2018
Galluzzi, L., Vitale, I., Aaronson, SA., Abrams, JM., Adam, D., Agostinis, P., Alnemri, ES., Altucci, L., Amelio, I., Andrews, DW., Annicchiarico-Petruzzelli, M., Antonov, AV., Arama, E., Baehrecke, EH., Barlev, NA., Bazan, NG., Bernassola, F., Bertrand, MJM., Bianchi, K., Blagosklonny, MV., Blomgren, K., Borner, C., Boya, P., Brenner, C., Campanella, M., Candi, E., Carmona-Gutierrez, D., Cecconi, F., Chan, FK-M., Chandel, NS., Cheng, EH., Chipuk, JE., Cidlowski, JA., Ciechanover, A., Cohen, GM., Conrad, M., Cubillos-Ruiz, JR., Czabotar, PE., D'Angiolella, V., Dawson, TM., Dawson, VL., De Laurenzi, V., De Maria, R., Debatin, K-M., DeBerardinis, RJ., Deshmukh, M., Di Daniele, N., Di Virgilio, F., Dixit, VM., Dixon, SJ., Duckett, CS., Dynlacht, BD., El-Deiry, WS., Elrod, JW., Fimia, GM., Fulda, S., García-Sáez, AJ., Garg, AD., Garrido, C., Gavathiotis, E., Golstein, P., Gottlieb, E., Green, DR., Greene, LA., Gronemeyer, H., Gross, A., Hajnoczky, G., Hardwick, JM., Harris, IS., Hengartner, MO., Hetz, C., Ichijo, H., Jäättelä, M., Joseph, B., Jost, PJ., Juin, PP., Kaiser, WJ., Karin, M., Kaufmann, T., Kepp, O., Kimchi, A., Kitsis, RN., Klionsky, DJ., Knight, RA., Kumar, S., Lee, SW., Lemasters, JJ., Levine, B., Linkermann, A., Lipton, SA., Lockshin, RA., López-Otín, C., Lowe, SW., Luedde, T., Lugli, E., MacFarlane, M., Madeo, F., Malewicz, M., Malorni, W., Manic, G., Marine, J-C., Martin, SJ., Martinou, J-C., Medema, JP., Mehlen, P., Meier, P., Melino, S., Miao, EA., Molkentin, JD., Moll, UM., Muñoz-Pinedo, C., Nagata, S., Nuñez, G., Oberst, A., Oren, M., Overholtzer, M., Pagano, M., Panaretakis, T., Pasparakis, M., Penninger, JM., Pereira, DM., Pervaiz, S., Peter, ME., Piacentini, M., Pinton, P., Prehn, JHM., Puthalakath, H., Rabinovich, GA., Rehm, M., Rizzuto, R., Rodrigues, CMP., Rubinsztein, DC., Rudel, T., Ryan, KM., Sayan, E., Scorrano, L., Shao, F., Shi, Y., Silke, J., Simon, H-U., Sistigu, A., Stockwell, BR., Strasser, A., Szabadkai, G., Tait, SWG., Tang, D., Tavernarakis, N., Thorburn, A., Tsujimoto, Y., Turk, B., Vanden Berghe, T., Vandenabeele, P., Vander Heiden, MG., Villunger, A., Virgin, HW., Vousden, KH., Vucic, D., Wagner, EF., Walczak, H., Wallach, D., Wang, Y., Wells, JA., Wood, W., Yuan, J., Zakeri, Z., Zhivotovsky, B., Zitvogel, L., Melino, G. and Kroemer, G., 2018. Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018. Cell Death Differ, v. 25
Doi: http://doi.org/10.1038/s41418-017-0012-4
Estornes, Y., Dondelinger, Y., Weber, K., Bruggeman, I., Peall, A., MacFarlane, M., Lebecque, S., Vandenabeele, P. and Bertrand, MJM., 2018. N-glycosylation of mouse TRAIL-R restrains TRAIL-induced apoptosis. Cell Death Dis, v. 9
Doi: http://doi.org/10.1038/s41419-018-0544-7
2017
Chernova, T., Murphy, FA., Galavotti, S., Sun, X-M., Powley, IR., Grosso, S., Schinwald, A., Zacarias-Cabeza, J., Dudek, KM., Dinsdale, D., Le Quesne, J., Bennett, J., Nakas, A., Greaves, P., Poland, CA., Donaldson, K., Bushell, M., Willis, AE. and MacFarlane, M., 2017. Long-Fiber Carbon Nanotubes Replicate Asbestos-Induced Mesothelioma with Disruption of the Tumor Suppressor Gene Cdkn2a (Ink4a/Arf). Curr Biol, v. 27
Doi: 10.1016/j.cub.2017.09.007
Karekla, E., Liao, W-J., Sharp, B., Pugh, J., Reid, H., Quesne, JL., Moore, D., Pritchard, C., MacFarlane, M. and Pringle, JH., 2017. Ex Vivo Explant Cultures of Non-Small Cell Lung Carcinoma Enable Evaluation of Primary Tumor Responses to Anticancer Therapy. Cancer Res, v. 77
Doi: http://doi.org/10.1158/0008-5472.CAN-16-1121
Horn, S., Hughes, MA., Schilling, R., Sticht, C., Tenev, T., Ploesser, M., Meier, P., Sprick, MR., MacFarlane, M. and Leverkus, M., 2017. Caspase-10 Negatively Regulates Caspase-8-Mediated Cell Death, Switching the Response to CD95L in Favor of NF-κB Activation and Cell Survival. Cell Rep, v. 19
Doi: http://doi.org/10.1016/j.celrep.2017.04.010
2016
Busacca, S., Law, EWP., Powley, IR., Proia, DA., Sequeira, M., Le Quesne, J., Klabatsa, A., Edwards, JM., Matchett, KB., Luo, JL., Pringle, JH., El-Tanani, M., MacFarlane, M. and Fennell, DA., 2016. Resistance to HSP90 inhibition involving loss of MCL1 addiction. Oncogene, v. 35
Doi: 10.1038/onc.2015.213
Chernova, T., Sun, XM., Powley, IR., Galavotti, S., Grosso, S., Murphy, FA., Miles, GJ., Cresswell, L., Antonov, AV., Bennett, J., Nakas, A., Dinsdale, D., Cain, K., Bushell, M., Willis, AE. and MacFarlane, M., 2016. Molecular profiling reveals primary mesothelioma cell lines recapitulate human disease. Cell Death Differ, v. 23
Doi: 10.1038/cdd.2015.165
Fox, JL. and MacFarlane, M., 2016. Targeting cell death signalling in cancer: minimising 'Collateral damage'. Br J Cancer, v. 115
Doi: 10.1038/bjc.2016.111
Powley, IR., Hughes, MA., Cain, K. and MacFarlane, M., 2016. Caspase-8 tyrosine-380 phosphorylation inhibits CD95 DISC function by preventing procaspase-8 maturation and cycling within the complex. Oncogene, v. 35
Doi: http://doi.org/10.1038/onc.2016.99
Hughes, MA., Powley, IR., Jukes-Jones, R., Horn, S., Feoktistova, M., Fairall, L., Schwabe, JWR., Leverkus, M., Cain, K. and MacFarlane, M., 2016. Co-operative and Hierarchical Binding of c-FLIP and Caspase-8: A Unified Model Defines How c-FLIP Isoforms Differentially Control Cell Fate. Mol Cell, v. 61
Doi: 10.1016/j.molcel.2016.02.023
2015
Naik, S., MacFarlane, M. and Sarin, A., 2015. Notch4 Signaling Confers Susceptibility to TRAIL-Induced Apoptosis in Breast Cancer Cells. J Cell Biochem, v. 116
Doi: http://doi.org/10.1002/jcb.25094
Langlais, C., Hughes, MA., Cain, K. and MacFarlane, M., 2015. In Vitro Assembly and Analysis of the Apoptosome Complex. Cold Spring Harb Protoc, v. 2015
Doi: 10.1101/pdb.prot087080
Langlais, C., Hughes, MA., Cain, K. and MacFarlane, M., 2015. Biochemical Analysis of Initiator Caspase-Activating Complexes: The Apoptosome and the Death-Inducing Signaling Complex. Cold Spring Harb Protoc, v. 2015
Doi: 10.1101/pdb.top070326
Hughes, MA., Langlais, C., Cain, K. and MacFarlane, M., 2015. Activation, Isolation, and Analysis of the Death-Inducing Signaling Complex. Cold Spring Harb Protoc, v. 2015
Doi: 10.1101/pdb.prot087098
2014
Elia, A., Powley, IR., MacFarlane, M. and Clemens, MJ., 2014. Modulation of the sensitivity of Jurkat T-cells to inhibition of protein synthesis by tumor necrosis factor α-related apoptosis-inducing ligand. J Interferon Cytokine Res, v. 34
Doi: 10.1089/jir.2013.0061
Horvilleur, E., Sbarrato, T., Hill, K., Spriggs, RV., Screen, M., Goodrem, PJ., Sawicka, K., Chaplin, LC., Touriol, C., Packham, G., Potter, KN., Dirnhofer, S., Tzankov, A., Dyer, MJS., Bushell, M., MacFarlane, M. and Willis, AE., 2014. A role for eukaryotic initiation factor 4B overexpression in the pathogenesis of diffuse large B-cell lymphoma. Leukemia, v. 28
Doi: 10.1038/leu.2013.295
2013
Simpson, KL., Cawthorne, C., Zhou, C., Hodgkinson, CL., Walker, MJ., Trapani, F., Kadirvel, M., Brown, G., Dawson, MJ., MacFarlane, M., Williams, KJ., Whetton, AD. and Dive, C., 2013. A caspase-3 'death-switch' in colorectal cancer cells for induced and synchronous tumor apoptosis in vitro and in vivo facilitates the development of minimally invasive cell death biomarkers. Cell Death Dis, v. 4
Doi: http://doi.org/10.1038/cddis.2013.137
Melis, MHM., Simpson, KL., Dovedi, SJ., Welman, A., MacFarlane, M., Dive, C., Honeychurch, J. and Illidge, TM., 2013. Sustained tumour eradication after induced caspase-3 activation and synchronous tumour apoptosis requires an intact host immune response. Cell Death Differ, v. 20
Doi: http://doi.org/10.1038/cdd.2013.8
Donaldson, K., Poland, CA., Murphy, FA., MacFarlane, M., Chernova, T. and Schinwald, A., 2013. Pulmonary toxicity of carbon nanotubes and asbestos - similarities and differences. Adv Drug Deliv Rev, v. 65
Doi: 10.1016/j.addr.2013.07.014
2012
Robinson, GL., Dinsdale, D., Macfarlane, M. and Cain, K., 2012. Switching from aerobic glycolysis to oxidative phosphorylation modulates the sensitivity of mantle cell lymphoma cells to TRAIL. Oncogene, v. 31
Doi: http://doi.org/10.1038/onc.2012.13
MacFarlane, M., Robinson, GL. and Cain, K., 2012. Glucose--a sweet way to die: metabolic switching modulates tumor cell death. Cell Cycle, v. 11
Doi: http://doi.org/10.4161/cc.21804
Dickens, LS., Boyd, RS., Jukes-Jones, R., Hughes, MA., Robinson, GL., Fairall, L., Schwabe, JWR., Cain, K. and Macfarlane, M., 2012. A death effector domain chain DISC model reveals a crucial role for caspase-8 chain assembly in mediating apoptotic cell death. Mol Cell, v. 47
Doi: http://doi.org/10.1016/j.molcel.2012.05.004
2011
Feoktistova, M., Geserick, P., Kellert, B., Dimitrova, DP., Langlais, C., Hupe, M., Cain, K., MacFarlane, M., Häcker, G. and Leverkus, M., 2011. cIAPs block Ripoptosome formation, a RIP1/caspase-8 containing intracellular cell death complex differentially regulated by cFLIP isoforms. Mol Cell, v. 43
Doi: http://doi.org/10.1016/j.molcel.2011.06.011
Tenev, T., Bianchi, K., Darding, M., Broemer, M., Langlais, C., Wallberg, F., Zachariou, A., Lopez, J., MacFarlane, M., Cain, K. and Meier, P., 2011. The Ripoptosome, a signaling platform that assembles in response to genotoxic stress and loss of IAPs. Mol Cell, v. 43
Doi: http://doi.org/10.1016/j.molcel.2011.06.006
Tenev, T., Bianchi, K., Darding, M., Broemer, M., Langlais, C., Wallberg, F., Zachariou, A., Lopez, J., MacFarlane, M., Cain, K. and Meier, P., 2011. The Ripoptosome, a Signaling Platform that Assembles in Response to Genotoxic Stress and Loss of IAPs Molecular Cell, v. 43
Doi: http://doi.org/10.1016/j.molcel.2011.08.005
Vaishnav, M., MacFarlane, M. and Dickens, M., 2011. Disassembly of the JIP1/JNK molecular scaffold by caspase-3-mediated cleavage of JIP1 during apoptosis. Exp Cell Res, v. 317
Doi: http://doi.org/10.1016/j.yexcr.2011.01.011
2010
Stadel, D., Mohr, A., Ref, C., MacFarlane, M., Zhou, S., Humphreys, R., Bachem, M., Cohen, G., Möller, P., Zwacka, RM., Debatin, K-M. and Fulda, S., 2010. TRAIL-induced apoptosis is preferentially mediated via TRAIL receptor 1 in pancreatic carcinoma cells and profoundly enhanced by XIAP inhibitors. Clin Cancer Res, v. 16
Doi: http://doi.org/10.1158/1078-0432.CCR-10-0985
Young, KW., Piñón, LGP., Dhiraj, D., Twiddy, D., Macfarlane, M., Hickman, J. and Nicotera, P., 2010. Mitochondrial fragmentation and neuronal cell death in response to the Bcl-2/Bcl-x(L)/Bcl-w antagonist ABT-737. Neuropharmacology, v. 58
Doi: http://doi.org/10.1016/j.neuropharm.2010.03.008
2009
Hughes, MA., Harper, N., Butterworth, M., Cain, K., Cohen, GM. and MacFarlane, M., 2009. Reconstitution of the death-inducing signaling complex reveals a substrate switch that determines CD95-mediated death or survival. Mol Cell, v. 35
Doi: http://doi.org/10.1016/j.molcel.2009.06.012
2007
Volkmann, X., Fischer, U., Bahr, MJ., Ott, M., Lehner, F., Macfarlane, M., Cohen, GM., Manns, MP., Schulze-Osthoff, K. and Bantel, H., 2007. Increased hepatotoxicity of tumor necrosis factor-related apoptosis-inducing ligand in diseased human liver. Hepatology, v. 46
Doi: http://doi.org/10.1002/hep.21846
Natoni, A., MacFarlane, M., Inoue, S., Walewska, R., Majid, A., Knee, D., Stover, DR., Dyer, MJS. and Cohen, GM., 2007. TRAIL signals to apoptosis in chronic lymphocytic leukaemia cells primarily through TRAIL-R1 whereas cross-linked agonistic TRAIL-R2 antibodies facilitate signalling via TRAIL-R2. Br J Haematol, v. 139
Doi: http://doi.org/10.1111/j.1365-2141.2007.06852.x
Williams, AC., Smartt, H., H-Zadeh, AM., Macfarlane, M., Paraskeva, C. and Collard, TJ., 2007. Insulin-like growth factor binding protein 3 (IGFBP-3) potentiates TRAIL-induced apoptosis of human colorectal carcinoma cells through inhibition of NF-kappaB. Cell Death Differ, v. 14
Doi: http://doi.org/10.1038/sj.cdd.4401919
2006
Twiddy, D., Cohen, GM., Macfarlane, M. and Cain, K., 2006. Caspase-7 is directly activated by the approximately 700-kDa apoptosome complex and is released as a stable XIAP-caspase-7 approximately 200-kDa complex. J Biol Chem, v. 281
Doi: http://doi.org/10.1074/jbc.M507393200
2005
MacFarlane, M., Inoue, S., Kohlhaas, SL., Majid, A., Harper, N., Kennedy, DBJ., Dyer, MJS. and Cohen, GM., 2005. Chronic lymphocytic leukemic cells exhibit apoptotic signaling via TRAIL-R1. Cell Death Differ, v. 12
Doi: http://doi.org/10.1038/sj.cdd.4401649
Hague, A., Hicks, DJ., Hasan, F., Smartt, H., Cohen, GM., Paraskeva, C. and MacFarlane, M., 2005. Increased sensitivity to TRAIL-induced apoptosis occurs during the adenoma to carcinoma transition of colorectal carcinogenesis. Br J Cancer, v. 92
Doi: http://doi.org/10.1038/sj.bjc.6602387
MacFarlane, M., Kohlhaas, SL., Sutcliffe, MJ., Dyer, MJS. and Cohen, GM., 2005. TRAIL receptor-selective mutants signal to apoptosis via TRAIL-R1 in primary lymphoid malignancies. Cancer Res, v. 65
Doi: http://doi.org/10.1158/0008-5472.CAN-05-2801
2004
Hague, A., Eveson, JW., MacFarlane, M., Huntley, S., Janghra, N. and Thavaraj, S., 2004. Caspase-3 expression is reduced, in the absence of cleavage, in terminally differentiated normal oral epithelium but is increased in oral squamous cell carcinomas and correlates with tumour stage. J Pathol, v. 204
Doi: http://doi.org/10.1002/path.1630
Inoue, S., MacFarlane, M., Harper, N., Wheat, LMC., Dyer, MJS. and Cohen, GM., 2004. Histone deacetylase inhibitors potentiate TNF-related apoptosis-inducing ligand (TRAIL)-induced apoptosis in lymphoid malignancies. Cell Death Differ, v. 11 Suppl 2
Doi: http://doi.org/10.1038/sj.cdd.4401535
Twiddy, D., Brown, DG., Adrain, C., Jukes, R., Martin, SJ., Cohen, GM., MacFarlane, M. and Cain, K., 2004. Pro-apoptotic proteins released from the mitochondria regulate the protein composition and caspase-processing activity of the native Apaf-1/caspase-9 apoptosome complex. J Biol Chem, v. 279
Doi: http://doi.org/10.1074/jbc.M311388200
Sun, X-M., Butterworth, M., MacFarlane, M., Dubiel, W., Ciechanover, A. and Cohen, GM., 2004. Caspase activation inhibits proteasome function during apoptosis. Mol Cell, v. 14
Doi: http://doi.org/10.1016/s1097-2765(04)00156-x
2003
Turner, C., Devitt, A., Parker, K., MacFarlane, M., Giuliano, M., Cohen, GM. and Gregory, CD., 2003. Macrophage-mediated clearance of cells undergoing caspase-3-independent death. Cell Death Differ, v. 10
Doi: http://doi.org/10.1038/sj.cdd.4401170
Harper, N., Hughes, M., MacFarlane, M. and Cohen, GM., 2003. Fas-associated death domain protein and caspase-8 are not recruited to the tumor necrosis factor receptor 1 signaling complex during tumor necrosis factor-induced apoptosis. J Biol Chem, v. 278
Doi: http://doi.org/10.1074/jbc.M303399200
Harper, N., Hughes, MA., Farrow, SN., Cohen, GM. and MacFarlane, M., 2003. Protein kinase C modulates tumor necrosis factor-related apoptosis-inducing ligand-induced apoptosis by targeting the apical events of death receptor signaling. J Biol Chem, v. 278
Doi: http://doi.org/10.1074/jbc.M307376200
2002
MacFarlane, M., Harper, N., Snowden, RT., Dyer, MJS., Barnett, GA., Pringle, JH. and Cohen, GM., 2002. Mechanisms of resistance to TRAIL-induced apoptosis in primary B cell chronic lymphocytic leukaemia. Oncogene, v. 21
Doi: http://doi.org/10.1038/sj.onc.1205853
Sun, X-M., Bratton, SB., Butterworth, M., MacFarlane, M. and Cohen, GM., 2002. Bcl-2 and Bcl-xL inhibit CD95-mediated apoptosis by preventing mitochondrial release of Smac/DIABLO and subsequent inactivation of X-linked inhibitor-of-apoptosis protein. J Biol Chem, v. 277
Doi: http://doi.org/10.1074/jbc.M109893200
van Loo, G., Saelens, X., van Gurp, M., MacFarlane, M., Martin, SJ. and Vandenabeele, P., 2002. The role of mitochondrial factors in apoptosis: a Russian roulette with more than one bullet. Cell Death Differ, v. 9
Doi: http://doi.org/10.1038/sj.cdd.4401088
MacFarlane, M., Merrison, W., Bratton, SB. and Cohen, GM., 2002. Proteasome-mediated degradation of Smac during apoptosis: XIAP promotes Smac ubiquitination in vitro. J Biol Chem, v. 277
Doi: http://doi.org/10.1074/jbc.M200317200
2001
Bouchier-Hayes, L., Conroy, H., Egan, H., Adrain, C., Creagh, EM., MacFarlane, M. and Martin, SJ., 2001. CARDINAL, a novel caspase recruitment domain protein, is an inhibitor of multiple NF-kappa B activation pathways. J Biol Chem, v. 276
Doi: http://doi.org/10.1074/jbc.M107373200
Greaves, P., Edwards, R., Cohen, GM. and MacFarlane, M., 2001. "Have you seen this?" Diffuse hepatic apoptosis. Toxicol Pathol, v. 29
Doi: 10.1080/019262301316905363
Harper, N., Farrow, SN., Kaptein, A., Cohen, GM. and MacFarlane, M., 2001. Modulation of tumor necrosis factor apoptosis-inducing ligand- induced NF-kappa B activation by inhibition of apical caspases. J Biol Chem, v. 276
Doi: http://doi.org/10.1074/jbc.M105693200
Roberts, DL., Merrison, W., MacFarlane, M. and Cohen, GM., 2001. The inhibitor of apoptosis protein-binding domain of Smac is not essential for its proapoptotic activity. J Cell Biol, v. 153
Doi: http://doi.org/10.1083/jcb.153.1.221
2000
Bratton, SB., MacFarlane, M., Cain, K. and Cohen, GM., 2000. Protein complexes activate distinct caspase cascades in death receptor and stress-induced apoptosis. Exp Cell Res, v. 256
Doi: http://doi.org/10.1006/excr.2000.4835
MacFarlane, M., Cohen, GM. and Dickens, M., 2000. JNK (c-Jun N-terminal kinase) and p38 activation in receptor-mediated and chemically-induced apoptosis of T-cells: differential requirements for caspase activation. Biochem J, v. 348 Pt 1
Stoneley, M., Chappell, SA., Jopling, CL., Dickens, M., MacFarlane, M. and Willis, AE., 2000. c-Myc protein synthesis is initiated from the internal ribosome entry segment during apoptosis. Mol Cell Biol, v. 20
Doi: 10.1128/MCB.20.4.1162-1169.2000
Coldwell, MJ., Mitchell, SA., Stoneley, M., MacFarlane, M. and Willis, AE., 2000. Initiation of Apaf-1 translation by internal ribosome entry. Oncogene, v. 19
Doi: 10.1038/sj.onc.1203407
MacFarlane, M., Merrison, W., Dinsdale, D. and Cohen, GM., 2000. Active caspases and cleaved cytokeratins are sequestered into cytoplasmic inclusions in TRAIL-induced apoptosis. J Cell Biol, v. 148
Doi: http://doi.org/10.1083/jcb.148.6.1239
1999
Chow, SC., Slee, EA., MacFarlane, M. and Cohen, GM., 1999. Caspase-1 is not involved in CD95/Fas-induced apoptosis in Jurkat T cells. Exp Cell Res, v. 246
Doi: http://doi.org/10.1006/excr.1998.4333
Yang, AL., Smith, AG., Akhtar, R., Clothier, B., Robinson, S., MacFarlane, M. and Festing, MF., 1999. Low levels of p53 are associated with resistance to tetrachlorodibenzo-p-dioxin toxicity in DBA/2 mice. Pharmacogenetics, v. 9
Inayat-Hussain, SH., Osman, AB., Din, LB., Ali, AM., Snowden, RT., MacFarlane, M. and Cain, K., 1999. Caspases-3 and -7 are activated in goniothalamin-induced apoptosis in human Jurkat T-cells. FEBS Lett, v. 456
Doi: http://doi.org/10.1016/s0014-5793(99)00984-9
Sun, XM., MacFarlane, M., Zhuang, J., Wolf, BB., Green, DR. and Cohen, GM., 1999. Distinct caspase cascades are initiated in receptor-mediated and chemical-induced apoptosis. J Biol Chem, v. 274
Doi: http://doi.org/10.1074/jbc.274.8.5053
1998
Chandler, JM., Cohen, GM. and MacFarlane, M., 1998. Different subcellular distribution of caspase-3 and caspase-7 following Fas-induced apoptosis in mouse liver. J Biol Chem, v. 273
Doi: http://doi.org/10.1074/jbc.273.18.10815
Srinivasula, SM., Ahmad, M., MacFarlane, M., Luo, Z., Huang, Z., Fernandes-Alnemri, T. and Alnemri, ES., 1998. Generation of constitutively active recombinant caspases-3 and -6 by rearrangement of their subunits. J Biol Chem, v. 273
Doi: http://doi.org/10.1074/jbc.273.17.10107
Browne, SJ., MacFarlane, M., Cohen, GM. and Paraskeva, C., 1998. The adenomatous polyposis coli protein and retinoblastoma protein are cleaved early in apoptosis and are potential substrates for caspases. Cell Death Differ, v. 5
Doi: http://doi.org/10.1038/sj.cdd.4400331
Déas, O., Dumont, C., MacFarlane, M., Rouleau, M., Hebib, C., Harper, F., Hirsch, F., Charpentier, B., Cohen, GM. and Senik, A., 1998. Caspase-independent cell death induced by anti-CD2 or staurosporine in activated human peripheral T lymphocytes. J Immunol, v. 161
1997
MacFarlane, M., Ahmad, M., Srinivasula, SM., Fernandes-Alnemri, T., Cohen, GM. and Alnemri, ES., 1997. Identification and molecular cloning of two novel receptors for the cytotoxic ligand TRAIL. J Biol Chem, v. 272
Doi: http://doi.org/10.1074/jbc.272.41.25417
MacFarlane, M., Cain, K., Sun, XM., Alnemri, ES. and Cohen, GM., 1997. Processing/activation of at least four interleukin-1beta converting enzyme-like proteases occurs during the execution phase of apoptosis in human monocytic tumor cells. J Cell Biol, v. 137
Doi: http://doi.org/10.1083/jcb.137.2.469
Chandler, JM., Alnemri, ES., Cohen, GM. and MacFarlane, M., 1997. Activation of CPP32 and Mch3 alpha in wild-type p53-induced apoptosis. Biochem J, v. 322 ( Pt 1)
Doi: http://doi.org/10.1042/bj3220019
1996
Slee, EA., MacFarlane, M., Zhu, H., Chow, SC. and Cohen, GM., 1996. Inhibition of apoptosis by prevention of CPP32 processing - A study of ice-like protease activity and its inhibition using an AV vitro system Biochemical Society Transactions, v. 24
MacFarlane, M., Cain, KC., Chow, S. and Cohen, GM., 1996. Cleavage of more than one ice homologue is required for the execution of apoptosis Biochemical Society Transactions, v. 24
Doi: http://doi.org/10.1042/bst024559s
Cain, K., MacFarlane, M. and Cohen, GM., 1996. Characterisation of ice-like proteolytic activity in apoptotic human monocytic tumour (THP.l) cells Biochemical Society Transactions, v. 24
MacFarlane, M., Jones, NA., Dive, C. and Cohen, GM., 1996. DNA-damaging agents induce both p53-dependent and p53-independent apoptosis in immature thymocytes. Mol Pharmacol, v. 50
Slee, EA., Zhu, H., Chow, SC., MacFarlane, M., Nicholson, DW. and Cohen, GM., 1996. Benzyloxycarbonyl-Val-Ala-Asp (OMe) fluoromethylketone (Z-VAD.FMK) inhibits apoptosis by blocking the processing of CPP32. Biochem J, v. 315 ( Pt 1)
Doi: http://doi.org/10.1042/bj3150021
1995
1994
Cohen, GM., Sun, XM., Fearnhead, H., MacFarlane, M., Brown, DG., Snowden, RT. and Dinsdale, D., 1994. Formation of large molecular weight fragments of DNA is a key committed step of apoptosis in thymocytes. J Immunol, v. 153
Norbury, C., MacFarlane, M., Fearnhead, H. and Cohen, GM., 1994. Cdc2 activation is not required for thymocyte apoptosis. Biochem Biophys Res Commun, v. 202
Doi: http://doi.org/10.1006/bbrc.1994.2086