Circadian Rhythm Dysfunction Accelerates Disease Progression in a Mouse Model With Amyotrophic Lateral Sclerosis
Open accessAbstract
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease caused by interactions between environmental factors and genetic susceptibility. Circadian rhythm dysfunction (CRD) is a significant contributor to neurodegenerative conditions such as Alzheimer's disease and Parkinson's disease. However, whether CRD contributes to the progression of ALS remains little known. We performed behavioral and physiological tests on SOD1G93A ALS model mice with and without artificially induced CRD, and on wild-type controls; we also analyzed spinal cord samples histologically for differences between groups. We found that CRD accelerated the disease onset and progression of ALS in model mice, as demonstrated by aggravated functional deficits and weight loss, as well as increased motor neuron loss, activated gliosis, and nuclear factor κB-mediated inflammation in the spinal cord. We also found an increasing abundance of enteric cyanobacteria in the ALS model mice shortly after disease onset that was further enhanced by CRD. Our study provides initial evidence on the CRD as a risk factor for ALS, and intestinal cyanobacteria may be involved.
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Environmental and biological disruptions to circadian and sleep systems do seem to worsen progression of neurodegenerative diseases.
“environmental and biological disruptions to these systems do seem to worsen progression of these diseases293–295”
From Rhythms of life: circadian disruption and brain disorders across the lifespan (2019) · cites this paper as [295]
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Motor Neuron Degeneration in Mice that Express a Human Cu,Zn Superoxide Dismutase Mutation
Gurney, M. E., Pu, H., Chiu, A. Y., Dal Canto, M. C., Polchow, C. Y., Alexander, D. D., Caliendo, J., Hentati, A., Kwon, Y. W., Deng, H.-X., et al. (1994) · Science · doi:10.1126/science.8209258 · Cited by 4,143 · see citing works
Self-citationGut microbiota regulate motor deficits and neuroinflammation in a model of Parkinson's disease
Sampson, T. R., Debelius, J. W., Thron, T., Janssen, S., Shastri, G. G., Ilhan, Z. E., Challis, C., Schretter, C. E., Rocha, S., Gradinaru, V., et al. (2016) · Cell · doi:10.1016/j.cell.2016.11.018 · Cited by 3,622 · see citing works
Decoding ALS: from genes to mechanism
Taylor, J. P., Brown, R. H., & Cleveland, D. W. (2016) · Nature · doi:10.1038/nature20413 · Cited by 2,047 · see citing works
Resetting central and peripheral circadian oscillators in transgenic rats
Yamazaki, S., Numano, R., Abe, M., Hida, A., Takahashi, R.-I., Ueda, M., Block, G. D., Sakaki, Y., Menaker, M., & Tei, H. (2000) · Science · doi:10.1126/science.288.5466.682 · Cited by 1,907 · see citing works
Extensive and divergent circadian gene expression in liver and heart
Storch, K.-F., Lipan, O., Leykin, I., Viswanathan, N., Davis, F. C., Wong, W. H., & Weitz, C. J. (2002) · Nature · doi:10.1038/nature744 · Cited by 1,509 · see citing works
Mutations of optineurin in amyotrophic lateral sclerosis
Maruyama, H., Morino, H., Ito, H., Izumi, Y., Kato, H., Watanabe, Y., Kinoshita, Y., Kamada, M., Nodera, H., Suzuki, H., et al. (2010) · Nature · doi:10.1038/nature08971 · Cited by 1,265 · see citing works
Suprachiasmatic Nucleus: Cell Autonomy and Network Properties
Welsh, D. K., Takahashi, J. S., & Kay, S. A. (2010) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021909-135919 · Cited by 1,216 · see citing works
Physiology of Circadian Entrainment
Golombek, D. A., & Rosenstein, R. E. (2010) · Physiological Reviews · doi:10.1152/physrev.00009.2009 · Cited by 1,103 · see citing works
Wild-Type Nonneuronal Cells Extend Survival of SOD1 Mutant Motor Neurons in ALS Mice
Clement, A. M., Nguyen, M. D., Roberts, E. A., Garcia, M. L., Boillée, S., Rule, M., McMahon, A. P., Doucette, W. T., Siwek, D. F., Ferrante, R. J., et al. (2003) · Science · doi:10.1126/science.1086071 · Cited by 1,101 · see citing works
The epidemiology of ALS: a conspiracy of genes, environment and time
Al‐Chalabi, A., & Hardiman, O. M. (2013) · Nature Reviews Neurology · doi:10.1038/nrneurol.2013.203 · Cited by 928 · see citing works
Mechanisms linking circadian clocks, sleep, and neurodegeneration
Musiek, E. S., & Holtzman, D. M. (2016) · Science · doi:10.1126/science.aah4968 · Cited by 878 · see citing works
Microbiota Diurnal Rhythmicity Programs Host Transcriptome Oscillations
Thaiss, C. A., Levy, M., Korem, T., Dohnalová, L., Shapiro, H., Jaitin, D. A., David, E., Winter, D. R., Gury-BenAri, M., Tatirovsky, E., et al. (2016) · Cell · doi:10.1016/j.cell.2016.11.003 · Cited by 870 · see citing works
Post-translational modifications regulate the ticking of the circadian clock
Gallego, M., & Virshup, D. M. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2106 · Cited by 863 · see citing works
Microglia Induce Motor Neuron Death via the Classical NF-κB Pathway in Amyotrophic Lateral Sclerosis
Frakes, A. E., Ferraiuolo, L., Haidet-Phillips, A. M., Schmelzer, L., Braun, L., Miranda, C. J., Ladner, K. J., Bevan, A. K., Foust, K. D., Godbout, J. P., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.01.013 · Cited by 638 · see citing works
Cox, P. A., Banack, S. A., & Murch, S. J. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2235808100 · Cited by 637 · see citing works
Roles for NF-κB in nerve cell survival, plasticity, and disease
Mattson, M. P., & Meffert, M. K. (2006) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401837 · Cited by 597 · see citing works
Rhythmicity of the intestinal microbiota is regulated by gender and the host circadian clock
Liang, X., Bushman, F. D., & FitzGerald, G. A. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1501305112 · Cited by 578 · see citing works
Roh, J. H., Huang, Y., Bero, A. W., Kasten, T., Stewart, F. R., Bateman, R. J., & Holtzman, D. M. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3004291 · Cited by 563 · see citing works
Disruption of circadian clocks has ramifications for metabolism, brain, and behavior
Karatsoreos, I. N., Bhagat, S., Bloss, E. B., Morrison, J. H., & McEwen, B. S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1018375108 · Cited by 547 · see citing works
T H 17 Cell Differentiation Is Regulated by the Circadian Clock
Yu, X., Rollins, D., Ruhn, K. A., Stubblefield, J. J., Green, C. B., Kashiwada, M., Rothman, P. B., Takahashi, J. S., & Hooper, L. V. (2013) · Science · doi:10.1126/science.1243884 · Cited by 445 · see citing works
Sleep and Circadian Rhythm Regulation in Early Parkinson Disease
Breen, D. P., Vuono, R., Nawarathna, U., Fisher, K., Shneerson, J. M., Reddy, A. B., & Barker, R. A. (2014) · JAMA Neurology · doi:10.1001/jamaneurol.2014.65 · Cited by 440 · see citing works
Marked seasonal variation in the wild mouse gut microbiota
Maurice, C. F., Knowles, S. C. L., Ladau, J., Pollard, K. S., Fenton, A., Pedersen, A. B., & Turnbaugh, P. J. (2015) · The ISME Journal · doi:10.1038/ismej.2015.53 · Cited by 406 · see citing works
Cyanobacterial toxins: biosynthetic routes and evolutionary roots
Dittmann, E., Fewer, D. P., & Neilan, B. A. (2012) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2012.12000.x · Cited by 375 · see citing works
Swarup, V., Phaneuf, D., Dupré, N., Petri, S., Strong, M. J., Križ, J., & Julien, J. (2011) · The Journal of Experimental Medicine · doi:10.1084/jem.20111313 · Cited by 338 · see citing works
Core circadian protein CLOCK is a positive regulator of NF-κB–mediated transcription
Spengler, M. L., Kuropatwinski, K. K., Comas, M., Gasparian, A. V., Fedtsova, N. G., Gleiberman, A. S., Gitlin, I. I., Artemicheva, N. M., Deluca, K. A., Gudkov, A. V., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1206274109 · Cited by 331 · see citing works
Target intestinal microbiota to alleviate disease progression in amyotrophic lateral sclerosis
Zhang, Y.-G., Wu, S., Yi, J., Xia, Y., Jin, D., Zhou, J., & Sun, J. (2017) · Clinical Therapeutics · doi:10.1016/j.clinthera.2016.12.014 · Cited by 287 · cited 2× · see citing works
“The oral administration of butyrate restored intestinal microbiota homeostasis, and thus delayed disease onset and progression in the SOD1G93A mice (47).”
BackgroundAP-HP, H. D. L. P.-S., & Gordon, P. (2013) · Aging and Disease · doi:10.14336/ad.2013.0400295 · Cited by 278 · see citing works
Leaky intestine and impaired microbiome in an amyotrophic lateral sclerosis mouse model
Wu, S., Yi, J., Zhang, Y.-G., Zhou, J., & Sun, J. (2015) · Physiological Reports · doi:10.14814/phy2.12356 · Cited by 267 · see citing works
Assessing disease onset and progression in the SOD1 mouse model of ALS
Weydt, P., Hong, S. Y., Kliot, M., & Möller, T. (2003) · Neuroreport · doi:10.1097/01.wnr.0000073685.00308.89 · Cited by 227 · see citing works
The role of circadian clock genes in mental disorders
Lamont, E. W., Coutu, D. L., Cermakian, N., & Boivin, D. B. (2007) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2007.9.3/elamont · Cited by 224 · see citing works
A protein fold switch joins the circadian oscillator to clock output in cyanobacteria
Chang, Y.-G., Cohen, S. E., Phong, C., Myers, W. K., Kim, Y.-I., Tseng, R., Lin, J., Zhang, L., Boyd, J. S., Lee, Y., et al. (2015) · Science · doi:10.1126/science.1260031 · Cited by 212 · see citing works
(2011) · PubMed · Cited by 207 · see citing works
ALS: A bucket of genes, environment, metabolism and unknown ingredients
Zufiría, M., Gil-Bea, F. J., Fernández‐Torrón, R., Poza, J. J., Muñoz-Blanco, J. L., Rojas‐García, R., Riancho, J., & de Munaín, A. L. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2016.05.004 · Cited by 192 · see citing works
The circadian clock: a framework linking metabolism, epigenetics and neuronal function
Masri, S., & Sassone‐Corsi, P. (2012) · Nature reviews. Neuroscience · doi:10.1038/nrn3393 · Cited by 154 · see citing works
Respiratory function vs sleep-disordered breathing as predictors of QOL in ALS
Bourke, S. C., Shaw, P. J., & Gibson, G. J. (2001) · Neurology · doi:10.1212/wnl.57.11.2040 · Cited by 143 · see citing works
Mincheva-Tasheva, S., & Soler, R. M. (2012) · The Neuroscientist · doi:10.1177/1073858412444007 · Cited by 133 · see citing works
Ahmed, R. M., Irish, M., Piguet, O., Halliday, G. M., Ittner, L. M., Farooqi, I. S., Hodges, J. R., & Kiernan, M. C. (2016) · The Lancet Neurology · doi:10.1016/s1474-4422(15)00380-4 · Cited by 130 · see citing works
Nitrogen starvation of cyanobacteria results in the production of β-N-methylamino-L-alanine
Downing, S., Banack, S. A., Metcalf, J. S., Cox, P. A., & Downing, T. G. (2011) · Toxicon · doi:10.1016/j.toxicon.2011.05.017 · Cited by 119 · see citing works
Circadian rhythm dysfunction: a novel environmental risk factor for Parkinson’s disease
Lauretti, E., Meco, A. D., Merali, S., & Praticò, D. (2016) · Molecular Psychiatry · doi:10.1038/mp.2016.47 · Cited by 109 · see citing works
Oxyntomodulin regulates resetting of the liver circadian clock by food
Landgraf, D., Tsang, A. H. K., Leliavski, A., Koch, C. E., Barclay, J. L., Drucker, D. J., & Oster, H. (2015) · eLife · doi:10.7554/elife.06253 · Cited by 103 · see citing works
A survey of clinicians' practice in the symptomatic treatment of ALS
Forshew, D. A., & Bromberg, M. B. (2003) · Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders · doi:10.1080/14660820310017344 · Cited by 101 · see citing works
Optineurin suppression causes neuronal cell death via <scp>NF</scp>‐κB pathway
Akizuki, M., Yamashita, H., Uemura, K., Maruyama, H., Kawakami, H., Ito, H., & Takahashi, R. (2013) · Journal of Neurochemistry · doi:10.1111/jnc.12326 · Cited by 96 · see citing works
Lajeunesse, A., Segura, P. A., Gélinas, M., Hudon, C., Thomas, K. M., Quilliam, M. A., & Gagnon, C. (2011) · Journal of Chromatography A · doi:10.1016/j.chroma.2011.10.092 · Cited by 96 · see citing works
Bradley, W. G., Borenstein, A. R., Nelson, L. M., Codd, G. A., Rosen, B. H., Stommel, E. W., & Cox, P. A. (2013) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · doi:10.3109/21678421.2012.750364 · Cited by 88 · see citing works
Sleep disorders and respiratory function in amyotrophic lateral sclerosis
Ahmed, R. M., Newcombe, R., Piper, A. J., Lewis, S. J. G., Yee, B. J., Kiernan, M. C., & Grunstein, R. R. (2015) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2015.05.007 · Cited by 82 · see citing works
Long-term Cognitive Impairments in Adult Rats Treated Neonatally with β-N-Methylamino-L-Alanine
Karlsson, O., Roman, E., & Brittebo, E. B. (2009) · Toxicological Sciences · doi:10.1093/toxsci/kfp196 · Cited by 74 · see citing works
Circadian Clocks as Modulators of Metabolic Comorbidity in Psychiatric Disorders
Barandas, R., Landgraf, D., McCarthy, M. J., & Welsh, D. K. (2015) · Current Psychiatry Reports · doi:10.1007/s11920-015-0637-2 · Cited by 68 · see citing works
Suprachiasmatic astrocytes as an interface for immune‐circadian signalling
Leone, M. J., Marpegán, L., Bekinschtein, T. A., Costas, M. A., & Golombek, D. A. (2006) · Journal of Neuroscience Research · doi:10.1002/jnr.21042 · Cited by 55 · see citing works
Endoplasmic reticulum stress is accompanied by activation of NF-κB in amyotrophic lateral sclerosis
Prell, T., Lautenschläger, J., Weidemann, L., Ruhmer, J., Witte, O. W., & Großkreutz, J. (2014) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2014.03.005 · Cited by 49 · see citing works
Kerrin, E. S., White, R. L., & Quilliam, M. A. (2016) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-016-0091-y · Cited by 39 · see citing works
Hypothesis: A motor neuron toxin produced by a clostridial species residing in gut causes ALS
Longstreth, W. T., Jr., Meschke, J. S., Davidson, S. K., Smoot, L. M., Smoot, J. C., & Koepsell, T. D. (2005) · Medical Hypotheses · doi:10.1016/j.mehy.2004.07.041 · Cited by 38 · see citing works
Fidler, J. A., Treleaven, C. M., Frakes, A., Tamsett, T. J., McCrate, M., Cheng, S. H., Shihabuddin, L. S., Kaspar, B. K., & Dodge, J. C. (2011) · The FASEB Journal · doi:10.1096/fj.11-190819 · Cited by 35 · see citing works
It’s About Time: Clock Genes Unveiled in the Gut
Scheving, L. A., & Russell, W. E. (2007) · Gastroenterology · doi:10.1053/j.gastro.2007.08.068 · Cited by 19 · see citing works
Kuzuhara, S. (2007) · PubMed · Cited by 14 · see citing works
Hypothesis: Gut as source of motor neuron toxin in the development of ALS
Kaneko, K., & Hachiya, N. (2005) · Medical Hypotheses · doi:10.1016/j.mehy.2005.09.012 · Cited by 11 · see citing works
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Logan, R. W., & McClung, C. A. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0088-y · Cited by 713 · see citing works
Association between circadian rhythms and neurodegenerative diseases
Leng, Y., Musiek, E. S., Hu, K., Cappuccio, F. P., & Yaffe, K. S. (2019) · The Lancet Neurology · doi:10.1016/s1474-4422(18)30461-7 · Cited by 660 · see citing works
Golini, E., Rigamonti, M., Iannello, F., Rosa, C. D., Scavizzi, F., Raspa, M., & Mandillo, S. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00896 · Cited by 50 · see citing works
Circadian rhythm alterations affecting the pathology of neurodegenerative diseases
Canever, J. B., Queiroz, L. Y., Soares, E. S., de Avelar, N. C. P., & Cimarosti, H. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.15883 · Cited by 40 · see citing works
Cullell, N., Cárcel‐Márquez, J., Gallego-Fábrega, C., Muiño, E., Llucià‐Carol, L., Lledós, M., Uscamaita, K. E., Krupiński, J., & Fernández‐Cadenas, I. (2021) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2021.05.008 · Cited by 37 · see citing works
Molecular mechanisms and consequences of TDP-43 phosphorylation in neurodegeneration
Kellett, E. A., Bademosi, A. T., & Walker, A. K. (2025) · Molecular Neurodegeneration · doi:10.1186/s13024-025-00839-8 · Cited by 37 · see citing works
Integration of Melatonin Related Redox Homeostasis, Aging, and Circadian Rhythm
Yanar, K., Simsek, B., & Çakatay, U. (2018) · Rejuvenation Research · doi:10.1089/rej.2018.2159 · Cited by 37 · see citing works
Dedeene, L., Schoor, E. V., Vandenberghe, R. R., Damme, P. V., Poesen, K., & Thal, D. R. (2019) · Acta Neuropathologica Communications · doi:10.1186/s40478-019-0845-9 · Cited by 36 · see citing works
Anderson, G. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms24010587 · Cited by 36 · see citing works
Chronobiology of Parkinson's disease: Past, present and future
Asadpoordezaki, Z., Coogan, A. N., & Henley, B. M. (2022) · European Journal of Neuroscience · doi:10.1111/ejn.15859 · Cited by 31 · see citing works
Erber, A. C., Çetin, H., Berry, D., & Schernhammer, E. S. (2019) · International Journal of Neuroscience · doi:10.1080/00207454.2019.1702549 · Cited by 28 · see citing works
Study on sleep-wake disorders in patients with genetic and non-genetic amyotrophic lateral sclerosis
Sun, X., Zhao, X., Liu, Q., Liu, S., Zhang, K., Wang, Z., Yang, X., Shang, L., Huang, Y., Cui, L., et al. (2020) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2020-324544 · Cited by 25 · see citing works
Self-citationSleep, Pain, and Neurodegeneration: A Mendelian Randomization Study
Grover, S., & Sharma, M. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.765321 · Cited by 23 · see citing works
Neuro-Cognitive Profile of Morning and Evening Chronotypes at Different Times of Day
Venkat, N., Sinha, M., Sinha, R., Ghate, J. R., & Pande, B. (2020) · Annals of Neurosciences · doi:10.1177/0972753121990280 · Cited by 24 · see citing works
Zhang, W., Liu, D., Yuan, M., & Zhu, L. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102307 · Cited by 25 · see citing works
Hypothalamus and amyotrophic lateral sclerosis: potential implications in sleep disorders
Gnoni, V., Zoccolella, S., Giugno, A., Urso, D., Tamburrino, L., Filardi, M., & Logroscino, G. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1193483 · Cited by 20 · see citing works
Hiew, J. Y., Lim, Y.-B., Liu, H., & Ng, C. S. (2025) · Communications Biology · doi:10.1038/s42003-025-07790-w · Cited by 16 · see citing works
Walter, L. M., Koch, C. E., Betts, C., Ahlskog, N., Meijboom, K. E., van Westering, T. L. E., Hazell, G., Bhomra, A., Claus, P., Oster, H., et al. (2018) · Human Molecular Genetics · doi:10.1093/hmg/ddy249 · Cited by 13 · see citing works
Combinatory biotechnological intervention for gut microbiota
Khangwal, I., & Shukla, P. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-09727-w · Cited by 14 · see citing works
Di, H., Zhu, Y., Xia, W., Meng, X., Zhang, M., Xu, M., Feng, J., Tian, Q., Yan, H., Cao, S., et al. (2022) · Sleep Medicine · doi:10.1016/j.sleep.2022.03.024 · Cited by 13 · see citing works
Application of mesenchymal stem cells for neurodegenerative diseases therapy discovery
Trinh, Q. D., Nhu, H., & Pham, D. T. (2024) · Regenerative Therapy · doi:10.1016/j.reth.2024.09.014 · Cited by 13 · see citing works
Baek, S., Tae, W., Park, J., & Kim, B. (2025) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2025.1570327 · Cited by 10 · see citing works
Sleep disturbance in rodent models and its sex-specific implications
Deng, Q., Li, Y., Sun, Z., Gao, X., Zhou, J., Ma, G., Qu, W., & Li, R. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105810 · Cited by 11 · see citing works
Smith, S. K., & Musiek, E. S. (2020) · International review of neurobiology · doi:10.1016/bs.irn.2020.02.005 · Cited by 9 · see citing works
Liu, W., Ma, R., Sun, C., Xu, Y., Liu, Y., Hu, J., Ma, Y., Wang, D., Wen, D., & Yu, Y. (2023) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2023.101789 · Cited by 8 · see citing works
Huang, B., Liao, G., Lee, P. M. Y., Chan, C. K., Tai, L.-B., Tsang, C. Y. J., Leung, C. C., & Tse, L. A. (2023) · Scientific Reports · doi:10.1038/s41598-023-28832-5 · Cited by 7 · see citing works
Sleep in neurodegenerative diseases: A focus on melatonin, melanin‐concentrating hormone and orexin
Guillot, S. J., Luppi, P., Dupuis, L., & Bolborea, M. (2025) · Journal of Neuroendocrinology · doi:10.1111/jne.70085 · Cited by 6 · see citing works
Mosna, S., & Dormann, D. (2025) · BioEssays · doi:10.1002/bies.70084 · Cited by 6 · see citing works
Jiang, G., Yuan, L., Liu, X., Wu, H., Yu, H., Zhang, W., Zhang, S., & Huang, Y. (2024) · Ageing and Neurodegenerative Diseases · doi:10.20517/and.2024.15 · Cited by 6 · see citing works
Rouibate, A. D., Benhafri, N., Ouali‐Hassenaoui, S., & Dekar-Madoui, A. (2020) · Folia Histochemica et Cytobiologica · doi:10.5603/fhc.a2020.0021 · Cited by 5 · see citing works
Maidh, A., Kalra, P., Khan, H., Silakari, P., & Grewal, A. K. (2026) · Metabolic Brain Disease · doi:10.1007/s11011-026-01813-z · Cited by 2 · see citing works
Zhang, H., Chen, C., Zhang, E. E., & Huang, X. (2024) · iScience · doi:10.1016/j.isci.2024.109522 · Cited by 2 · see citing works
Huang, B., Liao, G., Lee, P. M. Y., Chan, C. K., Tai, L.-B., Tsang, C. Y. J., Leung, C. C., & Tse, L. A. (2022) · Research Square · doi:10.21203/rs.3.rs-1259617/v1 · Cited by 1 · see citing works
Şenel, G. B. (2021) · Journal of Turkish Sleep Medicine · doi:10.4274/jtsm.galenos.2021.39306
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Zantinge, D. C., Havekes, R., Meerlo, P., & Gervais, N. J. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-27340-7.00009-7
Ralph, L. T., Kang, S., Joe, L. A., Tidball, P., Israwi, A. R., Tian, M., Kadia, A., Zhang, L., Jin, F., Ingram, R., et al. (2026) · Hippocampus · doi:10.1002/hipo.70118
- Authors
- Huang, Z., Liu, Q., Peng, Y., Dai, J., Xie, Y., Chen, W., Long, S., Pei, Z., Su, H., & Yao, X.
- Affiliations
- Sun Yat-sen University (CN)
- University of Macau (MO)
- Corresponding author
- Su, Huanxing
- Yao, Xiaoli
- Venue
- Frontiers in Neurology
- Publisher
- Frontiers Media SA
- Published
- 2018-04-24
- Volume
- 9
- Pages
- 218-218
- ISSN
- 1664-2295 (ISSN-L)
- PMC
- PMC5928145
- OpenAlex
- W2801800670
- Cited by
- 38
- References
- 55
- Citations by year
- 2026: 3 · 2025: 6 · 2024: 6 · 2023: 4 · 2022: 5 · 2021: 2 · 2020: 5 · 2019: 4 · 2018: 3
- FWCI
- 2.38
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Frontiers in Neurology (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Key Research and Development Program of China (2017YFA0105104, 2015B050501003, 2017YFC0907703)
- Topics
- Health Sciences › Medicine › Neurology › Amyotrophic Lateral Sclerosis Research
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Keywords
- amyotrophic lateral sclerosis, SOD1 G93A mice, disease progression, motor neuron degeneration, gliosis, spinal cord, gut microbiota, neurodegeneration, circadian clock
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 ›
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