The DOI matches its Crossref record; 797 of the 797 references it cites were found in a registry or an index.
Neuronal Cell Death
Open accessAbstract
Neuronal cell death occurs extensively during development and pathology, where it is especially important because of the limited capacity of adult neurons to proliferate or be replaced. The concept of cell death used to be simple as there were just two or three types, so we just had to work out which type was involved in our particular pathology and then block it. However, we now know that there are at least a dozen ways for neurons to die, that blocking a particular mechanism of cell death may not prevent the cell from dying, and that non-neuronal cells also contribute to neuronal death. We review here the mechanisms of neuronal death by intrinsic and extrinsic apoptosis, oncosis, necroptosis, parthanatos, ferroptosis, sarmoptosis, autophagic cell death, autosis, autolysis, paraptosis, pyroptosis, phagoptosis, and mitochondrial permeability transition. We next explore the mechanisms of neuronal death during development, and those induced by axotomy, aberrant cell-cycle reentry, glutamate (excitoxicity and oxytosis), loss of connected neurons, aggregated proteins and the unfolded protein response, oxidants, inflammation, and microglia. We then reassess which forms of cell death occur in stroke and Alzheimer’s disease, two of the most important pathologies involving neuronal cell death. We also discuss why it has been so difficult to pinpoint the type of neuronal death involved, if and why the mechanism of neuronal death matters, the molecular overlap and interplay between death subroutines, and the therapeutic implications of these multiple overlapping forms of neuronal death.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
2 retracted
Items 401–600 of 797
Gp91phox (NOX2) in classically activated microglia exacerbates traumatic brain injury
Dohi, K., Ohtaki, H., Nakamachi, T., Yofu, S., Satoh, K., Miyamoto, K., Song, D., Tsunawaki, S., Shioda, S., & Aruga, T. (2010) · Journal of Neuroinflammation · doi:10.1186/1742-2094-7-41 · Cited by 188
Alleviation of Neurotoxicity by Microglial Human Siglec-11
Wang, Y., & Neumann, H. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.3940-09.2010 · Cited by 188
Andreyev, A., & Fiskum, G. (1999) · Cell Death & Differentiation · doi:10.1038/sj.cdd.4400565 · Cited by 187
Yang, J., Weimer, R. M., Kallop, D., Olsen, O., Wu, Z., Renier, N., Uryu, K., & Tessier-Lavigne, M. (2013) · Neuron · doi:10.1016/j.neuron.2013.08.034 · Cited by 186
The role of lysosomal rupture in neuronal death
Yamashima, T., & Oikawa, S. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.09.003 · Cited by 185
Tan, C.-C., Zhang, J.-G., Tan, M.-S., Chen, H., Meng, D.-W., Jiang, T., Meng, X.-F., Li, Y., Sun, Z., Li, M.-M., et al. (2015) · Journal of Neuroinflammation · doi:10.1186/s12974-014-0233-0 · Cited by 185
Edwards, S., & Tolkovsky, A. (1994) · The Journal of cell biology · doi:10.1083/jcb.124.4.537 · Cited by 183
Self-citationMitochondrial Dysfunction Induces Sarm1-Dependent Cell Death in Sensory Neurons
Summers, D. W., DiAntonio, A., & Milbrandt, J. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0877-14.2014 · Cited by 181
Neuroprotection with a calpain inhibitor in a model of focal cerebral ischemia.
Hong, S. C., Goto, Y., Lanzino, G., Soleau, S., Kassell, N. F., & Lee, K. S. (1994) · Stroke · doi:10.1161/01.str.25.3.663 · Cited by 180
Calpain Mediates Excitotoxic DNA Fragmentation via Mitochondrial Pathways in Adult Brains
Takano, J., Tomioka, M., Tsubuki, S., Higuchi, M., Iwata, N., Itohara, S., Maki, M., & Saido, T. C. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m414552200 · Cited by 180
Beclin orthologs: integrative hubs of cell signaling, membrane trafficking, and physiology
Levine, B., Liu, R., Dong, X., & Zhong, Q. (2015) · Trends in Cell Biology · doi:10.1016/j.tcb.2015.05.004 · Cited by 178
NADPH Oxidase 1-Mediated Oxidative Stress Leads to Dopamine Neuron Death in Parkinson's Disease
Choi, D.-H., Cristóvão, A. C., Guhathakurta, S., Lee, J., Joh, T. H., Beal, M. F., & Kim, Y.-S. (2012) · Antioxidants & Redox Signaling · doi:10.1089/ars.2011.3960 · Cited by 178
AIF‐mediated caspase‐independent necroptosis: A new chance for targeted therapeutics
Delavallée, L., Cabon, L., Galán‐Malo, P., Lorenzo, H. K., & Susin, S. A. (2011) · IUBMB Life · doi:10.1002/iub.432 · Cited by 178
Hetz, C., Vitte, P.-A., Bombrun, A., Rostovtseva, T. K., Montessuit, S., Hiver, A., Schwarz, M. K., Church, D. J., Korsmeyer, S. J., Martinou, J.-C., et al. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m505843200 · Cited by 176
Xu, X., Chua, C. C., Kong, J., Kostrzewa, R. M., Kumaraguru, U., Hamdy, R. C., & Chua, B. H. L. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04884.x · Cited by 176
Su, J. H., Deng, G., & Cotman, C. W. (1997) · Brain Research · doi:10.1016/s0006-8993(97)81703-9 · Cited by 175
bax Deficiency Prevents the Increased Cell Death of Immature Neurons in bcl-x-Deficient Mice
Shindler, K. S., Latham, C. B., & Roth, K. A. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-09-03112.1997 · Cited by 175
11C-PBR28 binding to translocator protein increases with progression of Alzheimer's disease
Kreisl, W. C., Lyoo, C. H., Liow, J.-S., Wei, M., Snow, J., Page, E., Jenko, K. J., Morse, C. L., Zoghbi, S. S., Pike, V. W., et al. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.04.011 · Cited by 174
Differential retrotranslocation of mitochondrial Bax and Bak
Todt, F., Cakir, Z., Reichenbach, F., Emschermann, F., Lauterwasser, J., Kaiser, A., Ichim, G., Tait, S. W., Frank, S., Langer, H. F., et al. (2015) · The EMBO Journal · doi:10.15252/embj.201488806 · Cited by 172
Cell Degeneration in the Larval Ventral Horn of Xenopus laevis (Daudin)
Hughes, A. (1961) · Development · doi:10.1242/dev.9.2.269 · Cited by 172
Bartus, R. T., Baker, K. L., Heiser, A. D., Sawyer, S. D., Dean, R. L., Elliott, P. J., & Straub, J. A. (1994) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1994.67 · Cited by 171
Membrane Trafficking Pathways in Alzheimer's Disease
Rajendran, L., & Annaert, W. (2012) · Traffic · doi:10.1111/j.1600-0854.2012.01332.x · Cited by 171
Chu, C. T., Zhu, J.-H., & Dagda, R. (2007) · Autophagy · doi:10.4161/auto.4625 · Cited by 170
Mature neurons: equipped for survival
Kole, A. J., Annis, R. P., & Deshmukh, M. (2013) · Cell Death & Disease · doi:10.1038/cddis.2013.220 · Cited by 170
Amyloid-β signals through tau to drive ectopic neuronal cell cycle re-entry in Alzheimer's disease
Seward, M. E., Swanson, E., Norambuena, A., Reimann, A., Cochran, J. N., Li, R., Roberson, E. D., & Bloom, G. S. (2013) · Journal of Cell Science · doi:10.1242/jcs.1125880 · Cited by 169
Macroautophagy deficiency mediates age-dependent neurodegeneration through a phospho-tau pathway
Inoue, K., Rispoli, J., Kaphzan, H., Klann, E., Chen, E. I., Kim, J., Komatsu, M., & Abeliovich, A. (2012) · Molecular Neurodegeneration · doi:10.1186/1750-1326-7-48 · Cited by 168
Microglial secreted cathepsin B induces neuronal apoptosis
Kingham, P. J., & Pocock, J. M. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00146.x · Cited by 167
Coupling of extrasynaptic NMDA receptors to a CREB shut-off pathway is developmentally regulated
Hardingham, G. E., & Bading, H. (2002) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/s1570-9639(02)00455-7 · Cited by 167
Nitric‐Oxide‐Induced Necrosis and Apoptosis in PC12 Cells Mediated by Mitochondria
Bal‐Price, A., & Brown, G. C. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.0751455.x · Cited by 167
Self-citationRami, A., & Krieglstein, J. (1993) · Brain Research · doi:10.1016/0006-8993(93)90856-i · Cited by 166
Interleukin-1 and acute brain injury
Murray, K. N., Parry-Jones, A. R., & Allan, S. M. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00018 · Cited by 166
Cell death mechanisms in neurodegeneration
Jellinger, K. A. (2001) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2001.tb00134.x · Cited by 165
Vandenabeele, P., Grootjans, S., Callewaert, N., & Takahashi, N. (2013) · Cell Death & Differentiation · doi:10.1038/cdd.2012.151 · Cited by 163
Zhou, Z.-D., Chan, C. H.-S., Ma, Q.-H., Xu, X.-H., Xiao, Z.-C., & Tan, E.-K. (2011) · Cell Adhesion & Migration · doi:10.4161/cam.5.4.16986 · Cited by 162
Tumour necrosis factor alpha‐induced neuronal loss is mediated by microglial phagocytosis
Neniškytė, U., Vilalta, A., & Brown, G. C. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.05.046 · Cited by 162
Self-citationManabat, C., Han, B. H., Wendland, M., Derugin, N., Fox, C. K., Choi, J., Holtzman, D. M., Ferriero, D. M., & Vexler, Z. S. (2003) · Stroke · doi:10.1161/01.str.0000047101.87575.3c · Cited by 161
Yap, Y. W., Whiteman, M., Bay, B. H., Li, Y., Sheu, F., Qi, R. Z., Tan, C. H., & Cheung, N. S. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03996.x · Cited by 161
Gasdermin D: the long-awaited executioner of pyroptosis
Man, S. M., & Kanneganti, T. (2015) · Cell Research · doi:10.1038/cr.2015.124 · Cited by 160
Hernández-Tiedra, S., Fabriàs, G., Dávila, D., Salanueva, Í. J., Casas, J., Montes, L. R., Antón, Z., García-Taboada, E., Salazar-Roa, M., Lorente, M., et al. (2016) · Autophagy · doi:10.1080/15548627.2016.1213927 · Cited by 160
Almeida, Á., & Bolaños, J. P. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00276.x · Cited by 159
Involvement of autophagy in hypoxic-excitotoxic neuronal death
Ginet, V., Spiehlmann, A., Rummel, C., Rudinskiy, N., Grishchuk, Y., Luthi-Carter, R., Clarke, P. G., Truttmann, A. C., & Puyal, J. (2014) · Autophagy · doi:10.4161/auto.28264 · Cited by 159
Xing, S., Zhang, Y., Li, J., Zhang, J., Li, Y., Dang, C., Li, C., Fan, Y., Yu, J., Pei, Z., et al. (2012) · Autophagy · doi:10.4161/auto.8.1.18217 · Cited by 158
Neves, A. A., & Brindle, K. M. (2014) · Journal of Nuclear Medicine · doi:10.2967/jnumed.112.114264 · Cited by 158
Suppression of the Intrinsic Apoptosis Pathway by Synaptic Activity
Léveillé, F., Papadia, S., Fricker, M., Bell, K. F. S., Soriano, F. X., Martel, M., Puddifoot, C. A., Habel, M., Wyllie, D. J. A., Ikonomidou, C., et al. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5115-09.2010 · Cited by 157
Self-citationTissue acidosis induces neuronal necroptosis via ASIC1a channel independent of its ionic conduction
Wang, Y., Wang, J.-J., Huang, Y., Liu, F., Zeng, W.-Z., Li, Y., Xiong, Z.-G., Zhu, M. X., & Xu, T.-L. (2015) · eLife · doi:10.7554/elife.05682 · Cited by 157
Invited review: Prion‐like transmission and spreading of tau pathology
Clavaguera, F., Hench, J., Goedert, M., & Tolnay, M. (2015) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12197 · Cited by 156
Uchino, H., Minamikawa‐Tachino, R., Kristián, T., Perkins, G. A., Narazaki, M., Siesjö, B. K., & Shibasaki, F. (2002) · Neurobiology of Disease · doi:10.1006/nbdi.2002.0514 · Cited by 155
Peripheral administration of tau aggregates triggers intracerebral tauopathy in transgenic mice
Clavaguera, F., Hench, J., Lavenir, I., Schweighauser, G., Frank, S., Goedert, M., & Tolnay, M. (2013) · Acta Neuropathologica · doi:10.1007/s00401-013-1231-5 · Cited by 153
Sánchez-Migallón, M. C., Valiente‐Soriano, F. J., Nadal-Nicolás, F. M., Vidal‐Sanz, M., & Agudo‐Barriuso, M. (2016) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.15-17841 · Cited by 153
Caspase Inhibitors Reduce Neuronal Injury After Focal but Not Global Cerebral Ischemia in Rats
Li, H., Colbourne, F., Sun, P., Zhao, Z., & Buchan, A. M. (2000) · Stroke · doi:10.1161/01.str.31.1.176 · Cited by 152
Gill, R., Soriano, M. A., Blomgren, K., Hagberg, H., Wybrect, R., Miss, M.-T., Hoefer, S., Adam, G., Niederhauser, O., Kemp, J. A., et al. (2002) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200204000-00006 · Cited by 152
Deckwerth, T. L., & Johnson, E. M. (1994) · Developmental Biology · doi:10.1006/dbio.1994.1234 · Cited by 152
Caspase blockade induces RIP3-mediated programmed necrosis in Toll-like receptor-activated microglia
Kim, S. J., & Li, J. (2013) · Cell Death and Disease · doi:10.1038/cddis.2013.238 · Cited by 152
Glial cells are increased proportionally in transgenic optic nerves with increased numbers of axons
Burne, J. F., Staple, J., & RAFF, M. C. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-06-02064.1996 · Cited by 151
Genomics of Alzheimer Disease: A Review
Rosenberg, R. N., Lambracht‐Washington, D., Yu, G., & Xia, W. (2016) · JAMA Neurology · doi:10.1001/jamaneurol.2016.0301 · Cited by 151
Endo‐lysosomal and autophagic dysfunction: a driving factor in Alzheimer's disease?
Whyte, L. S., Lau, A. A., Hemsley, K. M., Hopwood, J. J., & Sargeant, T. J. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.13935 · Cited by 150
Barcia, C., Ros, C. M., Annese, V., Carrillo-de Sauvage, M. A., Ros-Bernal, F., Gómez, A., Yuste, J. E., Campuzano, C. M., de Pablos, V., Fernandez-Villalba, E., et al. (2012) · Scientific Reports · doi:10.1038/srep00809 · Cited by 150
Akt and mTOR mediate programmed necrosis in neurons
Liu, Q., Qiu, J., Liang, M., Golinski, J., van Leyen, K., Jung, J. E., You, Z., Lo, E. H., Degterev, A., & Whalen, M. J. (2014) · Cell Death and Disease · doi:10.1038/cddis.2014.69 · Cited by 150
Neher, J. J., Neniškytė, U., Hornik, T. C., & Brown, G. C. (2014) · Glia · doi:10.1002/glia.22693 · Cited by 150
Self-citationAnti-apoptotic Effect of cGMP in Cultured Astrocytes
Takuma, K., Phuagphong, P., Lee, E., Mori, K., Baba, A., & Matsuda, T. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m108622200 · Cited by 149
Concannon, C. G., Tuffy, L. P., Weisová, P., Bonner, H. P., Dávila, D., Bonner, C., Devocelle, M. C., Strasser, A., Ward, M. W., & Prehn, J. H. M. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.200909166 · Cited by 149
Yelamanchili, S. V., Lamberty, B. G., Rennard, D. A., Morsey, B., Hochfelder, C. G., Meays, B. M., Levy, E., & Fox, H. S. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1005032 · Cited by 147
Ballooned neurons in select neurodegenerative diseases contain phosphorylated neurofilament epitopes
Dickson, D. W., Yen, S. H., Suzuki, K., Davies, P., García, J. H., & Hirano, A. (1986) · Acta Neuropathologica · doi:10.1007/bf00688042 · Cited by 146
Wang, Y., Briz, V., Chishti, A. H., Bi, X., & Baudry, M. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3293-13.2013 · Cited by 146
Role of Cell Cycle Re-Entry in Neurons: A Common Apoptotic Mechanism of Neuronal Cell Death
Folch, J., Junyent, F., Verdaguer, E., Auladell, C., Pizarro, J. G., Beas‐Zárate, C., Pallàs, M., & Camins, A. (2011) · Neurotoxicity Research · doi:10.1007/s12640-011-9277-4 · Cited by 145
Mukherjee, P., Woods, T. A., Moore, R. A., & Peterson, K. E. (2013) · Immunity · doi:10.1016/j.immuni.2013.02.013 · Cited by 145
Yamashima, T., Saido, T. C., Takita, M., Miyazawa, A., Yamano, J., Miyakawa, A., Nishijyo, H., Yamashita, J., Kawashima, S., Ono, T., et al. (1996) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1996.tb01337.x · Cited by 145
Loss of OMA1 delays neurodegeneration by preventing stress-induced OPA1 processing in mitochondria
Korwitz, A., Merkwirth, C., Richter‐Dennerlein, R., Tröder, S. E., Sprenger, H., Quirós, P. M., López-Otín, C., Rugarli, E. I., & Langer, T. (2016) · The Journal of Cell Biology · doi:10.1083/jcb.201507022 · Cited by 145
Posttreatment with the immunosuppressant cyclosporin A in transient focal ischemia
Yoshimoto, T., & Siesjö, B. K. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01733-3 · Cited by 144
Moroni, F., Meli, E., Peruginelli, F., Chiarugi, A., Cozzi, A., Picca, R., Romagnoli, P., Pellicciari, R., & Pellegrini-Giampietro, D. E. (2001) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4400884 · Cited by 144
WldS requires Nmnat1 enzymatic activity and N16–VCP interactions to suppress Wallerian degeneration
Avery, M. A., Sheehan, A. E., Kerr, K. S., Wang, J., & Freeman, M. R. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200808042 · Cited by 144
Yip, P. K., Carrillo-Jiménez, A., King, P., Vilalta, A., Nomura, K., Chau, C. C. C., Scott-Egerton, A. M., Liu, Z., Shetty, A. J., Tremoleda, J. L., et al. (2017) · Scientific Reports · doi:10.1038/srep41689 · Cited by 144
Self-citationBid-induced release of AIF from mitochondria causes immediate neuronal cell death
Landshamer, S., Hoehn, M., Barth, N. D., Duvezin‐Caubet, S., Schwake, G., Tobaben, S., Kazhdan, I., Becattini, B., Stefan Zahler, A., Vollmar, A. M., et al. (2008) · Cell Death and Differentiation · doi:10.1038/cdd.2008.78 · Cited by 143
Role of necroptosis in the pathogenesis of solid organ injury
Zhao, H., Jaffer, T., Eguchi, S., Wang, Z., Linkermann, A., & Ma, D. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.316 · Cited by 143
Loss of tau elicits axonal degeneration in a mouse model of Alzheimer's disease
Dawson, H. N., Cantillana, V., Jansen, M., Wang, H., Vitek, M. P., Wilcock, D. M., Lynch, J., & Laskowitz, D. T. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.04.037 · Cited by 142
Rodríguez‐Muela, N., Hernández‐Pinto, A. M., Serrano‐Puebla, A., García‐Ledo, L., Latorre, S., de la Rosa, E. J., & Boya, P. (2014) · Cell Death and Differentiation · doi:10.1038/cdd.2014.203 · Cited by 142
Puma Is a Dominant Regulator of Oxidative Stress Induced Bax Activation and Neuronal Apoptosis
Steckley, D., Karajgikar, M., Dale, L. B., Fuerth, B. J., Swan, P., Drummond-Main, C., Poulter, M. O., Ferguson, S. S. G., Strasser, A., & Cregan, S. P. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3400-07.2007 · Cited by 142
The WldS gene delays axonal but not somatic degeneration in a rat glaucoma model
Beirowski, B., Babetto, E., Coleman, M. P., & Martin, K. R. G. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06426.x · Cited by 140
Self-citationAutophagosome–lysosome fusion in neurons requires INPP5E, a protein associated with Joubert syndrome
Hasegawa, J., Iwamoto, R., Otomo, T., Nezu, A., Hamasaki, M., & Yoshimori, T. (2016) · The EMBO Journal · doi:10.15252/embj.201593148 · Cited by 140
Akt Suppresses Retrograde Degeneration of Dopaminergic Axons by Inhibition of Macroautophagy
Cheng, H.-C., Kim, S. R., Oo, T. F., Kareva, T., Yarygina, O., Rzhetskaya, M., Wang, C., During, M. J., Tallóczy, Z., Tanaka, K., et al. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5519-10.2011 · Cited by 139
Inhibition of Pro-Apoptotic BAX by a Noncanonical Interaction Mechanism
Barclay, L. A., Wales, T. E., Garner, T. P., Wachter, F., Lee, S., Guerra, R. M., Stewart, M. L., Braun, C. R., Bird, G. H., Gavathiotis, E., et al. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.01.014 · Cited by 139
Cysteine protease inhibition prevents mitochondrial apoptosis-inducing factor (AIF) release
Yuste, V. J., Moubarak, R. S., Delettre, C., Bras, M., Sancho, P., Robert, N., d’Alayer, J., & Susín, S. A. (2005) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401687 · Cited by 138
Fricker, M., Oliva-Martín, M. J., & Brown, G. C. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-196 · Cited by 137
Self-citationSankarapandi, S., Zweier, J. L., Mukherjee, G., Quinn, M. T., & Huso, D. L. (1998) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1998.0658 · Cited by 136
Clinical Trials of Immunomodulation in Ischemic Stroke
Veltkamp, R. C., & Gill, D. (2016) · Neurotherapeutics · doi:10.1007/s13311-016-0458-y · Cited by 136
Xkr8 phospholipid scrambling complex in apoptotic phosphatidylserine exposure
Suzuki, J., Imanishi, E., & Nagata, S. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1610403113 · Cited by 135
Kieran, D., Woods, I., Villunger, A., Strasser, A., & Prehn, J. H. M. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0707906105 · Cited by 134
Linnartz, B., Kopatz, J., Tenner, A. J., & Neumann, H. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.3830-11.2012 · Cited by 134
Loreto, A., Stefano, M. D., Gering, M., & Conforti, L. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.11.032 · Cited by 134
Energy Requirement for Caspase Activation and Neuronal Cell Death
Nicotera, P., Leist, M., Fava, E., Berliocchi, L., & Volbracht, C. (2000) · Brain Pathology · doi:10.1111/j.1750-3639.2000.tb00261.x · Cited by 133
Ramanan, V. K., Risacher, S. L., Nho, K., Kim, S., Shen, L., McDonald, B. C., Yoder, K. K., Hutchins, G. D., West, J. D., Tallman, E. F., et al. (2015) · Brain · doi:10.1093/brain/awv231 · Cited by 133
Stoica, B. A., Loane, D. J., Zhao, Z., Kabadi, S. V., Hanscom, M., Byrnes, K. R., & Faden, A. I. (2013) · Journal of Neurotrauma · doi:10.1089/neu.2013.3194 · Cited by 133
Gibson, M. E., Han, B. H., Choi, J., Knudson, C. M., Korsmeyer, S. J., Parsadanian, M., & Holtzman, D. M. (2001) · Molecular Medicine · doi:10.1007/bf03401871 · Cited by 132
Rubin, L. L., Philpott, K. L., & Brooks, S. F. (1993) · Current Biology · doi:10.1016/0960-9822(93)90211-6 · Cited by 132
Excitotoxic neuronal death in the immature brain is an apoptosis-necrosis morphological continuum.
Portera‐Cailliau, C., Price, D. L., & Martin, L. J. (1997) · PubMed · Cited by 131
Rescue of Peripheral and CNS Axon Defects in Mice Lacking NMNAT2
Gilley, J., Adalbert, R., Yu, G., & Coleman, M. P. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1534-13.2013 · Cited by 131
Self-citationCutDB: a proteolytic event database
Igarashi, Y., Eroshkin, A. M., Gramatikova, S. I., Gramatikoff, K., Zhang, Y., Smith, J. W., Osterman, A. L., & Godzik, A. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl813 · Cited by 131
Yamashima, T., Tonchev, A. B., Tsukada, T., Saido, T. C., Imajoh‐Ohmi, S., Momoi, T., & Kominami, E. (2003) · Hippocampus · doi:10.1002/hipo.10127 · Cited by 131
The mitochondrial permeability transition pore in AD 2016: An update
Biasutto, L., Azzolini, M., Szabó, I., & Zoratti, M. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2016.02.012 · Cited by 131
Extrasynaptic glutamate release through cystine/glutamate antiporter contributes to ischemic damage
Soria, F. N., Pérez‐Samartín, A., Martín, A., Gona, K. B., Llop, J., Szczupak, B., Chara, J. C., Matute, C., & Domercq, M. (2014) · Journal of Clinical Investigation · doi:10.1172/jci71886 · Cited by 130
Yu-Long, W. A. N. G., Wang, H., Tao, Y., Zhang, S., Wang, J., & Feng, X. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.02.007 · Cited by 130
Gan, L., Ye, S., Chu, A., Anton, K., Yi, S.-L., Vincent, V. A. M., von Schack, D., Chin, D. J., Murray, J. C., Lohr, S., et al. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m306183200 · Cited by 130
Jekabsone, A., Mander, P. K., Tickler, A. K., Sharpe, M. A., & Brown, G. C. (2006) · Journal of Neuroinflammation · doi:10.1186/1742-2094-3-24 · Cited by 129
Self-citationJack, C. R., Therneau, T. M., Wiste, H. J., Weigand, S. D., Knopman, D. S., Lowe, V. J., Mielke, M. M., Vemuri, P., Roberts, R. O., Machulda, M. M., et al. (2016) · The Lancet Neurology · doi:10.1016/s1474-4422(15)00323-3 · Cited by 129
Thal, D. R., Tredici, K. D., Ludolph, A. C., Hoozemans, J. J. M., Rozemüller, A. J. M., Braak, H., & Knippschild, U. (2011) · Acta Neuropathologica · doi:10.1007/s00401-011-0871-6 · Cited by 128
PERK activation mitigates tau pathology in vitro and in vivo
Bruch, J., Xu, H. W., Rösler, T. W., Andrade, A. D., Kuhn, P., Lichtenthaler, S. F., Arzberger, T., Winklhofer, K. F., Müller, U., & Höglinger, G. U. (2017) · EMBO Molecular Medicine · doi:10.15252/emmm.201606664 · Cited by 128
Pathophysiology of the Ischemic Penumbra—Revision of a Concept
Back, T. (1998) · Cellular and Molecular Neurobiology · doi:10.1023/a:1020629818207 · Cited by 127
Vieira, M. M., Fernandes, J., Carreto, L. C., Soto, B. A., Santos, M. A. S., Han, J., Fernández‐López, A., Duarte, C. B., Carvalho, A. L., & Santos, A. E. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.04.002 · Cited by 127
Liu, M., Wu, W., Li, H., Li, S., Huang, L.-T., Yang, Y., Sun, Q., Wang, C.-X., Zhuang, Y., & Hang, C. (2014) · Journal of Spinal Cord Medicine · doi:10.1179/2045772314y.0000000224 · Cited by 127
Axon Degeneration Gated by Retrograde Activation of Somatic Pro-apoptotic Signaling
Simon, D. J., Pitts, J., Hertz, N. T., Yang, J. H., Yamagishi, Y., Olsen, O., Mark, M. T., Molina, H., & Tessier‐Lavigne, M. (2016) · Cell · doi:10.1016/j.cell.2016.01.032 · Cited by 127
Funk, K. E., Mrak, R. E., & Kuret, J. (2010) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.2010.01135.x · Cited by 126
Mechanisms and Potential Therapeutic Applications of Microglial Activation after Brain Injury
Kim, J. Y., Kim, N., & Yenari, M. A. (2014) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12360 · Cited by 126
The unfolded protein response in Alzheimer’s disease
Cornejo, V. H., & Hetz, C. A. (2013) · Seminars in Immunopathology · doi:10.1007/s00281-013-0373-9 · Cited by 125
Connecting the dots between tau dysfunction and neurodegeneration
Frost, B., Götz, J., & Feany, M. B. (2015) · Trends in Cell Biology · doi:10.1016/j.tcb.2014.07.005 · Cited by 124
Calpain inhibition mediates autophagy-dependent protection against polyglutamine toxicity
Menzies, F. M., García-Arencibia, M., Imarisio, S., O’Sullivan, N. C., Ricketts, T., Kent, B. A., Rao, M. V., Lam, W., Green-Thompson, Z. W., Nixon, R. A., et al. (2014) · Cell Death and Differentiation · doi:10.1038/cdd.2014.151 · Cited by 124
Westphal, D., Dewson, G., Menard, M. J., Frederick, P., Iyer, S., Bartolo, R. C., Gibson, L., Czabotar, P. E., Smith, B. J., Adams, J. M., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1415142111 · Cited by 124
ER stress and Parkinson's disease: Pathological inputs that converge into the secretory pathway
Mercado, G., Castillo, V., Soto, P., & Sidhu, A. (2016) · Brain Research · doi:10.1016/j.brainres.2016.04.042 · Cited by 124
Histamine induces microglia activation and dopaminergic neuronal toxicity via H1 receptor activation
Rocha, S. M., Saraiva, T., Cristóvão, A. C., Ferreira, R., Santos, T., Esteves, M., Saraiva, C., Je, G., Cortes, L., Valero, J., et al. (2016) · Journal of Neuroinflammation · doi:10.1186/s12974-016-0600-0 · Cited by 124
Thomas, S. N., Funk, K. E., Wan, Y., Liao, Z., Davies, P., Kuret, J., & Yang, A. J. (2012) · Acta Neuropathologica · doi:10.1007/s00401-011-0893-0 · Cited by 123
Yamanaka, K., Saito, Y., Yamamori, T., Urano, Y., & Noguchi, N. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.236273 · Cited by 123
Dihné, M., Grommes, C., Lutzenburg, M., Witte, O. W., & Block, F. (2002) · Stroke · doi:10.1161/01.str.0000039406.64644.cb · Cited by 123
Signaling by death receptors in the nervous system
Haase, G., Pettmann, B., Raoul, C., & Henderson, C. E. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.07.013 · Cited by 122
Bal‐Price, A., Matthias, A., & Brown, G. C. (2001) · Journal of Neurochemistry · doi:10.1046/j.0022-3042.2001.00675.x · Cited by 122
Self-citationÜber Untergang von Zellen während der normalen Entwicklung bei Wirbeltieren
Ernst, M. (1926) · Anatomy and Embryology · doi:10.1007/bf02118264 · Cited by 121
Mellén, M., de la Rosa, E. J., & Boya, P. (2008) · Cell Death and Differentiation · doi:10.1038/cdd.2008.40 · Cited by 121
The extent and time course of motoneuron involvement in amyotrophic lateral sclerosis
Dantes, M., & McComas, A. J. (1991) · Muscle & Nerve · doi:10.1002/mus.880140506 · Cited by 121
Reyes, R. C., Brennan, A. M., Shen, Y., Baldwin, Y., & Swanson, R. A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1597-12.2012 · Cited by 120
Epistatic and independent functions of Caspase-3 and Bcl-X L in developmental programmed cell death
Roth, K. A., Kuan, C.-Y., Haydar, T. F., D’Sa-Eipper, C., Shindler, K. S., Zheng, T. S., Kuida, K., Flavell, R. A., & RAKIC, P. T. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.1.466 · Cited by 119
Clarke, P. G. H., & Puyal, J. (2012) · Autophagy · doi:10.4161/auto.20380 · Cited by 119
Reexamination of granulovacuolar degeneration
Okamoto, K., Hirai, S., Iizuka, T., Yanagisawa, T., & Watanabe, M. (1991) · Acta Neuropathologica · doi:10.1007/bf00296544 · Cited by 119
Heterogeneity of microglia and TNF signaling as determinants for neuronal death or survival
Kraft, A. D., McPherson, C. A., & Harry, G. J. (2009) · NeuroToxicology · doi:10.1016/j.neuro.2009.07.001 · Cited by 119
Mechanisms and consequences of entosis
Krishna, S., & Overholtzer, M. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2207-0 · Cited by 118
Kristián, T., Gertsch, J., Bates, T. E., & Siesjö, B. K. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.0741999.x · Cited by 117
WldS protein requires Nmnat activity and a short N-terminal sequence to protect axons in mice
Conforti, L., Wilbrey, A. L., Morreale, G., Janečková, L., Beirowski, B., Adalbert, R., Mazzola, F., Stefano, M. D., Hartley, R., Babetto, E., et al. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200807175 · Cited by 117
Self-citationCalcineurin and glial signaling: neuroinflammation and beyond
Furman, J. L., & Norris, C. M. (2014) · Journal of Neuroinflammation · doi:10.1186/s12974-014-0158-7 · Cited by 117
LC3-Associated Phagocytosis (LAP): Connections with Host Autophagy
Lai, S.-C., & Devenish, R. J. (2012) · Cells · doi:10.3390/cells1030396 · Cited by 116 · cited 1×
“This is especially true now that there is evidence that certain ATG genes can have roles in other cell processes (124, 368, 375, 800) and that some types of autophagy may possibly bypass key ATG genes (114, 368), such as Beclin-1 in neurons (114).”
Oligomeropathies and pathogenesis of Alzheimer and Parkinson's diseases
Forloni, G., Artuso, V., Vitola, P. L., & Balducci, C. (2016) · Movement Disorders · doi:10.1002/mds.26624 · Cited by 116
The Role of Excitotoxic Programmed Necrosis in Acute Brain Injury
Fujikawa, D. G. (2015) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2015.03.004 · Cited by 114
Johnson, M. D., Xiang, H., London, S., Kinoshita, Y., Knudson, C. M., Mayberg, M. R., Korsmeyer, S. J., & Morrison, R. S. (1998) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19981215)54:6<721::aid-jnr1>3.0.co;2-1 · Cited by 114
Hwang, J.-Y., Gertner, M. J., Pontarelli, F., Court-Vazquez, B. L., Bennett, M. V. L., Ofengeim, D., & Zukin, R. S. (2016) · Cell Death and Differentiation · doi:10.1038/cdd.2016.140 · Cited by 114
Pathogenesis of hippocampal neuronal death after hypoxia–ischemia changes during brain development
Liu, C. L., Siesjö, B. K., & Hu, B. R. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.03.062 · Cited by 113
Chavez‐Valdez, R., Martin, L. J., Flock, D. L., & Northington, F. J. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.05.002 · Cited by 113
Huang, Y., Zhao, L., Jia, B., Wu, L., Li, Y., Curthoys, N. P., & Zheng, J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2051-11.2011 · Cited by 113
Xu, S.-Y., & Pan, S.-Y. (2013) · Medical science monitor basic research/Medical science monitor. Basic research · doi:10.12659/msmbr.883750 · Cited by 112
Li, B., Chauvin, C., Paulis, D. D., Oliveira, F. D., Gharib, A., Vial, G., Lablanche, S., Leverve, X. M., Bernardi, P., Ovize, M., et al. (2012) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2012.05.011 · Cited by 112
Nomura, K., Vilalta, A., Allendorf, D. H., Hornik, T. C., & Brown, G. C. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1502532 · Cited by 111
Self-citationPark, H.-Y. L., Park, Y. G., Cho, A.-H., & Park, C. K. (2013) · Ophthalmology · doi:10.1016/j.ophtha.2012.11.021 · Cited by 111
Ciliary neurotrophic factor: A review
Richardson, P. M. (1994) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(94)90045-0 · Cited by 111
Ballooned neurons in several neurodegenerative diseases and stroke contain αB crystallin
Lowe, J. S., ERRINGTON, D. R., Lennox, G. G., et al. (1992) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.1992.tb00796.x · Cited by 111
The DNA Replication Stress Hypothesis of Alzheimer’s Disease
Yurov, Y. B., Vorsanova, S. G., & Iourov, I. Y. (2011) · The Scientific World JOURNAL · doi:10.1100/2011/625690 · Cited by 110
Henshall, D. C., Bonislawski, D. P., Skradski, S. L., Lan, J., Meller, R., & Simon, R. P. (2001) · Neurobiology of Disease · doi:10.1006/nbdi.2001.0415 · Cited by 110
Microglial EP2 is critical to neurotoxicity from activated cerebral innate immunity
Shie, F., Montine, K. S., Breyer, R. M., & Montine, T. J. (2005) · Glia · doi:10.1002/glia.20220 · Cited by 110
Poly(ADP-ribose) Polymerase-1 in Amyloid Beta Toxicity and Alzheimer's Disease
Strosznajder, J. B., Czapski, G. A., Adamczyk, A., & Strosznajder, R. P. (2012) · Molecular Neurobiology · doi:10.1007/s12035-012-8258-9 · Cited by 110
Rao, M. V., Mohan, P. S., Peterhoff, C. M., Yang, D., Schmidt, S., Stavrides, P. H., Campbell, J., Chen, Y., Jiang, Y., Paskevich, P. A., et al. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4119-08.2008 · Cited by 110
Vosler, P. S., Sun, D., Wang, S., Gao, Y., Kintner, D. B., Signore, A. P., Cao, G., & Chen, J. (2009) · Experimental Neurology · doi:10.1016/j.expneurol.2009.04.032 · Cited by 110
Biswas, S. C., Shi, Y., Vonsattel, J., Leung, C. L., Troy, C. M., & Greene, L. A. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3524-06.2007 · Cited by 109
Ramonet, D., Perier, C., Recasens, A., Dehay, B., Bové, J., Costa, V., Scorrano, L., & Vila, M. (2012) · Cell Death and Differentiation · doi:10.1038/cdd.2012.95 · Cited by 109
Calpain 1 induce lysosomal permeabilization by cleavage of lysosomal associated membrane protein 2
Rodriguez, G. E. V., & Torriglia, A. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2013.05.019 · Cited by 107
Calpain-mediated Hsp70.1 cleavage in hippocampal CA1 neuronal death
Sahara, S., & Yamashima, T. (2010) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2010.02.087 · Cited by 105
Role of synaptic and nonsynaptic glutamate receptors in ischaemia induced neurotoxicity
Brassai, A., Suvanjeiev, R.-G., Bán, E.-G., & Lakatos, M. (2014) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2014.12.007 · Cited by 105
DRAM1 regulates apoptosis through increasing protein levels and lysosomal localization of BAX
Guan, J.-J., Zhang, X.-D., Sun, W., Qi, L., Wu, J.-C., & Qin, Z.-H. (2015) · Cell Death & Disease · doi:10.1038/cddis.2014.546 · Cited by 105
Pathologic role of glial nitric oxide in adult and pediatric neuroinflammatory diseases
Ghasemi, M., & Fatemi, A. S. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.06.002 · Cited by 104
The ins and outs of programmed cell death during C. elegans development
Hengartner, M. O., & Horvitz, H. R. (1994) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1994.0100 · Cited by 104
Nonomura, K., Yamaguchi, Y., Hamachi, M., Koike, M., Uchiyama, Y., Nakazato, K., Mochizuki, A., Sakaue-Sawano, A., Miyawaki, A., Yoshida, H., et al. (2013) · Developmental Cell · doi:10.1016/j.devcel.2013.11.015 · Cited by 104
PERK-opathies: An Endoplasmic Reticulum Stress Mechanism Underlying Neurodegeneration
Bell, M. C., Meier, S. E., Ingram, A., & Abisambra, J. F. (2015) · Current Alzheimer Research · doi:10.2174/1567205013666151218145431 · Cited by 104
Tau physiology and pathomechanisms in frontotemporal lobar degeneration
Bodea, L., Eckert, A., Ittner, L. M., Piguet, O., & Götz, J. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13600 · Cited by 104
From the Gla domain to a novel small-molecule detector of apoptosis
Cohen, A., Shirvan, A., Levin, G., Grimberg, H., Reshef, A., & Ziv, I. (2009) · Cell Research · doi:10.1038/cr.2009.17 · Cited by 103
Inflammation in Ischemic Stroke: Mechanisms, Consequences and Possible Drug Targets
Ahmad, M., Dar, N. J., Bhat, Z. S., Hussain, A., Shah, A., Liu, H., & Graham, S. H. (2014) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527313666141023094720 · Cited by 102
Dujardin, S., Colin, M., & Buée, L. (2014) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12200 · Cited by 101
Rao, M. V., McBrayer, M. K., Campbell, J., Kumar, A., Hashim, A. T., Sershen, H. W., Stavrides, P. H., Ohno, M., Hutton, M., & Nixon, R. A. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1132-14.2014 · Cited by 101
Problems of cell death in neurodegeneration and Alzheimer's Disease
Jellinger, K. A., & Stadelmann, C. (2001) · Journal of Alzheimer s Disease · doi:10.3233/jad-2001-3106 · Cited by 101
Angelova, P. R., & Abramov, A. Y. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.07.103 · Cited by 100
Selective neuronal loss in rescued penumbra relates to initial hypoperfusion
Guadagno, J. V., Jones, P. S., Aigbirhio, F. I., Wang, D., Fryer, T. D., Day, D. J., Antoun, N. M., Nimmo‐Smith, I., Warburton, E. A., & Baron, J. (2008) · Brain · doi:10.1093/brain/awn175 · Cited by 99
Seglen, P. O., & Gordon, P. B. (1980) · Molecular Pharmacology · doi:10.1016/s0026-895x(25)14541-0 · Cited by 99
Nadph Oxidase Mediates Striatal Neuronal Injury after Transient Global Cerebral Ischemia
Yoshioka, H., Niizuma, K., Katsu, M., Okami, N., Sakata, H., Kim, G. S., Narasimhan, P., & Chan, P. H. (2010) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2010.166 · Cited by 98
Vela, L., Gonzalo, Ó., Naval, J., & Marzo, I. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.422204 · Cited by 98
Wright, K. M., Linhoff, M. W., Potts, P. R., & Deshmukh, M. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200406073 · Cited by 98
BCL-2 family members in the development and degenerative pathologies of the nervous system
Sadoul, R. (1998) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4400438 · Cited by 97
Martin, L. J., Adams, N. A., Pan, Y., Price, A., & Wong, M. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.2225-10.2011 · Cited by 96
Kim, T. W., Cho, H. M., Choi, S. Y., Suguira, Y., Hayasaka, T., Setou, M., Koh, H. C., Hwang, E. M., Park, J., Kang, S. J., et al. (2013) · Cell Death and Disease · doi:10.1038/cddis.2013.447 · Cited by 96
Wießner, C., ALLEGRINI, P. R., Rupalla, K., Sauer, D., Oltersdorf, T., McGregor, A. L., Bischoff, S. F., Böttiger, B. W., & van der Putten, H. (1999) · Neuroscience Letters · doi:10.1016/s0304-3940(99)00392-4 · Cited by 95
Wang, Q., Zhang, X., Chen, S., Zhang, X., Zhang, S., Youdium, M. B. H., & Le, W. (2011) · Neurodegenerative Diseases · doi:10.1159/000323469 · Cited by 95
DEVELOPMENT OF THE NERVOUS SYSTEM
Hamburger, V. (1952) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1952.tb26527.x · Cited by 95
Lysosome and calcium dysregulation in Alzheimer's disease: partners in crime
McBrayer, M. K., & Nixon, R. A. (2013) · Biochemical Society Transactions · doi:10.1042/bst20130201 · Cited by 93
Caspase Inhibitors Protect Neurons by Enabling Selective Necroptosis of Inflamed Microglia
Fricker, M., Vilalta, A., Tolkovsky, A. M., & Brown, G. C. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.427880 · Cited by 92
Self-citationTaming Glutamate Excitotoxicity: Strategic Pathway Modulation for Neuroprotection
Jia, M., Njapo, S. A. N., Rastogi, V., & Hedna, V. S. (2015) · CNS Drugs · doi:10.1007/s40263-015-0225-3 · Cited by 91
Windelborn, J. A., & Lipton, P. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05349.x · Cited by 91
BH 3‐only proteins: a 20‐year stock‐take
Doerflinger, M., Glab, J., & Puthalakath, H. (2015) · FEBS Journal · doi:10.1111/febs.13190 · Cited by 91
Wyttenbach, A., & Tolkovsky, A. M. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03676.x · Cited by 90
Self-citationThe toxicity of tau in Alzheimer disease: turnover, targets and potential therapeutics
Pritchard, S. M., Dolan, P. J., Vitkus, A., & Johnson, G. V. W. (2011) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2011.01273.x · Cited by 89
BAX channel activity mediates lysosomal disruption linked to Parkinson disease
Bové, J., Martínez-Vicente, M., Dehay, B., Perier, C., Recasens, A., Bombrun, A., Antonsson, B., & Vila, M. (2014) · Autophagy · doi:10.4161/auto.28286 · Cited by 89
Caspase mRNA expression in a rat model of focal cerebral ischemia
Harrison, D. C., Davis, R. P., Bond, B. C., Campbell, C. A., James, M. F., Parsons, A. A., & Philpott, K. L. (2001) · Molecular Brain Research · doi:10.1016/s0169-328x(01)00058-4 · Cited by 89
Necroptosis Mediates TNF-Induced Toxicity of Hippocampal Neurons
Liu, S., Wang, X., Li, Y., Xu, L., Yu, X., Ge, L., Li, J., Zhu, Y., & He, S. (2014) · BioMed Research International · doi:10.1155/2014/290182 · Cited by 89
Pehar, M., O’Riordan, K. J., Burns‐Cusato, M., Andrzejewski, M. E., del Alcazar, C. R. G., Bürger, C., Scrable, H. J., & Puglielli, L. (2010) · Aging Cell · doi:10.1111/j.1474-9726.2010.00547.x · Cited by 89
Puyal, J., Ginet, V., Grishchuk, Y., Truttmann, A. C., & Clarke, P. G. H. (2011) · The Neuroscientist · doi:10.1177/1073858411404948 · Cited by 89
T-cell death following immune activation is mediated by mitochondria-localized SARM
Panneerselvam, P., Singh, L. P., Selvarajan, V., Chng, W. J., Ng, S., Tan, N. S., Ho, B., Chen, J., & Ding, J. L. (2012) · Cell Death and Differentiation · doi:10.1038/cdd.2012.144 · Cited by 88
Endonuclease G mediates α‐synuclein cytotoxicity during Parkinson's disease
Büttner, S., Habernig, L., Broeskamp, F., Ruli, D., Vögtle, F. N., Vlachos, M., Macchi, F., Küttner, V., Carmona‐Gutierrez, D., Eisenberg, T., et al. (2013) · The EMBO Journal · doi:10.1038/emboj.2013.228 · Cited by 87
Causal Role of Apoptosis-Inducing Factor for Neuronal Cell Death Following Traumatic Brain Injury
Slemmer, J. E., Zhu, C., Landshamer, S., Trabold, R., Grohm, J., Ardeshiri, A., Wagner, E., Sweeney, M. I., Blomgren, K., Culmsee, C., et al. (2008) · American Journal Of Pathology · doi:10.2353/ajpath.2008.080168 · Cited by 87
Gordon, P. B. (1982) · Experimental Cell Research · doi:10.1016/0014-4827(82)90402-5 · Cited by 87
Weber, A., Paschen, S. A., Heger, K., Wilfling, F., Frankenberg, T., Bauerschmitt, H., Seiffert, B. M., Kirschnek, S., Wagner, H., & Häcker, G. A. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200610148 · Cited by 87
Cited by
Hallmarks of neurodegenerative diseases
Wilson, D. M., Cookson, M. R., Van Den Bosch, L., Zetterberg, H., Holtzman, D. M., & Dewachter, I. (2023) · Cell · doi:10.1016/j.cell.2022.12.032 · Cited by 1,789
Signaling pathways involved in ischemic stroke: molecular mechanisms and therapeutic interventions
Qin, C., Yang, S., Chu, Y.-H., Zhang, H., Pang, X.-W., Chen, L., Zhou, L.-Q., Chen, M., Tian, D.-S., & Wang, W. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01064-1 · Cited by 939
Lee, J.-H., Yang, D.-S., Goulbourne, C. N., Im, E., Stavrides, P., Pensalfini, A., Chan, H., Bouchet-Marquis, C., Bleiwas, C., Berg, M. J., et al. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01084-8 · Cited by 638
Wang, Y., & Kanneganti, T.-D. (2021) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2021.07.038 · Cited by 545
The endotoxin hypothesis of neurodegeneration
Brown, G. C. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1564-7 · Cited by 457
Self-citation
Metadata
- Authors
- Fricker, M., Tolkovsky, A. M., Borutaite, V., Coleman, M., & Brown, G. C.
- Venue
- Physiological Reviews
- Publisher
- American Physiological Society
- Published
- 2018-04-01
- Volume
- 98
- Issue
- 2
- Pages
- 813-880
- ISSN
- 0031-9333 (ISSN-L)
- 1522-1210
- OpenAlex
- W2789018622
- Cited by
- 1,108
- References
- 797
- FWCI
- 6.95
- Type
- journal article
- Language
- en
- Open access
- green
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.