen CS, Hansen LT, Fugger K, Lundin C, Johansson F, et al. Inhibition of human Chk1 causes increased initiation of DNA replication, phosphorylation of ATR targets and DNA breakage. Mol Cell Biol 2005; 25:3553-62; PMID:15831461; DOI:10.1128/MCB.25.9.3553-62.2005.
-
(2005)
Mol Cell Biol
, vol.25
, pp. 3553-3562
-
-
Syljuåsen, R.G.1
Sorensen, C.S.2
Hansen, L.T.3
Fugger, K.4
Lundin, C.5
Johansson, F.6
-
10
-
-
33749599776
-
Evidence that the ATR/ Chk1 pathway maintains normal replication fork progression during unperturbed S phase
-
PMID:16969104; DOI:10.4161/cc.5.19.3256
-
Petermann E, Caldecott KW. Evidence that the ATR/ Chk1 pathway maintains normal replication fork progression during unperturbed S phase. Cell Cycle 2006; 5:2203-9; PMID:16969104; DOI:10.4161/cc.5.19.3256.
-
(2006)
Cell Cycle
, vol.5
, pp. 2203-2209
-
-
Petermann, E.1
Caldecott, K.W.2
-
11
-
-
80051887747
-
Single-agent inhibition of Chk1 is antiproliferative in human cancer cell lines in vitro and inhibits tumor xenograft growth in vivo
-
DOI:10.3727/096504011X13079697132961
-
Davies KD, Humphries MJ, Sullivan FX, von Carlowitz I, Le Huerou Y, Mohr PJ, et al. Single-agent inhibition of Chk1 is antiproliferative in human cancer cell lines in vitro and inhibits tumor xenograft growth in vivo. Oncol Res 2011; 19;349-63. DOI:10.3727/096504011X13079697132961
-
(2011)
Oncol Res
, vol.19
, pp. 349-363
-
-
Davies, K.D.1
Humphries, M.J.2
Sullivan, F.X.3
Von Carlowitz, I.4
Le Huerou, Y.5
Mohr, P.J.6
-
12
-
-
79952775174
-
RNAi screen of the protein kinome identifies checkpoint kinase 1 (CHK1) as a therapeutic target in neuroblastoma
-
PMID:21289283; DOI:10.1073/pnas.1012351108
-
Cole KA, Huggins J, Laquaglia M, Hulderman CE, Russell MR, Bosse K, et al. RNAi screen of the protein kinome identifies checkpoint kinase 1 (CHK1) as a therapeutic target in neuroblastoma. Proc Natl Acad Sci USA 2011; 108:3336-41; PMID:21289283; DOI:10.1073/pnas.1012351108.
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 3336-3341
-
-
Cole, K.A.1
Huggins, J.2
Laquaglia, M.3
Hulderman, C.E.4
Russell, M.R.5
Bosse, K.6
-
13
-
-
74549189337
-
New insights into checkpoint kinase 1 in the DNA damage response signaling network
-
PMID:20068082; DOI:10.1158/1078-0432.CCR-09-1029
-
Dai Y, Grant S. New insights into checkpoint kinase 1 in the DNA damage response signaling network. Clin Cancer Res 2010; 16:376-83; PMID:20068082; DOI:10.1158/1078-0432.CCR-09-1029.
-
(2010)
Clin Cancer Res
, vol.16
, pp. 376-383
-
-
Dai, Y.1
Grant, S.2
-
14
-
-
17244373777
-
Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy
-
PMID:15829967; DOI:10.1038/nature03445
-
Farmer H, McCabe N, Lord CJ, Tutt AN, Johnson DA, Richardson TB, et al. Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy. Nature 2005; 434:917-21; PMID:15829967; DOI:10.1038/nature03445.
-
(2005)
Nature
, vol.434
, pp. 917-921
-
-
Farmer, H.1
McCabe, N.2
Lord, C.J.3
Tutt, A.N.4
Johnson, D.A.5
Richardson, T.B.6
-
15
-
-
17244375049
-
Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADPribose) polymerase
-
PMID:15829966; DOI:10.1038/nature03443
-
Bryant HE, Schultz N, Thomas HD, Parker KM, Flower D, Lopez E, et al. Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADPribose) polymerase. Nature 2005; 434:913-7; PMID:15829966; DOI:10.1038/nature03443.
-
(2005)
Nature
, vol.434
, pp. 913-917
-
-
Bryant, H.E.1
Schultz, N.2
Thomas, H.D.3
Parker, K.M.4
Flower, D.5
Lopez, E.6
-
16
-
-
66349086978
-
Combined inhibition of MEK and mammalian target of rapamycin abolishes phosphorylation of cyclin-dependent kinase 4 in glioblastoma cell lines and prevents their proliferation
-
PMID:19458076; DOI:10.1158/0008-5472.CAN-08-3260
-
Paternot S, Roger PP. Combined inhibition of MEK and mammalian target of rapamycin abolishes phosphorylation of cyclin-dependent kinase 4 in glioblastoma cell lines and prevents their proliferation. Cancer Res 2009; 69:4577-81; PMID:19458076; DOI:10.1158/0008-5472.CAN-08-3260.
-
(2009)
Cancer Res
, vol.69
, pp. 4577-4581
-
-
Paternot, S.1
Roger, P.P.2
-
17
-
-
51349111250
-
Targeting AKT/mTOR and ERK MAPK signaling inhibits hormone-refractory prostate cancer in a preclinical mouse model
-
PMID:18725989
-
Kinkade CW, Castillo-Martin M, Puzio-Kuter A, Yan J, Foster TH, Gao H, et al. Targeting AKT/mTOR and ERK MAPK signaling inhibits hormone-refractory prostate cancer in a preclinical mouse model. J Clin Invest 2008; 118:3051-64; PMID:18725989.
-
(2008)
J Clin Invest
, vol.118
, pp. 3051-3064
-
-
Kinkade, C.W.1
Castillo-Martin, M.2
Puzio-Kuter, A.3
Yan, J.4
Foster, T.H.5
Gao, H.6
-
18
-
-
0030768948
-
Cdc25 mitotic inducer targeted by chk1 DNA damage checkpoint kinase
-
PMID:9278510; DOI:10.1126/science.277.5331.1495
-
Furnari B, Rhind N, Russell P. Cdc25 mitotic inducer targeted by chk1 DNA damage checkpoint kinase. Science 1997; 277:1495-7; PMID:9278510; DOI:10.1126/science.277.5331.1495.
-
(1997)
Science
, vol.277
, pp. 1495-1497
-
-
Furnari, B.1
Rhind, N.2
Russell, P.3
-
19
-
-
0030867582
-
Conservation of the Chk1 checkpoint pathway in mammals: Linkage of DNA damage to Cdk regulation through Cdc25
-
PMID:9278511; DOI:10.1126/science.277.5331.1497
-
Sanchez Y, Wong C, Thoma RS, Richman R, Wu Z, Piwnica-Worms H, et al. Conservation of the Chk1 checkpoint pathway in mammals: linkage of DNA damage to Cdk regulation through Cdc25. Science 1997; 277:1497-501; PMID:9278511; DOI:10.1126/science.277.5331.1497.
-
(1997)
Science
, vol.277
, pp. 1497-1501
-
-
Sanchez, Y.1
Wong, C.2
Thoma, R.S.3
Richman, R.4
Wu, Z.5
Piwnica-Worms, H.6
-
20
-
-
0026616796
-
Inactivation of the p34cdc2-cyclin B complex by the human WEE1 tyrosine kinase
-
PMID:1384126; DOI:10.1126/science.1384126
-
Parker LL, Piwnica-Worms H. Inactivation of the p34cdc2-cyclin B complex by the human WEE1 tyrosine kinase. Science 1992; 257:1955-7; PMID:1384126; DOI:10.1126/science.1384126.
-
(1992)
Science
, vol.257
, pp. 1955-1957
-
-
Parker, L.L.1
Piwnica-Worms, H.2
-
21
-
-
79952117003
-
Targeting Wee1-like protein kinase to treat cancer
-
PMID:20862394
-
Stathis A, Oza A. Targeting Wee1-like protein kinase to treat cancer. Drug News Perspect 2010; 23:425-9; PMID:20862394.
-
(2010)
Drug News Perspect
, vol.23
, pp. 425-429
-
-
Stathis, A.1
Oza, A.2
-
22
-
-
70949083026
-
Small-molecule inhibition of Wee1 kinase by MK-1775 selectively sensitizes p53-deficient tumor cells to DNA-damaging agents
-
PMID:19887545; DOI:10.1158/1535-7163.MCT-09-0463
-
Hirai H, Iwasawa Y, Okada M, Arai T, Nishibata T, Kobayashi M, et al. Small-molecule inhibition of Wee1 kinase by MK-1775 selectively sensitizes p53-deficient tumor cells to DNA-damaging agents. Mol Cancer Ther 2009; 8:2992-3000; PMID:19887545; DOI:10.1158/1535-7163.MCT-09-0463.
-
(2009)
Mol Cancer Ther
, vol.8
, pp. 2992-3000
-
-
Hirai, H.1
Iwasawa, Y.2
Okada, M.3
Arai, T.4
Nishibata, T.5
Kobayashi, M.6
-
23
-
-
77953711939
-
MK-1775, a small molecule Wee1 inhibitor, enhances anti-tumor efficacy of various DNA-damaging agents, including 5-fluorouracil
-
PMID:20107315; DOI:10.4161/cbt.9.7.11115
-
Hirai H, Arai T, Okada M, Nishibata T, Kobayashi M, Sakai N, et al. MK-1775, a small molecule Wee1 inhibitor, enhances anti-tumor efficacy of various DNA-damaging agents, including 5-fluorouracil. Cancer Biol Ther 2010; 9:514-22; PMID:20107315; DOI:10.4161/cbt.9.7.11115.
-
(2010)
Cancer Biol Ther
, vol.9
, pp. 514-522
-
-
Hirai, H.1
Arai, T.2
Okada, M.3
Nishibata, T.4
Kobayashi, M.5
Sakai, N.6
-
24
-
-
79955492036
-
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 JW, Brooks D, Demuth T, et al. MK-1775, a potent Wee1 inhibitor, synergizes with gemcitabine to achieve tumor regressions, selectively in p53-deficient pancreatic cancer xenografts. Clin Cancer Res 2011; 17:2799-806.
-
(2011)
Clin Cancer Res
, vol.17
, pp. 2799-2806
-
-
Rajeshkumar, N.V.1
De Oliveira, E.2
Ottenhof, N.3
Watters, J.W.4
Brooks, D.5
Demuth, T.6
-
25
-
-
30044440857
-
Chk1 and p21 cooperate to prevent apoptosis during DNA replication fork stress
-
PMID:16280359; DOI:10.1091/mbc.E05-07-0594
-
Rodriguez R, Meuth M. Chk1 and p21 cooperate to prevent apoptosis during DNA replication fork stress. Mol Biol Cell 2006; 17:402-12; PMID:16280359; DOI:10.1091/mbc.E05-07-0594.
-
(2006)
Mol Biol Cell
, vol.17
, pp. 402-412
-
-
Rodriguez, R.1
Meuth, M.2
-
26
-
-
33746495515
-
Depletion of CHK1, but not CHK2, induces chromosomal instability and breaks at common fragile sites
-
PMID:16732333; DOI:10.1038/sj.onc.1209466
-
Durkin SG, Arlt MF, Howlett NG, Glover TW. Depletion of CHK1, but not CHK2, induces chromosomal instability and breaks at common fragile sites. Oncogene 2006; 25:4381-8; PMID:16732333; DOI:10.1038/sj.onc.1209466.
-
(2006)
Oncogene
, vol.25
, pp. 4381-4388
-
-
Durkin, S.G.1
Arlt, M.F.2
Howlett, N.G.3
Glover, T.W.4
-
27
-
-
0037415735
-
Chk1-deficient tumour cells are viable but exhibit multiple checkpoint and survival defects
-
PMID:12554671; DOI:10.1093/emboj/cdg060
-
Zachos G, Rainey MD, Gillespie DA. Chk1-deficient tumour cells are viable but exhibit multiple checkpoint and survival defects. EMBO J 2003; 22:713-23; PMID:12554671; DOI:10.1093/emboj/cdg060.
-
(2003)
EMBO J
, vol.22
, pp. 713-723
-
-
Zachos, G.1
Rainey, M.D.2
Gillespie, D.A.3
-
28
-
-
28244497051
-
Depletion of Chk1 leads to premature activation of Cdc2-cyclin B and mitotic catastrophe
-
PMID:16159883; DOI:10.1074/jbc.M505009200
-
Niida H, Tsuge S, Katsuno Y, Konishi A, Takeda N, Nakanishi M. Depletion of Chk1 leads to premature activation of Cdc2-cyclin B and mitotic catastrophe. J Biol Chem 2005; 280:39246-52; PMID:16159883; DOI:10.1074/jbc.M505009200.
-
(2005)
J Biol Chem
, vol.280
, pp. 39246-39252
-
-
Niida, H.1
Tsuge, S.2
Katsuno, Y.3
Konishi, A.4
Takeda, N.5
Nakanishi, M.6
-
29
-
-
77955655940
-
Identification of WEE1 as a potential molecular target in cancer cells by RNAi screening of the human tyrosine kinome
-
PMID:19821025; DOI:10.1007/s10549-009-0571-2
-
Murrow LM, Garimella SV, Jones TL, Caplen NJ, Lipkowitz S. Identification of WEE1 as a potential molecular target in cancer cells by RNAi screening of the human tyrosine kinome. Breast Cancer Res Treat 2010; 122:347-57; PMID:19821025; DOI:10.1007/s10549-009-0571-2.
-
(2010)
Breast Cancer Res Treat
, vol.122
, pp. 347-357
-
-
Murrow, L.M.1
Garimella, S.V.2
Jones, T.L.3
Caplen, N.J.4
Lipkowitz, S.5
-
30
-
-
0037303640
-
Depletion of Wee-1 kinase is necessary for both human immunodeficiency virus type 1 Vpr- and gamma irradiation-induced apoptosis
-
PMID:12525641; DOI:10.1128/JVI.77.3.2063-70.2003
-
Yuan H, Xie YM, Chen IS. Depletion of Wee-1 kinase is necessary for both human immunodeficiency virus type 1 Vpr- and gamma irradiation-induced apoptosis. J Virol 2003; 77:2063-70; PMID:12525641; DOI:10.1128/JVI.77.3.2063- 70.2003.
-
(2003)
J Virol
, vol.77
, pp. 2063-2070
-
-
Yuan, H.1
Xie, Y.M.2
Chen, I.S.3
-
31
-
-
33744905789
-
Murine Wee1 plays a critical role in cell cycle regulation and preimplantation stages of embryonic development
-
PMID:16810330
-
Tominaga Y, Li C, Wang RH, Deng CX. Murine Wee1 plays a critical role in cell cycle regulation and preimplantation stages of embryonic development. Int J Biol Sci 2006; 2:161-70; PMID:16810330.
-
(2006)
Int J Biol Sci
, vol.2
, pp. 161-170
-
-
Tominaga, Y.1
Li, C.2
Wang, R.H.3
Deng, C.X.4
-
32
-
-
77949410508
-
Regulators of cyclin-dependent kinases are crucial for maintaining genome integrity in S phase
-
PMID:20194642; DOI:10.1083/jcb.200905059
-
Beck H, Nahse V, Larsen MS, Groth P, Clancy T, Lees M, et al. Regulators of cyclin-dependent kinases are crucial for maintaining genome integrity in S phase. J Cell Biol 2010; 188:629-38; PMID:20194642; DOI:10.1083/jcb.200905059.
-
(2010)
J Cell Biol
, vol.188
, pp. 629-638
-
-
Beck, H.1
Nahse, V.2
Larsen, M.S.3
Groth, P.4
Clancy, T.5
Lees, M.6
-
33
-
-
3142552523
-
Chk1 is haploinsufficient for multiple functions critical to tumor suppression
-
PMID:15261141; DOI:10.1016/j.ccr.2004.06.015
-
Lam MH, Liu Q, Elledge SJ, Rosen JM. Chk1 is haploinsufficient for multiple functions critical to tumor suppression. Cancer Cell 2004; 6:45-59; PMID:15261141; DOI:10.1016/j.ccr.2004.06.015.
-
(2004)
Cancer Cell
, vol.6
, pp. 45-59
-
-
Lam, M.H.1
Liu, Q.2
Elledge, S.J.3
Rosen, J.M.4
-
34
-
-
22844436238
-
Chk1 is essential for tumor cell viability following activation of the replication checkpoint
-
PMID:15539958; DOI:10.4161/ cc.4.1.1299
-
Cho SH, Toouli CD, Fujii GH, Crain C, Parry D. Chk1 is essential for tumor cell viability following activation of the replication checkpoint. Cell Cycle 2005; 4:131-9; PMID:15539958; DOI:10.4161/ cc.4.1.1299.
-
(2005)
Cell Cycle
, vol.4
, pp. 131-139
-
-
Cho, S.H.1
Toouli, C.D.2
Fujii, G.H.3
Crain, C.4
Parry, D.5
-
35
-
-
65449142073
-
CHK1 inhibition as a strategy for targeting Fanconi Anemia (FA) DNA repair pathway deficient tumors
-
PMID:19371427; DOI:10.1186/1476-4598-8-24
-
Chen CC, Kennedy RD, Sidi S, Look AT, D'Andrea A. CHK1 inhibition as a strategy for targeting Fanconi Anemia (FA) DNA repair pathway deficient tumors. Mol Cancer 2009; 8:24; PMID:19371427; DOI:10.1186/1476-4598-8-24.
-
(2009)
Mol Cancer
, vol.8
, pp. 24
-
-
Chen, C.C.1
Kennedy, R.D.2
Sidi, S.3
Look, A.T.4
D'Andrea, A.5
-
36
-
-
33749626550
-
Phosphorylation of Chk1 by ATR is antagonized by a Chk1-regulated protein phosphatase 2A circuit
-
PMID:17015476; DOI:10.1128/MCB.00447-06
-
Leung-Pineda V, Ryan CE, Piwnica-Worms H. Phosphorylation of Chk1 by ATR is antagonized by a Chk1-regulated protein phosphatase 2A circuit. Mol Cell Biol 2006; 26:7529-38; PMID:17015476; DOI:10.1128/MCB.00447-06.
-
(2006)
Mol Cell Biol
, vol.26
, pp. 7529-7538
-
-
Leung-Pineda, V.1
Ryan, C.E.2
Piwnica-Worms, H.3
-
37
-
-
77649083117
-
Enhanced H2AX phosphorylation, DNA replication fork arrest and cell death in the absence of Chk1
-
PMID:20053681; DOI:10.1091/mbc.E09-07-0618
-
Gagou ME, Zuazua-Villar P, Meuth M. Enhanced H2AX phosphorylation, DNA replication fork arrest and cell death in the absence of Chk1. Mol Biol Cell 2010; 21:739-52; PMID:20053681; DOI:10.1091/mbc.E09-07-0618.
-
(2010)
Mol Biol Cell
, vol.21
, pp. 739-752
-
-
Gagou, M.E.1
Zuazua-Villar, P.2
Meuth, M.3
-
38
-
-
34147206546
-
Specific role of Chk1 phosphorylations in cell survival and checkpoint activation
-
PMID:17242188; DOI:10.1128/MCB.01611-06
-
Niida H, Katsuno Y, Banerjee B, Hande MP, Nakanishi M. Specific role of Chk1 phosphorylations in cell survival and checkpoint activation. Mol Cell Biol 2007; 27:2572-81; PMID:17242188; DOI:10.1128/MCB.01611-06.
-
(2007)
Mol Cell Biol
, vol.27
, pp. 2572-2581
-
-
Niida, H.1
Katsuno, Y.2
Banerjee, B.3
Hande, M.P.4
Nakanishi, M.5
-
39
-
-
79955758170
-
Context Dependence of Checkpoint Kinase 1 as a Therapeutic Target for Pancreatic Cancers Deficient in the BRCA2 Tumor Suppressor
-
PMID:21289082; DOI:10.1158/1535-7163.MCT-10-0781
-
Hattori H, Skoulidis F, Russell P, Venkitaraman AR. Context Dependence of Checkpoint Kinase 1 as a Therapeutic Target for Pancreatic Cancers Deficient in the BRCA2 Tumor Suppressor. Mol Cancer Ther 2011; 10:670-8; PMID:21289082; DOI:10.1158/1535-7163.MCT-10-0781.
-
(2011)
Mol Cancer Ther
, vol.10
, pp. 670-678
-
-
Hattori, H.1
Skoulidis, F.2
Russell, P.3
Venkitaraman, A.R.4
-
40
-
-
67649710471
-
Discovery of gene expression-based pharmacodynamic biomarker for a p53 context-specific anti-tumor drug Wee1 inhibitor
-
PMID:19500427; DOI:10.1186/1476-4598-8-34
-
Mizuarai S, Yamanaka K, Itadani H, Arai T, Nishibata T, Hirai H, et al. Discovery of gene expression-based pharmacodynamic biomarker for a p53 context-specific anti-tumor drug Wee1 inhibitor. Mol Cancer 2009; 8:34; PMID:19500427; DOI:10.1186/1476-4598-8-34.
-
(2009)
Mol Cancer
, vol.8
, pp. 34
-
-
Mizuarai, S.1
Yamanaka, K.2
Itadani, H.3
Arai, T.4
Nishibata, T.5
Hirai, H.6
-
41
-
-
16544392882
-
Knockdown of Chk1, Wee1 and Myt1 by RNA interference abrogates G2 checkpoint and induces apoptosis
-
PMID:14726685; DOI:10.4161/cbt.3.3.697
-
Wang Y, Decker SJ, Sebolt-Leopold J. Knockdown of Chk1, Wee1 and Myt1 by RNA interference abrogates G2 checkpoint and induces apoptosis. Cancer Biol Ther 2004; 3:305-13; PMID:14726685; DOI:10.4161/cbt.3.3.697.
-
(2004)
Cancer Biol Ther
, vol.3
, pp. 305-313
-
-
Wang, Y.1
Decker, S.J.2
Sebolt-Leopold, J.3
-
42
-
-
13944266820
-
The cell cycle checkpoint kinase Chk1 is required for mammalian homologous recombination repair
-
PMID:15665856; DOI:10.1038/ncb1212
-
Sørensen CS, Hansen LT, Dziegielewski J, Syljuasen RG, Lundin C, Bartek J, et al. The cell cycle checkpoint kinase Chk1 is required for mammalian homologous recombination repair. Nat Cell Biol 2005; 7:195-201; PMID:15665856; DOI:10.1038/ncb1212.
-
(2005)
Nat Cell Biol
, vol.7
, pp. 195-201
-
-
Sørensen, C.S.1
Hansen, L.T.2
Dziegielewski, J.3
Syljuasen, R.G.4
Lundin, C.5
Bartek, J.6
-
43
-
-
33846636785
-
Chk1 is required for spindle checkpoint function
-
PMID:17276342; DOI:10.1016/j.devcel.2007.01.003
-
Zachos G, Black EJ, Walker M, Scott MT, Vagnarelli P, Earnshaw WC, et al. Chk1 is required for spindle checkpoint function. Dev Cell 2007; 12:247-60; PMID:17276342; DOI:10.1016/j.devcel.2007.01.003.
-
(2007)
Dev Cell
, vol.12
, pp. 247-260
-
-
Zachos, G.1
Black, E.J.2
Walker, M.3
Scott, M.T.4
Vagnarelli, P.5
Earnshaw, W.C.6
-
44
-
-
34047190253
-
Chk1-mediated phosphorylation of FANCE is required for the Fanconi anemia/ BRCA pathway
-
PMID:17296736; DOI:10.1128/MCB.02357-06
-
Wang X, Kennedy RD, Ray K, Stuckert P, Ellenberger T, D'Andrea AD. Chk1-mediated phosphorylation of FANCE is required for the Fanconi anemia/ BRCA pathway. Mol Cell Biol 2007; 27:3098-108; PMID:17296736; DOI:10.1128/MCB.02357- 06.
-
(2007)
Mol Cell Biol
, vol.27
, pp. 3098-3108
-
-
Wang, X.1
Kennedy, R.D.2
Ray, K.3
Stuckert, P.4
Ellenberger, T.5
D'Andrea, A.D.6
-
45
-
-
0029895439
-
UCN-01: A potent abrogator of G2 checkpoint function in cancer cells with disrupted p53
-
PMID:8667426; DOI:10.1093/jnci/88.14.956
-
Wang Q, Fan S, Eastman A, Worland PJ, Sausville EA, O'Connor PM. UCN-01: a potent abrogator of G2 checkpoint function in cancer cells with disrupted p53. J Natl Cancer Inst 1996; 88:956-65; PMID:8667426; DOI:10.1093/jnci/88.14.956.
-
(1996)
J Natl Cancer Inst
, vol.88
, pp. 956-965
-
-
Wang, Q.1
Fan, S.2
Eastman, A.3
Worland, P.J.4
Sausville, E.A.5
O'Connor, P.M.6
-
46
-
-
39749185974
-
Defective p53 signaling in p53 wild-type tumors attenuates p21waf1 induction and cyclin B repression rendering them sensitive to Chk1 inhibitors that abrogate DNA damage-induced S and G2 arrest
-
PMID:18281511; DOI:10.1158/1535-7163.MCT-07-2066
-
Levesque AA, Fanous AA, Poh A, Eastman A. Defective p53 signaling in p53 wild-type tumors attenuates p21waf1 induction and cyclin B repression rendering them sensitive to Chk1 inhibitors that abrogate DNA damage-induced S and G2 arrest. Mol Cancer Ther 2008; 7:252-62; PMID:18281511; DOI:10.1158/1535-7163. MCT-07-2066.
-
(2008)
Mol Cancer Ther
, vol.7
, pp. 252-262
-
-
Levesque, A.A.1
Fanous, A.A.2
Poh, A.3
Eastman, A.4
-
47
-
-
72249108356
-
Constitutive activation of the DNA damage signaling pathway in acute myeloid leukemia with complex karyotype: Potential importance for checkpoint targeting therapy
-
PMID:19843865; DOI:10.1158/0008-5472.CAN-09-0939
-
Cavelier C, Didier C, Prade N, Mansat-De Mas V, Manenti S, Recher C, et al. Constitutive activation of the DNA damage signaling pathway in acute myeloid leukemia with complex karyotype: potential importance for checkpoint targeting therapy. Cancer Res 2009; 69:8652-61; PMID:19843865; DOI:10.1158/0008-5472.CAN- 09-0939.
-
(2009)
Cancer Res
, vol.69
, pp. 8652-8661
-
-
Cavelier, C.1
Didier, C.2
Prade, N.3
Mansat-De Mas, V.4
Manenti, S.5
Recher, C.6
|