Cell death modalities: classification and pathophysiological implications

Apoptosis: A Basic Biological Phenomenon with Wideranging Implications in Tissue Kinetics

Kerr, J. F. R., Wyllie, A. H., & Currie, A. R. (1972) · British Journal of Cancer · doi:10.1038/bjc.1972.33 · Cited by 15,673 · see citing works

Caspases: the executioners of apoptosis

Cohen, G. M. (1997) · Biochemical Journal · doi:10.1042/bj3260001 · Cited by 4,720 · see citing works

Mitochondrial membrane permeabilization in cell death

Kroemer, G., Galluzzi, L., & Brenner, C. (2007) · Physiological Reviews · doi:10.1152/physrev.00013.2006 · Cited by 3,598 · see citing works

Calreticulin exposure dictates the immunogenicity of cancer cell death

Obeid, M., Tesniere, A., Ghiringhelli, F., Fimia, G. M., Apetoh, L., Perfettini, J.-L., Castedo, M., Mignot, G., Panaretakis, T., Casares, N., et al. (2007) · Nature Medicine · doi:10.1038/nm1523 · Cited by 3,216 · see citing works

Two CD95 (APO‐1/Fas) signaling pathways

Scaffidi, C., Fulda, S., Srinivasan, A., Friesen, C., Li, F., Tomaselli, K. J., Debatin, K., Krammer, P. H., & Peter, M. E. (1998) · The EMBO Journal · doi:10.1093/emboj/17.6.1675 · Cited by 3,000 · see citing works

Autophagy promotes tumor cell survival and restricts necrosis, inflammation, and tumorigenesis

Degenhardt, K., Mathew, R., Beaudoin, B., Bray, K., Anderson, D., Chen, G., Mukherjee, C., Shi, Y., Gélinas, C., Fan, Y., et al. (2006) · Cancer Cell · doi:10.1016/j.ccr.2006.06.001 · Cited by 2,013 · see citing works

THE MITOCHONDRIAL DEATH/LIFE REGULATOR IN APOPTOSIS AND NECROSIS

Kroemer, G., Dallaporta, B., & Resche-Rigon, M. (1998) · Annual Review of Physiology · doi:10.1146/annurev.physiol.60.1.619 · Cited by 1,971 · see citing works

Intracellular adenosine triphosphate (ATP) concentration: A switch in the decision between apoptosis and necrosis

Leist, M., Single, B., Castoldi, A. F., Kühnle, S., & Nicotera, P. (1997) · The Journal of Experimental Medicine · doi:10.1084/jem.185.8.1481 · Cited by 1,871 · see citing works

Endonuclease G is an apoptotic DNase when released from mitochondria

Li, L. Y., Luo, X., & Wang, X. (2001) · Nature · doi:10.1038/35083620 · Cited by 1,787 · see citing works

CD95's deadly mission in the immune system

Krammer, P. H. (2000) · Nature · doi:10.1038/35037728 · Cited by 1,710 · see citing works

Autophagy in cell death: an innocent convict?

Levine, B. (2005) · Journal of Clinical Investigation · doi:10.1172/jci26390 · Cited by 1,671 · see citing works

Inhibition of Macroautophagy Triggers Apoptosis

Boya, P., González‐Polo, R. A., Casares, N., Perfettini, J., Dessen, P., Larochette, N., Métivier, D., Meley, D., Souquère, S., Yoshimori, T., et al. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.3.1025-1040.2005 · Cited by 1,629 · see citing works

Caspase-dependent immunogenicity of doxorubicin-induced tumor cell death

Casares, N., Pequignot, M. O., Tesniere, A., Ghiringhelli, F., Roux, S., Chaput, N., Schmitt, E., Hamai, A., Hervas-Stubbs, S., Obeid, M., et al. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20050915 · Cited by 1,512 · see citing works

Role of Bcl-2 family proteins in a non-apoptotic programmed cell death dependent on autophagy genes

Shimizu, S., Kanaseki, T., Mizushima, N., Mizuta, T., Arakawa-Kobayashi, S., Thompson, C. B., & Tsujimoto, Y. (2004) · Nature Cell Biology · doi:10.1038/ncb1192 · Cited by 1,358 · see citing works

Lysosomes and autophagy in cell death control

Kroemer, G., & Jäättelä, M. (2005) · Nature reviews. Cancer · doi:10.1038/nrc1738 · Cited by 1,291 · see citing works

Cell death by mitotic catastrophe: a molecular definition

Castedo, M., Perfettini, J.-L., Roumier, T., Andreau, K., Medema, R., & Kroemer, G. (2004) · Oncogene · doi:10.1038/sj.onc.1207528 · Cited by 1,269 · see citing works

Caspases 3 and 7: Key Mediators of Mitochondrial Events of Apoptosis

Lakhani, S. A., Masud, A. J., Kuida, K., Porter, G. A., Jr., Booth, C. J., Mehal, W. Z., Inayat, I., & Flavell, R. A. (2006) · Science · doi:10.1126/science.1115035 · Cited by 1,175 · see citing works

A decade of caspases

Degterev, A., Boyce, M., & Yuan, J. (2003) · Oncogene · doi:10.1038/sj.onc.1207107 · Cited by 1,118 · see citing works

A Serine Protease, HtrA2, Is Released from the Mitochondria and Interacts with XIAP, Inducing Cell Death

Suzuki, Y., Imai, Y., Nakayama, H., Takahashi, K., Takio, K., & Takahashi, R. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00341-0 · Cited by 1,116 · see citing works

Cell death by necrosis: towards a molecular definition

Golstein, P., & Kroemer, G. (2007) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2006.11.001 · Cited by 1,044 · see citing works

Autophagy: dual roles in life and death?

Baehrecke, E. H. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1666 · Cited by 986 · see citing works

Necrotic death as a cell fatePreprint

Zong, W., & Thompson, C. B. (2006) · Genes & Development · doi:10.1101/gad.1376506 · Cited by 912 · see citing works

Classification of cell death: recommendations of the Nomenclature Committee on Cell Death

Kroemer, G., El-Deiry, W. S., Golstein, P., Peter, M. E., Vaux, D., Vandenabeele, P., Zhivotovsky, B., Blagosklonny, M. V., Malorni, W., Knight, R. A., et al. (2005) · Cell Death & Differentiation · doi:10.1038/sj.cdd.4401724 · Cited by 843 · see citing works

Caspase-independent cell death

Kroemer, G., & Martin, S. J. (2005) · Nature Medicine · doi:10.1038/nm1263 · Cited by 719 · see citing works

Necrosis, a well-orchestrated form of cell demise: Signalling cascades, important mediators and concomitant immune response

Festjens, N., Vanden Berghe, T., & Vandenabeele, P. (2006) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2006.06.014 · Cited by 710 · see citing works

Inflammation and necrosis promote tumour growth

Vakkila, J., & Lotze, M. T. (2004) · Nature reviews. Immunology · doi:10.1038/nri1415 · Cited by 692 · see citing works

HtrA2 Promotes Cell Death through Its Serine Protease Activity and Its Ability to Antagonize Inhibitor of Apoptosis Proteins

Verhagen, A. M., Silke, J., Ekert, P. G., Pakusch, M., Kaufmann, H., Connolly, L. M., Day, C. L., Tikoo, A., Burke, R., Wrobel, C. N., et al. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m109891200 · Cited by 558 · see citing works

Death Receptor Recruitment of Endogenous Caspase-10 and Apoptosis Initiation in the Absence of Caspase-8

Kischkel, F. C., Lawrence, D. A., Tinel, A., LeBlanc, H. N., Virmani, A. K., Schow, P. W., Gazdar, A. F., Blenis, J., Arnott, D. P., & Ashkenazi, A. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m105102200 · Cited by 536 · see citing works

Endoplasmic Reticulum Stress-induced Apoptosis

Li, J., Lee, B. A., & Lee, A. S. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m509868200 · Cited by 500 · see citing works

Programmed cell death—I. Cytology of degeneration in the intersegmental muscles of the Pernyi silkmoth

Lockshin, R. A., & Williams, C. M. (1965) · Journal of Insect Physiology · doi:10.1016/0022-1910(65)90099-5 · Cited by 487 · see citing works

Mitochondrial release of AIF and EndoG requires caspase activation downstream of Bax/Bak‐mediated permeabilization

Arnoult, D., Gaume, B. R., Karbowski, M., Sharpe, J. C., Cecconi, F., & Youle, R. J. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg423 · Cited by 451 · see citing works

Initiator caspases in apoptosis signaling pathways

Chen, M., & Wang, J. (2002) · APOPTOSIS · doi:10.1023/a:1016167228059 · Cited by 448 · see citing works

The Apaf-1 apoptosome: a large caspase-activating complex

Cain, K., Bratton, S. B., & Cohen, G. M. (2002) · Biochimie · doi:10.1016/s0300-9084(02)01376-7 · Cited by 439 · see citing works

Calpain I Induces Cleavage and Release of Apoptosis-inducing Factor from Isolated Mitochondria

Polster, B. M., Basáñez, G., Etxebarria, A., Hardwick, J. M., & Nicholls, D. G. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m413269200 · Cited by 438 · see citing works

Cathepsin-regulated apoptosis

Chwieralski, C. E., Welte, T., & Bühling, F. (2006) · APOPTOSIS · doi:10.1007/s10495-006-3486-y · Cited by 427 · see citing works

The CD95 Type I/Type II model

Barnhart, B. C., Alappat, E. C., & Peter, M. E. (2003) · Seminars in Immunology · doi:10.1016/s1044-5323(03)00031-9 · Cited by 419 · see citing works

Granzyme A Induces Caspase-Independent Mitochondrial Damage, a Required First Step for Apoptosis

Martinvalet, D., Zhu, P., & Lieberman, J. (2005) · Immunity · doi:10.1016/j.immuni.2005.02.004 · Cited by 411 · see citing works

Mitochondria as therapeutic targets for cancer chemotherapy

Galluzzi, L., Larochette, N., Zamzami, N., & Kroemer, G. (2006) · Oncogene · doi:10.1038/sj.onc.1209598 · Cited by 342 · see citing works

Mitochondrial release of apoptosis-inducing factor occurs downstream of cytochrome c release in response to several proapoptotic stimuli

Arnoult, D., Parone, P. A., Martinou, J., Antonsson, B. E., Estaquier, J., & Martinou, J. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200207071 · Cited by 312 · see citing works

Apoptotic and necrotic cell death induced by death domain receptors

Denecker, G., Vercammen, D., Declercq, W., & Vandenabeele, P. (2001) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000863 · Cited by 279 · see citing works

Dominant cell death induction by extramitochondrially targeted apoptosis‐inducing factor

Loeffler, M. W., Daugas, É., Susín, S. A., Zamzami, N., Métivier, D., Nieminen, A., Brothers, G. M., Penninger, J. M., & Kroemer, G. (2001) · The FASEB Journal · doi:10.1096/fj.00-0388com · Cited by 241 · see citing works

Pharmacological manipulation of cell death: clinical applications in sight?

Green, D. R. (2005) · Journal of Clinical Investigation · doi:10.1172/jci26321 · Cited by 239 · see citing works

Discovery, regulation, and action of the major apoptotic nucleases DFF40/CAD and endonuclease G

Widłak, P., & Garrard, W. T. (2005) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20409 · Cited by 225 · see citing works

Methods for the assessment of mitochondrial membrane permeabilization in apoptosis

Galluzzi, L., Zamzami, N., Rouge, T. D. L. M., Lemaire, C., Brenner, C., & Kroemer, G. (2007) · APOPTOSIS · doi:10.1007/s10495-007-0720-1 · Cited by 224 · see citing works

A Salmonella protein causes macrophage cell death by inducing autophagy

Hernandez, L. D., Pypaert, M., Flavell, R. A., & Galán, J. E. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200309161 · Cited by 214 · see citing works

Cytofluorometric detection of mitochondrial alterations in early CD95/Fas/APO-1-triggered apoptosis of Jurkat T lymphoma cells. Comparison of seven mitochondrion-specific fluorochromes

Métivier, D., Dallaporta, B., Zamzami, N., Larochette, N., Susín, S. A., Marzo, I., & Kroemer, G. (1998) · Immunology Letters · doi:10.1016/s0165-2478(98)00013-3 · Cited by 190 · see citing works

Origin and early evolution of the vertebrates: New insights from advances in molecular biology, anatomy, and palaeontology

Holland, N. D., & Chen, J. (2001) · BioEssays · doi:10.1002/1521-1878(200102)23:2 · Cited by 185 · see citing works

Bid acts on the permeability transition pore complex to induce apoptosis

Zamzami, N., Hamel, C. E., Maisse, C., Brenner, C., Muñoz-Pinedo, C., Belzacq, A.-S., Costantini, P., Vieira, H., Loeffler, M., Molle, G., et al. (2000) · Oncogene · doi:10.1038/sj.onc.1204030 · Cited by 178 · see citing works

Ultraviolet B Radiation-Induced Cell Death: Critical Role of Ultraviolet Dose in Inflammation and Lupus Autoantigen Redistribution

Caricchio, R., McPhie, L., & Cohen, P. L. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.11.5778 · Cited by 163 · see citing works

Apoptosis and necrosis: different execution of the same death

Nicotera, P., Leist, M., & Ferrando‐May, E. (1999) · Biochemical Society Symposia · doi:10.1042/bss0660069 · Cited by 153 · see citing works

Apoptotic Cells Deliver Processed Antigen to Dendritic Cells for Cross-Presentation

Blachère, N. E., Darnell, R. B., & Albert, M. L. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030185 · Cited by 153 · see citing works

Acidic Sphingomyelinase (ASM) Is Necessary for Fas-induced GD3 Ganglioside Accumulation and Efficient Apoptosis of Lymphoid Cells

Maria, R. D., Rippo, M. R., Schuchman, E. H., & Testi, R. (1998) · The Journal of Experimental Medicine · doi:10.1084/jem.187.6.897 · Cited by 145 · see citing works

A Central Role for Bid in Granzyme B-induced Apoptosis

Waterhouse, N. J., Sedelies, K. A., Browne, K. A., Wowk, M. E., Newbold, A., Sutton, V. R., Clarke, C., Oliaro, J., Lindemann, R. K., Bird, P. I., et al. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m410985200 · Cited by 134 · see citing works

Immune Response Against Dying Tumor Cells

Zitvogel, L., Casares, N., Péquignot, M. O., Chaput, N., Albert, M. L., & Kroemer, G. (2004) · Advances in immunology · doi:10.1016/s0065-2776(04)84004-5 · Cited by 129 · see citing works

Apoptosis Following Photodynamic Tumor Therapy: Induction, Mechanisms and Detection

Plaetzer, K., Kiesslich, T., Oberdanner, C. B., & Krammer, B. E. (2005) · Current Pharmaceutical Design · doi:10.2174/1381612053507648 · Cited by 122 · see citing works

Physiological cell death of chondrocytes in vivo is not confined to apoptosis

Roach, H. I., & Clarke, N. (2000) · Journal of Bone and Joint Surgery - British Volume · doi:10.1302/0301-620x.82b4.9846 · Cited by 121 · see citing works

Energy supply and the shape of death in neurons and lymphoid cells

Nicotera, P., & Leist, M. (1997) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4400265 · Cited by 121 · see citing works

Apoptosis caused by p53-induced protein with death domain (PIDD) depends on the death adapter protein RAIDD

Berube, C., Boucher, L.-M., Ma, W., Wakeham, A. C., Salmena, L., Hakem, R., Yeh, W., Mak, T. W., & Benchimol, S. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506475102 · Cited by 105 · see citing works

Caspases and calpain are independent mediators of cisplatin-induced endothelial cell necrosis

Dursun, B., He, Z., Somerset, H., Oh, D., Faubel, S. G., & Edelstein, C. L. (2006) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00455.2005 · Cited by 92 · see citing works

The fate of epithelial cells in the human large intestine

Barkla, D. H., & Gibson, P. R. (1999) · Pathology · doi:10.1080/003130299105043 · Cited by 88 · see citing works

Redundant cell death mechanisms as relics and backups

Golstein, P., & Kroemer, G. (2005) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401607 · Cited by 85 · see citing works

Disruption of Mcl-1·Bim Complex in Granzyme B-mediated Mitochondrial Apoptosis

Han, J., Goldstein, L. A., Gastman, B., Rabinovitz, A., & Rabinowich, H. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m411377200 · Cited by 73 · see citing works

Divergence from a Dedicated Cellular Suicide Mechanism: Exploring the Evolution of Cell Death

Yuan, J. (2006) · Molecular Cell · doi:10.1016/j.molcel.2006.06.008 · Cited by 73 · see citing works

Activation of calcium‐independent phospholipase A2 (iPLA2) in brain mitochondria and release of apoptogenic factors by BAX and truncated BID

Brustovetsky, T., Antonsson, B. E., Jemmerson, R., Dubinsky, J. M., & Brustovetsky, N. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03248.x · Cited by 61 · see citing works

Mitochondria and calpains mediate caspase-dependent apoptosis induced by doxycycline in HeLa cells

Jia Rui, W. U., Liu, T., Xie, J., et al. (2006) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-005-5565-6 · Cited by 45 · see citing works

Cell death induced by 131I in a differentiated thyroid carcinoma cell line in vitro: Necrosis or apoptosis?

Marx, K., Moka, D., Schomäcker, K., Fischer, T. H., Gabruk-Szostak, B., Kobe, C., Dietlein, M., & Schicha, H. (2006) · Nuclear Medicine Communications · doi:10.1097/01.mnm.0000199475.08407.e2 · Cited by 23 · see citing works

Mechanism of cytosol phospholipase C and sphingomyelinase-induced lysosome destabilization

Wang, X., Zhao, H.-F., & Zhang, G. (2006) · Biochimie · doi:10.1016/j.biochi.2006.02.005 · Cited by 13 · see citing works

Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018.

Galluzzi, L., Vitale, I., Aaronson, S. A., Abrams, J. M., Adam, D., Agostinis, P., Alnemri, E. S., Altucci, L., Amelio, I., Andrews, D. W., et al. (2018) · Cell Death & Differentiation · doi:10.1038/s41418-017-0012-4 · Cited by 6,680 · see citing works

Classification of cell death: recommendations of the Nomenclature Committee on Cell Death 2009

Kroemer, G., Galluzzi, L., Vandenabeele, P., Abrams, J., Alnemri, E. S., Baehrecke, E. H., Blagosklonny, M. V., El-Deiry, W. S., Golstein, P., Green, D. R., et al. (2009) · Cell Death & Differentiation · doi:10.1038/cdd.2008.150 · Cited by 3,399 · see citing works

Molecular definitions of cell death subroutines: recommendations of the Nomenclature Committee on Cell Death 2012

Galluzzi, L., Vitale, I., Abrams, J. M., Alnemri, E. S., Baehrecke, E. H., Blagosklonny, M. V., Dawson, T. M., Dawson, V. L., El-Deiry, W. S., Fulda, S., et al. (2012) · Cell Death & Differentiation · doi:10.1038/cdd.2011.96 · Cited by 2,421 · see citing works

Autophagic cell death: the story of a misnomer

Kroemer, G., & Levine, B. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2529 · Cited by 1,453 · see citing works

Immunogenic and tolerogenic cell death

Green, D. R., Ferguson, T., Zitvogel, L., & Kroemer, G. (2009) · Nature Reviews Immunology · doi:10.1038/nri2545 · Cited by 1,176 · see citing works

Essential versus accessory aspects of cell death: recommendations of the NCCD 2015

Galluzzi, L., Bravo-San Pedro, J. M., Vitale, I., Aaronson, S. A., Abrams, J. M., Adam, D., Alnemri, E. S., Altucci, L., Andrews, D., Annicchiarico-Petruzzelli, M., et al. (2015) · Cell Death & Differentiation · doi:10.1038/cdd.2014.137 · Cited by 1,002 · see citing works

Consensus guidelines for the detection of immunogenic cell death

Kepp, O., Senovilla, L., Vitale, I., Vacchelli, E., Adjemian, S., Agostinis, P., Apetoh, L., Aranda, F., Barnaba, V., Bloy, N., et al. (2014) · OncoImmunology · doi:10.4161/21624011.2014.955691 · Cited by 832 · see citing works

Caloric restriction and resveratrol promote longevity through the Sirtuin-1-dependent induction of autophagy

Morselli, E., Maiuri, M. C., Markaki, M., Megalou, E., Pasparaki, A., Palikaras, K., Criollo, A., Galluzzi, L., Malik, S. A., Vitale, I., et al. (2010) · Cell Death & Disease · doi:10.1038/cddis.2009.8 · Cited by 613 · see citing works

Environmental toxicity, oxidative stress and apoptosis: Ménage à Trois

Franco, R., Sánchez-Olea, R., Reyes-Reyes, E. M., & Panayiotidis, M. I. (2009) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/j.mrgentox.2008.11.012 · Cited by 541 · see citing works

Calreticulin exposure is required for the immunogenicity of γ-irradiation and UVC light-induced apoptosis

Obeid, M., Panaretakis, T., Joza, N., Tufi, R., Tesniere, A., van Endert, P., Zitvogel, L., & Kroemer, G. (2007) · Cell Death & Differentiation · doi:10.1038/sj.cdd.4402201 · Cited by 474 · see citing works

Glyphosate Formulations Induce Apoptosis and Necrosis in Human Umbilical, Embryonic, and Placental Cells

Benachour, N., & Séralini, G.-E. (2009) · Chemical Research in Toxicology · doi:10.1021/tx800218n · Cited by 428 · see citing works

Autophagy in cardiovascular biology

Lavandero, S., Chiong, M., Rothermel, B. A., & Hill, J. A. (2015) · Journal of Clinical Investigation · doi:10.1172/jci73943 · Cited by 331 · see citing works

The inositol 1,4,5-trisphosphate receptor regulates autophagy through its interaction with Beclin 1

Vicencio, J. M., Ortiz, C., Criollo, A., Jones, A. W. E., Kepp, O., Galluzzi, L., Joza, N., Vitale, I., Morselli, E., Tailler, M., et al. (2009) · Cell Death & Differentiation · doi:10.1038/cdd.2009.34 · Cited by 289 · see citing works

Molecular mechanisms of regulated necrosis

Galluzzi, L., Kepp, O., Krautwald, S., Kroemer, G., & Linkermann, A. (2014) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2014.02.006 · Cited by 258 · see citing works

Autophagy mediates pharmacological lifespan extension by spermidineand resveratrol

Morselli, E., Galluzzi, L., Kepp, O., Criollo, A., Maiuri, M. C., Tavernarakis, N., Madeo, F., & Kroemer, G. (2009) · Aging · doi:10.18632/aging.100110 · Cited by 213 · see citing works

Ecto‐calreticulin in immunogenic chemotherapy

Obeid, M., Tesniere, A., Panaretakis, T., Tufi, R., Joza, N., Van Endert, P., Ghiringhelli, F., Apetoh, L., Chaput, N., Flament, C., et al. (2007) · Immunological Reviews · doi:10.1111/j.1600-065x.2007.00567.x · Cited by 202 · see citing works

A Novel Epidermal Growth Factor Receptor Inhibitor Promotes Apoptosis in Non–Small Cell Lung Cancer Cells Resistant to Erlotinib

de La Motte Rouge, T., Galluzzi, L., Olaussen, K. A., Zermati, Y., Tasdemir, E., Robert, T., Ripoche, H., Lazar, V., Dessen, P., Harper, F., et al. (2007) · Cancer Research · doi:10.1158/0008-5472.can-07-0538 · Cited by 141 · see citing works

Reactive oxygen species-mediated pancreatic β-cell death is regulated by interactions between stress-activated protein kinases, p38 and c-Jun N-terminal kinase, and mitogen-activated protein kinase phosphatases.

Hou, N., Torii, S., Saito, N., Hosaka, M., & Takeuchi, T. (2008) · Endocrinology · doi:10.1210/en.2007-0988 · Cited by 141 · see citing works

The role of nitric oxide in intestinal epithelial injury and restitution in neonatal necrotizing enterocolitis

Chokshi, N. K., Guner, Y. S., Hunter, C. J., Upperman, J. S., Grishin, A., & Ford, H. R. (2008) · Seminars in Perinatology · doi:10.1053/j.semperi.2008.01.002 · Cited by 137 · see citing works

Fatty Acids - Induced Lipotoxicity and Inflammation

Savary, S., Trompier, D., Andreoletti, P., Le Borgne, F., Demarquoy, J., & Lizard, G. (2012) · Current Drug Metabolism · doi:10.2174/138920012803762729 · Cited by 111 · see citing works

L-amino acid oxidase from Bothrops atrox snake venom triggers autophagy, apoptosis and necrosis in normal human keratinocytes

Costal-Oliveira, F., Stransky, S., Guerra-Duarte, C., Naves de Souza, D. L., Vivas-Ruiz, D. E., Yarlequé, A., Sanchez, E. F., Chávez-Olórtegui, C., & Braga, V. M. M. (2019) · Scientific Reports · doi:10.1038/s41598-018-37435-4 · Cited by 86 · see citing works

Elimination of Self-Reactive T Cells in the Thymus: A Timeline for Negative Selection

Dzhagalov, I. L., Chen, K. G., Herzmark, P., & Robey, E. A. (2013) · PLoS Biology · doi:10.1371/journal.pbio.1001566 · Cited by 82 · see citing works

Cell Death–Stimulated Cell Proliferation: A Tissue Regeneration Mechanism Usurped by Tumors During Radiotherapy

Zimmerman, M. A., Huang, Q., Li, F., Liu, X., & Li, C.-Y. (2013) · Seminars in Radiation Oncology · doi:10.1016/j.semradonc.2013.05.003 · Cited by 59 · see citing works

Mechanisms of Myofibre Death in Muscular Dystrophies: The Emergence of the Regulated Forms of Necrosis in Myology

Bencze, M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms24010362 · Cited by 20 · see citing works

The Effect of Teaching Practical Physical Modalities on the Ordering Skills of Physical Medicine and Rehabilitation Residents

Sadat, B. E., Babaei-Ghazani, A., Alizadeh, M., et al. (2013) · DOAJ (DOAJ: Directory of Open Access Journals) · doi:10.5681/rdme.2013.009

SHAPE: An Unified Approach to Evaluate the Contribution and Cooperation of Individual ModalitiesPreprint

Hu, P., Li, X., & Zhou, Y. X. (2022) · arXiv (Cornell University) · doi:10.48550/arxiv.2205.00302

Some Issues on Choices of Modalities for Multimodal Biometric Systems

Imran, M., Rao, A., Shaffi, N., et al. (2014) · Advances in intelligent systems and computing · doi:10.1007/978-81-322-1602-5_151 · Cited by 1 · see citing works

Interruptions as multimodal outputs: which are the less disruptive?

Arroyo, E., Selker, T., & Stouffs, A. (2003) · INTERNATIONAL CONFERENCE ON MULTIMODAL INTERACTION · doi:10.1109/icmi.2002.1167043 · Cited by 70 · see citing works

Beyond a Generic Complementary and Alternative Medicine: The Holistic Health Care- Conventional Medicine Continuum

Robinson, A., Chesters, J., & Cooper, S. J. (2009) · Complementary health practice review · doi:10.1177/1533210109360016 · Cited by 8 · see citing works