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Neuronal cell death in neurodegenerative diseases: recurring themes around protein handling
Open accessAbstract
Neuronal cell death plays a role in many chronic neurodegenerative diseases with the loss of particular subsets of neurons. The loss of the neurons occurs during a period of many years, which can make the mode(s) of cell death and the initiating factors difficult to determine. In vitro and in vivo models have proved invaluable in this regard, yielding insight into cell death pathways. This review describes the main mechanisms of neuronal cell death, particularly apoptosis, necrosis, excitotoxicity and autophagic cell death, and their role in neurodegenerative diseases such as ischaemia, Alzheimer's, Parkinson's and Huntington's diseases. Crosstalk between these death mechanisms is also discussed. The link between cell death and protein mishandling, including misfolded proteins, impairment of protein degradation, protein aggregation is described and finally, some pro‐survival strategies are discussed.
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“AD is a neurodegenerative disorder marked by neuronal loss, especially in the hippocampus and cerebral cortex (49, 50).”
From Modeling late-onset Alzheimer’s disease neuropathology via direct neuronal reprogramming (2024) · cites this paper as [50]
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Cites
Spillantini, M. G., Schmidt, M. L., Lee, V. M.-Y., Trojanowski, J. Q., Jakes, R., & Goedert, M. (1997) · Nature · doi:10.1038/42166 · Cited by 8,382
Li, P., Nijhawan, D., Budihardjo, I., Srinivasula, S. M., Ahmad, M., Alnemri, E. S., & Wang, X. (1997) · Cell · doi:10.1016/s0092-8674(00)80434-1 · Cited by 7,289
Autophagy in the Pathogenesis of Disease
Levine, B., & Kroemer, G. (2008) · Cell · doi:10.1016/j.cell.2007.12.018 · Cited by 7,069
Alzheimer's Disease: Genes, Proteins, and Therapy
Selkoe, D. J. (2001) · Physiological Reviews · doi:10.1152/physrev.2001.81.2.741 · Cited by 6,063
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
Kitada, T., Asakawa, S., Hattori, N., Matsumine, H., Yamamura, Y., Minoshima, S., Yokochi, M., Mizuno, Y., & Shimizu, N. (1998) · Nature · doi:10.1038/33416 · Cited by 5,227
Molecular characterization of mitochondrial apoptosis-inducing factor
Susin, S. A., Lorenzo, H. K., Zamzami, N., Marzo, I., Snow, B. E., Brothers, G. M., Mangion, J., Jacotot, E., Costantini, P., Loeffler, M., et al. (1999) · Nature · doi:10.1038/17135 · Cited by 4,060
The Bcl2 family: regulators of the cellular life-or-death switch
Cory, S., & Adams, J. M. (2002) · Nature Reviews Cancer · doi:10.1038/nrc883 · Cited by 4,032
Self-eating and self-killing: crosstalk between autophagy and apoptosis
Maiuri, M. C., Zalckvar, E., Kimchi, A., & Kroemer, G. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2239 · Cited by 3,638
Bcl-2 Antiapoptotic Proteins Inhibit Beclin 1-Dependent Autophagy
Pattingre, S., Tassa, A., Qu, X., Garuti, R., Liang, X. H., Mizushima, N., Packer, M., Schneider, M. D., & Levine, B. (2005) · Cell · doi:10.1016/j.cell.2005.07.002 · Cited by 3,536
Molecular Chaperones in the Cytosol: from Nascent Chain to Folded Protein
Hartl, F. U., & Hayer-Hartl, M. K. (2002) · Science · doi:10.1126/science.1068408 · Cited by 3,335
Research works printed but not linked: 1
- 10.1002/(SICI)1096-9861(19970203)378:1<10::AID-CNE4>3.0.CO;2-N · DOI
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Fulda, S., Gorman, A. M., Hori, O., & Samali, A. (2010) · International Journal of Cell Biology · doi:10.1155/2010/214074 · Cited by 1,590
Self-citationMolecular mechanisms of cell death in neurological diseases
Moujalled, D., Strasser, A., & Liddell, J. R. (2021) · Cell Death & Differentiation · doi:10.1038/s41418-021-00814-y · Cited by 749
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Jellinger, K. A. (2010) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2010.01010.x · Cited by 640
Find-me and eat-me signals in apoptotic cell clearance: progress and conundrums
Ravichandran, K. S. (2010) · The Journal of Experimental Medicine · doi:10.1084/jem.20101157 · Cited by 572
Cohen, R. M., Rezai-Zadeh, K. P., Weitz, T. M., Rentsendorj, A., Gate, D., Spivak, I. E., Bholat, Y., Vasilevko, V., Glabe, C. G., Breunig, J. J., et al. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3672-12.2013 · Cited by 555
Resveratrol-Activated AMPK/SIRT1/Autophagy in Cellular Models of Parkinson’s Disease
Wu, Y., Li, X., Zhu, J. X., Xie, W., Le, W., Fan, Z., Jankovic, J. J., & Pan, T. (2011) · Neurosignals · doi:10.1159/000328516 · Cited by 496
Development of Polymeric Nanoparticles for Blood–Brain Barrier Transfer—Strategies and Challenges
Zhang, W., Mehta, A., Tong, Z., Esser, L., & Voelcker, N. H. (2021) · Advanced Science · doi:10.1002/advs.202003937 · Cited by 430
Neuronal Cell Death Mechanisms in Major Neurodegenerative Diseases
Chi, H., Chang, H.-Y., & Sang, T.-K. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19103082 · Cited by 412
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Doyle, K., Kennedy, D. C., Gorman, A. M., Gupta, S., Healy, S., & Samali, A. (2011) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2011.01374.x · Cited by 329
Self-citationRole of AIM2 inflammasome in inflammatory diseases, cancer and infection
Sharma, B. R., Karki, R., & Kanneganti, T. (2019) · European Journal of Immunology · doi:10.1002/eji.201848070 · Cited by 301
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Christgen, S. L., Tweedell, R. E., & Kanneganti, T. (2021) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.108010 · Cited by 298
Recent advances in our understanding of neurodegeneration
Jellinger, K. A. (2009) · Journal of Neural Transmission · doi:10.1007/s00702-009-0240-y · Cited by 274
Stress-induced self-cannibalism: on the regulation of autophagy by endoplasmic reticulum stress
Deegan, S., Saveljeva, S., Gorman, A. M., & Samali, A. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-1173-4 · Cited by 280
Self-citationSairazi, N. S. M., & Sirajudeen, K. N. S. (2020) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2020/6565396 · Cited by 260
Neuronal cell death mechanisms in Alzheimer’s disease: An insight
Goel, P., Chakrabarti, S., Goel, K., Bhutani, K., Chopra, T., & Bali, S. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.937133 · Cited by 248
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Volkman, R., & Offen, D. (2017) · Stem Cells · doi:10.1002/stem.2651 · Cited by 222
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Zhang, F., Zhao, X., Shen, H., & Zhang, C. (2016) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2016.2573 · Cited by 230
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Castle, A. R., & Gill, A. C. (2017) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2017.00019 · Cited by 232
Nimgampalle, M., Chakravarthy, H., Sharma, S., Shree, S., Bhat, A. R., Pradeepkiran, J. A., & Devanathan, V. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101994 · Cited by 207
Bejarano, E., & Cuervo, A. M. (2010) · Proceedings of the American Thoracic Society · doi:10.1513/pats.200909-102js · Cited by 200
Ubiquitin/proteasome pathway impairment in neurodegeneration: therapeutic implications
Huang, Q., & Figueiredo‐Pereira, M. E. (2010) · APOPTOSIS · doi:10.1007/s10495-010-0466-z · Cited by 177
Dynamics of Dynamin-Related Protein 1 in Alzheimer’s Disease and Other Neurodegenerative Diseases
Oliver, D., & Reddy, P. H. (2019) · Cells · doi:10.3390/cells8090961 · Cited by 172
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Mullin, S., & Schapira, A. H. V. (2013) · Molecular Neurobiology · doi:10.1007/s12035-013-8394-x · Cited by 158
Wuolikainen, A., Jonsson, P., Ahnlund, M., Antti, H., Marklund, S. L., Möritz, T., Forsgren, L., Andersen, P. M., & Trupp, M. (2016) · Molecular BioSystems · doi:10.1039/c5mb00711a · Cited by 138
Crashing the computer: apoptosis vs. necroptosis in neuroinflammation
Heckmann, B. L., Tummers, B., & Green, D. R. (2018) · Cell Death and Differentiation · doi:10.1038/s41418-018-0195-3 · Cited by 136
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Gabandé‐Rodríguez, E., Keane, L., & Capasso, M. (2020) · Journal of Neuroscience Research · doi:10.1002/jnr.24419 · Cited by 127
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Gogvadze, V. G., Orrenius, S., & Zhivotovsky, B. (2009) · APOPTOSIS · doi:10.1007/s10495-009-0323-0 · Cited by 127
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Wuwongse, S., Chang, R. C., & Law, A. C. K. (2010) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2010.04.005 · Cited by 126
Autophagy–lysosomal-associated neuronal death in neurodegenerative disease
Nixon, R. A. (2024) · Acta Neuropathologica · doi:10.1007/s00401-024-02799-7 · Cited by 126
Zhao, Y., Cong, L., & Lukiw, W. J. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00407 · Cited by 116
Wu, S., Xu, R., Duan, B., & Jiang, P. (2017) · Journal of Materials Chemistry B · doi:10.1039/c7tb00721c · Cited by 111
Ayeni, E. A., Aldossary, A. M., Ayejoto, D. A., Gbadegesin, L. A., Alshehri, A. A., Alfassam, H. A., Afewerky, H. K., Almughem, F. A., Saidu, M. B., & Tawfik, E. A. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph191912495 · Cited by 121
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Venza, M., Visalli, M., Beninati, C., Gaetano, G. V. D., Teti, D. V., & Venza, I. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2015/481782 · Cited by 110
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Park, H., Kam, T., Dawson, T. M., & Dawson, V. L. (2020) · International review of cytology · doi:10.1016/bs.ircmb.2019.12.009 · Cited by 105
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Very, N., Vercoutter‐Edouart, A., Lefebvre, T., Hardivillé, S., & Yazidi‐Belkoura, I. E. (2018) · Frontiers in Endocrinology · doi:10.3389/fendo.2018.00602 · Cited by 96
Moreira, R., Nóbrega, C., de Almeida, L. P., & Mendonça, L. S. (2024) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-02511-7 · Cited by 98
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Turner, M. R., Barnwell, J., Al‐Chalabi, A., & Eisen, A. (2012) · Brain · doi:10.1093/brain/aws144 · Cited by 88
Kim, N., Chen, D., Zhou, X. Z., & Lee, T. H. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20133131 · Cited by 89
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Tenreiro, S., Munder, M. C., Alberti, S., & Outeiro, T. F. (2013) · Journal of Neurochemistry · doi:10.1111/jnc.12271 · Cited by 88
Adak, A., Das, G., Barman, S., Mohapatra, S., Bhunia, D., Jana, B., & Ghosh, S. (2017) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.6b12114 · Cited by 84
Thundyil, J., & Lim, K. (2014) · Ageing Research Reviews · doi:10.1016/j.arr.2014.11.003 · Cited by 85
Panchal, K., & Tiwari, A. K. (2017) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2017.03.001 · Cited by 85
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Guo, D., Liu, Z., Zhou, J., Ke, C., & Li, D. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25189947 · Cited by 83
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Qiu, W., Ai, W., Zhu, F., Zhang, Y., Guo, M., Law, B. Y. K., Wu, J., Wong, V. K. W., Tang, Y., Yu, L., et al. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.12.263 · Cited by 81
Balakrishnan, R., Cho, D.-Y., Kim, I., Seol, S.-H., & Choi, D. (2022) · Antioxidants · doi:10.3390/antiox11020281 · Cited by 83
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Leong, Y. Q., Ng, K. Y., Chye, S. M., Ling, A. P. K., & Koh, R. Y. (2019) · Metabolic Brain Disease · doi:10.1007/s11011-019-00516-y · Cited by 80
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Sun, Z., Kwon, J.-S., Ren, Y., Chen, S., Walker, C. K., Lu, X., Cates, K., Karahan, H., Sviben, S., Fitzpatrick, J. A. J., et al. (2024) · Science · doi:10.1126/science.adl2992 · Cited by 77
“AD is a neurodegenerative disorder marked by neuronal loss, especially in the hippocampus and cerebral cortex (49, 50).”
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Watkins, S., & Sontheimer, H. W. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.05.001 · Cited by 76
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Memon, A., Coleman, J., & Amara, A. W. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.104859 · Cited by 77
Olesen, M. A., Villavicencio-Tejo, F., & Quintanilla, R. A. (2022) · Translational Neurodegeneration · doi:10.1186/s40035-022-00308-y · Cited by 80
Kim, M. W., Abid, N. B., Jo, M. G., Jo, M. G., Yoon, G. H., & Kim, M. O. (2017) · Scientific Reports · doi:10.1038/s41598-017-12632-9 · Cited by 72
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Lumkwana, D., du Toit, A., Kinnear, C. J., & Loos, B. (2017) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2017.03.006 · Cited by 69
Guo, W., Zhang, B., Mu, K., Feng, S., Dong, Z., Ning, G., Li, H., Liu, S., Zhao, L., Li, Y., et al. (2018) · Cell Death and Disease · doi:10.1038/s41419-017-0232-z · Cited by 67
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Agrawal, L., Louboutin, J., Marusich, E., Reyes, B. A. S., Bockstaele, E. J. V., & Strayer, D. S. (2009) · Brain Research · doi:10.1016/j.brainres.2009.09.113 · Cited by 66
Khan, Y. F., Kaushik, B., Chowdhary, C. L., & Srivastava, G. (2022) · Diagnostics · doi:10.3390/diagnostics12123193 · Cited by 65
Francis, N. L., Bennett, N. K., Halikere, A., Pang, Z. P., & Moghe, P. V. (2016) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.6b00156 · Cited by 63
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Soni, D., Sagar, P., & Takkar, B. (2021) · International Ophthalmology · doi:10.1007/s10792-021-01864-4 · Cited by 66
Bansal, R., & Singh, R. (2017) · Medicinal Research Reviews · doi:10.1002/med.21458 · Cited by 62
Ravera, S., Colombo, E., Pasquale, C., Benedicenti, S., Solimei, L., Signore, A., & Amaroli, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094347 · Cited by 58
Reddy, D. S., & Abeygunaratne, H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231911734 · Cited by 58
Keeney, J. T. R., Swomley, A. M., Harris, J. L., Fiorini, A., Mitov, M. I., Marzia Perluigi, A., Rukhsana Sultana, A., & Butterfield, D. A. (2011) · Neurotoxicity Research · doi:10.1007/s12640-011-9287-2 · Cited by 56
Azarashvili, T., Stricker, R., & Reiser, G. (2010) · Biological Chemistry · doi:10.1515/bc.2010.070 · Cited by 57
Harrell, C. R., Volarević, V., Djonov, V., & Volarevic, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094487 · Cited by 59
Bayram-Weston, Z., Jones, L., Dunnett, S. B., & Brooks, S. P. (2011) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2011.07.009 · Cited by 60
Zhang, H.-P., Yuan, L., Rui-ni, Z., Li, T., Ma, R., Dong, H., & Xiong, L. (2010) · Anesthesia & Analgesia · doi:10.1213/ane.0b013e3181e45519 · Cited by 56
Xu, D., Zhao, H., Gao, H. T., Zhao, H., Liu, D., & Li, J. (2018) · Molecular Pain · doi:10.1177/1744806918783535 · Cited by 56
Intermittent hypoxia improves cognition and reduces anxiety‐related behavior in APP/PS1 mice
Meng, S., Wang, B., & Li, W. (2019) · Brain and Behavior · doi:10.1002/brb3.1513 · Cited by 56
Recent insights into the roles of circular RNAs in human brain development and neurologic diseases
Najafi, S., Zarch, S. M. A., Majidpoor, J., Pordel, S., Aghamiri, S., Rasul, M. F., Asemani, Y., Vakili, O., Mohammadi, V., Movahedpour, A., et al. (2022) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2022.11.166 · Cited by 56
Tian, Y., Chen, K., Liu, L., Dong, Y.-X., Zhao, P., & Guo, S. (2018) · Mediators of Inflammation · doi:10.1155/2018/3802324 · Cited by 53
Loss of Quinone Reductase 2 Function Selectively Facilitates Learning Behaviors
Benoit, C.-É., Bastianetto, S., Brouillette, J., Tse, Y. C., Boutin, J. A., Delagrange, P., Wong, T. P., Sarret, P., & Quirion, R. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2808-10.2010 · Cited by 54
Gut microbiota in neurological diseases: Melatonin plays an important regulatory role
Ahmadi, S., Taghizadieh, M., Mehdizadehfar, E., Hasani, A., Fard, J. K., Feizi, H., Hamishehkar, H., Ansarin, M., Yekani, M., & Memar, M. Y. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116487 · Cited by 62
Pieper, I., Wehe, C. A., Bornhorst, J., Ebert, F., Leffers, L., Holtkamp, M., Höseler, P., Weber, T., Mangerich, A., Bürkle, A., et al. (2014) · Metallomics · doi:10.1039/c3mt00337j · Cited by 52
Neuroinflammation and central PI3K/Akt/mTOR signal pathway contribute to bone cancer pain
Zhang, J., Wang, L., Wang, H., Su, Z., & Pang, X. (2019) · Molecular Pain · doi:10.1177/1744806919830240 · Cited by 52
Inflammatory, Apoptotic, and Survival Gene Signaling in Alzheimer’s Disease
Lukiw, W. J., & Bazan, N. G. (2010) · Molecular Neurobiology · doi:10.1007/s12035-010-8126-4 · Cited by 50
Yasuda, T., & Mochizuki, H. (2010) · APOPTOSIS · doi:10.1007/s10495-010-0486-8 · Cited by 51
DNA double-strand breaks: a potential therapeutic target for neurodegenerative diseases
Thadathil, N., Hori, R. T., Xiao, J., & Khan, M. M. (2019) · Chromosome Research · doi:10.1007/s10577-019-09617-x · Cited by 51
Controlling properties of human neural progenitor cells using 2D and 3D conductive polymer scaffolds
Song, S., Amores, D., Chen, C., McConnell, K. W., Oh, B., Poon, A. S. Y., & George, P. M. (2019) · Scientific Reports · doi:10.1038/s41598-019-56021-w · Cited by 49
D’souza, A. A., Nozohouri, S., Bleier, B. S., & Amiji, M. M. (2022) · Pharmaceutical Research · doi:10.1007/s11095-022-03433-5 · Cited by 49
Cabeza-Arvelaiz, Y., & Schiestl, R. H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0044700 · Cited by 45
Mechanistic roles for altered O-GlcNAcylation in neurodegenerative disorders
Balana, A. T., & Pratt, M. R. (2021) · Biochemical Journal · doi:10.1042/bcj20200609 · Cited by 46
Lee, S. Y., & Hur, S. J. (2019) · Comprehensive Reviews in Food Science and Food Safety · doi:10.1111/1541-4337.12451 · Cited by 47
Inestrosa, N. C., Ríos, J. A., Cisternas, P., Tapia‐Rojas, C., Rivera, D. S., Braidy, N., Zolezzi, J. M., Godoy, J. A., Carvajal, F. J., Ardiles, Á. O., et al. (2014) · Brain Pathology · doi:10.1111/bpa.12226 · Cited by 47
Chung, H., Chung, H.-Y., Bae, C.-W., Kim, C.-J., & Park, S. (2011) · Endocrine Journal · doi:10.1507/endocrj.k10e-396 · Cited by 44
Quantitative Proteomics Analysis of Inborn Errors of Cholesterol Synthesis
Jiang, X.-S., Backlund, P. S., Wassif, C. A., Yergey, A. L., & Porter, F. D. (2010) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m900548-mcp200 · Cited by 44
Sharifi-Rad, J., Bahukhandi, A., Dhyani, P., Sati, P., Capanoglu, E., Docea, A. O., Al-Harrasi, A., Dey, A., & Calina, D. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.664197 · Cited by 43
Li, R., Wang, L., Duan, H., Zhang, Q., Guo, X., Wu, C., & Peng, W. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.937289 · Cited by 48
Prasansuklab, A., Meemon, K., Sobhon, P., & Tencomnao, T. (2017) · BMC Complementary and Alternative Medicine · doi:10.1186/s12906-017-2050-3 · Cited by 42
Whether short peptides are good candidates for future neuroprotective therapeutics?
Perlikowska, R. (2021) · Peptides · doi:10.1016/j.peptides.2021.170528 · Cited by 43
Heat shock protein 27 in neuronal survival and neurite outgrowth
Read, D. E., & Gorman, A. M. (2009) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2009.02.114 · Cited by 41
Self-citationŽivančević, K., Baralić, K., Jorgovanović, D., Djordjević, A. B., Ćurčić, M., Miljaković, E. A., Antonijević, B., Bulat, Z., & Đukić-Ćosić, D. (2021) · Environmental Research · doi:10.1016/j.envres.2021.110727 · Cited by 39
Adiponectin and sporadic Alzheimer’s disease: Clinical and molecular links
Letra, L., Rodrigues, T., Matafome, P. N., Santana, I. J., & Seiça, R. M. F. (2017) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2017.10.002 · Cited by 38
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Metadata
- Authors
- Gorman, A. M.
- Affiliations
- Ollscoil na Gaillimhe – University of Galway (IE)
- Corresponding author
- Gorman, Adrienne M.
- ORCID
- Gorman, Adrienne M.
- Venue
- Journal of Cellular and Molecular Medicine
- Publisher
- Wiley
- Published
- 2008-07-10
- Volume
- 12
- Issue
- 6a
- Pages
- 2263-2280
- ISSN
- 1582-1838 (ISSN-L)
- 1582-4934
- PMC
- PMC4514105
- OpenAlex
- W1965453486
- Cited by
- 362
- References
- 222
- Citations by year
- 2026: 18 · 2025: 28 · 2024: 35 · 2023: 34 · 2022: 38 · 2021: 36 · 2020: 11 · 2019: 26 · 2018: 28 · 2017: 26 · 2016: 11 · 2015: 6 · 2014: 8 · 2013: 9 · 2012: 10
- FWCI
- 0.98
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Journal of Cellular and Molecular Medicine (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Arrow@dit (Dublin Institute of Technology) (acceptedVersion)
- ARAN (University of Galway Research Repository) (Ollscoil na Gaillimhe – University of Galway) (acceptedVersion, cc-by-nc-nd)
- ARAN (University of Galway Research Repository) (Ollscoil na Gaillimhe – University of Galway) (submittedVersion, cc-by-nc-nd)
- Arrow@dit (Dublin Institute of Technology) (submittedVersion, cc-by-nc-nd)
- Research Repository UCD (University College Dublin) (cc-by)
- Funders
- National University of Ireland
- University of Galway
- Irish Research Council
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- neuronal cell death, neurodegenerative diseases, apoptosis, necrosis, excitotoxicity, autophagic cell death, protein misfolding, protein aggregation, protein degradation, ischemia, Alzheimer's disease, Parkinson's disease, Huntington's disease, neuroprotection
- MeSH terms
- Alzheimer Disease, Autophagy, Brain Ischemia, Endoplasmic Reticulum, Humans, Huntington Disease, Models, Neurological, Necrosis, Nerve Tissue Proteins, Neurons, Parkinson Disease, Stress, Physiological, Receptors, N-Methyl-D-Aspartate, Cell Death, Apoptosis, Neurodegenerative Diseases, Ubiquitin, Proteasome Endopeptidase Complex
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