Coordination of circadian timing in mammals

Phototransduction by retinal ganglion cells that set the circadian clock

Berson, D. M., Dunn, F. A., & Takao, M. (2002) · Science · doi:10.1126/science.1067262 · Cited by 3,629

Melanopsin-Containing Retinal Ganglion Cells: Architecture, Projections, and Intrinsic Photosensitivity

Hattar, S., Liao, H.-W., Takao, M., Berson, D. M., & Yau, K.-W. (2002) · Science · doi:10.1126/science.1069609 · Cited by 2,734

Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus

Damiola, F., Le Minh, N., Preitner, N., Kornmann, B., Fleury-Olela, F., & Schibler, U. (2000) · Genes & Development · doi:10.1101/gad.183500 · Cited by 2,394

Coordinated Transcription of Key Pathways in the Mouse by the Circadian Clock

Panda, S., Antoch, M. P., Miller, B. H., Su, A. I., Schook, A. C., Straume, M., Schultz, P. G., Kay, S. A., Takahashi, J. S., & Hogenesch, J. B. (2002) · Cell · doi:10.1016/s0092-8674(02)00722-5 · Cited by 2,310

The Orphan Nuclear Receptor REV-ERBα Controls Circadian Transcription within the Positive Limb of the Mammalian Circadian Oscillator

Preitner, N., Damiola, F., Luis-Lopez-Molina, Zakany, J., Duboule, D., Albrecht, U., & Schibler, U. (2002) · Cell · doi:10.1016/s0092-8674(02)00825-5 · Cited by 2,198

Role of the CLOCK Protein in the Mammalian Circadian Mechanism

Gekakis, N., Staknis, D., Nguyen, H. B., Davis, F. C., Wilsbacher, L. D., King, D. P., Takahashi, J. S., & Weitz, C. J. (1998) · Science · doi:10.1126/science.280.5369.1564 · Cited by 2,035

A Serum Shock Induces Circadian Gene Expression in Mammalian Tissue Culture Cells

Balsalobre, A., Damiola, F., & Schibler, U. (1998) · Cell · doi:10.1016/s0092-8674(00)81199-x · Cited by 2,001

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

Resetting of circadian time in peripheral tissues by glucocorticoid signaling

Balsalobre, A., Brown, S. A., Marcacci, L., Tronche, F., Kellendonk, C., Reichardt, H. M., Schütz, G., & Schibler, U. (2000) · Science · doi:10.1126/science.289.5488.2344 · Cited by 1,859

Entrainment of the circadian clock in the liver by feeding

Stokkan, K.-A., Yamazaki, S., Tei, H., Sakaki, Y., & Menaker, M. (2001) · Science · doi:10.1126/science.291.5503.490 · Cited by 1,800

High‐Fat Feeding Exerts Minimal Effects on Rhythmic mRNA Expression of Clock Genes in Mouse Peripheral Tissues

Yanagihara, H., Ando, H., Hayashi, Y., Obi, Y., & Fujimura, A. (2006) · Chronobiology International · doi:10.1080/07420520600827103 · Cited by 99

Circadian rhythms, Wnt/beta-catenin pathway and PPAR alpha/gamma profiles in diseases with primary or secondary cardiac dysfunction

Lecarpentier, Y., CLAES, V. A., Duthoit, G., & Hébert, J. (2014) · Frontiers in Physiology · doi:10.3389/fphys.2014.00429 · Cited by 98

Circadian clock cryptochrome proteins regulate autoimmunity

Cao, Q., Zhao, X., Bai, J., Gery, S., Sun, H., Lin, D., Chen, Q., Chen, Z., Mack, L. A., Yang, H. H., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1619119114 · Cited by 99

Clock Protein Bmal1 and Nrf2 Cooperatively Control Aging or Oxidative Response and Redox Homeostasis by Regulating Rhythmic Expression of Prdx6

Chhunchha, B., Kubo, E., & Singh, D. P. (2020) · Cells · doi:10.3390/cells9081861 · Cited by 98

AMP-activated protein kinase as a key molecular link between metabolism and clockwork

Lee, Y., & Kim, E. K. (2013) · Experimental & Molecular Medicine · doi:10.1038/emm.2013.65 · Cited by 100

The circadian clock is functional in eosinophils and mast cells

Baumann, A., Gönnenwein, S., Bischoff, S. C., Sherman, H., Chapnik, N., Froy, O., & Lorentz, A. (2013) · Immunology · doi:10.1111/imm.12157 · Cited by 98

Molecular Clocks in Mouse Skin

Tanioka, M., Yamada, H., Doi, M., Bando, H., Yamaguchi, Y., Nishigori, C., & Okamura, H. (2008) · Journal of Investigative Dermatology · doi:10.1038/jid.2008.345 · Cited by 98

Ultrastructural plasticity in the rat suprachiasmatic nucleus. Possible involvement in clock entrainment

Becquet, D., Girardet, C., Guillaumond, F., François‐Bellan, A., & Bosler, O. (2007) · Glia · doi:10.1002/glia.20613 · Cited by 98

Minireview: The Nuclear Hormone Receptor Family Round the Clock

Teboul, M., Guillaumond, F., Gréchez‐Cassiau, A., & Delaunay, F. (2008) · Molecular Endocrinology · doi:10.1210/me.2007-0521 · Cited by 98

A Transdiagnostic Intervention for Youth Sleep and Circadian Problems

Harvey, A. G. (2015) · Cognitive and Behavioral Practice · doi:10.1016/j.cbpra.2015.06.001 · Cited by 98

Neuroendocrine-immune interaction: Evolutionarily conserved mechanisms that maintain allostasis in an ever-changing environment

Kemenade, B. M. L. V.-V., Cohen, N., & Chadzińska, M. (2016) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2016.05.015 · Cited by 98

Interplay between the endocrine and circadian systems in fishes

Isorna, E., de Pedro, N., Valenciano, A. I., Alonso-Gómez, A. L., & Delgado, M. J. (2016) · Journal of Endocrinology · doi:10.1530/joe-16-0330 · Cited by 98

The SCN‐independent clocks, methamphetamine and food restriction

Honma, K., & Honma, S. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06976.x · Cited by 97

The Circadian Clock in the Regulation of Renal Rhythms

Solocinski, K., & Gumz, M. L. (2015) · Journal of Biological Rhythms · doi:10.1177/0748730415610879 · Cited by 97

The reduced Morningness–Eveningness Questionnaire: Psychometric properties and related factors in a young Swedish population

Danielsson, K., Sakarya, A., & Jansson‐Fröjmark, M. (2019) · Chronobiology International · doi:10.1080/07420528.2018.1564322 · Cited by 97

Maternal-Fetal Circadian Communication During Pregnancy

Bates, K., & Herzog, E. D. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.00198 · Cited by 97

Modified Cortisol Circadian Rhythm: The Hidden Toll of Night-Shift Work

Andreadi, A., Andreadi, S., Todaro, F., Ippoliti, L., Bellia, A., Magrini, A., Chrousos, G. P., & Lauro, D. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26052090 · Cited by 102

Contrary to other non-photic cues, acute melatonin injection does not induce immediate changes of clock gene mrna expression in the rat suprachiasmatic nuclei

Poirel, V., Boggio, V., Dardente, H., Pévet, P., Masson‐Pévet, M., & Gauer, F. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00344-0 · Cited by 97

Chronobiology and Anesthesia

Warltier, D. C., CHASSARD, D., & Bruguerolle, B. (2004) · Anesthesiology · doi:10.1097/00000542-200402000-00034 · Cited by 97

Characterization of the equine skeletal muscle transcriptome identifies novel functional responses to exercise training

McGivney, B. A., McGettigan, P., Browne, J. A., Evans, A. C. O., Fonseca, R. G., Loftus, B., Lohan, A. J., MacHugh, D. E., Murphy, B. A., Katz, L. M., et al. (2010) · BMC Genomics · doi:10.1186/1471-2164-11-398 · Cited by 97

A Circadian Clock in HaCaT Keratinocytes

Spörl, F., Schellenberg, K., Blatt, T., Wenck, H., Wittern, K., Schrader, A., & Kramer, A. (2010) · Journal of Investigative Dermatology · doi:10.1038/jid.2010.315 · Cited by 96

Phenolic compounds and biological rhythms: Who takes the lead?

Ávila‐Román, J., Soliz‐Rueda, J. R., Bravo, F. I., Aragonès, G., Suárez, M., Arola‐Arnal, A., Mulero, M., Salvadó, M. J., Arola, L., Torres‐Fuentes, C., et al. (2021) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2021.04.050 · Cited by 96

Caffeine lengthens circadian rhythms in mice

Oike, H., Kobori, M., Suzuki, T., & Ishida, N. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.06.049 · Cited by 96

Postnatal ontogenesis of the circadian clock within the rat liver

Sládek, M., Jindráková, Z., Bendová, Z., & Sumová, A. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00184.2006 · Cited by 96

Peripheral oscillators: the driving force for food‐anticipatory activity

Escobar, C., Cailotto, C., Castellanos, A., Delgado, R. S., & Buijs, R. M. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06972.x · Cited by 96

A Novel Heme-Regulatory Motif Mediates Heme-Dependent Degradation of the Circadian Factor Period 2

Yang, J., Kim, K. D., Lucas, A. T., Drahos, K. E., Santos, C. S., Mury, S. P., Capelluto, D. G. S., & Finkielstein, C. V. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.00236-08 · Cited by 96

Relationship between Oxidative Stress, Circadian Rhythms, and AMD

Fanjul‐Moles, M. L., & López-Riquelme, G. O. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/7420637 · Cited by 97

PER1 prevents excessive innate immune response during endotoxin-induced liver injury through regulation of macrophage recruitment in mice

Wang, T., Wang, Z., Yang, P., Xia, L., Zhou, M., Wang, S., Du, J., & Zhang, J. (2016) · Cell Death and Disease · doi:10.1038/cddis.2016.9 · Cited by 96

Sensors Capabilities, Performance, and Use of Consumer Sleep Technology

de Zambotti, M., Cellini, N., Menghini, L., Sarlo, M., & Baker, F. C. (2020) · Sleep Medicine Clinics · doi:10.1016/j.jsmc.2019.11.003 · Cited by 95

Mammalian synthetic biology: Engineering of sophisticated gene networks

Greber, D., & Fussenegger, M. (2007) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2007.05.014 · Cited by 95

Photoperiod regulates multiple gene expression in the suprachiasmatic nuclei and pars tuberalis of the Siberian hamster (Phodopus sungorus)

Johnston, J. D., Ebling, F. J. P., & Hazlerigg, D. G. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04148.x · Cited by 95

Light-at-Night-Induced Circadian Disruption, Cancer and Aging

Anisimov, V. N., Vinogradova, I. A., Панченко, А. В., Popovich, I. G., & Zabezhinski, M. A. (2013) · Current Aging Science · doi:10.2174/1874609811205030002 · Cited by 95

A Network of (Autonomic) Clock Outputs

Kalsbeek, A., Perreau‐Lenz, S., & Buijs, R. M. (2006) · Chronobiology International · doi:10.1080/07420520600651073 · Cited by 95

Clock Genes and the Long‐Term Regulation of Prolactin Secretion: Evidence for a Photoperiod/Circannual Timer in the Pars Tuberalis

Lincoln, G. A., Andersson, H., & Hazlerigg, D. G. (2003) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2003.00990.x · Cited by 95

Primate enamel evinces long period biological timing and regulation of life history

Bromage, T. G., Hogg, R. T., Lacruz, R. S., & Hou, C. (2012) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2012.04.007 · Cited by 94

The Circadian Timing System: Making Sense of day/night gene expression

Richter, H. G., Torres‐Farfan, C., Rojas-Garcia, P. P., Campino, C., Torrealba, F., & Serón‐Ferré, M. (2004) · Biological Research · doi:10.4067/s0716-97602004000100003 · Cited by 94

Sleep and circadian disruption and incident breast cancer risk: An evidence-based and theoretical review

Samuelsson, L. B., Bovbjerg, D. H., Roecklein, K. A., & Hall, M. H. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.10.011 · Cited by 94

Targeting the Canonical WNT/β-Catenin Pathway in Cancer Treatment Using Non-Steroidal Anti-Inflammatory Drugs

Vallée, A., Lecarpentier, Y., & Vallée, J.-N. (2019) · Cells · doi:10.3390/cells8070726 · Cited by 94

Circadian Rhythm: Potential Therapeutic Target for Atherosclerosis and Thrombosis

Man, A. W. C., Li, H., & Xia, N. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22020676 · Cited by 96

Light at Night and Disrupted Circadian Rhythms Alter Physiology and Behavior

Bumgarner, J. R., & Nelson, R. J. (2021) · Integrative and Comparative Biology · doi:10.1093/icb/icab017 · Cited by 96

Reciprocal Control of the Circadian Clock and Cellular Redox State - a Critical Appraisal

Putker, M., & O'Neill, J. S. (2016) · Molecules and Cells · doi:10.14348/molcells.2016.2323 · Cited by 94

Circadian control of pain and neuroinflammation

Segal, J. P., Tresidder, K. A., Bhatt, C., Gilron, I., & Ghasemlou, N. (2017) · Journal of Neuroscience Research · doi:10.1002/jnr.24150 · Cited by 97

Rhythms in clock proteins in the mouse pars tuberalis depend on MT1 melatonin receptor signalling

Jilg, A., Moek, J., Weaver, D. R., Korf, H., Stehle, J. H., & von Gall, C. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04485.x · Cited by 94

Reversible Protein Phosphorylation Regulates Circadian RhythmsPreprint

Virshup, D. M., Eide, E. J., Forger, D. B., Gallego, M., & Vielhaber, E. L. (2007) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2007.72.048 · Cited by 94

Consequences of Circadian and Sleep Disturbances for the Cardiovascular System

Alibhai, F. J., Tsimakouridze, E. V., Reitz, C. J., Pyle, W. G., & Martino, T. A. (2015) · Canadian Journal of Cardiology · doi:10.1016/j.cjca.2015.01.015 · Cited by 93

Circadian nutritional behaviours and cancer risk: New insights from the NutriNet‐santé prospective cohort study: Disclaimers

Srour, B., Plancoulaine, S., Andreeva, V. A., Fassier, P., Julia, C., Galan, P., Herçberg, S., Deschasaux, M., Latino‐Martel, P., & Touvier, M. (2018) · International Journal of Cancer · doi:10.1002/ijc.31584 · Cited by 93

Melatonina en los trastornos de sueño

Poza, J. J., Pujol, M., Ortega-Albás, J. J., & Romero, O. (2018) · Neurología · doi:10.1016/j.nrl.2018.08.002 · Cited by 93

Inducible cell-to-cell signaling for tunable dynamics in microbial communities

Miano, A., Liao, M. J., & Hasty, J. (2020) · Nature Communications · doi:10.1038/s41467-020-15056-8 · Cited by 93

Endocrine regulation of circadian rhythms

Begemann, K., Rawashdeh, O., Olejniczak, I., Pilorz, V., de Assis, L. V. M., Osorio-Mendoza, J., & Oster, H. (2025) · npj Biological Timing and Sleep · doi:10.1038/s44323-025-00024-6 · Cited by 93

Prokineticin 2 and circadian clock output

Zhou, Q., & Cheng, M. (2005) · FEBS Journal · doi:10.1111/j.1742-4658.2005.04984.x · Cited by 93

Reduced Expression of Circadian Clock Genes in Male Alcoholic Patients

Huang, M., Ho, C., Chen, C.-Y. O., Liu, S., Chen, C., & Leu, S. (2010) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.2010.01278.x · Cited by 93

Retinoid‐related orphan receptors (RORs): Roles in cellular differentiation and development

Jetten, A. M., & Joo, J. H. (2006) · Advances in developmental biology · doi:10.1016/s1574-3349(06)16010-x · Cited by 93

Cryptochromes impair phosphorylation of transcriptional activators in the clock: a general mechanism for circadian repression

Dardente, H., Fortier, E. E., Martineau, V., & Cermakian, N. (2007) · Biochemical Journal · doi:10.1042/bj20060827 · Cited by 93

What keeps C. elegans regular: the genetics of defecation

Branicky, R. S., & Hekimi, S. (2006) · Trends in Genetics · doi:10.1016/j.tig.2006.08.006 · Cited by 93

Influence of the Corticosterone Rhythm on Photic Entrainment of Locomotor Activity in Rats

Ciocca, D., Ganem, J., Guillaumond, F., Laforge-Anglade, G., François‐Bellan, A., Bosler, O., & Becquet, D. (2004) · Journal of Biological Rhythms · doi:10.1177/0748730403261894 · Cited by 93

Impact of behavior on central and peripheral circadian clocks in the common vole Microtus arvalis , a mammal with ultradian rhythms

van der Veen, D. R., Minh, N. L., Gos, P., Arnerić, M., Gerkema, M. P., & Schibler, U. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0507825103 · Cited by 93

Suprachiasmatic Nucleus Clock Time in the Mammalian Circadian SystemPreprint

Okamura, H. (2007) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2007.72.033 · Cited by 93

Delayed first active-phase meal, a breakfast-skipping model, led to increased body weight and shifted the circadian oscillation of the hepatic clock and lipid metabolism-related genes in rats fed a high-fat diet

Shimizu, H., Hanzawa, F., Kim, D., Sun, S., Laurent, T., Umeki, M., Ikeda, S., Mochizuki, S., & Oda, H. (2018) · PLoS ONE · doi:10.1371/journal.pone.0206669 · Cited by 92

Circadian oscillator proteins across the kingdoms of life: structural aspects

Saini, R. V., Jaskólski, M., & Davis, S. J. (2019) · BMC Biology · doi:10.1186/s12915-018-0623-3 · Cited by 92

Roles of Neuropeptides, VIP and AVP, in the Mammalian Central Circadian Clock

Ono, D., Honma, K., & Honma, S. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.650154 · Cited by 92

Deficiency of intestinal Bmal1 prevents obesity induced by high-fat feeding

Yu, F., Wang, Z., Zhang, T., Chen, X., Xu, H., Wang, F., Guo, L., Chen, M., Liu, K., & Wu, B. (2021) · Nature Communications · doi:10.1038/s41467-021-25674-5 · Cited by 92

Determination of reference genes for circadian studies in different tissues and mouse strains

Košir, R., Ačimovič, J., Goličnik, M., Perše, M., Majdič, G., Fink, M., & Rozman, D. (2010) · BMC Molecular Biology · doi:10.1186/1471-2199-11-60 · Cited by 92

The circadian mutation PER2S662G is linked to cell cycle progression and tumorigenesis

Gu, X., Xing, L., Shi, G., Liu, Z., Wang, X., Qu, Z., Wu, X., Dong, Z., Gao, X., Liu, G., et al. (2011) · Cell Death and Differentiation · doi:10.1038/cdd.2011.103 · Cited by 92

Spatiotemporal Heterogeneity in the Electrical Activity of Suprachiasmatic Nuclei Neurons and their Response to Photoperiod

Brown, T. M., & Piggins, H. D. (2009) · Journal of Biological Rhythms · doi:10.1177/0748730408327918 · Cited by 92

Alterations of Circadian Expressions of Clock Genes in Dahl Salt-Sensitive Rats Fed a High-Salt Diet

Mohri, T., Emoto, N., Nonaka, H., Fukuya, H., Yagita, K., Okamura, H., & Yokoyama, M. (2003) · Hypertension · doi:10.1161/01.hyp.0000082766.63952.49 · Cited by 92

Circadian and ultradian rhythms of clock gene expression in the suprachiasmatic nucleus of freely moving mice

Ono, D., Honma, K., & Honma, S. (2015) · Scientific Reports · doi:10.1038/srep12310 · Cited by 91

FAD Regulates CRYPTOCHROME Protein Stability and Circadian Clock in Mice

Hirano, A., Braas, D., Fu, Y., & Ptáček, L. J. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.03.041 · Cited by 91

The proteasome: A key modulator of nervous system function, brain aging, and neurodegenerative disease

Davidson, K., & Pickering, A. M. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1124907 · Cited by 91

Circadian clocks

Idda, M. L., Bertolucci, C., Vallone, D., Gothilf, Y., Sánchez‐Vázquez, F. J., & Foulkes, N. S. (2012) · Progress in brain research · doi:10.1016/b978-0-444-59427-3.00003-4 · Cited by 91

Twenty-Four-Hour Rhythmic Gene Expression in the Rhesus Macaque Adrenal Gland

Lemos, D. R., Downs, J. L., & Urbanski, H. F. (2006) · Molecular Endocrinology · doi:10.1210/me.2005-0361 · Cited by 91

Circadian Expression of Adiponectin and Its Receptors in Human Adipose Tissue

Gómez-Abellán, P., Gómez‐Santos, C., Madrid, J. A., Milagro, F. I., Campión, J., Martínez, J. A., Ordovás, J. M., & Garaulet, M. (2009) · Endocrinology · doi:10.1210/en.2009-0647 · Cited by 91

Encoding the Ins and Outs of Circadian Pacemaking

Kuhlman, S. J., & McMahon, D. G. (2006) · Journal of Biological Rhythms · doi:10.1177/0748730406294316 · Cited by 91

Circadian Regulation and Function of Voltage-Dependent Calcium Channels in the Suprachiasmatic Nucleus

Nahm, S., Farnell, Y. Z., Griffith, W. H., & Earnest, D. J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2733-05.2005 · Cited by 91

Photic regulation of the mTOR signaling pathway in the suprachiasmatic circadian clock

Cao, R., Lee, B., Cho, H.-Y., Saklayen, S. S., & Obrietan, K. H. (2008) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2008.03.005 · Cited by 91

The functional significance of the skeletal muscle clock: lessons from Bmal1 knockout models

Schiaffino, S., Blaauw, B., & Dyar, K. A. (2016) · Skeletal Muscle · doi:10.1186/s13395-016-0107-5 · Cited by 92

The Transcriptional Repressor STRA13 Regulates a Subset of Peripheral Circadian Outputs

Gréchez‐Cassiau, A., Panda, S., Lacoche, S., Teboul, M., Azmi, S., Laudet, V., Hogenesch, J. B., Taneja, R., & Delaunay, F. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m305369200 · Cited by 91

Loss of circadian rhythmicity in agingmPer1-/-mCry2-/-mutant micePreprint

Oster, H., Baeriswyl, S., van der Horst, G. T. J., & Albrecht, U. (2003) · Genes & Development · doi:10.1101/gad.256103 · Cited by 91

The Circadian Clock, the Immune System, and Viral Infections: The Intricate Relationship Between Biological Time and Host-Virus Interaction

Mazzoccoli, G., Vinciguerra, M., Carbone, A., & Relógio, A. (2020) · Pathogens · doi:10.3390/pathogens9020083 · Cited by 91

Circadian timing in health and disease

Maywood, E. S., O'Neill, J. S., Wong, G. K. Y., Reddy, A. B., & Hastings, M. H. (2006) · Progress in brain research · doi:10.1016/s0079-6123(06)53015-8 · Cited by 90

Function and Pharmacology of Spinally-Projecting Sympathetic Pre-Autonomic Neurones in the Paraventricular Nucleus of the Hypothalamus

Barrett‐Jolley, R., Nunn, N., Womack, M. D., & Dart, C. (2011) · Current Neuropharmacology · doi:10.2174/157015911795596531 · Cited by 90

Protein phosphatase 1 regulates the stability of the circadian protein PER2

Gallego, M., Kang, H., & Virshup, D. M. (2006) · Biochemical Journal · doi:10.1042/bj20060678 · Cited by 90

Expression of the gene for Dec2, a basic helix–loop–helix transcription factor, is regulated by a molecular clock system

Hamaguchi, H., Fujimoto, K., Kawamoto, T., Noshiro, M., Maemura, K., Takeda, N., Nagai, R., Furukawa, M., Honma, S., Honma, K., et al. (2004) · Biochemical Journal · doi:10.1042/bj20031760 · Cited by 90

Expression Levels of Estrogen Receptor β Are Modulated by Components of the Molecular Clock

Cai, W., Rambaud, J., Teboul, M., Masse, I., Benoit, G., Gustafsson, J.-Å., Delaunay, F., Laudet, V., & Pongratz, I. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.00233-07 · Cited by 90

Suprachiasmatic Nucleus Interaction with the Arcuate Nucleus; Essential for Organizing Physiological Rhythms

Buijs, F. N., Guzmán‐Ruiz, M. A., Mercado, L. L., Basualdo, M. C., Escobar, C., Kalsbeek, A., & Buijs, R. M. (2017) · eNeuro · doi:10.1523/eneuro.0028-17.2017 · Cited by 90

Circadian regulation of mammalian target of rapamycin signaling in the mouse suprachiasmatic nucleus

Cao, R., Anderson, F. E., Jung, Y. J., Dziema, H., & Obrietan, K. H. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.03.005 · Cited by 89

Thermoregulation as a disease tolerance defense strategy

Schieber, A. M. P., & Ayres, J. S. (2016) · Pathogens and Disease · doi:10.1093/femspd/ftw106 · Cited by 89

The Circadian Clock Regulates Adipogenesis by a Per3 Crosstalk Pathway to Klf15

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