Suprachiasmatic nucleus

Coordination of circadian timing in mammals

Reppert, S. M., & Weaver, D. R. (2002) · Nature · doi:10.1038/nature00965 · Cited by 4,379 · see citing works

PERIOD2::LUCIFERASE real-time reporting of circadian dynamics reveals persistent circadian oscillations in mouse peripheral tissues

Yoo, S.-H., Yamazaki, S., Lowrey, P. L., Shimomura, K., Ko, C. H., Buhr, E. D., Siepka, S. M., Hong, H.-K., Oh, W. J., Yoo, O. J., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308709101 · Cited by 2,329 · see citing works

A functional analysis of circadian pacemakers in nocturnal rodents

Pittendrigh, C. S., & Daan, S. (1976) · Journal of Comparative Physiology A · doi:10.1007/bf01417856 · Cited by 2,129 · 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

A functional analysis of circadian pacemakers in nocturnal rodents: V. Pacemaker structure: A clock for all seasons

Pittendrigh, C. S., & Daan, S. (1976) · Journal of Comparative Physiology ? A · doi:10.1007/bf01417860 · Cited by 1,636 · see citing works

Mutagenesis and Mapping of a Mouse Gene, <i>Clock</i> , Essential for Circadian Behavior

Vitaterna, M. H., King, D. P., Chang, A.-M., Kornhauser, J. M., Lowrey, P. L., McDonald, J. D., Dove, W. F., Pinto, L. H., Turek, F. W., & Takahashi, J. S. (1994) · Science · doi:10.1126/science.8171325 · Cited by 1,632 · see citing works

Individual neurons dissociated from rat suprachiasmatic nucleus express independently phased circadian firing rhythms.

Welsh, D. K., Logothetis, D., Meister, M., & Reppert, S. (1995) · Neuron · doi:10.1016/0896-6273(95)90214-7 · Cited by 1,535 · see citing works

Synchronization of Cellular Clocks in the Suprachiasmatic Nucleus

Yamaguchi, S., Isejima, H., Matsuo, T., Okura, R., Yagita, K., Kobayashi, M., & Okamura, H. (2003) · Science · doi:10.1126/science.1089287 · Cited by 934 · see citing works

Suprachiasmatic nucleus in the mouse: retinal innervation, intrinsic organization and efferent projections

Abrahamson, E. E., & Moore, R. Y. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02890-6 · Cited by 788 · see citing works

Intercellular Coupling Confers Robustness against Mutations in the SCN Circadian Clock Network

Liu, A. C., Welsh, D. K., Ko, C. H., Tran, H. G., Zhang, E. E., Priest, A. A., Buhr, E. D., Singer, O., Meeker, K., Verma, I. M., et al. (2007) · Cell · doi:10.1016/j.cell.2007.02.047 · Cited by 694 · see citing works

The hypothalamic suprachiasmatic nucleus of rat: Intrinsic anatomy

van den Pol, A. N. (1980) · The Journal of comparative neurology · doi:10.1002/cne.901910410 · Cited by 447 · see citing works

Synchronization and Maintenance of Timekeeping in Suprachiasmatic Circadian Clock Cells by Neuropeptidergic Signaling

Maywood, E. S., Reddy, A. B., Wong, G. K. Y., O'Neill, J. S., O'Brien, J. A., McMahon, D. G., Harmar, A. J., Okamura, H., & Hastings, M. H. (2006) · Current Biology · doi:10.1016/j.cub.2006.02.023 · Cited by 438 · see citing works

Coupling governs entrainment range of circadian clocks

Abraham, U., Granada, A. E., Westermark, P. O., Heine, M., Kramer, A., & Herzel, H. (2010) · Molecular Systems Biology · doi:10.1038/msb.2010.92 · Cited by 349 · see citing works

A diversity of paracrine signals sustains molecular circadian cycling in suprachiasmatic nucleus circuits

Maywood, E. S., Chesham, J. E., O’Brien, J., & Hastings, M. H. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1101767108 · Cited by 284 · see citing works

Temporal Precision in the Mammalian Circadian System: A Reliable Clock from Less Reliable Neurons

Herzog, E. D., Aton, S. J., Numano, R., Sakaki, Y., & Tei, H. (2004) · Journal of Biological Rhythms · doi:10.1177/0748730403260776 · Cited by 281 · see citing works

Separate oscillating cell groups in mouse suprachiasmatic nucleus couple photoperiodically to the onset and end of daily activity

Inagaki, N., Honma, S., Ono, D., Tanahashi, Y., & Honma, K. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0607713104 · Cited by 274 · see citing works

An Abrupt Shift in the Day/Night Cycle Causes Desynchrony in the Mammalian Circadian Center

Nagano, M., Adachi, A. A., Nakahama, K., Nakamura, T., Tamada, M., Meyer-Bernstein, E. L., Sehgal, A., & Shigeyoshi, Y. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-14-06141.2003 · Cited by 273 · see citing works

Circadian Dynamics of Cytosolic and Nuclear Ca2+ in Single Suprachiasmatic Nucleus Neurons

Ikeda, M., Sugiyama, T., Wallace, C. S., Gompf, H. S., Yoshioka, T., Miyawaki, A., & Allen, C. N. (2003) · Neuron · doi:10.1016/s0896-6273(03)00164-8 · Cited by 273 · see citing works

Intrinsic, nondeterministic circadian rhythm generation in identified mammalian neurons

Webb, A. B., Angelo, N., Huettner, J. E., & Herzog, E. D. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0902768106 · Cited by 236 · see citing works

Two distinct oscillators in the rat suprachiasmatic nucleus in vitro.

Shinohara, K., Honma, S., Katsuno, Y., Abe, H., & Honma, K.-I. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.16.7396 · Cited by 215 · see citing works

Emergence of Noise-Induced Oscillations in the Central Circadian Pacemaker

Ko, C. H., Yamada, Y., Welsh, D. K., Buhr, E. D., Liu, A. C., Zhang, E. E., Ralph, M. R., Kay, S. A., Forger, D. B., & Takahashi, J. S. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000513 · Cited by 212 · see citing works

Assembling a Clock for All Seasons: Are There M and E Oscillators in the Genes?

Daan, S., Albrecht, U., van der Horst, G. T. J., Illnerová, H., Roenneberg, T., Wehr, T. A., & Schwartz, W. J. (2001) · Journal of Biological Rhythms · doi:10.1177/074873001129001809 · Cited by 204 · see citing works

Circadian periods of single suprachiasmatic neurons in rats

Honma, S., Shirakawa, T., Katsuno, Y., Namihira, M., & Honma, K. (1998) · Neuroscience Letters · doi:10.1016/s0304-3940(98)00464-9 · Cited by 184 · see citing works

Diversity in the circadian periods of single neurons of the rat suprachiasmatic nucleus depends on nuclear structure and intrinsic period

Honma, S., Nakamura, W., Shirakawa, T., & Honma, K. (2004) · Neuroscience Letters · doi:10.1016/j.neulet.2004.01.022 · Cited by 145 · see citing works

Clock mutation lengthens the circadian period without damping rhythms in individual SCN neurons

Nakamura, W., Honma, S., Shirakawa, T., & Honma, K. (2002) · Nature Neuroscience · doi:10.1038/nn843 · Cited by 136 · see citing works

Circadian rhythms in mouse suprachiasmatic nucleus explants on multimicroelectrode plates.

Herzog, E., Geusz, M., Khalsa, S. B., Straume, M., & Block, G. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00337-5 · Cited by 133 · see citing works

GFP fluorescence reports Period 1 circadian gene regulation in the mammalian biological clock

Kuhlman, S. J., Quintero, J. E., & McMahon, D. G. (2000) · Neuroreport · doi:10.1097/00001756-200005150-00024 · Cited by 132 · see citing works

Synchronization of circadian firing rhythms in cultured rat suprachiasmatic neurons

Shirakawa, T., Honma, S., Katsuno, Y., Oguchi, H., & Honma, K. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00170.x · Cited by 120 · see citing works

Regional pacemakers composed of multiple oscillator neurons in the rat suprachiasmatic nucleus

Nakamura, W., Honma, S., Shirakawa, T., & Honma, K.-I. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01684.x · Cited by 113 · see citing works

Neuronal Activity Is Required for the Circadian Rhythm of Vasopressin Gene Transcription in the Suprachiasmatic Nucleusin Vitro

Arima, H., House, S. B., Gainer, H., & Aguilera, G. (2002) · Endocrinology · doi:10.1210/en.2002-220393 · Cited by 58 · see citing works

Synaptic communication of cellular oscillations in the rat suprachiasmatic neurons

Honma, S., Shirakawa, T., Nakamura, W., & Honma, K.-I. (2000) · Neuroscience Letters · doi:10.1016/s0304-3940(00)01558-5 · Cited by 56 · see citing works

Fourier-based spatial mapping of oscillatory phenomena in fungi

Fricker, M. D., Tlalka, M., Bebber, D. P., Tagaki, S., Watkinson, S. C., & Darrah, P. R. (2007) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2007.02.012 · Cited by 28 · see citing works

Clock mechanisms for seasonal adaptation: Morning and evening oscillators in the suprachiasmatic nucleus

Honma, S., INAGAKI, N., Ono, D., Yoshikawa, T., Hashimoto, S., & Honma, K. (2008) · Sleep and Biological Rhythms · doi:10.1111/j.1479-8425.2008.00347.x · Cited by 1 · see citing works

Three period Homologs in Mammals: Differential Light Responses in the Suprachiasmatic Circadian Clock and Oscillating Transcripts Outside of Brain

Zylka, M. J., Shearman, L. P., Weaver, D. R., & Reppert, S. M. (1998) · Neuron · doi:10.1016/s0896-6273(00)80492-4 · Cited by 865 · see citing works

Circadian Rhythms, Sleep, and Disorders of Aging

Mattis, J., & Sehgal, A. (2016) · Trends in Endocrinology &amp; Metabolism · doi:10.1016/j.tem.2016.02.003 · Cited by 369 · see citing works

Seasonal Regulation of Reproduction in Mammals

Hazlerigg, D. G., & Simonneaux, V. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-397175-3.00034-x · Cited by 281 · see citing works

The hallmarks of fibroblast ageing

Tigges, J., Krutmann, J., Fritsche, E., Haendeler, J., Schaal, H., Fischer, J. W., Kalfalah, F., Reinke, H., Reifenberger, G., Stühler, K., et al. (2014) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2014.03.004 · Cited by 250 · see citing works

The mammalian circadian system: a hierarchical multi-oscillator structure for generating circadian rhythm

Honma, S. (2018) · The Journal of Physiological Sciences · doi:10.1007/s12576-018-0597-5 · Cited by 233 · see citing works

Total and Cause-Specific Mortality of U.S. Nurses Working Rotating Night Shifts

Gu, F., Han, J., Laden, F., Pan, A., Caporaso, N. E., Stampfer, M. J., Kawachi, I., Rexrode, K. M., Willett, W. C., Hankinson, S. E., et al. (2015) · American Journal of Preventive Medicine · doi:10.1016/j.amepre.2014.10.018 · Cited by 202 · see citing works

Activity Patterns in Small Mammals

(2000) · Ecological studies · doi:10.1007/978-3-642-18264-8 · Cited by 159 · see citing works

Age-Related Changes in the Circadian System Unmasked by Constant Conditions

Nakamura, T. J., Nakamura, W., Tokuda, I. T., Ishikawa, T., Kudo, T., Colwell, C. S., & Block, G. D. (2015) · eNeuro · doi:10.1523/eneuro.0064-15.2015 · Cited by 109 · see citing works

Synchrony and desynchrony in circadian clocks: impacts on learning and memoryPreprint

Krishnan, H. C., & Lyons, L. C. (2015) · Learning & Memory · doi:10.1101/lm.038877.115 · Cited by 91 · see citing works

Constructing the suprachiasmatic nucleus: a watchmaker's perspective on the central clockworks

Bedont, J. L., & Blackshaw, S. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00074 · Cited by 86 · see citing works

Melatonin: From Seasonal to Circadian Signal

Pévet, P. (2003) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2003.01017.x · Cited by 87 · see citing works

A landscape view on the interplay between EMT and cancer metastasis

Li, C., & Balázsi, G. (2018) · npj Systems Biology and Applications · doi:10.1038/s41540-018-0068-x · Cited by 76 · see citing works

The Concept of Coupling in the Mammalian Circadian Clock Network

Pilorz, V., Astiz, M., Heinen, K. O., Rawashdeh, O., & Oster, H. (2020) · Journal of Molecular Biology · doi:10.1016/j.jmb.2019.12.037 · Cited by 70 · see citing works

Circadian expression of Period 1, Period 2, and Arylalkylamine N-acetyltransferase mRNA in the rat pineal gland under different light conditions

Fukuhara, C., Dirden, J. C., & Tosini, G. (2000) · Neuroscience Letters · doi:10.1016/s0304-3940(00)01129-0 · Cited by 59 · see citing works

CRY Drives Cyclic CK2-Mediated BMAL1 Phosphorylation to Control the Mammalian Circadian Clock

Tamaru, T., Hattori, M., Honda, K., Nakahata, Y., Sassone‐Corsi, P., van der Horst, G. T. J., Ozawa, T., & Takamatsu, K. (2015) · PLoS Biology · doi:10.1371/journal.pbio.1002293 · Cited by 50 · see citing works

Photoperiodic and circadian bifurcation theories of depression and mania

Kripke, D. F., Elliott, J. A., Welsh, D. K., & Youngstedt, S. D. (2015) · F1000Research · doi:10.12688/f1000research.6444.1 · Cited by 48 · see citing works

Molecular Mechanisms that Regulate the Coupled Period of the Mammalian Circadian Clock

Kim, J. K., Kilpatrick, Z. P., Bennett, M. R., & Josić́, K. (2014) · Biophysical Journal · doi:10.1016/j.bpj.2014.02.039 · Cited by 47 · see citing works

Brain Neurons Partly Expressing Dopaminergic Phenotype

Ugrumov, M. V. (2013) · Advances in pharmacology · doi:10.1016/b978-0-12-411512-5.00004-x · Cited by 39 · see citing works

Control of neural network patterning using collagen gel photothermal etching

Odawara, A., Gotoh, M., & Suzuki, I. (2013) · Lab on a Chip · doi:10.1039/c3lc00036b · Cited by 34 · see citing works

Circadian Polymorphisms in Night Owls, in Bipolars, and in Non-24-Hour Sleep Cycles

Kripke, D. F., Klimecki, W. T., Nievergelt, C. M., Rex, K. M., Murray, S. S., Shekhtman, T., Tranah, G. J., Loving, R. T., Lee, H.-J., Rhee, M. K., et al. (2014) · Psychiatry Investigation · doi:10.4306/pi.2014.11.4.345 · Cited by 30 · see citing works

Neurophysiological Analysis of the Suprachiasmatic Nucleus

Meijer, J. H., & Michel, S. H. (2014) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/bs.mie.2014.11.001 · Cited by 27 · see citing works

Neuropeptidergic Organization of the Suprachiasmatic Nucleus in the Blind Mole Rat (Spalax ehrenbergi)

Negroni, J., Nevo, E., & Cooper, H. M. (1997) · Brain Research Bulletin · doi:10.1016/s0361-9230(97)00306-7 · Cited by 26 · see citing works

Understanding Quantitative Circadian Regulations Are Crucial Towards Advancing Chronotherapy

Chowdhury, D., Wang, C., Lü, A., & Zhu, H. (2019) · Cells · doi:10.3390/cells8080883 · Cited by 24 · see citing works

Measuring Synchrony in the Mammalian Central Circadian Circuit

Herzog, E. D., Kiss, I. Z., & Mazuski, C. N. (2014) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/bs.mie.2014.10.042 · Cited by 24 · see citing works

A suprachiasmatic-independent circadian clock(s) in the habenula is affected by Per gene mutations and housing light conditions in mice

Salaberry, N. L., Hamm, H., Felder‐Schmittbuhl, M., & Mendoza, J. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1756-4 · Cited by 23 · see citing works

Mutual coupling of neurons in the circadian master clock: What we can learn from fruit flies

Helfrich‐Förster, C., & Reinhard, N. (2025) · Neurobiology of Sleep and Circadian Rhythms · doi:10.1016/j.nbscr.2025.100112 · Cited by 22 · see citing works

Cell cycle time series gene expression data encoded as cyclic attractors in Hopfield systems

Szedlak, A., Sims, S., Smith, N. H., Paternostro, G., & Piermarocchi, C. (2017) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005849 · Cited by 20 · see citing works

Delineating the regulation of energy homeostasis using hypothalamic cell models

Wellhauser, L., Gojska, N. M., & Belsham, D. D. (2014) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2014.09.001 · Cited by 17 · see citing works

Perforated Multi-Electrode Array Recording in Hypothalamic Brain Slices

Belle, M. D. C., Baño‐Otálora, B., & Piggins, H. D. (2020) · Methods in molecular biology · doi:10.1007/978-1-0716-0381-9_20 · Cited by 16 · see citing works

Exosomes rich in Wnt5 improved circadian rhythm dysfunction via enhanced PPARγ activity in the 6-hydroxydopamine model of Parkinson's disease

Li, Z., Li, Y., Xu, X., Gu, J., Chen, H., & Gui, Y. (2023) · Neuroscience Letters · doi:10.1016/j.neulet.2023.137139 · Cited by 16 · see citing works

Hypothalamic neurons fully or partially expressing the dopaminergic phenotype: development, distribution, functioning and functional significance. A review

Ugrumov, M. V. (2024) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2024.101153 · Cited by 15 · see citing works

Genetic Advances in Ophthalmology: The Role of Melanopsin-Expressing, Intrinsically Photosensitive Retinal Ganglion Cells in the Circadian Organization of the Visual System

Ramsey, D. J., Ramsey, K. M., & Vavvas, D. G. (2013) · Seminars in Ophthalmology · doi:10.3109/08820538.2013.825294 · Cited by 15 · see citing works

Chronobiology of transient global amnesia

Hoyer, C., Higashida, K., Fabbian, F., Giorgi, A. D., Sandikci, V., Ebert, A., Platten, M., Okazaki, S., Manfredini, R., & Szabo, K. (2021) · Journal of Neurology · doi:10.1007/s00415-021-10639-x · Cited by 15 · see citing works

Disrupted Ultradian Activity Rhythms and Differential Expression of Several Clock Genes in Interleukin-6-Deficient Mice

Monje, F. J., Cicvaric, A., Aguilar, J. P. A., Elbau, I., Horváth, O., Diao, W., Glat, M. J., & Pollak, D. D. (2017) · Frontiers in Neurology · doi:10.3389/fneur.2017.00099 · Cited by 14 · see citing works

N-Nitrosomelatonin

Turjanski, A. G., Chaia, Z. D., Doctorovich, F. A., Estrin, D. A., Rosenstein, R. E., & Piro, O. E. (2000) · Acta Crystallographica Section C Crystal Structure Communications · doi:10.1107/s010827010000456x · Cited by 14 · see citing works

The anterior paraventricular thalamus modulates neuronal excitability in the suprachiasmatic nuclei of the rat

Alamilla, J., Granados‐Fuentes, D., & Aguilar‐Roblero, R. A. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.13088 · Cited by 11 · see citing works

The role of the circadian rhythms in critical illness with a focus on acute pancreatitis

Waddell, H., Stevenson, T. J., & Mole, D. J. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e15335 · Cited by 11 · see citing works

Phase Gradients and Anisotropy of the Suprachiasmatic Network: Discovery of Phaseoids

Yoshikawa, T., Pauls, S. D., Foley, N. C., Taub, A., LeSauter, J., Foley, D. K., Honma, K., Honma, S., & Silver, R. (2021) · eNeuro · doi:10.1523/eneuro.0078-21.2021 · Cited by 10 · see citing works

A synthetic multi-cellular network of coupled self-sustained oscillators

Fernández‐Niño, M., Giraldo, D., Gomez‐Porras, J. L., Drèyer, I., Barrios, A. F. G., & Arévalo-Ferro, C. (2017) · PLoS ONE · doi:10.1371/journal.pone.0180155 · Cited by 8 · see citing works

Collective Oscillations in Coupled-Cell Systems

Chen, K., & Shih, C.-W. (2021) · Bulletin of Mathematical Biology · doi:10.1007/s11538-021-00883-7 · Cited by 8 · see citing works

Weak synchronization can alter circadian period length: implications for aging and disease conditions

Myung, J., Hong, S., Schmal, C., Vitet, H., & Wu, M. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1242800 · Cited by 7 · see citing works

Circadian rhythms and autoregulatory transcription loops—going round in circles?

Carter, D., & Murphy, D. (1996) · Molecular and Cellular Endocrinology · doi:10.1016/s0303-7207(96)03962-7 · Cited by 7 · see citing works

Unique food-entrained circadian rhythm in cysteine414-alanine mutant mCRY1 transgenic mice

Okano, S., Yasui, A., Hayasaka, K., & Nakajima, O. (2016) · Sleep and Biological Rhythms · doi:10.1007/s41105-016-0050-1 · Cited by 6 · see citing works

Temporal Orchestration of Immunity: How Circadian Clocks Coordinate Immune Responses

Jiang, Y., Liu, C., & Zhong, Y. (2025) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl39948 · Cited by 5 · see citing works

Toward dissection of diverse neural components in the suprachiasmatic nucleus (SCN) pacemaker network

Izumo, M., Cox, K. H., & Takahashi, J. S. (2026) · Neurobiology of Sleep and Circadian Rhythms · doi:10.1016/j.nbscr.2026.100143 · Cited by 4 · see citing works

Characteristic of Dopamine-Producing System and Dopamine Receptors in the Suprachiasmatic Nucleus in Rats in Ontogenesis

Pronina, T. S., Kolacheva, A. A., Dil’muhametova, L. K., Nikishina, Y. O., Suhinich, K. K., & Ugrumov, M. V. (2020) · Doklady Biochemistry and Biophysics · doi:10.1134/s1607672920010123 · Cited by 4 · see citing works

Effects of Circadian Disruption on Physiology and Pathology: From Bench to Clinic (and Back)

Chiesa, J. J., Duhart, J. M., Casiraghi, L. P., Paladino, N., Bussi, I. L., & Golombek, D. A. (2014) · Springer eBooks · doi:10.1007/978-3-319-08945-4_15 · Cited by 4 · see citing works

The Apparently Blind Infant

Brodsky, M. C. (2016) · Springer eBooks · doi:10.1007/978-1-4939-3384-6_1 · Cited by 4 · see citing works

Neuronal reprogramming of mouse and human fibroblasts using transcription factors involved in suprachiasmatic nucleus development

Hirayama, M., Mure, L. S., Le, H. D., & Panda, S. (2024) · iScience · doi:10.1016/j.isci.2024.109051 · Cited by 3 · see citing works

Oxygen glucose deprivation impairs circadian clock genes expressions in Neuro 2A neuroblastoma cells unlike C6 glioma

Roy, K., Maji, D., & Deb, I. (2021) · Biological Rhythm Research · doi:10.1080/09291016.2021.1911551 · Cited by 2 · see citing works

Sleep and Circadian Rhythms in the Blind

Emens, J. S., & Lewy, A. J. (2006) · Springer eBooks · doi:10.1007/0-387-23692-9_16 · Cited by 2 · see citing works

It is About Time: Circadian Clock in the Pancreas

Wan, W. J. R. (2015) · Pancreatic Disorders and Therapy · doi:10.4172/2165-7092.1000155 · Cited by 2 · see citing works

Circadian System and Ageing in Rodent Models

Rizvi, S. I., & Majumdar, G. (2024) · Springer eBooks · doi:10.1007/978-981-97-6695-6_4 · Cited by 1 · see citing works

Identifying Chronotype for the Preservation of Muscle Mass, Quality and Strength

Barrientos-Salinas, R., Dahdah, N., Alvarez-Luis, J., Vilarrasa, N., & García-Rovés, P. M. (2026) · Nutrients · doi:10.3390/nu18020221 · Cited by 1 · see citing works

Circadian System and Aging in Rodent Models

Панченко, А. В., Александровна, Г. Е., & Anisimov, V. N. (2017) · Healthy ageing and longevity · doi:10.1007/978-3-319-64543-8_5 · Cited by 1 · see citing works

Synthesis of Dopamine by Non-Dopaminergic Neurons Containing Aromatic Amino Acid Decarboxylase in the Suprachiasmatic Nucleus of Rats in Ontogeny

Pronina, T. S., Dil’mukhametova, L. K., Nikishina, Y. O., Муртазина, А. Р., & Ugryumov, M. V. (2020) · Neurochemical Journal · doi:10.1134/s1819712420020099 · Cited by 1 · see citing works

Phase Gradients and Anisotropy of the Suprachiasmatic NetworkPreprint

Yoshikawa, T., Pauls, S. D., Foley, N. C., Taub, A., LeSauter, J., Foley, D. K., Honma, K., Honma, S., & Silver, R. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.02.01.429173 · Cited by 1 · see citing works

THE STUDY OF CIRCADIAN RHYTHMS IN OVARIAN CANCER RAT MODEL: IS THERE CONNECTION BETWEEN TUMOR DEVELOPMENT AND RHYTHMICITY DISRUPTION IN INTACT TISSUES?

Kireeva, G. S., Александровна, Г. Е., Mitiushkina, N. V., Панченко, А. В., Александрович, М. М., Тындык, М. Л., Гаврилов, И. А., Круглов, С. С., Kharchenko, Y., & Anisimov, V. N. (2019) · Voprosy Onkologii · doi:10.37469/0507-3758-2019-65-6-889-897

Caractérisation moléculaire et pharmacologique de l'horloge circadienne située dans l'habénula

Salaberry, N. L. (2018) · doi:10.70675/8d54db3cz09e1z4999zbcb5za35dc04505ca

Cell autonomy and synchrony of suprachiasmatic nucleus circadian oscillators

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