References
- J. Biol. Chem. v.277 ATM is activated in response to N-methyl-N'-nitro-N-nitrosoguanidine-induced DNA alkylation Adamson,A.W.;Kim,W.J.;Shangary,S.;Baskaran,R.;Brown,K.D. https://doi.org/10.1074/jbc.M204409200
- Exp. Cell. Res. v.256 The Bcl-2 protein family Antonsson,B.;Martinou,J.C. https://doi.org/10.1006/excr.2000.4839
- J. Clin. Invest. v.98 Competency in mismatch repair prohibits clonal expansion of cancer cells treated with N-methyl-N'-nitro-N-nitrosoguanidine Carethers,J.M.;Hawn,M.T.;Chauhan,D.P.;Luce,M.C.;Marra,G.;Koi,M.;Boland,C.R. https://doi.org/10.1172/JCI118767
- Cell Mol Biol. Res. v.40 Apoptosis and the cell cycle Chiarugi,V.;Magnelli,L.;Clinelli,M.;Basi,G.
- Exp. Mol. Med. v.33 Research technics for the cell cycle study Choi.Y.H. https://doi.org/10.1038/emm.2001.3
- Int. J. Oncol. v.18 Apoptotic activity of novel bile acid derivatives in human leukemic T cells through the activation of caspases Choi,Y.H.;Im,E.O.;Suh,H.S.;Jin.Y.E.;Lee,W.H.;Yoo,Y.H.;Kim,K.W.;Kim,N.D.
- J. Biol. Chem. v.272 Regulation of cyclin D1 by calpain protease Choi,Y.H.;Lee,S.J.;Nguyen,P.;Jang,J.S.;Lee,J.;Wu,M.L.;Takano,E.;Maki,M.;Henkart,P.A.;Trepel,J.B. https://doi.org/10.1074/jbc.272.45.28479
- Jpn. J. Cancer Res. v.91 p53-independent induction of p21 (WAF1/CIP1), reduction of cyclin B1 and G2/M arrest by the isoflavone genistein in human prostate carcinoma cells Choi,Y.H.;Lee,W.H.;Park,K.Y.;Zhang,L. https://doi.org/10.1111/j.1349-7006.2000.tb00928.x
- Proc. Natl. Acad. Sci. v.96 hMutSalpha- and hMutLalpha-dependent phosphorylation of p53 in response to DNA methylator damage Duckett,D.R.;Bronstein,S.M.;Taya,Y.;Modrich,P. https://doi.org/10.1073/pnas.96.22.12384
- Toxicology v.163 Cell cycle was disturbed in the MNNG-induced initiation stage during in vitro two-stage transformation of Balb/3T3 cells Fang,M.Z.;Mar,W.C.;Cho,M.H. https://doi.org/10.1016/S0300-483X(01)00400-0
- Int. J. Biochem. Cell. Biol. v.31 Apoptosis-associated cleavate of β-catenin in human colon cancer and rat hepatoma cells Fukuda,K. https://doi.org/10.1016/S1357-2725(98)00119-8
- J. Biol. Chem. v.274 Survival and proliferation of cells expressing caspase-uncleavable Poly(ADP-ribose) polymerase in response to death-inducing DNA damage by an alkylating agent Halappanavar,S.S.;Rhun,Y.L.;Mounir,S.;Martins,L.M.;Huot,J.;Earnshaw,W.C.;Shah,G.M. https://doi.org/10.1074/jbc.274.52.37097
- Blood Rev. v.6 Mechanisms of action of, and modes of resistance to, alkylating agents used in the treatment of haematological malignancies Hall,A.G.;Tilby,M.J. https://doi.org/10.1016/0268-960X(92)90028-O
- Cancer Res. v.55 Evidence for a connection between the mismatch repair system and the G2 cell cycle checkpoint Hawn,M.T.;Umar,A.;Carethers,J.M.;Marra,G.;Kunkel,T.A.;Boland,C.R.;Koi,M.
- Proc. Natl. Acad. Sci. v.96 Role of DNA mismatch repair and p53 in signaling induction of apoptosis by alkylating agents Hickman,M.J.;Samson,L.D. https://doi.org/10.1073/pnas.96.19.10764
- Apoptosis v.6 XIAP: apoptotic brake and promising therapeutic target Holcik,M.;Gibson,H.;Komeluk,R.G. https://doi.org/10.1023/A:1011379307472
- J. Pathol. v.199 Apoptosis and melanoma: molecular mechanisms Hussein,M.R.;Haemel,A.K.;Wood,G.S. https://doi.org/10.1002/path.1300
- Mutat. Res. v.500 SN2 DNA-alkylating agent-induced phosphorylation of p53 and activation of p21 gene expression Jaiswal,A.S.;Narayan,S. https://doi.org/10.1016/S0027-5107(01)00296-2
- Cancer Metastasis Rev. v.8 Cell adhesion molecules in the development and progression of malignant melanoma Johnson,J.P.
- Proc. Natl. Acad. Sci. v.95 Bax directly induces release of cytochrome c from isolated mitochondria Jurgensmeier,J.M.;Xie,Z.;Deveraux,Q.;Ellerby,L.;Bredesen,D.;Reed,J.C. https://doi.org/10.1073/pnas.95.9.4997
- Proc. Natl. Acad. Sci. v.90 An alkylation-tolerant, mutator human cell line is deficient in strand-specific mismatch repair Kat,A.;Thilly,W.G.;Fang.W.H.;Longley,M.J.;Li,G.M.;Modrich,P. https://doi.org/10.1073/pnas.90.14.6424
- Cancer Res. v.53 Specific proteolytic cleavage of poly(ADP-ribose) polymerase: an early marker of chemotherapy-induced apoptosis Kaufmann,S.H.;Desnoyers,S.;Ottaviano,Y.;Davidson,N.E.;Poirier,G.G.
- Carcinogenesis v.21 Diverse chemical carcinogens fail to induce G(1) arrest in MCF-7 cells Khan,Q.A.;Dipple,A. https://doi.org/10.1093/carcin/21.8.1611
- Science v.275 The release of cytochrome c from mitochondria: a primary site for Bcl-2 regulation of apoptosis Kluck,R.M.;Bossy-Wetzel,E.;Green,D.R.;Newmeyer,D.D. https://doi.org/10.1126/science.275.5303.1132
- Cancer Invest. v.13 Current chemotherapy and future directions in research for the treatment of advanced hormone-refractory prostate cancer Kreis,W. https://doi.org/10.3109/07357909509094465
- Nature v.371 Cleavage of poly(ADP-ribose) polymerase by a proteinase with properties like ICE Lazebnik,Y.A.;Kaufmann.S.H.;Desnoyers,S.;Poirier,G.G.;Earnshaw,W.C. https://doi.org/10.1038/371346a0
- Acta. Biochim. Pol. v.46 Mitochondria, oxidative stress, and antioxidant defences Lanaz,G.;Bovina,C.;Formiggini,G.;Castelli,G.P.
- Semin. Nephrol. v.18 Necrosis and apoptosis in acute renal failure Lieberthal,W.;Koh,J.S.;Levine,J.S.
- Cell v.88 Apopotosis by death factor Nagata,S. https://doi.org/10.1016/S0092-8674(00)81874-7
- Br. J. Cancer v.85 DNA damage-induced cell cycle checkpoints involve both p53-dependent and -independent pathways: role of telomere repeat binding factor 2 Narayan,S.;Jaiswal,A.S.;Multani,A.S.;Pathak,S. https://doi.org/10.1054/bjoc.2001.2002
- J. Biol. Chem. v.276 p53 Phosphorylation at serine 15 is required for transcriptional induction of the plasminogen activator inhibitor-1 (PAI-1) gene by the alkylating agent N-methyl-N'-nitro-N-nitrosoguanidine Parra,M.;Jardi,M.;Koziczak,M.;Nagamine,Y.;Munoz-Canoves,P. https://doi.org/10.1074/jbc.M103735200
- Exp. Cell Res. v.257 The human cyclin B1 protein modulates sensitivity of DNA mismatch repair deficient prostate cancer cell lines to alkylating agents Rasmussen,L.J.;Rasmussen,M.;Lutzen.A.;Bisgaard,H.C.;Singh,K.K. https://doi.org/10.1006/excr.2000.4865
- Oncogene v.17 Bcl-2 family proteins Reed,J.C. https://doi.org/10.1038/sj.onc.1202591
- Nature v.391 Bcl-2 prolongs cell survival after Bax-induced release of cytochrome c Rosse,T.;Olivier,R.;Monney,L.;Rager,M.;Conus,S.;Fellay,I.;Jansen,B.;Borner,C. https://doi.org/10.1038/35160
- Rev. Reprod v.5 Cadherins: crucial regulators of structure and function in reproductive tissues Rowlands,T.M.;Symonds,J.M.;Farookhi,R.;Blaschuk,O.W. https://doi.org/10.1530/ror.0.0050053
- Nat. Rev. Mol. Cell. Biol. v.3 IAP proteins; blocking the road to death's door Salvesen,G.S.;Duckett,C.S. https://doi.org/10.1038/nrm830
- Eur. J. Biochem. v.254 Apoptosis signaling by death receptors Schulze-Osthoff,K.;Ferrai,D.;Los,M.;Wesselborg,S.;Peter,M.E. https://doi.org/10.1046/j.1432-1327.1998.2540439.x
- Pathol. Annu. v.17 Necrosis and apoptosis: distinct modes of cell death with fundamentally different significance Searle,J.;Kerr,J.F.;Bishop,C.J.
- Oncogene v.12 Oncogenic transformation of HPV-immortalized human oral keratinocytes is associated with the genetic instability of cells Shin,K.H.;Tannyhill,R.J.;Liu,X.;Park,N.H.
- J. Biol. Chem. v.275 Apoptosis-induced cleavage of β-catenin by caspase-3 results in proteolytic fragments with reduced transactivation potential Steinhusen,U.;Badock,V.;Bauer,A.;Behrens,J.;Wittman-Liebold,B.;Dorken,B.;Bommert,K. https://doi.org/10.1074/jbc.M001458200
- Cell v.79 DNA damage can induce apoptosis in proliferating lymphoid cells via p53-independent mechanisms inhibitable by Bcl-2 Strasser,A.;Harris,A.W.;Jacks,T.;Cory,S. https://doi.org/10.1016/0092-8674(94)90201-1
- Cell v.81 Yama/CPP32 β, a mammalian homolog of CED-3, is a CrmA-inhibitable protease that cleaves the death substrate poly(ADP-ribose) polymerase Tewari,M.;Quan,L.T.;O'Rourke,K;Desnoyers,S.;Zeng,Z.;Beidler,D.R.;Poirier,G.G.;Salvesen,G.S.;Dixit,V.M. https://doi.org/10.1016/0092-8674(95)90541-3
- Prostate v.47 Widely used prostate carcinoma cell lines share common origins van Bokhoven,A.;Varella-Garcia,M.;Korch,C.;Hessels,D.;Miller,G.J. https://doi.org/10.1002/pros.1045
- Crit. Rev. Toxicol. v.24 Intragenomic heterogeneity of DNA damage formation and repair: a review of cellular responses to covalent drug DNA interaction Wassermann,K. https://doi.org/10.3109/10408449409017921
- Br. J. Surg. v.87 Ecadherin-catenin cell-cell adhesion complex and human cancer Wijnhoven,B.P.;Dinjens,W.N.;Pignatelli,M. https://doi.org/10.1046/j.1365-2168.2000.01513.x
- Int. Rev. Cytol. v.68 Cell death: the significance of apoptosis Wyllie,A.H.;Kerr,J.F.;Currie,A.R. https://doi.org/10.1016/S0074-7696(08)62312-8
- J. Biol. Chem. v.276 Activation of a p53-independent, sphingolipid-mediated cytolytic pathway in p53-negative mouse fibroblast cells treated with Nmethyl-N-nitro-N-nitrosoguanidine Yang,J.;Duerksen-Hughes,P.J. https://doi.org/10.1074/jbc.M100729200
- Pharmacol. Ther. v.92 The machinery of programmed cell death Zimmermann,K.C.;Bonzon,C.;Green,D.R. https://doi.org/10.1016/S0163-7258(01)00159-0