Blood-Borne Circadian Signal Stimulates Daily Oscillations in Actin Dynamics and SRF Activity

Molecular Cloning: A Laboratory Manual

Sambrook, J., Fritsch, E., & Maniatis, T. (1989) · UCLA - Biblioteca de Ciencias de la Salud · Cited by 133,589 · see citing works

The mammalian circadian timing system: organization and coordination of central and peripheral clocks

Dibner, C., Schibler, U., & Albrecht, U. (2010) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021909-135821 · Cited by 2,421 · see citing works

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 · 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

Actin, a Central Player in Cell Shape and Movement

Pollard, T. D., & Cooper, J. A. (2009) · Science · doi:10.1126/science.1175862 · Cited by 2,094 · see citing works

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 · see citing works

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 · see citing works

Epidemiology of the human circadian clock

Roenneberg, T., Kuehnle, T., Juda, M., Kantermann, T., Allebrandt, K., Gordijn, M., & Merrow, M. (2007) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2007.07.005 · Cited by 1,545 · see citing works

Actin dynamics control SRF activity by regulation of its coactivator MAL

Miralles, F., Posern, G., Zaromytidou, A.-I., & Treisman, R. (2003) · Cell · doi:10.1016/s0092-8674(03)00278-2 · Cited by 1,327 · see citing works

Linking actin dynamics and gene transcription to drive cellular motile functions

Olson, E. N., & Nordheim, A. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2890 · Cited by 958 · see citing works

Mammalian genes are transcribed with widely different bursting kinetics

Suter, D. M., Molina, N., Gatfield, D., Schneider, K., Schibler, U., & Naef, F. (2011) · Science · doi:10.1126/science.1198817 · Cited by 927 · see citing works

Temperature as a Universal Resetting Cue for Mammalian Circadian Oscillators

Buhr, E. D., Yoo, S.-H., & Takahashi, J. S. (2010) · Science · doi:10.1126/science.1195262 · Cited by 917 · see citing works

Phagocytosis and the actin cytoskeleton

May, R. C., & Machesky, L. M. (2001) · Journal of Cell Science · doi:10.1242/jcs.114.6.1061 · Cited by 715 · see citing works

Nuclear Actin Regulates Dynamic Subcellular Localization and Activity of the SRF Cofactor MAL

Vartiainen, M., Guettler, S., Larijani, B., & Treisman, R. (2007) · Science · doi:10.1126/science.1141084 · Cited by 672 · see citing works

System-Driven and Oscillator-Dependent Circadian Transcription in Mice with a Conditionally Active Liver Clock

Kornmann, B., Schaad, O., Bujard, H., Takahashi, J. S., & Schibler, U. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050034 · Cited by 658 · see citing works

Rhythmic CLOCK-BMAL1 binding to multiple E-box motifs drives circadian Dbp transcription and chromatin transitions

Ripperger, J. A., & Schibler, U. (2006) · Nature Genetics · doi:10.1038/ng1738 · Cited by 593 · see citing works

Serum response factor: toggling between disparate programs of gene expression

Miano, J. M. (2003) · Journal of Molecular and Cellular Cardiology · doi:10.1016/s0022-2828(03)00110-x · Cited by 588 · see citing works

Genetics of Circadian Rhythms in Mammalian Model Organisms

Lowrey, P. L., & Takahashi, J. S. (2011) · Advances in genetics · doi:10.1016/b978-0-12-387690-4.00006-4 · Cited by 578 · see citing works

Actin' together: serum response factor, its cofactors and the link to signal transduction.

Posern, G., & Treisman, R. (2006) · Trends in Cell Biology · doi:10.1016/j.tcb.2006.09.008 · Cited by 560 · see citing works

A solvent system for delipidation of plasma or serum without protein precipitation

Cham, B. E., & Knowles, B. R. (1976) · Journal of Lipid Research · doi:10.1016/s0022-2275(20)37003-6 · Cited by 515 · see citing works

Genome-Wide and Phase-Specific DNA-Binding Rhythms of BMAL1 Control Circadian Output Functions in Mouse Liver

Rey, G., Cesbron, F., Rougemont, J., Reinke, H., Brunner, M., & Naef, F. (2011) · PLoS Biology · doi:10.1371/journal.pbio.1000595 · Cited by 473 · see citing works

Identification of the circadian transcriptome in adult mouse skeletal muscle

McCarthy, J. J., Andrews, J. L., McDearmon, E. L., Campbell, K. S., Barber, B. K., Miller, B. H., Walker, J. R., Hogenesch, J. B., Takahashi, J. S., & Esser, K. A. (2007) · Physiological Genomics · doi:10.1152/physiolgenomics.00066.2007 · Cited by 363 · see citing works

Circadian transcription of the cholesterol 7 alpha hydroxylase gene may involve the liver-enriched bZIP protein DBP.Preprint

Lavery, D. J., & Schibler, U. (1993) · Genes & Development · doi:10.1101/gad.7.10.1871 · Cited by 300 · see citing works

Protein synthesis inhibitors differentially superinduce c‐fos and c‐jun by three distinct mechanisms: lack of evidence for labile repressors.

Edwards, D. R., & Mahadevan, L. C. (1992) · The EMBO Journal · doi:10.1002/j.1460-2075.1992.tb05306.x · Cited by 280 · see citing works

Glucocorticoid signaling synchronizes the liver circadian transcriptome

Reddy, A. B., Maywood, E. S., Karp, N. A., King, V. M., Inoue, Y., Gonzalez, F. J., Lilley, K. S., Kyriacou, C. P., & Hastings, M. H. (2007) · Hepatology · doi:10.1002/hep.21571 · Cited by 261 · see citing works

Differential control of peripheral circadian rhythms by suprachiasmatic-dependent neural signals

Guo, H., Brewer, J. M., Champhekar, A. S., Harris, R. B. S., & Bittman, E. L. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409734102 · Cited by 258 · see citing works

Simulated body temperature rhythms reveal the phase-shifting behavior and plasticity of mammalian circadian oscillatorsPreprint

Saini, C., Morf, J., Stratmann, M., Gos, P., & Schibler, U. (2012) · Genes & Development · doi:10.1101/gad.183251.111 · Cited by 248 · see citing works

Protein Synthesis Inhibitors Reveal Differential Regulation of Mitogen-Activated Protein Kinase and Stress-Activated Protein Kinase Pathways That Converge on Elk-1

Zinck, R., Cahill, M. A., Kracht, M., Sachsenmaier, C., Hipskind, R. A., & Nordheim, A. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.9.4930 · Cited by 243 · see citing works

Differential display of DNA-binding proteins reveals heat-shock factor 1 as a circadian transcription factorPreprint

Reinke, H., Saini, C., Fleury-Olela, F., Dibner, C., Benjamin, I. J., & Schibler, U. (2008) · Genes & Development · doi:10.1101/gad.453808 · Cited by 228 · see citing works

Differential Usage of Signal Transduction Pathways Defines Two Types of Serum Response Factor Target Gene

Gineitis, D., & Treisman, R. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m102678200 · Cited by 197 · see citing works

Nuclear actin and actin‐binding proteins in the regulation of transcription and gene expression

Zheng, B., Han, M., Bernier, M., & Wen, J. (2009) · FEBS Journal · doi:10.1111/j.1742-4658.2009.06986.x · Cited by 152 · see citing works

Nuclear actin and myosins: Life without filaments

de Lanerolle, P., & Serebryannyy, L. (2011) · Nature Cell Biology · doi:10.1038/ncb2364 · Cited by 144 · see citing works

Rapid and Sensitive Detection of Severe Acute Respiratory Syndrome Coronavirus by Rolling Circle Amplification

Wang, B., Potter, S. J., Lin, Y., Cunningham, A. L., Dwyer, D. E., Su, Y., Ma, X., Hou, Y.-D., & Saksena, N. K. (2005) · Journal of Clinical Microbiology · doi:10.1128/jcm.43.5.2339-2344.2005 · Cited by 142 · see citing works

Negative Regulation of the EGFR-MAPK Cascade by Actin-MAL-Mediated Mig6/Errfi-1 Induction

Descot, A., Hoffmann, R., Shaposhnikov, D., Reschke, M., Ullrich, A., & Posern, G. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.07.015 · Cited by 128 · see citing works

Sympathetic input modulates, but does not determine, phase of peripheral circadian oscillators

Vujović, N., Davidson, A. J., & Menaker, M. (2008) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00498.2007 · Cited by 116 · see citing works

Purification from Bovine Serum of a Survival-Promoting Factor for Cultured Central Neurons and Its Identification as Selenoprotein-P

Yan, J., & Barrett, J. N. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-21-08682.1998 · Cited by 107 · see citing works

Purification of plasmid DNA using selective precipitation by compaction agents

Murphy, J. C., Wibbenmeyer, J. A., Fox, G. E., & Willson, R. C. (1999) · Nature Biotechnology · doi:10.1038/11777 · Cited by 100 · see citing works

Regulation of Circadian Gene Expression in Liver by Systemic Signals and Hepatocyte OscillatorsPreprint

Kornmann, B., Schaad, O., Reinke, H., Saini, C., & Schibler, U. (2007) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2007.72.041 · Cited by 99 · see citing works

Mapping of epidermal growth factor-, serum-, and phorbol ester-responsive sequence elements in the c-jun promoter.

Han, T.-H., Lamph, W. W., & Prywes, R. (1992) · Molecular and Cellular Biology · doi:10.1128/mcb.12.10.4472 · Cited by 98 · see citing works

A steroid-inducible promoter for the controlled overexpression of cloned genes in eukaryotic cells.

Mader, S., & White, J. H. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.12.5603 · Cited by 89 · see citing works

Light-dark oscillations in the lung transcriptome: implications for lung homeostasis, repair, metabolism, disease, and drug action

Sukumaran, S., Jusko, W. J., DuBois, D. C., & Almon, R. R. (2011) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00079.2011 · Cited by 82 · see citing works

Transcriptional Profiling of Circadian Patterns of mRNA Expression in the Chick Retina

Bailey, M. J., Beremand, P. D., Hammer, R., Reidel, E., Thomas, T. L., & Cassone, V. M. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m405679200 · Cited by 66 · see citing works

A bHLH transcriptional network regulating the specification of retinal ganglion cells

Matter-Sadzinski, L., Puzianowska‐Kuźnicka, M., Hernandez, J., Ballivet, M., & Matter, J. (2005) · Development · doi:10.1242/dev.01960 · Cited by 66 · see citing works

An improved method for determining the actin filament content of nonmuscle cells by the DNase I inhibition assay

Fox, J. E. B., Dockter, M. E., & Phillips, D. R. (1981) · Analytical Biochemistry · doi:10.1016/0003-2697(81)90707-7 · Cited by 52 · see citing works

Regulation of Immediate Early Gene Expression

Cochran, B. (1993) · PsycEXTRA Dataset · doi:10.1037/e496052006-003 · Cited by 38 · see citing works

F‐actin‐based Ca signaling—a critical comparison with the current concept of Ca signaling

Lange, K., & Gartzke, J. (2006) · Journal of Cellular Physiology · doi:10.1002/jcp.20717 · Cited by 37 · see citing works

A Chimeric Reporter Gene Allowing for Clone Selection and High-Throughput Screening of Reporter Cell Lines Expressing G-Protein-Coupled Receptors

Kotarsky, K., Owman, C., & Olde, B. (2001) · Analytical Biochemistry · doi:10.1006/abio.2000.4898 · Cited by 36 · see citing works

Daytime food restriction alters liver glycogen, triacylglycerols, and cell size. A histochemical, morphometric, and ultrastructural study

Díaz‐Muñoz, M., Martínez, O. V., Báez‐Ruíz, A., Martı́nez-Cabrera, G., Soto-Abraham, M. V., Avila-Casado, M. C., & Larriva-Sahd, J. A. (2010) · Comparative Hepatology · doi:10.1186/1476-5926-9-5 · Cited by 26 · see citing works

Nongradient blue native gel analysis of serum proteins and in-gel detection of serum esterase activities

Thangthaeng, N., Sumien, N., Forster, M. J., Shah, R. A., & Yan, L. (2011) · Journal of Chromatography B · doi:10.1016/j.jchromb.2010.12.026 · Cited by 23 · see citing works

Rhythms in morphology and function of hepatocytes

Uchiyama, Y. (1990) · Journal of Gastroenterology and Hepatology · doi:10.1111/j.1440-1746.1990.tb01634.x · Cited by 22 · see citing works

Circadian Rhythm of Liver Parameters (Cellular Structures, Mitotic Activity, Glycogen and Lipids in Liver and Serum) During Three Consecutive Cycles in Phenobarbital-Treated Rats

Kast, A., Nishikawa, J., Yabe, T., Nanri, H., & Albert, H. (1988) · Chronobiology International · doi:10.3109/07420528809067782 · Cited by 18 · see citing works

Circadian phagocytic activity of neutrophils and its modulation by light

Hriscu, M. (2004) · Journal of Applied Biomedicine · doi:10.32725/jab.2004.024 · Cited by 15 · see citing works

Transcriptional architecture of the mammalian circadian clock

Takahashi, J. S. (2016) · Nature Reviews Genetics · doi:10.1038/nrg.2016.150 · Cited by 2,639 · see citing works

Molecular mechanisms and physiological importance of circadian rhythms

Patke, A., Young, M. W., & Axelrod, S. (2020) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-019-0179-2 · Cited by 1,388 · see citing works

Generation of circadian rhythms in the suprachiasmatic nucleus

Hastings, M. H., Maywood, E. S., & Brancaccio, M. (2018) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0026-z · Cited by 1,065 · see citing works

Circadian time signatures of fitness and disease

Bass, J. T., & Lazar, M. A. (2016) · Science · doi:10.1126/science.aah4965 · Cited by 616 · see citing works

Crosstalk between metabolism and circadian clocks

Reinke, H., & Asher, G. (2019) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-018-0096-9 · Cited by 598 · see citing works

Rho-actin signaling to the MRTF coactivators dominates the immediate transcriptional response to serum in fibroblastsPreprint

Esnault, C., Stewart, A., Gualdrini, F., East, P., Horswell, S. D., Matthews, N., & Treisman, R. (2014) · Genes & Development · doi:10.1101/gad.239327.114 · Cited by 355 · see citing works

Circadian Clock Control of Liver Metabolic Functions

Reinke, H., & Asher, G. (2016) · Gastroenterology · doi:10.1053/j.gastro.2015.11.043 · Cited by 321 · see citing works

Clock-Talk: Interactions between Central and Peripheral Circadian Oscillators in MammalsPreprint

Schibler, U., Gotić, I., Saini, C., Gos, P., Curie, T., Emmenegger, Y., Sinturel, F., Gosselin, P., Gerber, A., Fleury-Olela, F., et al. (2015) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2015.80.027490 · Cited by 313 · see citing works

Communicating clocks shape circadian homeostasis

Koronowski, K. B., & Sassone‐Corsi, P. (2021) · Science · doi:10.1126/science.abd0951 · Cited by 299 · see citing works

Dosing-Time Makes the Poison: Circadian Regulation and Pharmacotherapy

Dallmann, R., Okyar, A., & Lévi, F. (2016) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2016.03.004 · Cited by 295 · see citing works

The circadian clock in cancer development and therapy

Fu, L., & Kettner, N. M. (2013) · Progress in Molecular Biology and Translational Science · doi:10.1016/b978-0-12-396971-2.00009-9 · Cited by 251 · see citing works

Functional Long Non-coding RNAs Evolve from Junk Transcripts

Palazzo, A. F., & Koonin, E. V. (2020) · Cell · doi:10.1016/j.cell.2020.09.047 · Cited by 240 · see citing works

Chronopharmacology: New Insights and Therapeutic Implications

Dallmann, R., Brown, S. A., & Gachon, F. (2013) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-011613-135923 · Cited by 244 · see citing works

Diurnal Oscillations in Liver Mass and Cell Size Accompany Ribosome Assembly Cycles

Sinturel, F., Gerber, A., Mauvoisin, D., Wang, J., Gatfield, D., Stubblefield, J. J., Green, C. B., Gachon, F., & Schibler, U. (2017) · Cell · doi:10.1016/j.cell.2017.04.015 · Cited by 222 · see citing works

Circadian actin dynamics drive rhythmic fibroblast mobilization during wound healing

Hoyle, N. P., Seinkmane, E., Putker, M., Feeney, K. A., Krogager, T. P., Chesham, J. E., Bray, L. K., Thomas, J. M., Dunn, K., Blaikley, J., et al. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aal2774 · Cited by 205 · see citing works

Chronobiology and nutrition

Tahara, Y., & Shibata, S. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.08.049 · Cited by 198 · see citing works

Nuclear Proteomics Uncovers Diurnal Regulatory Landscapes in Mouse Liver

Wang, J., Mauvoisin, D., Martín, E., Atger, F., Galindo, A. N., Dayon, L., Sizzano, F., Palini, A. G., Kussmann, M., Waridel, P., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.10.003 · Cited by 185 · see citing works

A basal-like breast cancer-specific role for SRF–IL6 in YAP-induced cancer stemness

Kim, T., Yang, S.-J., Hwang, D., Song, J., Kim, M., Kim, S. K., Kang, K., Ahn, J., Lee, D., Kim, M., et al. (2015) · Nature Communications · doi:10.1038/ncomms10186 · Cited by 181 · see citing works

Differential effects of light and feeding on circadian organization of peripheral clocks in a forebrain Bmal1 mutant

Izumo, M., Pejchal, M., Schook, A. C., Lange, R. P., Walisser, J. A., Sato, T., Wang, X., Bradfield, C. A., & Takahashi, J. S. (2014) · eLife · doi:10.7554/elife.04617 · Cited by 180 · see citing works

Synchronization of the mammalian circadian timing system: Light can control peripheral clocks independently of the SCN clock

Husse, J., Gregor Eichele, C., & Oster, H. (2015) · BioEssays · doi:10.1002/bies.201500026 · Cited by 156 · see citing works

Circadian rhythms – from genes to physiology and disease

Bollinger, T., & Schibler, U. (2014) · Swiss Medical Weekly · doi:10.4414/smw.2014.13984 · Cited by 152 · see citing works

Circadian gene variants in cancer

Kettner, N. M., Katchy, C. A., & Fu, L. (2014) · Annals of Medicine · doi:10.3109/07853890.2014.914808 · Cited by 147 · see citing works

Actin cytoskeleton remodeling drives epithelial‐mesenchymal transition for hepatoma invasion and metastasis in mice

Peng, J., Bera, R., Chiou, C., Yu, M., Chen, T., Chen, C., Wang, T.-H., Chiang, W., Chai, S., Wei, Y., et al. (2017) · Hepatology · doi:10.1002/hep.29678 · Cited by 147 · see citing works

The cost of circadian desynchrony: Evidence, insights and open questions

West, A. C., & Bechtold, D. A. (2015) · BioEssays · doi:10.1002/bies.201400173 · Cited by 143 · see citing works

The clock gene Bmal1 inhibits macrophage motility, phagocytosis, and impairs defense against pneumonia

Kitchen, G. B., Cunningham, P. S., Poolman, T. M., Iqbal, M., Maidstone, R. J., Baxter, M. D., Bagnall, J., Begley, N., Saer, B., Hussell, T., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1915932117 · Cited by 140 · see citing works

Excitable Dynamics and Yap-Dependent Mechanical Cues Drive the Segmentation Clock

Hubaud, A., Regev, I., Mahadevan, L., & Pourquié, O. (2017) · Cell · doi:10.1016/j.cell.2017.08.043 · Cited by 139 · see citing works

Circadian disruption in the pathogenesis of metabolic syndrome

Maury, E., Hong, H. K., & Bass, J. (2014) · Diabetes & Metabolism · doi:10.1016/j.diabet.2013.12.005 · Cited by 132 · see citing works

Pan-Cancer Analysis Reveals Disrupted Circadian Clock Associates With T Cell Exhaustion

Wu, Y. C., Tao, B., Zhang, T., Fan, Y., & Mao, R. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02451 · Cited by 126 · see citing works

Integration of feeding behavior by the liver circadian clock reveals network dependency of metabolic rhythms

Greco, C. M., Koronowski, K. B., Smith, J. G., Shi, J., Kunderfranco, P., Carriero, R., Chen, S., Samad, M., Welz, P.-S., Zinna, V. M., et al. (2021) · Science Advances · doi:10.1126/sciadv.abi7828 · Cited by 124 · see citing works

Timing of circadian genes in mammalian tissues

Korenčič, A., Košir, R., Bordyugov, G., Lehmann, R., Rozman, D., & Herzel, H. (2014) · Scientific Reports · doi:10.1038/srep05782 · Cited by 117 · see citing works

Circadian Metabolism: From Mechanisms to Metabolomics and Medicine

Brown, S. A. (2016) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2016.03.015 · Cited by 118 · see citing works

Cellular mechano-environment regulates the mammary circadian clock

Yang, N., Williams, J. L., Pekovic‐Vaughan, V., Wang, P., Olabi, S., McConnell, J. C., Gossan, N. C., Hughes, A. T. L., Cheung, J., Streuli, C. H., et al. (2017) · Nature Communications · doi:10.1038/ncomms14287 · Cited by 118 · see citing works

Mammalian circadian systems: Organization and modern life challenges

Finger, A., & Kramer, A. (2021) · Acta Physiologica · doi:10.1111/apha.13548 · Cited by 117 · see citing works

Requirement for NF-κB in maintenance of molecular and behavioral circadian rhythms in micePreprint

Hong, H., Maury, E., Ramsey, K. M., Perelis, M., Marcheva, B., Omura, C., Kobayashi, Y., D, D. C. G., Barish, G. D., & Bass, J. T. (2018) · Genes & Development · doi:10.1101/gad.319228.118 · Cited by 114 · see citing works

Spatiotemporal Metabolic Liver Zonation and Consequences on Pathophysiology

Martini, T., Naef, F., & Tchorz, J. S. (2023) · Annual Review of Pathology: Mechanisms of Disease · doi:10.1146/annurev-pathmechdis-031521-024831 · Cited by 113 · see citing works

Circadian Rhythms in Rho1 Activity Regulate Neuronal Plasticity and Network Hierarchy

Petsakou, A., Sapsis, T. P., & Blau, J. (2015) · Cell · doi:10.1016/j.cell.2015.07.010 · Cited by 101 · see citing works

In pancreatic islets from type 2 diabetes patients, the dampened circadian oscillators lead to reduced insulin and glucagon exocytosis

Petrenko, V., Gandasi, N. R., Sage, D., Tengholm, A., Barg, S., & Dibner, C. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1916539117 · Cited by 101 · see citing works

Rho, nuclear actin, and actin-binding proteins in the regulation of transcription and gene expression

Rajakylä, E. K., & Vartiainen, M. K. (2014) · Small GTPases · doi:10.4161/sgtp.27539 · Cited by 99 · see citing works

The circadian clock protein REVERBα inhibits pulmonary fibrosis development

Cunningham, P. S., Meijer, P., Nazgiewicz, A., Anderson, S. G., Borthwick, L. A., Bagnall, J., Kitchen, G. B., Lodyga, M., Begley, N., Venkateswaran, R., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1912109117 · Cited by 97 · see citing works

Coupled network of the circadian clocks: a driving force of rhythmic physiology

Finger, A., Dibner, C., & Kramer, A. (2020) · FEBS Letters · doi:10.1002/1873-3468.13898 · Cited by 99 · see citing works

Chrono-biology, Chrono-pharmacology and Chrono-nutrition

Tahara, Y., & Shibata, S. (2014) · Journal of Pharmacological Sciences · doi:10.1254/jphs.13r06cr · Cited by 94 · see citing works

Transcriptional regulatory logic of the diurnal cycle in the mouse liver

Sobel, J., Krier, I., Andersin, T., Raghav, S. K., Canella, D., Gilardi, F., Kalantzi, A., Rey, G., Weger, B. D., Gachon, F., et al. (2017) · PLoS Biology · doi:10.1371/journal.pbio.2001069 · Cited by 91 · see citing works

Central control of peripheral circadian oscillators

Menaker, M., Murphy, Z. C., & Sellix, M. T. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.03.003 · Cited by 85 · see citing works

ERK signaling pathway regulates sleep duration through activity-induced gene expression during wakefulness

Mikhail, C., Vaucher, A., Jimenez, S., & Tafti, M. (2017) · Science Signaling · doi:10.1126/scisignal.aai9219 · Cited by 82 · see citing works

A high-throughput screening and computation platform for identifying synthetic promoters with enhanced cell-state specificity (SPECS)

Wu, M.-R., Nissim, L., Stupp, D., Pery, E., Binder-Nissim, A., Weisinger, K., Enghuus, C., Palacios, S., Humphrey, M. R. M., Zhang, Z., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-10912-8 · Cited by 85 · see citing works

Diurnal suppression of EGFR signalling by glucocorticoids and implications for tumour progression and treatment

Lauriola, M., Enuka, Y., Zeisel, A., D’Uva, G., Roth, L. E., Sevilla-Sharon, M., Lindzen, M., Sharma, K., Nevo, N., Feldman, M. E., et al. (2014) · Nature Communications · doi:10.1038/ncomms6073 · Cited by 82 · see citing works

Endocrine regulation of circadian physiology

Tsang, A. H. K., Astiz, M., Friedrichs, M., & Oster, H. (2016) · Journal of Endocrinology · doi:10.1530/joe-16-0051 · Cited by 82 · see citing works

Temporal transcriptomics suggest that twin-peaking genes reset the clock

Pembroke, W. G., Babbs, A., Davies, K. E., Ponting, C. P., & Oliver, P. L. (2015) · eLife · doi:10.7554/elife.10518 · Cited by 81 · see citing works

Intercellular coupling between peripheral circadian oscillators by TGF-β signaling

Finger, A., Jäschke, S., del Olmo, M., HURWITZ, R. M., Granada, A. E., Herzel, H., & Kramer, A. (2021) · Science Advances · doi:10.1126/sciadv.abg5174 · Cited by 80 · see citing works

Non‐alcoholic fatty liver disease: the role of nuclear receptors and circadian rhythmicity

Mazzoccoli, G., Vinciguerra, M., Oben, J. A., Tarquini, R., & Cosmo, S. D. (2014) · Liver International · doi:10.1111/liv.12534 · Cited by 65 · see citing works

CLOCK and BMAL1 stabilize and activate RHOA to promote F-actin formation in cancer cells

Ma, T., Zhang, Z.-W., Lu, Y.-L., Zhang, Y., Tao, D., Liu, Y.-Q., & Ma, Y. (2018) · Experimental & Molecular Medicine · doi:10.1038/s12276-018-0156-4 · Cited by 59 · see citing works

Circadian transcription from beta cell function to diabetes pathophysiology

Perelis, M., Ramsey, K. M., Marcheva, B., & Bass, J. (2016) · Journal of Biological Rhythms · doi:10.1177/0748730416656949 · Cited by 57 · see citing works

Rhythms of the Genome: Circadian Dynamics from Chromatin Topology, Tissue-Specific Gene Expression, to Behavior

Yeung, J., & Naef, F. (2018) · Trends in Genetics · doi:10.1016/j.tig.2018.09.005 · Cited by 58 · see citing works

The Clock Protein Bmal1 Regulates Circadian Expression and Activity of Sulfotransferase 1a1 in Mice

Guo, L., Yu, F., Zhang, T., & Wu, B. (2018) · Drug Metabolism and Disposition · doi:10.1124/dmd.118.082503 · Cited by 56 · see citing works

Circadian Rhythms of PER2::LUC in Individual Primary Mouse Hepatocytes and Cultures

Guenthner, C. J., Luitje, M. E., Pyle, L. A., Molyneux, P. C., Yu, J. K., Li, A. S., Leise, T., & Harrington, M. E. (2014) · PLoS ONE · doi:10.1371/journal.pone.0087573 · Cited by 52 · see citing works

Epithelial and stromal circadian clocks are inversely regulated by their mechano-matrix environment

Williams, J. L., Yang, N., Wood, A., Zindy, E., Meng, Q., & Streuli, C. H. (2018) · Journal of Cell Science · doi:10.1242/jcs.208223 · Cited by 52 · see citing works

Circadian Redox and Metabolic Oscillations in Mammalian Systems

O'Neill, J. S., & Feeney, K. A. (2014) · Antioxidants & Redox Signaling · doi:10.1089/ars.2013.5582 · Cited by 51 · see citing works

SRF Regulates Craniofacial Development through Selective Recruitment of MRTF Cofactors by PDGF Signaling

Vasudevan, H. N., & Soriano, P. M. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.10.005 · Cited by 49 · see citing works

Interorgan rhythmicity as a feature of healthful metabolism

Bass, J. T. (2024) · Cell Metabolism · doi:10.1016/j.cmet.2024.01.009 · Cited by 49 · see citing works

Tissue physiology revolving around the clock: circadian rhythms as exemplified by the intervertebral disc

Morris, H., Gonçalves, C. F., Dudek, M., Hoyland, J. A., & Meng, Q. (2021) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2020-219515 · Cited by 47 · see citing works

The molecular clockwork of mammalian cells

Yi, J. S., Díaz, N. M., D’Souza, S. P., & Buhr, E. D. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.03.012 · Cited by 48 · see citing works

Organelles – understanding noise and heterogeneity in cell biology at an intermediate scale

Chang, A. Y., & Marshall, W. F. (2017) · Journal of Cell Science · doi:10.1242/jcs.181024 · Cited by 49 · see citing works

The Molecular Mechanism Regulating Diurnal Rhythm of Flavin-Containing Monooxygenase 5 in Mouse Liver

Chen, M., Guan, B., Xu, H., Yu, F., Zhang, T., & Wu, B. (2019) · Drug Metabolism and Disposition · doi:10.1124/dmd.119.088450 · Cited by 45 · see citing works

The importance of determining circadian parameters in pharmacological studies

Gaspar, L. S., Álvaro, A. R., Carmo‐Silva, S., Mendes, A. F., Relógio, A., & Cavadas, C. (2019) · British Journal of Pharmacology · doi:10.1111/bph.14712 · Cited by 44 · see citing works

Knitting Up the Raveled Sleave of Care

Yang, G., Paschos, G. K., Curtis, A. M., Musiek, E. S., McLoughlin, S. C., & FitzGerald, G. A. (2013) · Science Translational Medicine · doi:10.1126/scitranslmed.3007225 · Cited by 45 · see citing works

Mechanical loading and hyperosmolarity as a daily resetting cue for skeletal circadian clocks

Dudek, M., Pathiranage, D. R., Baño‐Otálora, B., Paszek, A., Rogers, N., Gonçalves, C. F., Lawless, C., Wang, D., Luo, Z., Yang, L., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-42056-1 · Cited by 44 · see citing works

Minimal upstream open reading frame of Per2 mediates phase fitness of the circadian clock to day/night physiological body temperature rhythm

Miyake, T., Inoue, Y., Shao, X., Seta, T., Aoki, Y., Pham, K. T. N., Shichino, Y., Sasaki, J., Sasaki, T., Ikawa, M., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112157 · Cited by 38 · see citing works

Untimely oxidative stress in β-cells leads to diabetes – Role of circadian clock in β-cell function

Lee, J. M., Ma, K., Moulik, M., & Yechoor, V. K. (2018) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.02.022 · Cited by 39 · see citing works

Rheumatoid arthritis reprograms circadian output pathways

Poolman, T. M., Gibbs, J. E., Walker, A. L., Dickson, S. H., Farrell, L. N., Hensman, J. J., Kendall, A. C., Maidstone, R. J., Warwood, S., Loudon, A. S. I., et al. (2019) · Arthritis Research & Therapy · doi:10.1186/s13075-019-1825-y · Cited by 39 · see citing works

Influence of the extracellular matrix on cell-intrinsic circadian clocks

Streuli, C. H., & Meng, Q. (2019) · Journal of Cell Science · doi:10.1242/jcs.207498 · Cited by 36 · see citing works

Translating around the clock: Multi-level regulation of post-transcriptional processes by the circadian clock

Parnell, A. A., Nobrega, A. K. D., & Lyons, L. C. (2020) · Cellular Signalling · doi:10.1016/j.cellsig.2020.109904 · Cited by 34 · see citing works

The actin cytoskeleton-MRTF/SRF cascade transduces cellular physical niche cues to entrain the circadian clock

Xiong, X., Li, W., Nam, J., Qu, M., Kay, S. A., & Ma, K. (2022) · Journal of Cell Science · doi:10.1242/jcs.260094 · Cited by 34 · see citing works

The systemic control of circadian gene expression

Gerber, A., Saini, C., Curie, T., Emmenegger, Y., Rando, G., Gosselin, P., Gotić, I., Gos, P., Franken, P., & Schibler, U. (2015) · Diabetes Obesity and Metabolism · doi:10.1111/dom.12512 · Cited by 33 · see citing works

Bmal1‐deficiency affects glial synaptic coverage of the hippocampal mossy fiber synapse and the actin cytoskeleton in astrocytes

Ali, A. A. H., Schwarz‐Herzke, B., Rollenhagen, A., Anstötz, M., Holub, M., Lübke, J. H. R., Rose, C. R., Schnittler, H., & von Gall, C. (2019) · Glia · doi:10.1002/glia.23754 · Cited by 32 · see citing works

The nature and intensity of mechanical stimulation drive different dynamics of MRTF-A nuclear redistribution after actin remodeling in myoblasts

Montel, L., Sotiropoulos, A., & Hénon, S. (2019) · PLoS ONE · doi:10.1371/journal.pone.0214385 · Cited by 31 · see citing works

Identification of rhythmic human CYPs and their circadian regulators using synchronized hepatoma cells

Chen, M., Zhou, C., Zhang, T., & Wu, B. (2020) · Xenobiotica · doi:10.1080/00498254.2020.1737890 · Cited by 31 · see citing works

Insulin Directly Regulates the Circadian Clock in Adipose Tissue

Tuvia, N., Pivovarova‐Ramich, O., Murahovschi, V., Lück, S., Grudziecki, A., Ost, A.-C., Kruse, M., Nikiforova, V. J., Osterhoff, M. A., Gottmann, P., et al. (2021) · Diabetes · doi:10.2337/db20-0910 · Cited by 31 · see citing works

The Liver in the Eyes of a Chronobiologist

Zwighaft, Z., Reinke, H., & Asher, G. (2016) · Journal of Biological Rhythms · doi:10.1177/0748730416633552 · Cited by 29 · see citing works

Hepatocyte SREBP signaling mediates clock communication within the liver

Guan, D., Bae, H., Zhou, D., Chen, Y., Jiang, C., La, C. M., Xiao, Y., Zhu, K., Hu, W., Trinh, T. M., et al. (2023) · Journal of Clinical Investigation · doi:10.1172/jci163018 · Cited by 29 · see citing works

Mechanical control of the mammalian circadian clock via YAP/TAZ and TEAD

Abenza, J. F., Rossetti, L., Mouelhi, M., Burgués, J., Andreu, I., Kennedy, K., Roca‐Cusachs, P., Marco, S., García‐Ojalvo, J., & Trepat, X. (2023) · The Journal of Cell Biology · doi:10.1083/jcb.202209120 · Cited by 28 · see citing works

The sleep-wake distribution contributes to the peripheral rhythms in PERIOD-2

Hoekstra, M. M., Jan, M., Katsioudi, G., Emmenegger, Y., & Franken, P. (2021) · eLife · doi:10.7554/elife.69773 · Cited by 28 · see citing works

Regulation of Intestinal Lipid Absorption by Clock Genes

Hussain, M. M. (2014) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-071813-105322 · Cited by 28 · see citing works

CRS: a circadian rhythm score model for predicting prognosis and treatment response in cancer patients

Liu, Y., Guo, S., Sun, Y., Zhang, C., Gan, J., Ning, S., & Wang, J. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-04013-w · Cited by 24 · see citing works

Circadian clock control of MRTF/SRF pathway suppresses beige adipocyte thermogenic recruitment

Xiong, X., Li, W., Liu, R., Saha, P., Yechoor, V., & Ma, K. (2023) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjac079 · Cited by 24 · see citing works

Circadian regulation of macromolecular complex turnover and proteome renewal

(2024) · doi:10.1038/s44318-024-00121-5 · Cited by 24 · see citing works

Deficiency of the clock gene Bmal1 affects neural progenitor cell migration

Ali, A. A. H., Schwarz‐Herzke, B., Mir, S., Sahlender, B., Victor, M. B., Görg, B., Schmuck, M. R., Dach, K., Fritsche, E., Kremer, A., et al. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1775-1 · Cited by 24 · see citing works

Type 2 diabetes disrupts circadian orchestration of lipid metabolism and membrane fluidity in human pancreatic islets

Petrenko, V., Sinturel, F., Loizides‐Mangold, U., Montoya, J. P., Chera, S., Riezman, H., & Dibner, C. (2022) · PLoS Biology · doi:10.1371/journal.pbio.3001725 · Cited by 21 · see citing works

Circadian Rhythm of Lipid Metabolism in Health and Disease

Zhang, Z., Xin, H., & Li, M. (2020) · Small Methods · doi:10.1002/smtd.201900601 · Cited by 21 · see citing works

Non-Darwinian Molecular Biology

Palazzo, A. F., & Kejiou, N. S. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.831068 · Cited by 17 · see citing works

Core circadian clock transcription factor BMAL1 regulates mammary epithelial cell growth, differentiation, and milk component synthesis

Casey, T., Suárez-Trujillo, A., Cummings, S., Huff, K., Crodian, J. S., Bhide, K. P., Aduwari, C., Teeple, K. M., Shamay, A., Mabjeesh, S. J., et al. (2021) · PLoS ONE · doi:10.1371/journal.pone.0248199 · Cited by 15 · see citing works

CRY1/2 regulate rhythmic CYP2A5 in mouse liver through repression of E4BP4

Lin, L., Huang, Y., Wang, J., Guo, X., Yu, F., He, D., Wu, C., Guo, L., & Wu, B. (2023) · Biochemical Pharmacology · doi:10.1016/j.bcp.2023.115843 · Cited by 14 · see citing works

Different levels of circadian (de)synchrony – where does it hurt?

Galinde, A. A., Al‐Μughales, F., Oster, H., & Heyde, I. (2022) · F1000Research · doi:10.12688/f1000research.127234.2 · Cited by 13 · see citing works

Development of circadian neurovascular function and its implications

Mitchell, J. W., & Gillette, M. U. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1196606 · Cited by 12 · see citing works

Clock gene Bmal1 controls diurnal rhythms in expression and activity of intestinal carboxylesterase 1

Chen, X., Yu, F., Guo, X., Su, C., Li, S., & Wu, B. (2021) · Journal of Pharmacy and Pharmacology · doi:10.1093/jpp/rgaa035 · Cited by 12 · see citing works

SRF in Neurochemistry: Overview of Recent Advances in Research on the Nervous System

Tabuchi, A., & Ihara, D. (2022) · Neurochemical Research · doi:10.1007/s11064-022-03632-x · Cited by 12 · see citing works

Disruption of daily rhythms in gene expression: The importance of being synchronised

Hughes, A. T. L., & Piggins, H. D. (2014) · BioEssays · doi:10.1002/bies.201400043 · Cited by 11 · see citing works

Liver size: Waning by day, Waxing by Night

Reinke, H., & Asher, G. (2017) · Hepatology · doi:10.1002/hep.29506 · Cited by 11 · see citing works

Serum cholesterol selectively regulates glucocorticoid sensitivity through activation of JNK

Yang, N., Caratti, G., Ince, L. M., Poolman, T. M., Trebble, P., Holt, C. M., Ray, D. W., & Matthews, L. C. (2014) · Journal of Endocrinology · doi:10.1530/joe-14-0456 · Cited by 11 · see citing works

Unbiased identification of signal-activated transcription factors by barcoded synthetic tandem repeat promoter screening (BC-STAR-PROM)Preprint

Gosselin, P., Rando, G., Fleury-Olela, F., & Schibler, U. (2016) · Genes & Development · doi:10.1101/gad.284828.116 · Cited by 11 · see citing works

Steven A. Brown and the synchronization of circadian rhythms by body temperature cycles

Schibler, U. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16431 · Cited by 10 · see citing works

Identification of circadian pathways by Synthetic TAndem Repeat PROMoter (STAR-PROM) screening

Gerber, A. (2012) · Archive ouverte UNIGE (University of Geneva) · doi:10.13097/archive-ouverte/unige:22149

The role of immediate early transcription factors in the regulation of peripheral circadian clocks

Hui, K. Y. (2015) · Archive ouverte UNIGE (University of Geneva) · doi:10.13097/archive-ouverte/unige:78838

Actin cytoskeleton signaling via MRTF/SRF entrains circadian clockPreprint

Xiong, X., Li, W., Nam, J., Qu, M., Kay, S. A., & Ma, K. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.04.29.490111 · Cited by 1 · see citing works

Rho-actin signaling to the MRTF coactivators dominates the immediate transcriptional response to serum in fibroblastsPreprint

Esnault, C., Stewart, A., Gualdrini, F., East, P., Horswell, S. D., Matthews, N., & Treisman, R. (2014) · Genes & Development · doi:10.1101/gad.239327.114 · Cited by 355 · see citing works

Integrin signaling via actin cytoskeleton activates MRTF/SRF to entrain circadian clockPreprint

Xiong, X., Li, W., Nam, J., & Ma, K. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.12.456061 · Cited by 4 · see citing works