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 3,570 · 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

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 2,272 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

Resetting central and peripheral circadian oscillators in transgenic rats

Yamazaki, S., Numano, R., Abe, M., Hida, A., Takahashi, R.-I., Ueda, M., Block, G. D., Sakaki, Y., Menaker, M., & Tei, H. (2000) · Science · doi:10.1126/science.288.5466.682 · Cited by 1,907 · see citing works

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

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 · 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

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 · see citing works

Suprachiasmatic nucleus : the mind's clock

Klein, D. C., Moore, R. Y., & Reppert, S. M. (1991) · Cited by 1,713 · see citing works

Molecular components of the mammalian circadian clock

Ko, C. H., & Takahashi, J. S. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl207 · Cited by 1,657 · see citing works

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

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

Extensive and divergent circadian gene expression in liver and heart

Storch, K.-F., Lipan, O., Leykin, I., Viswanathan, N., Davis, F. C., Wong, W. H., & Weitz, C. J. (2002) · Nature · doi:10.1038/nature744 · Cited by 1,509 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 1,003 · see citing works

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 934 · see citing works

Post-translational modifications regulate the ticking of the circadian clock

Gallego, M., & Virshup, D. M. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2106 · Cited by 863 · see citing works

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 · see citing works

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 · see citing works

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 786 · see citing works

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 · see citing works

A Web of Circadian Pacemakers

Schibler, U., & Sassone‐Corsi, P. (2002) · Cell · doi:10.1016/s0092-8674(02)01225-4 · Cited by 752 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

The “other” circadian system: food as a Zeitgeber

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

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 · see citing works

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 606 · see citing works

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× · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

Hypothalamic integration of central and peripheral clocks

Buijs, R. M., & Kalsbeek, A. (2001) · Nature reviews. Neuroscience · doi:10.1038/35081582 · Cited by 580 · see citing works

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 · see citing works

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× · see citing works

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 · see citing works

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 547 · see citing works

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 · see citing works

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 536 · see citing works

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 · see citing works

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 528 · see citing works

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 509 · see citing works

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 · see citing works

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 485 · see citing works

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 · see citing works

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 484 · see citing works

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 · see citing works

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 · see citing works

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 468 · see citing works

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 467 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 373 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 335 · see citing works

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 · see citing works

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 302 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

Clock genes in mammalian peripheral tissues

Balsalobre, A. (2002) · Cell and Tissue Research · doi:10.1007/s00441-002-0585-0 · Cited by 288 · see citing works

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 · see citing works

Serotonin and the regulation of mammalian circadian rhythmicity

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

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 · see citing works

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 · see citing works

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 274 · see citing works

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 · 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

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 · see citing works

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 · see citing works

Circadian clocks: setting time by food

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

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 231 · see citing works

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 231 · see citing works

Diurnal and Ultradian Rhythms in Human Endocrine Function: A Minireview

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

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 226 · see citing works

Chronobiology in the endocrine system

Haus, E. L. (2007) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2007.01.001 · Cited by 222 · see citing works

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 · see citing works

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 · see citing works

Intracellular Regeneration of Glucocorticoids by 11β-Hydroxysteroid Dehydrogenase (11β-HSD)-1 Plays a Key Role in Regulation of the Hypothalamic-Pituitary-Adrenal Axis: Analysis of 11β-HSD-1-Deficient Mice**The Wellcome Trust supported this work through a program grant (to J.J.M. and J.R.S.) and a Career Development Fellowship (to M.C.H.).

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 209 · see citing works

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 · see citing works

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 · see citing works

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× · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

EFFECTS OF LESIONS OF THE SUPRACHIASMATIC NUCLEI AND OF <i>p</i> -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× · see citing works

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 175 · see citing works

Phototransduction in ganglion-cell photoreceptors

Berson, D. M. (2007) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-007-0242-2 · Cited by 174 · see citing works

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 · see citing works

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 · see citing works

Circadian and Glucocorticoid Regulation of Rev-erbα Expression in Liver 1

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 169 · see citing works

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 · see citing works

Intraadrenal Interactions in the Regulation of Adrenocortical Steroidogenesis

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

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 160 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 132 · see citing works

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 · see citing works

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 128 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 120 · see citing works

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 · see citing works

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 118 · see citing works

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 · 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

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 · see citing works

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. (2007) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0030208 · Cited by 114 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 107 · see citing works

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 · see citing works

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 · see citing works

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 102 · see citing works

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 · see citing works

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 101 · see citing works

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 · see citing works

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

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

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 96 · see citing works

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 · see citing works

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 92 · see citing works

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 90 · see citing works

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 · see citing works

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 88 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 78 · see citing works

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 · see citing works

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 78 · see citing works

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 · see citing works

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 77 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 72 · see citing works

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 · see citing works

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 70 · see citing works

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 · see citing works

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 · see citing works

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

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

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 · see citing works

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 · see citing works

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 · see citing works

Circadian rhythms in the hypothalamo-pituitary-adrenal (HPA) axis

Kalsbeek, A., van der Spek, R., Lei, J., Endert, E., Buijs, R. M., & Fliers, E. (2012) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2011.06.042 · Cited by 380 · see citing works

Sex differences in circadian timing systems: implications for disease

Bailey, M., & Silver, R. (2014) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2013.11.003 · Cited by 348 · see citing works

Circadian rhythms, time-restricted feeding, and healthy aging

Manoogian, E. N. C., & Panda, S. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2016.12.006 · Cited by 330 · see citing works

Circadian rhythm of adrenal glucocorticoid: its regulation and clinical implications

Chung, S., Son, G. H., & Kim, K. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2011.02.003 · Cited by 305 · see citing works

Effects of diet, lifestyle, Chrononutrition and alternative dietary interventions on postprandial Glycemia and insulin resistance

Papakonstantinou, E., Oikonomou, C., Nychas, G., & Dimitriadis, G. D. (2022) · Nutrients · doi:10.3390/nu14040823 · Cited by 199 · see citing works

Circadian endocrine rhythms: the hypothalamic–pituitary–adrenal axis and its actions

Nicolaides, N. C., Charmandari, E., Chrousos, G. P., & Kino, T. (2014) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12464 · Cited by 183 · see citing works

Yoga practice improves executive function by attenuating stress levels

Gothe, N. P., Keswani, R. K., & McAuley, E. (2016) · Biological Psychology · doi:10.1016/j.biopsycho.2016.10.010 · Cited by 159 · see citing works

Dipper and Non-Dipper Blood Pressure 24-Hour Patterns: Circadian Rhythm–Dependent Physiologic and Pathophysiologic Mechanisms

Fabbian, F., Smolensky, M. H., Tiseo, R., Pala, M., Manfredini, R., & Portaluppi, F. (2013) · Chronobiology International · doi:10.3109/07420528.2012.715872 · Cited by 147 · see citing works

The circadian clock and glucocorticoids – interactions across many time scales

Dickmeis, T., Weger, B. D., & Weger, M. (2013) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2013.05.012 · Cited by 144 · see citing works

The adrenal peripheral clock: Glucocorticoid and the circadian timing system

Son, G. H., Chung, S., & Kim, K. (2011) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2011.07.003 · Cited by 136 · see citing works

Adverse effects of two nights of sleep restriction on the hypothalamic-pituitary-adrenal axis in healthy men

Guyon, A., Balbo, M., Morselli, L. L., Tasali, E., Leproult, R., L'Hermite-Balériaux, M., Van Cauter, E., & Spiegel, K. (2014) · The Journal of Clinical Endocrinology &amp; Metabolism · doi:10.1210/jc.2013-4254 · Cited by 127 · 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

Cortisol and anxiety response to a relaxing intervention on pregnant women awaiting amniocentesis

Ventura, T., Gomes, M. C., & Carreira, T. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2011.05.016 · Cited by 107 · see citing works

Suppression of the HPA axis during cholestasis can be attributed to hypothalamic bile acid signaling

McMillin, M., Frampton, G., Quinn, M., Divan, A., Grant, S., Patel, N., Newell-Rogers, K., & DeMorrow, S. (2015) · Molecular Endocrinology · doi:10.1210/me.2015-1087 · Cited by 82 · see citing works

Central and peripheral circadian clocks and their role in Alzheimer's disease

Chauhan, R., Chen, K.-F., Kent, B. A., & Crowther, D. C. (2017) · Disease Models &amp; Mechanisms · doi:10.1242/dmm.030627 · Cited by 58 · see citing works

The long-term abnormalities in circadian expression of Period 1 and Period 2 genes in response to stress is normalized by agomelatine administered immediately after exposure

Koresh, O., Kozlovsky, N., Kaplan, Z., Zohar, J., Matar, M. A., & Cohen, H. (2012) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2011.07.012 · Cited by 40 · see citing works

When time stands still: an integrative review on the role of chronodisruption in posttraumatic stress disorder

Agorastos, A., Kellner, M., Baker, D. G., & Otte, C. (2014) · Current Opinion in Psychiatry · doi:10.1097/yco.0000000000000079 · Cited by 33 · see citing works

Stress-Induced Changes in the Expression of the Clock Protein PERIOD1 in the Rat Limbic Forebrain and Hypothalamus: Role of Stress Type, Time of Day, and Predictability

Al-Safadi, S., Al-Safadi, A., Branchaud, M., Rutherford, S., Dayanandan, A., Robinson, B., & Amir, S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0111166 · Cited by 31 · see citing works

Altered Rhythm of Adrenal Clock Genes, StAR and Serum Corticosterone in VIP Receptor 2-Deficient Mice

Fahrenkrug, J., Georg, B., Hannibal, J., & Jørgensen, H. L. (2012) · Journal of Molecular Neuroscience · doi:10.1007/s12031-012-9804-7 · Cited by 27 · see citing works

Study of fecal glucocorticoid metabolites in captive Asian elephants in Kanchanaburi Province, Thailand

Nokkaew, W., Intarapuk, A., Sakulthai, A., Wajjwalku, W., & Thongtip, N. (2022) · Veterinary World · doi:10.14202/vetworld.2022.647-654 · Cited by 3 · see citing works

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 44 · see citing works

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 · see citing works

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 · see citing works

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 54 · see citing works

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 · see citing works