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

A retinohypothalamic projection in the rat

Moore, R. Y., & Lenn, N. J. (1972) · The Journal of Comparative Neurology · doi:10.1002/cne.901460102 · Cited by 1,263

Chronobiology

Halberg, F. E. (1969) · Annual Review of Physiology · doi:10.1146/annurev.ph.31.030169.003331 · Cited by 700

Advances in Neuroendocrinology.

Brodish, A. (1963) · JAMA · doi:10.1001/jama.1963.03710120088037 · Cited by 480

Hormone Secretion of the Anterior Pituitary Gland After Physical Interruption of All Nervous Pathways to the Hypophysiotrophic Area

Halász, B., & PUPP, L. (1965) · Endocrinology · doi:10.1210/endo-77-3-553 · Cited by 397

Visual Pathway Mediating Pineal Response to Environmental Light

Moore, R. Y., Heller, A., Wurtman, R. J., & Axelrod, J. (1967) · Science · doi:10.1126/science.155.3759.220 · Cited by 134

Central Control of the Pineal Gland: Visual Pathways

Moore, R. Y., Heller, A., Bhatnager, R. K., Wurtman, R. J., & Axelrod, J. (1968) · Archives of Neurology · doi:10.1001/archneur.1968.00470320110013 · Cited by 115

Adrenocorticotrophic Hormone Secretion in Rats after Partial or Total Deafferentation of the Medial Basal Hypothalamus

Halász, B., Slusher, M. A., & Gorski, R. A. (2008) · Neuroendocrinology · doi:10.1159/000121528 · Cited by 105

Effects of Light and Visual Stimuli on Endocrine Function

Wurtman, R. J. (1967) · Neuroendocrinology · doi:10.1016/b978-1-4832-3229-4.50009-9 · Cited by 80

Fluorimetric Analysis of Corticoids

SILBER, R. H. (1966) · Methods of biochemical analysis · doi:10.1002/9780470110324.ch3 · Cited by 60

Behavioral and neuroendocrine responses to light mediated by separate visual pathways in the rat

Chase, P. A., Seiden, L. S., & Moore, R. Y. (1969) · Physiology & Behavior · doi:10.1016/0031-9384(69)90046-8 · Cited by 18

Chronopharmaceutics: Pharmaceutics Focused on Biological Rhythm

Ohdo, S. (2010) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.33.159 · Cited by 51

Circadian rhythm in light response in suprachiasmatic nucleus neurons of freely moving rats

Meijer, J. H., Watanabe, K., Détári, L., & Schaap, J. (1996) · Brain Research · doi:10.1016/s0006-8993(96)01091-8 · Cited by 51

Persistence of nonphotic phase shifts in hamsters after serotonin depletion in the suprachiasmatic nucleus

Bobrzynska, K. J., Vrang, N., & Mrosovsky, N. (1996) · Brain Research · doi:10.1016/s0006-8993(96)00913-4 · Cited by 51

Changes in 24-hour fluctuations of feeding behavior during hypothalamic hyperphagia in rats

Rietveld, W. J., ten Hoor, F., Kooij, M., & Flory, W. (1978) · Physiology & Behavior · doi:10.1016/0031-9384(78)90139-7 · Cited by 51

The Mammalian Circadian Time-Keeping System

Patton, A. P., & Hastings, M. H. (2023) · Journal of Huntington s Disease · doi:10.3233/jhd-230571 · Cited by 50

Chrononutrition: Use of dissociated day/night infant milk formulas to improve the development of the wake–sleep rhythms. Effects of tryptophan

Aparicio, S., Garau, C., Esteban, S., Nicolau, M. C., Rivero, M., & Rial, R. V. (2007) · Nutritional Neuroscience · doi:10.1080/10284150701455916 · Cited by 50

Chapter 27 Peptidergic transmitters of the suprachiasmatic nuclei and the control of circadian rhythmicity

Kalsbeek, A., & Buijs, R. M. (1992) · Progress in brain research · doi:10.1016/s0079-6123(08)61186-3 · Cited by 50

Synaptic input from the retina to the suprachiasmatic nucleus changes with the light‐dark cycle in the Syrian hamster.

Cui, L.-N., & Dyball, R. (1996) · Journal of Physiology · doi:10.1113/jphysiol.1996.sp021782 · Cited by 48

Adipose tissue, adipocytes and the circadian timing system

Johnston, J. D., Frost, G. S., & Otway, D. T. (2009) · Obesity Reviews · doi:10.1111/j.1467-789x.2009.00665.x · Cited by 49

The Suprachiasmatic Nucleus at 50: Looking Back, Then Looking Forward

Ono, D., Weaver, D. R., Hastings, M. H., Honma, K., Honma, S., & Silver, R. (2024) · Journal of Biological Rhythms · doi:10.1177/07487304231225706 · Cited by 53

Hippocampal spine changes across the sleep–wake cycle: corticosterone and kinases

Ikeda, M., Hojo, Y., Komatsuzaki, Y., Okamoto, M., Kato, A., Takeda, T., & Kawato, S. (2015) · Journal of Endocrinology · doi:10.1530/joe-15-0078 · Cited by 49

Cancer Clocks Out for Lunch: Disruption of Circadian Rhythm and Metabolic Oscillation in Cancer

Altman, B. J. (2016) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2016.00062 · Cited by 54

Hypothalamic Dysfunction in Obesity and Metabolic Disorders

Carmo‐Silva, S., & Cavadas, C. (2017) · Advances in neurobiology · doi:10.1007/978-3-319-63260-5_4 · Cited by 53

Multimodal Regulation of Circadian Glucocorticoid Rhythm by Central and Adrenal Clocks

Son, G. H., Cha, H. K., Chung, S., & Kim, K. (2018) · Journal of the Endocrine Society · doi:10.1210/js.2018-00021 · Cited by 49

Biological clock dysfunction exacerbates contact hypersensitivity in mice

Takita, E., Yokota, S., Tahara, Y., Hirao, A., Aoki, N., Nakamura, Y., Nakao, A., & Shibata, S. (2012) · British Journal of Dermatology · doi:10.1111/j.1365-2133.2012.11176.x · Cited by 49

Circadian Rhythms in the Endocrine System

Kriegsfeld, L. J., LeSauter, J., Hamada, T., Pitts, S., & Silver, R. (2002) · Elsevier eBooks · doi:10.1016/b978-012532104-4/50020-2 · Cited by 50

Calcium Dynamics and Circadian Rhythms in Suprachiasmatic Nucleus Neurons

Ikeda, M. (2004) · The Neuroscientist · doi:10.1177/10738584031262149 · Cited by 49

Photoperiod Regulates Corticosterone Rhythms by Altered Adrenal Sensitivity via Melatonin-Independent Mechanisms in Fischer 344 Rats and C57BL/6J Mice

Otsuka, T., Goto, M., Kawai, M., Togo, Y., Sato, K., Katoh, K., Furuse, M., & Yasuo, S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0039090 · Cited by 49

Developing Mathematical Models of Neurobehavioral Performance for the “Real World”

Dean, D. A., Fletcher, A., Hursh, S. R., & Klerman, E. B. (2007) · Journal of Biological Rhythms · doi:10.1177/0748730407301376 · Cited by 49

Suprachiasmatic Nucleus

Moore, R. Y., & Leak, R. K. (2001) · Handbook of behavioral neurobiology · doi:10.1007/978-1-4615-1201-1_7 · Cited by 49

Suprachiasmatic nucleus in a patient with multiple system atrophy with abnormal circadian rhythm of arginine-vasopressin secretion into plasma

Ozawa, T., Oyanagi, K., Tanaka, H., Horikawa, Y., Takahashi, H., Morita, T., & Tsuji, S. (1998) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(97)00210-4 · Cited by 49

Circadian rhythm hypotheses of mixed features, antidepressant treatment resistance, and manic switching in bipolar disorder

Lee, H.-J., Son, G.-H., & Geum, D. (2013) · Psychiatry Investigation · doi:10.4306/pi.2013.10.3.225 · Cited by 48

Dysfunction of circadian and sleep rhythms in the early stages of Alzheimer's disease

Rigat, L., Ouk, K., Kramer, A., & Priller, J. (2023) · Acta Physiologica · doi:10.1111/apha.13970 · Cited by 50

The REV-ERB Nuclear Receptors: Timekeepers for the Core Clock Period and Metabolism

Adlanmérini, M., & Lazar, M. A. (2023) · Endocrinology · doi:10.1210/endocr/bqad069 · Cited by 54

Activity Patterns and the Biological Clock in Mammals

Bartness, T. J., & Albers, H. E. (2000) · Ecological studies · doi:10.1007/978-3-642-18264-8_3 · Cited by 48

Central and peripheral regulation of feeding and nutrition by the mammalian circadian clock

Cassone, V. M., & Stephan, F. K. (2002) · Nutrition · doi:10.1016/s0899-9007(02)00937-1 · Cited by 48

Sleep Pharmacogenetics: Personalized Sleep-Wake Therapy

Holst, S. C., Valomon, A., & Landolt, H. (2015) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-010715-103801 · Cited by 48

Absence of Normal Photic Integration in the Circadian Visual System: Response to Millisecond Light Flashes

Vidal, L., & Morin, L. P. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.5496-06.2007 · Cited by 49

Vestibular loss disrupts daily rhythm in rats

Martin, T., Mauvieux, B., Bulla, J., Quarck, G., Davenne, D., Denise, P., Philoxène, B., & Besnard, S. (2014) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00811.2014 · Cited by 48

Paradoxical function of orexin/hypocretin circuits in a mouse model of Huntington's disease

Williams, R. H., Morton, A. J., & Burdakov, D. (2011) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.02.006 · Cited by 49

Circadian system of mice integrates brief light stimuli

van den Pol, A. N., Cao, V. H., & Heller, H. C. (1998) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1998.275.2.r654 · Cited by 48

Long-term monitoring of circadian rhythms in c-fos gene expression from suprachiasmatic nucleus cultures

Geusz, M. E., Fletcher, C., Block, G. D., Straume, M., Copeland, N. G., Jenkins, N. A., Kay, S. A., & Day, R. N. (1997) · Current Biology · doi:10.1016/s0960-9822(06)00334-4 · Cited by 48

Structural features of the retinohypothalamic projection in the rat during normal development

Mason, C. A., Sparrow, N., & Lincoln, D. W. (1977) · Brain Research · doi:10.1016/0006-8993(77)90711-9 · Cited by 48

The diurnal rhythm in adrenocorticotropin responses to restraint in adrenalectomized rats is determined by caloric intake

Hanson, E. S., BRADBURY, M. J., Akana, S. F., SCRIBNER, K. S., Strack, A. M., & Dallman, M. F. (1994) · Endocrinology · doi:10.1210/endo.134.5.8156924 · Cited by 48

Time is of the essence: Coupling sleep-wake and circadian neurobiology to the antidepressant effects of ketamine

Kohtala, S., Alitalo, O., Rosenholm, M., Rozov, S. V., & Rantamäki, T. (2020) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2020.107741 · Cited by 47

The molecular clockwork of mammalian cells

Yi, J. S., Díaz, N. M., D’Souza, S. P., & Buhr, E. D. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.03.012 · Cited by 51

The circadian protein BMAL1 supports endothelial cell cycle during angiogenesis

Astone, M., Oberkersch, R. E., Tosi, G., Biscontin, A., & Santoro, M. M. (2023) · Cardiovascular Research · doi:10.1093/cvr/cvad057 · Cited by 49

Altered sleep and behavioral activity phenotypes in PER3-deficient mice

Hasan, S., van der Veen, D. R., Winsky‐Sommerer, R., Dijk, D., & Archer, S. N. (2011) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00260.2011 · Cited by 50

Circadian Insights into Motivated Behavior

Antle, M. C., & Silver, R. (2015) · Current topics in behavioral neurosciences · doi:10.1007/7854_2015_384 · Cited by 47

Early onset of behavioral alterations in senescence-accelerated mouse prone 8 (SAMP8)

Yanai, S., & Endo, S. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.04.026 · Cited by 47

The control of circadian rhythms and the levels of vasoactive intestinal peptide mRNA in the suprachiasmatic nucleus are altered in spontaneously hypertensive rats

Peters, R. V., Zoeller, R. T., Hennessey, A. C., Stopa, E. G., Anderson, G. P., & Albers, H. E. (1994) · Brain Research · doi:10.1016/0006-8993(94)91733-7 · Cited by 47

Circadian and Homeostatic Factors in Arousal

Silver, R., & LeSauter, J. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1417.032 · Cited by 48

Preservation of nucleus basalis neurons containing choline acetyltransferase and the vesicular acetylcholine transporter in the elderly with mild cognitive impairment and early Alzheimer's disease

Gilmor, M. L., Erickson, J. D., Varoqui, H., Hersh, L. B., Bennett, D. A., Cochran, E. J., Mufson, E. J., & Levey, A. I. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990906)411:4 · Cited by 243

Corticosterone-dependent driving influence of the suprachiasmatic nucleus on adrenal sensitivity to ACTH

Ciocca, D., Maurel, D., & Bosler, O. (2002) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00287.2001 · Cited by 47

The role of efferent connections of the suprachiasmatic nucleus in the control of circadian rhythms

Núñez, A. A., & Casati, M. J. (1979) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(79)90623-x · Cited by 47

Effects of genetically altered brain glucocorticoid receptor action on behavior and adrenal axis regulation in mice

Howell, M. P., & Muglia, L. J. (2006) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2006.05.001 · Cited by 46

Chronopharmacological strategies: Intra- and inter-individual variability of molecular clock☆

Ohdo, S., Koyanagi, S., & Matsunaga, N. (2010) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2010.04.005 · Cited by 47

Developmental and circadian changes in Ca2+ mobilization mediated by GABAA and NMDA receptors in the suprachiasmatic nucleus

Ikeda, M., Yoshioka, T., & Allen, C. N. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02427.x · Cited by 46

Additional evidence that the suprachiasmatic nucleus is the center for regulation of insulin secretion and glucose homeostasis

Yamamoto, H., Nagai, K., & Nakagawa, H. (1984) · Brain Research · doi:10.1016/0006-8993(84)90326-3 · Cited by 46

Circadian rhythm of adenosine-3',5'-monophosphate content in suprachiasmatic nucleus (SCN) and ventromedial hypothalamus (VMH) in the rat.

Murakami, N., & Takahashi, K. (1983) · Brain Research · doi:10.1016/0006-8993(83)90737-0 · Cited by 47

New Insights into the Diurnal Rhythmicity of Gut Microbiota and Its Crosstalk with Host Circadian Rhythm

Wang, H., Zhang, H., & Su, Y. (2022) · Animals · doi:10.3390/ani12131677 · Cited by 48

Projections of the suprachiasmatic nucleus and ventral subparaventricular zone in the Nile grass rat (Arvicanthis niloticus)

Schwartz, M. D., Urbanski, H. F., Núñez, A. A., & Smale, L. (2010) · Brain Research · doi:10.1016/j.brainres.2010.10.058 · Cited by 45

From clock to functional pacemaker

Michel, S. H., & Meijer, J. H. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14388 · Cited by 50

Multifaceted Control of GR Signaling and Its Impact on Hepatic Transcriptional Networks and Metabolism

Præstholm, S. M., Correia, C. M., & Grøntved, L. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.572981 · Cited by 45

Circadian clock synchrony and chronotherapy opportunities in cancer treatment

Damato, A. R., & Herzog, E. D. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.07.017 · Cited by 45

Labeling of human retinohypothalamic tract with the carbocyanine dye, DiI

Friedman, D. I., Johnson, J., Chorsky, R. L., & Stopa, E. G. (1991) · Brain Research · doi:10.1016/0006-8993(91)91246-w · Cited by 45

The retinohypothalamic tract in the cat: retinal ganglion cell morphology and pattern of projection

Murakami, D. M., Miller, J. D., & Fuller, C. A. (1989) · Brain Research · doi:10.1016/0006-8993(89)91191-8 · Cited by 45

Circadian locomotor rhythms in the desert iguana

Janik, D., Pickard, G. E., & Menaker, M. (1990) · Journal of Comparative Physiology A · doi:10.1007/bf00187327 · Cited by 45

The suprachiasmatic nucleus synchronizes growth hormone secretory rhythms with the light-dark cycle

Willoughby, J. O., & Martin, J. B. (1978) · Brain Research · doi:10.1016/0006-8993(78)90899-5 · Cited by 45

Circadian-independent light regulation of mammalian metabolism

Rao, F., & Xue, T. (2024) · Nature Metabolism · doi:10.1038/s42255-024-01051-6 · Cited by 46

Tissue‐type plasminogen activator‐plasmin‐BDNF modulate glutamate‐induced phase‐shifts of the mouse suprachiasmatic circadian clock in vitro

Mou, X., Peterson, C. B., & Prosser, R. A. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06946.x · Cited by 44

Bmal1Is an Essential Regulator for Circadian Cytosolic Ca2+Rhythms in Suprachiasmatic Nucleus Neurons

Ikeda, M., & Ikeda, M. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.5158-13.2014 · Cited by 44

Circadian clock signals in the adrenal cortex

Ota, T., Fustin, J., Yamada, H., Doi, M., & Okamura, H. (2011) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2011.08.010 · Cited by 44

Age-Related Sleep Disruption and Reduction in the Circadian Rhythm of Urine Output: Contribution to Nocturia?

Duffy, J. F., Scheuermaier, K. D., & Loughlin, K. R. (2015) · Current Aging Science · doi:10.2174/1874609809666151130220343 · Cited by 44

The stability of the transcriptome during the estrous cycle in four regions of the mouse brain

DiCarlo, L. M., Vied, C., & Nowakowski, R. S. (2017) · The Journal of Comparative Neurology · doi:10.1002/cne.24282 · Cited by 45

Neurobehavioral Performance in Young Adults Living on a 28-h Day for 6 Weeks

Lee, J. H., Wang, W., Silva, E. J., Chang, A., Scheuermaier, K. D., Cain, S. W., & Duffy, J. F. (2009) · SLEEP · doi:10.1093/sleep/32.7.905 · Cited by 44

Clock gene defect disrupts light-dependency of autonomic nerve activity

Ikeda, H., Yong, Q., Kurose, T., Todo, T., Mizunoya, W., Fushiki, T., Seino, Y., & Yamada, Y. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.10.058 · Cited by 44

Representation of time in time-place learning

Pizzo, M. J., & Crystal, J. D. (2002) · Animal Learning & Behavior · doi:10.3758/bf03195963 · Cited by 44

Circadian and Seasonal Variations of Plasma Insulin and Cortisol Concentrations in the Syrian Hamster,Mesocricetus Auratus

de Souza, C. J., & MEIER, A. H. (1987) · Chronobiology International · doi:10.3109/07420528709078520 · Cited by 44

Circadian Food Anticipation Persists in Capsaicin Deafferented Rats

Davidson, A. J., & Stephan, F. K. (1998) · Journal of Biological Rhythms · doi:10.1177/074873049801300507 · Cited by 44

Ontogenesis of circadian sleep-wakefulness rhythms and developmental changes of sleep in the altricial rat and in the precocial guinea pig.

Ibuka, N. (1984) · Behavioural Brain Research · doi:10.1016/0166-4328(84)90210-9 · Cited by 46

Rest-activity rhythm of the blind mole rat Spalax ehrenbergi under different lighting conditions

Tobler, I., Herrmann, M., Cooper, H. M., Negroni, J., Nevo, E., & Achermann, P. (1998) · Behavioural Brain Research · doi:10.1016/s0166-4328(98)00012-6 · Cited by 44

Physiology and regulation of biological rhythms in laboratory animals: an overview

Wollnik, F. (1989) · Laboratory Animals · doi:10.1258/002367789780863538 · Cited by 44

Participation of limbic-hypothalamic structures in circadian rhythm of slow wave sleep and paradoxical sleep in the rat

Yamaoka, S. (1978) · Brain Research · doi:10.1016/0006-8993(78)90883-1 · Cited by 44

Effects of suprachiasmatic lesions on circadian rhythms of blood pressure, heart rate and locomotor activity in the rat.

Sano, H., Hayashi, H., Makino, M., Takezawa, H., Hirai, M., Saito, H., & Ebihara, S. (1995) · Japanese circulation journal · doi:10.1253/jcj.59.565 · Cited by 49

Resetting the Dynamic Range of Hypothalamic‐Pituitary‐Adrenal Axis Stress Responses Through Pregnancy

Brunton, P. J. (2010) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2010.02067.x · Cited by 43

Sleep Health Education in Pediatric Community Settings: Rationale and Practical Suggestions for Incorporating Healthy Sleep Education into Pediatric Practice

Gruber, R., Cassoff, J., & Knaüper, B. (2011) · Pediatric Clinics of North America · doi:10.1016/j.pcl.2011.03.006 · Cited by 47

Mis-expression of the BK K+ channel disrupts suprachiasmatic nucleus circuit rhythmicity and alters clock-controlled behavior

Montgomery, J. R., Whitt, J. P., Wright, B. N., Lai, M. H., & Meredith, A. L. (2012) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00302.2012 · Cited by 44

Keeping Up With the Clock

Covassin, N., Singh, P., & Somers, V. K. (2016) · Hypertension · doi:10.1161/hypertensionaha.116.06588 · Cited by 44

Photoperiod-Induced Neuroplasticity in the Circadian System

Porcu, A., Riddle, M., Dulcis, D., & Welsh, D. K. (2018) · Neural Plasticity · doi:10.1155/2018/5147585 · Cited by 44

Extracellular Vesicles: Potential Participants in Circadian Rhythm Synchronization

Tao, S., & Guo, S. (2018) · International Journal of Biological Sciences · doi:10.7150/ijbs.26518 · Cited by 44

Circadian control of neuroendocrine function: implications for health and disease

Gotlieb, N., Moeller, J., & Kriegsfeld, L. J. (2018) · Current Opinion in Physiology · doi:10.1016/j.cophys.2018.11.001 · Cited by 43

Prevalence of allergic rhinitis and its impact on the use of emergency care services in a group of children and adolescents with moderate to severe persistent asthma

Lasmar, L. M. L. B. F., Camargos, P. A. M., Ordones, A. B., Gaspar, G. R., Campos, E. G., & Ribeiro, G. A. (2007) · Jornal de Pediatria · doi:10.2223/jped.1727 · Cited by 45

Methamphetamine induced locomotor rhythm entrains to restricted daily feeding in SCN lesioned rats

Honma, S., Honma, K., & Hiroshige, T. (1989) · Physiology & Behavior · doi:10.1016/0031-9384(89)90237-0 · Cited by 43

Measuring Seasonal Time within the Circadian System: Regulation of the Suprachiasmatic Nuclei by Photoperiod

Johnston, J. D. (2005) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2005.01326.x · Cited by 45

Bilateral lesions of suprachiasmatic nuclei affect circadian rhythms in [3H]‐thymidine incorporation into deoxyribonucleic acid in mouse intestinal tract, mitotic index of corneal epithelium, and serum corticosterone

Scheving, L. E., Tsai, T. H., Powell, E. W., Pasley, J. N., Franz Halberg, A., & Dunn, J. (1983) · The Anatomical Record · doi:10.1002/ar.1092050302 · Cited by 43

VIP‐ and CCK‐like‐immunoreactive neurons in the hedgehog (Erinaceus europaeus) and Sheep (Ovis aries) brain

Antonopoulos, J., Papadopoulos, G. C., Karamanlidis, A. N., Parnavelas, J. G., Dinopoulos, A., & Michaloudi, H. C. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902630211 · Cited by 42

ROLE OF THE SUPRACHIASMATIC NUCLEUS IN GLUCOSE HOMEOSTASIS

Yamamoto, H., Nagai, K., & Nakagawa, H. (1984) · Biomedical Research · doi:10.2220/biomedres.5.55 · Cited by 43

Thetau mutation shortens the period of rhythmic photoreceptor outer segment disk shedding in the hamster

Grace, M. S., Wang, L. A., Pickard, G. E., Besharse, J. C., & Menaker, M. (1996) · Brain Research · doi:10.1016/0006-8993(96)00600-2 · Cited by 42

Cholecystokinin neurons in mouse suprachiasmatic nucleus regulate the robustness of circadian clock

Xie, L., Xiong, Y., Ma, D., Shi, K., Chen, J., Yang, Q., & Yan, J. (2023) · Neuron · doi:10.1016/j.neuron.2023.04.016 · Cited by 42

The stress of losing sleep: Sex-specific neurobiological outcomes

Wright, C. J., Milosavljevic, S., & Pocivavsek, A. (2023) · Neurobiology of Stress · doi:10.1016/j.ynstr.2023.100543 · Cited by 47

Circadian Oscillations of Molecular Clock Components in the Cerebellar Cortex of the Rat

Rath, M. F., Rohde, K., & Møller, M. (2012) · Chronobiology International · doi:10.3109/07420528.2012.728660 · Cited by 42

Effects of early weaning on the circadian rhythm and behavioral satiety sequence in rats

Oliveira, L. D. S., da Silva, L. P., da Silva, A. I., Magalhães, C. P., de Souza, S. L., & Manhães‐de‐Castro, R. (2010) · Behavioural Processes · doi:10.1016/j.beproc.2010.10.001 · Cited by 43

Biological rhythms, chronodisruption and chrono-enhancement: The role of physical activity as synchronizer in correcting steroids circadian rhythm in metabolic dysfunctions and cancer

Vitale, J. A., Lombardi, G., Weydahl, A., & Banfi, G. (2018) · Chronobiology International · doi:10.1080/07420528.2018.1475395 · Cited by 43

Potential Pathways for Circadian Dysfunction and Sundowning-Related Behavioral Aggression in Alzheimer’s Disease and Related Dementias

Todd, W. D. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00910 · Cited by 46

Characterizing the behavioral and neuroendocrine features of susceptibility and resilience to social stress

Murra, D., Hilde, K. L., Fitzpatrick, A., Maras, P. M., Watson, S. J., & Akil, H. (2022) · Neurobiology of Stress · doi:10.1016/j.ynstr.2022.100437 · Cited by 48

Food-anticipatory activity persists after olfactory bulb ablation in the rat

Davidson, A. J., Aragona, B. J., Werner, R. M., Schroeder, E., Smith, J. C., & Stephan, F. K. (2001) · Physiology & Behavior · doi:10.1016/s0031-9384(00)00417-0 · Cited by 42

Circadian modulation of conditioned place avoidance in hamsters does not require the suprachiasmatic nucleus

Cain, S. W., & Ralph, M. R. (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.10.005 · Cited by 42

Melatonin, cortisol and body temperature rhythms in Lennox-Gastaut patients with or without circadian rhythm sleep disorders

Laakso, M. L., Leinonen, L. M., H�t�nen, T., Alila, A., & Heiskala, H. J. (1993) · Journal of Neurology · doi:10.1007/bf00867353 · Cited by 42

Melatonin and corticosterone regulation: Feeding time or the light:Dark cycle?

Holloway, W. R., Tsui, H. W., Grota, L. J., & Brown, G. M. (1979) · Life Sciences · doi:10.1016/0024-3205(79)90431-4 · Cited by 42

Reanalysis of primate brain circadian transcriptomics reveals connectivity-related oscillations

Lee, J., Chen, S., Monfared, R. V., Derdeyn, P., Leong, K., Chang, T. Y., Beier, K. T., Baldi, P., & Alachkar, A. (2023) · iScience · doi:10.1016/j.isci.2023.107810 · Cited by 8

Large‐scale analysis reveals spatiotemporal circadian patterns of cilia transcriptomes in the primate brain

Baldi, P., Alhassen, W., Chen, S., Nguyen, H. N., Khoudari, M., & Alachkar, A. (2021) · Journal of Neuroscience Research · doi:10.1002/jnr.24919 · Cited by 12

Identification of putative rat ribonuclease III by differential display: a novel rat mRNA expressed in a circadian manner in the rat suprachiasmatic nucleus

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Circadian rhythms and different photoresponses of Clock gene transcription in the rat suprachiasmatic nucleus and pineal gland.

Wang, G., Chun-ling, F., Li, J., Du, Y., & Tong, J. (2006) · PubMed · Cited by 2

Diurnal Patterns of Gene Expression in the Dorsal Vagal Complex and the Central Nucleus of the Amygdala – Non-rhythm-generating Brain Regions

Staehle, M. M., O’Sullivan, S. J., Vadigepalli, R., Kernan, K. F., Gonye, G. E., Ogunnaike, B. A., & Schwaber, J. S. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00375 · Cited by 7