Glucocorticoids and the circadian clock

The Neuroendocrinology of Stress: A Never Ending Story

Lightman, S. L. (2008) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2008.01711.x · Cited by 3,588

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

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

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

Loss of a circadian adrenal corticosterone rhythm following suprachiasmatic lesions in the rat

Moore, R. Y., & Eichler, V. B. (1972) · Brain Research · doi:10.1016/0006-8993(72)90054-6 · Cited by 2,135

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

Organization of ovine corticotropin-releasing factor immunoreactive cells and fibers in the rat brain: an immunohistochemical study

Swanson, L. W., Sawchenko, P. E., Rivier, J., & Vale, W. W. (2008) · Neuroendocrinology · doi:10.1159/000123454 · Cited by 1,953

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

Control of hepatic gluconeogenesis through the transcriptional coactivator PGC-1

Yoon, J. C., Puigserver, P., Chen, G., Donovan, J., Wu, Z., Rhee, J., Adelmant, G., Stafford, J., Kahn, C. R., Granner, D. K., et al. (2001) · Nature · doi:10.1038/35093050 · Cited by 1,821

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

Overview of steroidogenic enzymes in the pathway from cholesterol to active steroid hormones

Payne, A. H., & Hales, D. B. (2004) · Endocrine Reviews · doi:10.1210/er.2003-0030 · Cited by 1,766

Molecular components of the mammalian circadian clock

Ko, C. H., & Takahashi, J. S. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl207 · Cited by 1,725

Suprachiasmatic nucleus : the mind's clock

Klein, D. C., Moore, R. Y., & Reppert, S. M. (1991) · Cited by 1,715

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

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

Welsh, D. K., Logothetis, D. E., Meister, M., & Reppert, S. M. (1995) · Neuron · doi:10.1016/0896-6273(95)90214-7 · Cited by 1,481

Twenty-four hour pattern of the episodic secretion of cortisol in normal subjects

WEITZMAN, E. D., FUKUSHIMA, D., NOGEIRE, C., ROFFWARG, H., GALLAGHER, T. F., & HELLMAN, L. (1971) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-33-1-14 · Cited by 1,258

Control Mechanism of the Circadian Clock for Timing of Cell Division in Vivo

Matsuo, T., Yamaguchi, S., Mitsui, S., Emi, A., Shimoda, F., & Okamura, H. (2003) · Science · doi:10.1126/science.1086271 · Cited by 1,132

A pdf Neuropeptide Gene Mutation and Ablation of PDF Neurons Each Cause Severe Abnormalities of Behavioral Circadian Rhythms in Drosophila

Renn, S. C. P., Park, J. H., Rosbash, M., Hall, J. C., & Taghert, P. H. (1999) · Cell · doi:10.1016/s0092-8674(00)81676-1 · Cited by 1,117

Reconstitution of Circadian Oscillation of Cyanobacterial KaiC Phosphorylation in Vitro

Nakajima, M., Imai, K., Ito, H., Nishiwaki, T., Murayama, Y., Iwasaki, H., Oyama, T., & Kondo, T. (2005) · Science · doi:10.1126/science.1108451 · Cited by 1,110

Circadian Gene Expression in Individual Fibroblasts

Nagoshi, E., Saini, C., Bauer, C. R., Laroche, T., Naef, F., & Schibler, U. (2004) · Cell · doi:10.1016/j.cell.2004.11.015 · Cited by 1,031

Nuclear Receptor Expression Links the Circadian Clock to Metabolism

Yang, X., Downes, M., Yu, R. T., Bookout, A. L., He, W., Straume, M., Mangelsdorf, D. J., & Evans, R. M. (2006) · Cell · doi:10.1016/j.cell.2006.06.050 · Cited by 946

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 881

Circadian food-anticipatory activity: Formal models and physiological mechanisms

Mistlberger, R. E. (1994) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(94)90023-x · Cited by 857

System-level identification of transcriptional circuits underlying mammalian circadian clocks

Ueda, H. R., Hayashi, S., Chen, W., Sano, M., Machida, M., Shigeyoshi, Y., Iino, M., & Hashimoto, S. (2005) · Nature Genetics · doi:10.1038/ng1504 · Cited by 802

Feast and Famine: Critical Role of Glucocorticoids with Insulin in Daily Energy Flow

Dallman, M. F., Strack, A. M., Akana, S. F., Bradbury, M. J., Hanson, E. S., Scribner, K. A., & Smith, M. (1993) · Frontiers in Neuroendocrinology · doi:10.1006/frne.1993.1010 · Cited by 796

Circadian Cycling of the Mouse Liver Transcriptome, as Revealed by cDNA Microarray, Is Driven by the Suprachiasmatic Nucleus

Akhtar, R. A., Reddy, A. B., Maywood, E. S., Clayton, J. D., King, V. M., Smith, A. G., Gant, T. W., Hastings, M. H., & Kyriacou, C. P. (2002) · Current Biology · doi:10.1016/s0960-9822(02)00759-5 · Cited by 777

A Web of Circadian Pacemakers

Schibler, U., & Sassone‐Corsi, P. (2002) · Cell · doi:10.1016/s0092-8674(02)01225-4 · Cited by 761

Bioluminescence imaging of individual fibroblasts reveals persistent, independently phased circadian rhythms of clock gene expression

Welsh, D. K., Yoo, S.-H., Liu, A. C., Takahashi, J. S., & Kay, S. A. (2004) · Current Biology · doi:10.1016/j.cub.2004.11.057 · Cited by 726

Circadian rhythms in isolated brain regions

Abe, M., Herzog, E. D., Yamazaki, S., Straume, M., Tei, H., Sakaki, Y., Menaker, M., & Block, G. D. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-01-00350.2002 · Cited by 681

Efferent projections of the suprachiasmatic nucleus: I. Studies using anterograde transport of Phaseolus vulgaris leucoagglutinin in the rat

Watts, A. G., Swanson, L. W., & Sanchez‐Watts, G. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902580204 · Cited by 678

The “other” circadian system: food as a Zeitgeber

Stephan, F. K. (2002) · Journal of Biological Rhythms · doi:10.1177/074873002129002591 · Cited by 672

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

Transcriptional coactivator PGC-1α integrates the mammalian clock and energy metabolism

Liu, C., Li, S., Liu, T., Borjigin, J., & Lin, J. D. (2007) · Nature · doi:10.1038/nature05767 · Cited by 643

Microarray Analysis and Organization of Circadian Gene Expression in Drosophila

McDonald, M. J., & Rosbash, M. (2001) · Cell · doi:10.1016/s0092-8674(01)00545-1 · Cited by 614

Hypothalamic integration of central and peripheral clocks

Buijs, R. M., & Kalsbeek, A. (2001) · Nature reviews. Neuroscience · doi:10.1038/35081582 · Cited by 601

Intraadrenal interactions in the regulation of adrenocortical steroidogenesis.

Ehrhart-Bornstein, M., Hinson, J. P., Bornstein, S. R., Scherbaum, W. A., & Vinson, G. P. (1998) · Endocrine Reviews · doi:10.1210/edrv.19.2.0326 · Cited by 600 · cited 2×

The neuronal mineralocorticoid eeceptor as a mediator of glucocorticoid response

Arriza, J. L., Simerly, R. B., Swanson, L. W., & Evans, R. M. (1988) · Neuron · doi:10.1016/0896-6273(88)90136-5 · Cited by 591

Light activates the adrenal gland: Timing of gene expression and glucocorticoid release

Ishida, A., Mutoh, T., Ueyama, T., Bando, H., Masubuchi, S., Nakahara, D., Tsujimoto, G., & Okamura, H. (2005) · Cell Metabolism · doi:10.1016/j.cmet.2005.09.009 · Cited by 589

Rhythms of Mammalian Body Temperature Can Sustain Peripheral Circadian Clocks

Brown, S. A., Zumbrunn, G., Fleury-Olela, F., Preitner, N., & Schibler, U. (2002) · Current Biology · doi:10.1016/s0960-9822(02)01145-4 · Cited by 589

NPAS2: an analog of clock operative in the mammalian forebrain

Reick, M., Garcia, J. A., Dudley, C., & McKnight, S. L. (2001) · Science · doi:10.1126/science.1060699 · Cited by 572

Restricted feeding entrains liver clock without participation of the suprachiasmatic nucleus

Hara, R., Wan, K., Wakamatsu, H., Aida, R., Moriya, T., Akiyama, M., & Shibata, S. (2001) · Genes to Cells · doi:10.1046/j.1365-2443.2001.00419.x · Cited by 569 · cited 1×

The stress system in depression and neurodegeneration: Focus on the human hypothalamus

Bao, A., Meynen, G., & Swaab, D. F. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.04.005 · Cited by 565

Circadian orchestration of the hepatic proteome

Reddy, A. B., Karp, N. A., Maywood, E. S., Sage, E. A., Deery, M., O'Neill, J. S., Wong, G. K. Y., Chesham, J., Odell, M., Lilley, K. S., et al. (2006) · Current Biology · doi:10.1016/j.cub.2006.04.026 · Cited by 548

The hypothalamic integrator for circadian rhythms

Saper, C. B., Lü, J., Chou, T. C., & Gooley, J. J. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2004.12.009 · Cited by 548

Circadian Mutant Overtime Reveals F-box Protein FBXL3 Regulation of Cryptochrome and Period Gene Expression

Siepka, S. M., Yoo, S. H., Park, J., Song, W., Kumar, V., Hu, Y., Lee, C., & Takahashi, J. S. (2007) · Cell · doi:10.1016/j.cell.2007.04.030 · Cited by 545

Multiple signaling pathways regulating steroidogenesis and steroidogenic acute regulatory protein expression: more complicated than we thought

Stocco, D. M., Wang, X., Jo, Y., & Manna, P. R. (2005) · Molecular Endocrinology · doi:10.1210/me.2004-0532 · Cited by 538

The circadian rhythm of glucocorticoids is regulated by a gating mechanism residing in the adrenal cortical clock

Oster, H., Damerow, S., Kiessling, S., Jakubcakova, V., Abraham, D., Tian, J., Hoffmann, M. W., & Eichele, G. (2006) · Cell Metabolism · doi:10.1016/j.cmet.2006.07.002 · Cited by 528

SCF Fbxl3 Controls the Oscillation of the Circadian Clock by Directing the Degradation of Cryptochrome Proteins

Busino, L., Bassermann, F. C., Maiolica, A., Lee, C., Nolan, P. M., Godinho, S. I. H., Draetta, G. F., & Pagano, M. (2007) · Science · doi:10.1126/science.1141194 · Cited by 510

CLOCK and NPAS2 have overlapping roles in the suprachiasmatic circadian clock

DeBruyne, J. P., Weaver, D. R., & Reppert, S. M. (2007) · Nature Neuroscience · doi:10.1038/nn1884 · Cited by 496

SCN Outputs and the Hypothalamic Balance of Life

Kalsbeek, A., Palm, I. F., la Fleur, S., Scheer, F., Perreau‐Lenz, S., Ruiter, M., Kreier, F., Cailotto, C., & Buijs, R. (2006) · Journal of Biological Rhythms · doi:10.1177/0748730406293854 · Cited by 492

Anatomical and functional demonstration of a multisynaptic suprachiasmatic nucleus adrenal (cortex) pathway

Buijs, R. M., Wortel, J., Van Heerikhuize, J. J., Feenstra, M. G. P., Ter Horst, G. J., Romijn, H. J., & Kalsbeek, A. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00575.x · Cited by 485

Light acts directly on organs and cells in culture to set the vertebrate circadian clock

Whitmore, D., Foulkes, N. S., & Sassone‐Corsi, P. (2000) · Nature · doi:10.1038/35003589 · Cited by 481

Co-expression of corticotropin-releasing factor and vasopressin immunoreactivity in parvocellular neurosecretory neurons of the adrenalectomized rat.

Sawchenko, P. E., Swanson, L. W., & Vale, W. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.6.1883 · Cited by 481

The coming out of the brain mineralocorticoid receptor

Joëls, M., Karst, H., DeRijk, R., & de Kloet, E. R. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2007.10.005 · Cited by 481

Glucocorticoid hormones inhibit food‐induced phase‐shifting of peripheral circadian oscillators

Minh, N. L., Damiola, F., Tronche, F., Schütz, G., & Schibler, U. (2001) · The EMBO Journal · doi:10.1093/emboj/20.24.7128 · Cited by 480

The After-Hours Mutant Reveals a Role for Fbxl3 in Determining Mammalian Circadian Period

Godinho, S. I. H., Maywood, E. S., Shaw, L. E., Tucci, V., Barnard, A. R., Busino, L., Pagano, M., Kendall, R., Quwailid, M. M., Romero, M. R., et al. (2007) · Science · doi:10.1126/science.1141138 · Cited by 469

Orchestrating time: arrangements of the brain circadian clock

Antle, M. C., & Silver, R. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.01.003 · Cited by 463

Intrinsic circadian clock of the mammalian retina: importance for retinal processing of visual information

Storch, K.-F., Paz, C., Signorovitch, J., Raviola, E., Pawlyk, B., Li, T., & Weitz, C. J. (2007) · Cell · doi:10.1016/j.cell.2007.06.045 · Cited by 460

The dorsomedial hypothalamic nucleus is critical for the expression of food-entrainable circadian rhythms

Gooley, J. J., Schomer, A., & Saper, C. B. (2006) · Nature Neuroscience · doi:10.1038/nn1651 · Cited by 453

Circadian Regulation of Gene Expression Systems in the Drosophila Head

Claridge‐Chang, A., Wijnen, H., Naef, F., Boothroyd, C. E., Rajewsky, N., & Young, M. W. (2001) · Neuron · doi:10.1016/s0896-6273(01)00515-3 · Cited by 444

A clock shock: mouse CLOCK is not required for circadian oscillator function

DeBruyne, J. P., Noton, E., Lambert, C. M., Maywood, E. S., Weaver, D. R., & Reppert, S. M. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.041 · Cited by 430

Melanopsin: an exciting photopigment

Hankins, M. W., Peirson, S. N., & Foster, R. G. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2007.11.002 · Cited by 426

Circadian clocks: regulators of endocrine and metabolic rhythms

Hastings, M., O’Neill, J. S., & Maywood, E. S. (2007) · Journal of Endocrinology · doi:10.1677/joe-07-0378 · Cited by 426

The glucocorticoid responses are shaped by molecular chaperones

Grad, I., & Picard, D. (2007) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2007.05.018 · Cited by 423

Molecular mechanisms of glucocorticoid action and selective glucocorticoid receptor agonists

Stahn, C., Löwenberg, M., Hommes, D. W., & Buttgereit, F. (2007) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2007.05.019 · Cited by 419

Altered patterns of sleep and behavioral adaptability in NPAS2-deficient mice

Dudley, C. A., Erbel-Sieler, C., Estill, S. J., Reick, M., Franken, P., Pitts, S., & McKnight, S. L. (2003) · Science · doi:10.1126/science.1082795 · Cited by 415

Epigenetic programming of the stress response in male and female rats by prenatal restraint stress

Darnaudéry, M., & Maccari, S. (2008) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.11.004 · Cited by 412

The biological clock tunes the organs of the body: timing by hormones and the autonomic nervous system

Buijs, R. M., van Eden, C. G., Goncharuk, V. D., & Kalsbeek, A. (2003) · Journal of Endocrinology · doi:10.1677/joe.0.1770017 · Cited by 387

Feedback repression is required for mammalian circadian clock function

Sato, T. K., Yamada, R. G., Ukai, H., Baggs, J. E., Miraglia, L. J., Kobayashi, T., Welsh, D. K., Kay, S. A., Ueda, H. R., & Hogenesch, J. B. (2006) · Nature Genetics · doi:10.1038/ng1745 · Cited by 377

Circadian orchestration of gene expression in cyanobacteria.Preprint

Liu, Y., Tsinoremas, N. F., Johnson, C. H., Lebedeva, N. V., Golden, S. S., Ishiura, M., & Kondo, T. (1995) · Genes & Development · doi:10.1101/gad.9.12.1469 · Cited by 373

Functional subsets of serotonergic neurones: implications for control of the hypothalamic-pituitary-adrenal axis

Lowry, C. A. (2002) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2002.00861.x · Cited by 362

Zebrafish Clock rhythmic expression reveals independent peripheral circadian oscillators

Whitmore, D., Foulkes, N. S., Strähle, U., & Sassone‐Corsi, P. (1998) · Nature Neuroscience · doi:10.1038/3703 · Cited by 357

Dissociation of ACTH and glucocorticoids

Bornstein, S. R., Engeland, W. C., Ehrhart-Bornstein, M., & Herman, J. P. (2008) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2008.01.009 · Cited by 345

The Hypothalamic‐Pituitary‐Adrenal Axis Activity in Obesity and the Metabolic Syndrome

Pasquali, R., Vicennati, V., Cacciari, M., & Pagotto, U. (2006) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1367.009 · Cited by 334

Acute Physical Stress Elevates Mouse Period1 mRNA Expression in Mouse Peripheral Tissues via a Glucocorticoid-responsive Element

Yamamoto, T., Nakahata, Y., Tanaka, M., Yoshida, M., Soma, H., Shinohara, K., Yasuda, A., Mamine, T., & Takumi, T. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m509600200 · Cited by 309

Corticotropin-releasing factor: co-expression within distinct subsets of oxytocin-, vasopressin-, and neurotensin-immunoreactive neurons in the hypothalamus of the male rat

Sawchenko, P. E., Swanson, L. W., & Vale, W. (1984) · Journal of Neuroscience · doi:10.1523/jneurosci.04-04-01118.1984 · Cited by 305

Suprachiasmatic Nuclear Lesions Do Not Abolish Food-Shifted Circadian Adrenal and Temperature Rhythmicity

Krieger, D. T., Hauser, H., & Krey, L. C. (1977) · Science · doi:10.1126/science.877566 · Cited by 297

Adrenergic regulation of clock gene expression in mouse liver

Terazono, H., Mutoh, T., Yamaguchi, S., Kobayashi, M., Akiyama, M., Udo, R., Ohdo, S., Okamura, H., & Shibata, S. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0936797100 · Cited by 293

The dorsomedial hypothalamic nucleus as a putative food-entrainable circadian pacemaker

Mieda, M., Williams, S. C., Richardson, J. A., Tanaka, K., & Yanagisawa, M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604189103 · Cited by 290

Clock genes in mammalian peripheral tissues

Balsalobre, A. (2002) · Cell and Tissue Research · doi:10.1007/s00441-002-0585-0 · Cited by 289

A Tissue-Specific Coactivator of Steroid Receptors, Identified in a Functional Genetic Screen

Knutti, D., Kaul, A., & Kralli, A. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.7.2411-2422.2000 · Cited by 286

Serotonin and the regulation of mammalian circadian rhythmicity

Morin, L. P. (1999) · Annals of Medicine · doi:10.3109/07853899909019259 · Cited by 286

Crosstalk between the glucocorticoid receptor and other transcription factors: Molecular aspects

Kassel, O., & Herrlich, P. (2007) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2007.07.003 · Cited by 277

Ultradian rhythm of basal corticosterone release in the female rat: dynamic interaction with the response to acute stress

Windle, R. J., Wood, S. A., Shanks, N., Lightman, S. L., & Ingram, C. D. (1998) · Endocrinology · doi:10.1210/en.139.2.443 · Cited by 276

A Diurnal Rhythm of Stimulatory Input to the Hypothalamo–Pituitary–Adrenal System as Revealed by Timed Intrahypothalamic Administration of the Vasopressin V1Antagonist

Kalsbeek, A., van Heerikhuize, J. J., Wortel, J., & Buijs, R. M. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-17-05555.1996 · Cited by 275

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 272

The projections of the dorsomedial hypothalamic nucleus in the rat

Horst, G. J. T., & Luiten, P. G. M. (1986) · Brain Research Bulletin · doi:10.1016/0361-9230(86)90038-9 · Cited by 269

Output pathways of the mammalian suprachiasmatic nucleus: coding circadian time by transmitter selection and specific targeting

Kalsbeek, A., & Buijs, R. M. (2002) · Cell and Tissue Research · doi:10.1007/s00441-002-0577-0 · Cited by 261

Differential Rescue of Light- and Food-Entrainable Circadian Rhythms

Fuller, P. M., Lü, J., & Saper, C. B. (2008) · Science · doi:10.1126/science.1153277 · Cited by 260

Circadian clocks: setting time by food

Mendoza, J. (2007) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2006.01510.x · Cited by 257

The central and basolateral nuclei of the amygdala exhibit opposite diurnal rhythms of expression of the clock protein Period2

Lamont, E. W., Robinson, B., Stewart, J., & Amir, S. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0500901102 · Cited by 256

Factors affecting the circadian rhythm in plasma cortisol concentrations in the horse

IRVINE, C. H. G., & Alexander, S. L. (1994) · Domestic Animal Endocrinology · doi:10.1016/0739-7240(94)90030-2 · Cited by 253

Effects of Suprachiasmatic Transplants on Circadian Rhythms of Neuroendocrine Function in Golden Hamsters**This work was supported by NIH Grants MH-44132, KO2-MH-00914, and F32-HD-07673. A preliminary report of this research was presented at the 23rd Annual Meeting of the Society for Neuroscience (Neurosci Abstr 19:236.17, 1993).

Meyer-Bernstein, E. L., Jetton, A. E., Matsumoto, S., Markuns, J. F., Lehman, M. N., & Bittman, E. L. (1999) · Endocrinology · doi:10.1210/endo.140.1.6428 · Cited by 252

Hypothalamic-pituitary-adrenocortical axis regulation

Jacobson, L. (2005) · Endocrinology and Metabolism Clinics of North America · doi:10.1016/j.ecl.2005.01.003 · Cited by 248

Adrenal splanchnic innervation contributes to the diurnal rhythm of plasma corticosterone in rats by modulating adrenal sensitivity to ACTH

Ulrich‐Lai, Y. M., Arnhold, M. M., & Engeland, W. C. (2005) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00042.2003 · Cited by 247

Glucocorticoids, developmental ‘programming’ and the risk of affective dysfunction

Seckl, J. R. (2007) · Progress in Brain Research · doi:10.1016/s0079-6123(07)67002-2 · Cited by 245

The significance of glucocorticoid pulsatility

Lightman, S. L., Wiles, C. C., Atkinson, H. C., Henley, D. E., Russell, G. M., Leendertz, J. A., McKenna, M. A., Spiga, F., Wood, S. A., & Conway-Campbell, B. L. (2008) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2007.11.073 · Cited by 241

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 237

Studies of the Secretion of Corticotropin-Releasing Factor and Arginine Vasopressin into the Hypophysial-Portal Circulation of the Conscious Sheep

Engler, D., Pham, T., Fullerton, M. J., Ooi, G., Funder, J. W., & Clarke, I. J. (2008) · Neuroendocrinology · doi:10.1159/000125141 · Cited by 235

DNA microarray analyses of circadian timing: the genomic basis of biological time

Duffield, G. E. (2003) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2003.01082.x · Cited by 234

Transcriptional Profiling in the Adrenal Gland Reveals Circadian Regulation of Hormone Biosynthesis Genes and Nucleosome Assembly Genes

Oster, H., Damerow, S., Hut, R. A., & Gregor Eichele, C. (2006) · Journal of Biological Rhythms · doi:10.1177/0748730406293053 · Cited by 233

Diurnal and Ultradian Rhythms in Human Endocrine Function: A Minireview

Cauter, E. V. (2008) · Hormone Research · doi:10.1159/000181794 · Cited by 231

Co-localization of corticotropin-releasing factor and vasopressin in median eminence neurosecretory vesicles

Whitnall, M. H., Mezey, É., & Gainer, H. (1985) · Nature · doi:10.1038/317248a0 · Cited by 230

Vasopressin-containing neurons of the suprachiasmatic nuclei inhibit corticosterone release

Kalsbeek, A., Buijs, R. M., van Heerikhuize, J. J., Arts, M., & van der Woude, T. P. (1992) · Brain Research · doi:10.1016/0006-8993(92)90927-2 · Cited by 230

Chronobiology in the endocrine system

Haus, E. L. (2007) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2007.01.001 · Cited by 228

Efferent connections of the rat suprachiasmatic nucleus

Stephan, F. K., Berkley, K. J., & Moss, R. L. (1981) · Neuroscience · doi:10.1016/0306-4522(81)90108-1 · Cited by 216

Intracellular Regeneration of Glucocorticoids by 11 -Hydroxysteroid Dehydrogenase (11 -HSD)-1 Plays a Key Role in Regulation of the Hypothalamic-Pituitary-Adrenal Axis: Analysis of 11 -HSD-1-Deficient Mice

Harris, H. J., Kotelevtsev, Y. V., Mullins, J. J., Seckl, J. R., & Holmes, M. C. (2001) · Endocrinology · doi:10.1210/endo.142.1.7887 · Cited by 215

Riding Tandem: Circadian Clocks and the Cell Cycle

Hunt, T., & Sassone‐Corsi, P. (2007) · Cell · doi:10.1016/j.cell.2007.04.015 · Cited by 211

Lack of Food Anticipation in Per2 Mutant Mice

Feillet, C. A., Ripperger, J. A., Magnone, M. C., Dulloo, A. G., Albrecht, U., & Challet, É. (2006) · Current Biology · doi:10.1016/j.cub.2006.08.053 · Cited by 208

Amplitude, but not Frequency, Modulation of Adrenocorticotropin Secretory Bursts Gives Rise to the Nyctohemeral Rhythm of the Corticotropic Axis in Man*

Veldhuis, J. D., Iranmanesh, A., Johnson, M. L., & LIZARRALDE, G. (1990) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-71-2-452 · Cited by 203

The Pulsatile Characteristics of Hypothalamo-Pituitary-Adrenal Activity in Female Lewis and Fischer 344 Rats and Its Relationship to Differential Stress Responses*

Windle, R. J., Wood, S. A., Lightman, S. L., & Ingram, C. D. (1998) · Endocrinology · doi:10.1210/endo.139.10.6238 · Cited by 201 · cited 2×

Vasopressin Exhibits a Rhythmic Daily Pattern in Cerebrospinal Fluid But Not in Blood

Reppert, S. M., Artman, H. G., Swaminathan, S., & Fisher, D. A. (1981) · Science · doi:10.1126/science.7268432 · Cited by 201

From transcriptome to biological function: environmental stress in an ectothermic vertebrate, the coral reef fish Pomacentrus moluccensis

Kassahn, K. S., Crozier, R. H., Ward, A. C., Stone, G., & Caley, M. J. (2007) · BMC Genomics · doi:10.1186/1471-2164-8-358 · Cited by 199

An autoradiographic determination of the efferent projections of the suprachiasmatic nucleus of the hypothalamus

Berk, M. L., & Finkelstein, J. A. (1981) · Brain Research · doi:10.1016/0006-8993(81)91079-9 · Cited by 193

Genome-wide Expression Analysis Reveals 100 Adrenal Gland-dependent Circadian Genes in the Mouse Liver

Oishi, K., Amagai, N., Shirai, H., Kadota, K., Ohkura, N., & Ishida, N. (2005) · DNA Research · doi:10.1093/dnares/dsi003 · Cited by 192

The suprachiasmatic nucleus controls the daily variation of plasma glucose via the autonomic output to the liver: are the clock genes involved?

Cailotto, C., La Fleur, S. E., Van Heijningen, C., Wortel, J., Kalsbeek, A., Feenstra, M., Pévet, P., & Buijs, R. M. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04439.x · Cited by 191

Effects of Destruction of the Suprachiasmatic Nuclei on the Circadian Rhythms in Plasma Corticosterone, Body Temperature, Feeding and Plasma Thyrotropin

Abe, K., Kroning, J., Greer, M. A., & CRITCHLOW, V. (2008) · Neuroendocrinology · doi:10.1159/000122913 · Cited by 189

Suprachiasmatic nucleus: a central autonomic clock

Ueyama, T., Krout, K. E., Nguyen, X. V., Karpitskiy, V. V., Kollert, A., Mettenleiter, T. C., & Loewy, A. D. (1999) · Nature Neuroscience · doi:10.1038/15973 · Cited by 188

Light Regulates the Cell Cycle in Zebrafish

Dekens, M. P. S., Santoriello, C., Vallone, D., Grassi, G., Whitmore, D., & Foulkes, N. S. (2003) · Current Biology · doi:10.1016/j.cub.2003.10.022 · Cited by 187

Rhythmic Properties of the Hamster Suprachiasmatic Nucleus In Vivo

Yamazaki, S., Kerbeshian, M. C., Hocker, C. G., Block, G. D., & Menaker, M. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-24-10709.1998 · Cited by 184

Melanocortin receptors: their functions and regulation by physiological agonists and antagonists

ABDEL‐MALEK, Z. A. (2001) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000868 · Cited by 183

Immunoreactive Corticotropin-Releasing Hormone in the Hypothalamoinfundibular Tract

Antoni, F. A., Palkovits, M., Makara, G. B., Linton, E. A., Lowry, P. J., & Kiss, J. Z. (2008) · Neuroendocrinology · doi:10.1159/000123492 · Cited by 180

Persistence of a behavioral food-anticipatory circadian rhythm following dorsomedial hypothalamic ablation in rats

Landry, G. J., Simon, M. M., Webb, I. C., & Mistlberger, R. E. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00874.2005 · Cited by 179

A Circadian Rhythm in the Expression of PERIOD2 Protein Reveals a Novel SCN-Controlled Oscillator in the Oval Nucleus of the Bed Nucleus of the Stria Terminalis

Amir, S., Lamont, E. W., Robinson, B., & Stewart, J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4488-03.2004 · Cited by 179

Neural Circuitry in the Regulation of Adrenal Corticosterone Rhythmicity

Engeland, W. C., & Arnhold, M. M. (2005) · Endocrine · doi:10.1385/endo:28:3:325 · Cited by 178

Phototransduction in ganglion-cell photoreceptors

Berson, D. M. (2007) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-007-0242-2 · Cited by 177

Circadian and Glucocorticoid Regulation of Rev-erb Expression in Liver

Pineda‐Torra, I., Tsibulsky, V. P., Delaunay, F., Saladin, R., Laudet, V., Fruchart, J., Kosykh, V., & Staels, B. (2000) · Endocrinology · doi:10.1210/endo.141.10.7708 · Cited by 177

EFFECTS OF LESIONS OF THE SUPRACHIASMATIC NUCLEI AND OF p -CHLOROPHENYLALANINE ON THE CIRCADIAN RHYTHMS OF ADRENOCORTICOTROPHIC HORMONE AND CORTICOSTERONE IN THE PLASMA, AND ON LOCOMOTOR ACTIVITY OF RATS

SZAFARCZYK, A., IXART, G., MALAVAL, F., NOUGUIER-SOULÉ, J., & ASSENMACHER, I. (1979) · Journal of Endocrinology · doi:10.1677/joe.0.0830001 · Cited by 177 · cited 1×

Nycthemeral rhythm in adrenal responsiveness to ACTH

Dallman, M. F., Engeland, W. C., Rose, J. C., Wilkinson, C. W., Shinsako, J., & Siedenburg, F. (1978) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1978.235.5.r210 · Cited by 172

Evolution of circadian organization in vertebrates

Menaker, M., Moreira, L. F. S., & Tosini, G. (1997) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x1997000300003 · Cited by 171

Daily Rhythm of Tryptophan Hydroxylase-2 Messenger Ribonucleic Acid within Raphe Neurons Is Induced by Corticoid Daily Surge and Modulated by Enhanced Locomotor Activity

Malek, Z. S., Ciocca, D., Pévet, P., & Raison, S. (2007) · Endocrinology · doi:10.1210/en.2007-0526 · Cited by 169

Peripheral circadian oscillators require CLOCK

DeBruyne, J. P., Weaver, D. R., & Reppert, S. M. (2007) · Current Biology · doi:10.1016/j.cub.2007.05.067 · Cited by 162

Intraadrenal Interactions in the Regulation of Adrenocortical Steroidogenesis

Ehrhart‐Bornstein, M. (1998) · Endocrine Reviews · doi:10.1210/er.19.2.101 · Cited by 162

Projections of the suprachiasmatic nucleus to stress-related areas in the rat hypothalamus: A light and electron microscopic study

Buijs, R. M., Markman, M., Nunes‐Cardoso, B., Hou, Y., & Shinn, S. (1993) · Journal of Comparative Neurology · doi:10.1002/cne.903350104 · Cited by 153

The two PAR leucine zipper proteins, TEF and DBP, display similar circadian and tissue‐specific expression, but have different target promoter preferences.

Fonjallaz, P., Ossipow, V., Wanner, G., & Schibler, U. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00365.x · Cited by 151

Categorically Distinct Acute Stressors Elicit Dissimilar Transcriptional Profiles in the Paraventricular Nucleus of the Hypothalamus

Reyes, T. M., Walker, J. R., DeCino, C., Hogenesch, J. B., & Sawchenko, P. E. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-13-05607.2003 · Cited by 149

Suprachiasmatic nucleus lesion increases corticosterone secretion

Buijs, R. M., Kalsbeek, A., van der Woude, T. P., van Heerikhuize, J. J., & Shinn, S. (1993) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1993.264.6.r1186 · Cited by 149

Effects of Splanchnic Nerve Stimulation on the Adrenal Cortex May Be Mediated by Chromaffin Cells in a Paracrine Manner

Bornstein, S. R., Ehrhart‐Bornstein, M., Scherbaum, W. A., Pfeiffer, E. F., & Holst, J. J. (1990) · Endocrinology · doi:10.1210/endo-127-2-900 · Cited by 141

Glucocorticoid rhythms control the rhythm of expression of the clock protein, Period2, in oval nucleus of the bed nucleus of the stria terminalis and central nucleus of the amygdala in rats

Segall, L. A., Perrin, J. S., Walker, C. D., Stewart, J., & Amir, S. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.03.037 · Cited by 141

Rhythmic Expression of BMAL1 mRNA Is Altered in Clock Mutant Mice: Differential Regulation in the Suprachiasmatic Nucleus and Peripheral Tissues

Oishi, K., Fukui, H., & Ishida, N. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1999.2054 · Cited by 140

Decrease of Endogenous Vasopressin Release Necessary for Expression of the Circadian Rise in Plasma Corticosterone: a Reverse Microdialysis Study

Kalsbeek, A., van der Vliet, J., & Buijs, R. M. (1996) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1996.04597.x · Cited by 138

The nuclear receptors Rev-erbs and RORs integrate circadian rhythms and metabolism

Duez, H., & Staels, B. (2008) · Diabetes and Vascular Disease Research · doi:10.3132/dvdr.2008.0014 · Cited by 134

Imaging of single light-responsive clock cells reveals fluctuating free-running periods

Carr, A. F., & Whitmore, D. (2005) · Nature Cell Biology · doi:10.1038/ncb1232 · Cited by 133

Dual KaiC-based oscillations constitute the circadian system of cyanobacteriaPreprint

Kitayama, Y., Nishiwaki, T., Terauchi, K., & Kondo, T. (2008) · Genes & Development · doi:10.1101/gad.1661808 · Cited by 133

Glucocorticoids Play a Key Role in Circadian Cell Cycle Rhythms

Dickmeis, T., Lahiri, K., Nica, G., Vallone, D., Santoriello, C., Neumann, C. J., Hammerschmidt, M., & Foulkes, N. S. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050078 · Cited by 131

In vivo measurement of a diurnal variation in vasopressin release in the rat suprachiasmatic nucleus.

Kalsbeek, A., Buijs, R. M., Engelmann, M., Wotjak, C., & Landgraf, R. (1995) · Brain Research · doi:10.1016/0006-8993(95)00324-j · Cited by 131

Circadian and Ultradian Rhythms of Peripheral Cortisol Concentrations in Lactating Dairy Cows

Lefcourt, A. M., Bitman, J., Kahl, S., & Wood, D. L. (1993) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(93)77595-5 · Cited by 128

Food-entrained circadian rhythms are sustained in arrhythmic Clk/Clk mutant mice

Pitts, S., Perone, E. A., & Silver, R. (2003) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00023.2003 · Cited by 126

Proteasome-Dependent Down-Regulation of Activated Nuclear Hippocampal Glucocorticoid Receptors Determines Dynamic Responses to Corticosterone

Conway-Campbell, B. L., McKenna, M. A., Wiles, C. C., Atkinson, H. C., de Kloet, E. R., & Lightman, S. L. (2007) · Endocrinology · doi:10.1210/en.2007-0585 · Cited by 125

From Malthus to motive: How the HPA axis engineers the phenotype, yoking needs to wants

Pecoraro, N. C., Dallman, M. F., Warne, J. P., Ginsberg, A. B., Laugero, K. D., la Fleur, S. E., Houshyar, H., Gómez-Oliver, F., Bhargava, A., & Akana, S. F. (2006) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2006.07.004 · Cited by 125

Direct projection from the suprachiasmatic nucleus to hypophysiotrophic corticotropin-releasing factor immunoreactive cells in the paraventricular nucleus of the hypothalamus demonstrated by means ofPhaseolus vulgaris-leucoagglutinin tract tracing

Vrang, N., Larsen, P. J., & Mikkelsen, J. D. (1995) · Brain Research · doi:10.1016/0006-8993(95)00425-p · Cited by 123

The Dorsomedial Hypothalamic Nucleus Is Not Necessary for the Expression of Circadian Food-Anticipatory Activity in Rats

Landry, G. J., Yamakawa, G. R., Webb, I. C., Mear, R. J., & Mistlberger, R. E. (2007) · Journal of Biological Rhythms · doi:10.1177/0748730407307804 · Cited by 120

Minireview: The Circadian Clockwork of the Suprachiasmatic Nuclei—Analysis of a Cellular Oscillator that Drives Endocrine Rhythms

Maywood, E. S., O'Neill, J. S., Chesham, J. E., & Hastings, M. H. (2007) · Endocrinology · doi:10.1210/en.2007-0660 · Cited by 119

Adrenal Innervation May Be an Extrapituitary Mechanism Able to Regulate Adrenocortical Rhythmicity in Rats*

Ottenweller, J. E., & MEIER, A. H. (1982) · Endocrinology · doi:10.1210/endo-111-4-1334 · Cited by 119

Meta-Analysis of Drosophila Circadian Microarray Studies Identifies a Novel Set of Rhythmically Expressed Genes

Keegan, K. P., Pradhan, S., Wang, J.-P., & Allada, R. (2005) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0030208 · Cited by 117

Neural Connections of Hypothalamic Neuroendocrine Nuclei in the Rat

Saeb‐Parsy, K., Lombardelli, Khan, McDowall, Au‐Yong, & Dyball (2000) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2000.00503.x · Cited by 116

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

Reciprocal Regulation of a Glucocorticoid Receptor-Steroidogenic Factor-1 Transcription Complex on the Dax-1 Promoter by Glucocorticoids and Adrenocorticotropic Hormone in the Adrenal Cortex

Gummow, B. M., Scheys, J. O., Cancelli, V. R., & Hammer, G. D. (2006) · Molecular Endocrinology · doi:10.1210/me.2005-0461 · Cited by 114

Probing the Relative Importance of Molecular Oscillations in the Circadian Clock

Zheng, X., & Sehgal, A. (2008) · Genetics · doi:10.1534/genetics.107.088658 · Cited by 112

Increased Corticosterone Pulse Frequency During Adjuvant‐Induced Arthritis and its Relationship to Alterations in Stress Responsiveness

Windle, R., Wood, S. A., Kershaw, Y. M., Lightman, S. L., Ingram, C. D., & Harbuz, M. S. (2001) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2001.00715.x · Cited by 110

Synchronous ultradian rhythms in adrenocortical secretion detected by microdialysis in awake rats

Jasper, M. S., & Engeland, W. C. (1991) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1991.261.5.r1257 · Cited by 109

The suprachiasmatic nuclei stimulate evening ACTH secretion in the rat

Cascio, C. S., Shinsako, J., & Dallman, M. F. (1987) · Brain Research · doi:10.1016/0006-8993(87)90837-7 · Cited by 109

Corticotropin-Releasing Hormone and Arginine Vasopressin Gene Transcription in the Hypothalamic Paraventricular Nucleus of Unstressed Rats: Daily Rhythms and Their Interactions with Corticosterone

Watts, A. G., Tanimura, S. M., & Sanchez‐Watts, G. (2003) · Endocrinology · doi:10.1210/en.2003-0394 · Cited by 109

Period gene expression in mouse endocrine tissues

Bittman, E. L., Doherty, L. F., Huang, L., & Paroskie, A. (2003) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00783.2002 · Cited by 109

Circadian metabolic patterns in cultured hamster adrenal glands

Andrews, R. V., & Folk, G. E. (1964) · Comparative Biochemistry and Physiology · doi:10.1016/0010-406x(64)90006-4 · Cited by 109

The rat hepatic leukemia factor (HLF) gene encodes two transcriptional activators with distinct circadian rhythms, tissue distributions and target preferences.

Falvey, E., Fleury-Olela, F., & Schibler, U. (1995) · The EMBO Journal · doi:10.1002/j.1460-2075.1995.tb00105.x · Cited by 105

Circadian variation of cell proliferation and cell cycle protein expression in man: Clinical implications

Bjarnason, G. A., & Jordan, R. C. (2000) · Springer eBooks · doi:10.1007/978-1-4615-4253-7_17 · Cited by 105

Daily Rhythms in Metabolic Liver Enzymes and Plasma Glucose Require a Balance in the Autonomic Output to the Liver

Cailotto, C., Heijningen, C. L. V., van der Vliet, J., Plasse, G., Habold, C., Kalsbeek, A., Pévet, P., & Buijs, R. M. (2007) · Endocrinology · doi:10.1210/en.2007-0816 · Cited by 105

HOURLY FLUCTUATIONS IN THE BLOOD LEVELS OF MELATONIN, PROLACTIN, LUTEINIZING HORMONE, FOLLICLE-STIMULATING HORMONE, TESTOSTERONE, TRI-IODOTHYRONINE, THYROXINE AND CORTISOL IN RAMS UNDER ARTIFICIAL PHOTOPERIODS, AND THE EFFECTS OF CRANIAL SYMPATHECTOMY

Lincoln, G. A., Almeida, O. F. X., KLANDORF, H., & CUNNINGHAM, R. A. (1982) · Journal of Endocrinology · doi:10.1677/joe.0.0920237 · Cited by 101

Opposite actions of hypothalamic vasopressin on circadian corticosterone rhythm in nocturnal versus diurnal species

Kalsbeek, A., Verhagen, L. A. W., Schalij, I., Foppen, E., Saboureau, M., Bothorel, B., Buijs, R. M., & Pévet, P. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06057.x · Cited by 100

Glucocorticoid suppression of the sympathetic nervous system and adrenal medulla

Brown, M. R., & Fisher, L. A. (1986) · Life Sciences · doi:10.1016/0024-3205(86)90289-4 · Cited by 99

Late-night salivary cortisol measurement in the diagnosis of Cushing’s syndrome

Carroll, T., Raff, H., & Findling, J. W. (2008) · Nature Clinical Practice Endocrinology & Metabolism · doi:10.1038/ncpendmet0837 · Cited by 97

Diurnal Variation in the Responsiveness of the Hypothalamic‐Pituitary‐Adrenal Axis of the Male Rat to Noise Stress

Atkinson, H. C., Wood, S. A., Kershaw, Y. M., Bate, E., & Lightman, S. L. (2006) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2006.01444.x · Cited by 97

Age-related changes of the adrenal secretory pattern: possible role in pathological brain aging

Ferrari, E., Casarotti, D., Muzzoni, B., Albertelli, N., Cravello, L., Fioravanti, M., Solerte, S. B., & Magri, F. (2001) · Brain Research Reviews · doi:10.1016/s0165-0173(01)00133-3 · Cited by 97

The role of the transcriptional activator protein DBP in circadian liver gene expression

Wuarin, J., Falvey, E., Lavery, D. J., Talbot, D., Schmidt, E., Ossipow, V., Fonjallaz, P., & Schibler, U. (1992) · Journal of Cell Science · doi:10.1242/jcs.1992.supplement_16.15 · Cited by 96

Electrical stimulation of the median or dorsal raphe nuclei reduces light-induced FOS protein in the suprachiasmatic nucleus and causes circadian activity rhythm phase shifts

Meyer-Bernstein, E. L., & Morin, L. P. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00733-7 · Cited by 96

Transcriptional and post-transcriptional regulation of the circadian clock of cyanobacteria and NeurosporaPreprint

Brunner, M., & Schafmeier, T. (2006) · Genes & Development · doi:10.1101/gad.1410406 · Cited by 95

Daily Variation in Concentration of Plasma Corticosteroid in Hypophysectomized Rats

MEIER, A. H. (1976) · Endocrinology · doi:10.1210/endo-98-6-1475 · Cited by 95

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

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

The expression of the clock protein PER2 in the limbic forebrain is modulated by the estrous cycle

Perrin, J. S., Segall, L. A., Harbour, V. L., Woodside, B., & Amir, S. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601310103 · Cited by 88

Light enhances sympathetic and suppresses vagal outflows and lesions including the suprachiasmatic nucleus eliminate these changes in rats

Niijima, A., Nagai, K., Nagai, N., & Nakagawa, H. (1992) · Journal of the Autonomic Nervous System · doi:10.1016/0165-1838(92)90026-d · Cited by 86

Circadian clocks: Neural and peripheral pacemakers that impact upon the cell division cycle

Reddy, A. B., Wong, G. K. Y., O'Neill, J. S., Maywood, E. S., & Hastings, M. H. (2005) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2005.01.024 · Cited by 86

Effects of light stimulation on the activity of the autonomic nerves in anesthetized rats

Niijima, A., Nagai, K., Nagai, N., & Akagawa, H. (1993) · Physiology & Behavior · doi:10.1016/0031-9384(93)90249-f · Cited by 85

Synchronized Ultradian Cortisol Rhythms in Monkeys: Persistence During Corticotropin Infusion

Holaday, J. W., Martínez, H. M., & Natelson, B. H. (1977) · Science · doi:10.1126/science.197603 · Cited by 85

Editorial: Ultradian, circadian, and stress–related hypothalamic–pituitary–adrenal axis activity–a dynamic digital–to–analog Modulation

Chrousos, G. P. (1998) · Endocrinology · doi:10.1210/endo.139.2.5857 · Cited by 83

Intrauterine programming of the endocrine pancreas

Remacle, C., Dumortier, O., Bol, V., Goosse, K., Romanus, P., Theys, N., Bouckenooghe, T., & Reusens, B. (2007) · Diabetes Obesity and Metabolism · doi:10.1111/j.1463-1326.2007.00790.x · Cited by 81

Start the clock! Circadian rhythms and development

Vallone, D., Lahiri, K., Dickmeis, T., & Foulkes, N. S. (2006) · Developmental Dynamics · doi:10.1002/dvdy.20998 · Cited by 78

Altered food-anticipatory activity rhythm in Cryptochrome-deficient mice

Iijima, M., Yamaguchi, S., van der Horst, G. T. J., Bonnefont, X., Okamura, H., & Shibata, S. (2005) · Neuroscience Research · doi:10.1016/j.neures.2005.03.003 · Cited by 77

Evidence for an Overlapping Role of CLOCK and NPAS2 Transcription Factors in Liver Circadian Oscillators

Bertolucci, C., Cavallari, N., Colognesi, I., Aguzzi, J., Chen, Z., Caruso, P., Foà, A., Tosini, G., Bernardi, F., & Pinotti, M. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.01931-07 · Cited by 77

Diurnal variation in resting levels of corticosterone is not mediated by variation in adrenal responsiveness to adrenocorticotropin but involves splanchnic nerve integrity

Dijkstra, I., Binnekade, R., & Tilders, F. J. H. (1996) · Endocrinology · doi:10.1210/endo.137.2.8593800 · Cited by 75

Effects of Suprachiasmatic Transplants on Circadian Rhythms of Neuroendocrine Function in Golden Hamsters

Meyer-Bernstein, E. L. (1999) · Endocrinology · doi:10.1210/en.140.1.207 · Cited by 74

The Diurnal Modulation of Hormonal Responses in the Rat Varies with Different Stimuli

Kalsbeek, A., Ruiter, M., la Fleur, S. E., Heijningen, C. L. V., & Buijs, R. M. (2003) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2003.01112.x · Cited by 73

Diversity of zebrafish peripheral oscillators revealed by luciferase reporting

Kaneko, M. A. N., de Borsetti, N. H., & Cahill, G. M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0606563103 · Cited by 73

Diurnal Rhythmicity of the Canonical Clock Genes Per1, Per2 and Bmal1 in the Rat Adrenal Gland is Unaltered after Hypophysectomy

Fahrenkrug, J., Hannibal, J., & Georg, B. (2008) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2008.01651.x · Cited by 73

Plasma Adrenocorticotropic Hormone in the Rat Demonstrates Three Different Rhythms within 24 h

Carnes, M. L., Lent, S. J., Feyzi, J. M., & Hazel, D. K. (2008) · Neuroendocrinology · doi:10.1159/000125197 · Cited by 72

Diurnal Regulation of Glucocorticoid Receptor and Mineralocorticoid Receptor mRNAs in Rat Hippocampus

Herman, J. P., Watson, S. J., Chao, H. M., Coirini, H., & McEwen, B. S. (1993) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.1993.1022 · Cited by 72

Circadian Transcription Contributes to Core Period Determination in Drosophila

Kadener, S., Menet, J. S., Schoer, R. A., & Rosbash, M. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060119 · Cited by 71

Relationships between circadian rhythms and modulation of gene expression by glucocorticoids in skeletal muscle

Almon, R. R., Yang, E., Lai, W., Androulakis, I. P., Ghimbovschi, S. D., Hoffman, E. P., Jusko, W. J., & DuBois, D. C. (2008) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.90399.2008 · Cited by 70

Circadian control of the immune system

Scheiermann, C., Kunisaki, Y., & Frenette, P. S. (2013) · Nature Reviews Immunology · doi:10.1038/nri3386 · Cited by 1,135

The cortisol awakening response: More than a measure of HPA axis function

Clow, A., Hucklebridge, F., Stalder, T., Evans, P., & Thorn, L. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.12.011 · Cited by 635

The Functional and Clinical Significance of the 24-Hour Rhythm of Circulating Glucocorticoids

Oster, H., Challet, E., Ott, V., Arvat, E., de Kloet, E. R., Dijk, D.-J., Lightman, S., Vgontzas, A., & Van Cauter, E. (2017) · Endocrine Reviews · doi:10.1210/er.2015-1080 · Cited by 548

Dynamics and Correlation of Serum Cortisol and Corticosterone under Different Physiological or Stressful Conditions in Mice

Gong, S., Miao, Y.-L., Jiao, G.-Z., Sun, M.-J., Li, H., Lin, J., Luo, M.-J., & Tan, J.-H. (2015) · PLOS ONE · doi:10.1371/journal.pone.0117503 · Cited by 460

Developmental Trajectories of Early Life Stress and Trauma: A Narrative Review on Neurobiological Aspects Beyond Stress System Dysregulation

Agorastos, A., Pervanidou, P., Chrousos, G. P., & Baker, D. G. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00118 · Cited by 385

Exogenous Glucocorticoids and a High-Fat Diet Cause Severe Hyperglycemia and Hyperinsulinemia and Limit Islet Glucose Responsiveness in Young Male Sprague-Dawley Rats

Beaudry, J. L., D'souza, A. M., Teich, T., Tsushima, R. G., & Riddell, M. C. (2013) · Endocrinology · doi:10.1210/en.2012-2114 · Cited by 47

The Effect of Fasting on Tissue Cyclic cAMP and Plasma Glucagon in the Obese Hyperglycemic Mouse

VINE, R. L. L., Voyles, N. R., Perrino, P. V., & Recant, L. (1975) · Endocrinology · doi:10.1210/endo-97-3-615 · Cited by 38

Modulation of Adipoinsular Axis in Prediabetic Zucker Diabetic Fatty Rats by Diazoxide

Alemzadeh, R., & Tushaus, K. (2004) · Endocrinology · doi:10.1210/en.2003-1523 · Cited by 38

The Paraventricular Nucleus of the Hypothalamus Has a Major Role in Thyroid Hormone Feedback Regulation of Thyrotropin Synthesis and Secretion

Taylor, T., Wondisford, F. E., Blaine, T. A., & Weintraub, B. D. (1990) · Endocrinology · doi:10.1210/endo-126-1-317 · Cited by 55

Growth hormone binding protein in the rat: effects of gonadal steroids

Carmignac, D. F., Gabrielsson, B. G., & Robinson, I. C. A. F. (1993) · Endocrinology · doi:10.1210/endo.133.6.8243263 · Cited by 68