Two period Homologs: Circadian Expression and Photic Regulation in the Suprachiasmatic Nuclei

PAUP (phylogenetic analysis using parsimony)

(2008) · Springer eBooks · doi:10.1007/978-1-4020-6754-9_12413 · Cited by 4,424 · 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

Mutagenesis and Mapping of a Mouse Gene, <i>Clock</i> , Essential for Circadian Behavior

Vitaterna, M. H., King, D. P., Chang, A.-M., Kornhauser, J. M., Lowrey, P. L., McDonald, J. D., Dove, W. F., Pinto, L. H., Turek, F. W., & Takahashi, J. S. (1994) · Science · doi:10.1126/science.8171325 · Cited by 1,632 · see citing works

[22] Using CLUSTAL for multiple sequence alignments

Higgins, D. G., Thompson, J., & Gibson, T. J. (1996) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(96)66024-8 · Cited by 1,571 · 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

Positional Cloning of the Mouse Circadian Gene

King, D. P., Zhao, Y., Sangoram, A. M., Wilsbacher, L. D., Tanaka, M., Antoch, M. P., Steeves, T. D. L., Vitaterna, M. H., Kornhauser, J. M., Lowrey, P. L., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)80245-7 · Cited by 1,382 · see citing works

ALSCRIPT: a tool to format multiple sequence alignments

Barton, G. J. (1993) · Protein Engineering Design and Selection · doi:10.1093/protein/6.1.37 · Cited by 1,144 · see citing works

Temporal Organization: Reflections of a Darwinian Clock-Watcher

Pittendrigh, C. S. (1993) · Annual Review of Physiology · doi:10.1146/annurev.ph.55.030193.000313 · Cited by 1,023 · see citing works

Prediction of the Coding Sequences of Unidentified Human Genes. IX. The Complete Sequences of 100 New cDNA Clones from Brain Which Can Code for Large Proteins in vitro

Nagase, T. (1998) · DNA Research · doi:10.1093/dnares/5.1.31 · Cited by 845 · see citing works

Circadian oscillation of a mammalian homologue of the Drosophila period gene

Tei, H., Okamura, H., Shigeyoshi, Y., Fukuhara, C., Ozawa, R., Hirose, M., & Sakaki, Y. (1997) · Nature · doi:10.1038/39086 · Cited by 792 · see citing works

Circadian Rhythms in Cultured Mammalian Retina

Tosini, G., & Menaker, M. (1996) · Science · doi:10.1126/science.272.5260.419 · Cited by 716 · see citing works

RIGUI, a putative mammalian ortholog of the Drosophila period gene.

Sun, Z. S., Albrecht, U., Zhuchenko, O., Bailey, J., Eichele, G., & Lee, C.-C. (1997) · Cell · doi:10.1016/s0092-8674(00)80366-9 · Cited by 706 · see citing works

Functional Identification of the Mouse Circadian Clock Gene by Transgenic BAC Rescue

Antoch, M. P., Song, E.-J., Chang, A., Vitaterna, M. H., Zhao, Y., Wilsbacher, L. D., Sangoram, A. M., King, D. P., Pinto, L. H., & Takahashi, J. S. (1997) · Cell · doi:10.1016/s0092-8674(00)80246-9 · Cited by 665 · see citing works

Independent Photoreceptive Circadian Clocks Throughout Drosophila

Plautz, J. D., Kaneko, M. A. N., Hall, J. C., & Kay, S. A. (1997) · Science · doi:10.1126/science.278.5343.1632 · Cited by 640 · see citing works

Cellular Construction of a Circadian Clock: Period Determination in the Suprachiasmatic Nuclei

Liu, C., Weaver, D. R., Strogatz, S. H., & Reppert, S. M. (1997) · Cell · doi:10.1016/s0092-8674(00)80473-0 · Cited by 508 · see citing works

A light-entrainment mechanism for the Drosophila circadian clock

Zeng, H., Qian, Z., Myers, M. P., & Rosbash, M. (1996) · Nature · doi:10.1038/380129a0 · Cited by 479 · see citing works

Light-Induced Degradation of TIMELESS and Entrainment of the Drosophila Circadian Clock

Myers, M. P., Wager‐Smith, K., Rothenfluh, A., & Young, M. W. (1996) · Science · doi:10.1126/science.271.5256.1736 · Cited by 465 · see citing works

Regulation of the Drosophila Protein Timeless Suggests a Mechanism for Resetting the Circadian Clock by Light

Hunter-Ensor, M., Ousley, A. H., & Sehgal, A. (1996) · Cell · doi:10.1016/s0092-8674(00)81046-6 · Cited by 395 · see citing works

Light-induced resetting of a circadian clock is mediated by a rapid increase in frequency transcript

Crosthwaite, S. K., Loros, J., & Dunlap, J. (1995) · Cell · doi:10.1016/s0092-8674(05)80005-4 · Cited by 358 · see citing works

Expression of the period clock gene within different cell types in the brain of Drosophila adults and mosaic analysis of these cells' influence on circadian behavioral rhythms

Ewer, J., Frisch, B., Hamblen-Coyle, M., et al. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-09-03321.1992 · Cited by 333 · see citing works

Circadian timekeeping in BALB/c and C57BL/6 inbred mouse strains

Schwartz, W., & Zimmerman, P. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-11-03685.1990 · Cited by 315 · see citing works

Resetting the Drosophila Clock by Photic Regulation of PER and a PER-TIM Complex

Lee, C., Parikh, V., Itsukaichi, T., Bae, K., & Edery, I. (1996) · Science · doi:10.1126/science.271.5256.1740 · Cited by 274 · see citing works

A promoterless period gene mediates behavioral rhythmicity and cyclical per expression in a restricted subset of the drosophila nervous system

Frisch, B., Hardin, P. E., Hamblen-Coyle, M. J., et al. (1994) · Neuron · doi:10.1016/0896-6273(94)90212-7 · Cited by 259 · see citing works

Trippings along the trail to the molecular mechanisms of biological clocks

Hall, J. C. (1995) · Trends in Neurosciences · doi:10.1016/0166-2236(95)93908-g · Cited by 242 · see citing works

Circadian Clock Neurons in the Silkmoth Antheraea pernyi: Novel Mechanisms of Period Protein Regulation

Šauman, I., & Reppert, S. M. (1996) · Neuron · doi:10.1016/s0896-6273(00)80220-2 · Cited by 238 · see citing works

Prediction of the Coding Sequences of Unidentified Human Genes. VII. The Complete Sequences of 100 New cDNA Clones from Brain Which Can Code for Large Proteins in vitro

Nagase, T. (1997) · DNA Research · doi:10.1093/dnares/4.2.141 · Cited by 200 · see citing works

Molecular Neurobiology and Genetics of Circadian Rhythms in Mammals

Takahashi, J. S. (1995) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.18.030195.002531 · Cited by 199 · see citing works

Genetic Analysis of Circadian Clocks

Dunlap, J. (1993) · Annual Review of Physiology · doi:10.1146/annurev.ph.55.030193.003343 · Cited by 199 · see citing works

The suprachiasmatic nucleus

Patton, A. P., & Hastings, M. H. (2018) · Current Biology · doi:10.1016/j.cub.2018.06.052 · Cited by 168 · see citing works

Cloning of a structural and functional homolog of the circadian clock gene period from the giant silkmoth antheraea pernyi

Reppert, S. M., Tsai, T., Roca, A. L., & Saumant, I. (1994) · Neuron · doi:10.1016/0896-6273(94)90054-x · Cited by 132 · see citing works

Prediction of the Coding Sequences of Unidentified Human Genes. VIII. 78 New cDNA Clones from Brain Which Code for Large Proteins in vitro

Ishikawa, K.-I. (1997) · DNA Research · doi:10.1093/dnares/4.5.307 · Cited by 106 · see citing works

A1-adenosine receptor gene expression in fetal rat brain

Weaver, D. R. (1996) · Developmental Brain Research · doi:10.1016/s0165-3806(96)80013-7 · Cited by 82 · see citing works

Period Protein Is Necessary for Circadian Control of Egg Hatching Behavior in the Silkmoth Antheraea pernyi

Šauman, I., Tsai, T., Roca, A. L., et al. (1996) · Neuron · doi:10.1016/s0896-6273(00)80221-4 · Cited by 60 · see citing works

Forward Genetic Approach Strikes Gold: Cloning of a Mammalian Clock Gene

Reppert, S. M., & Weaver, D. R. (1997) · Cell · doi:10.1016/s0092-8674(00)80229-9 · Cited by 47 · see citing works

period and timeless Tango: A dance of two clock genes

Reppert, S. M., & Šauman, I. (1995) · Neuron · doi:10.1016/0896-6273(95)90086-1 · Cited by 40 · see citing works

Molecular Bases for Circadian Clocks

Dunlap, J. C. (1999) · Cell · doi:10.1016/s0092-8674(00)80566-8 · Cited by 2,900 · see citing works

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

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

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

Stability, precision, and near-24-hour period of the human circadian pacemaker

Czeisler, C. A., Duffy, J. F., Shanahan, T. L., Brown, E. N., Mitchell, J. F., Rimmer, D. W., Ronda, J. M., Silva, E. J., Allan, J. S., Emens, J. S., et al. (1999) · Science · doi:10.1126/science.284.5423.2177 · Cited by 1,705 · see citing works

mCRY1 and mCRY2 are essential components of the negative limb of the circadian clock feedback loop

Kume, K., Zylka, M. J., Sriram, S., Shearman, L. P., Weaver, D. R., Jin, X., Maywood, E. S., Hastings, M. H., & Reppert, S. M. (1999) · Cell · doi:10.1016/s0092-8674(00)81014-4 · Cited by 1,617 · see citing works

Molecular analysis of mammalian circadian rhythms

Reppert, S. M., & Weaver, D. R. (2001) · Annual Review of Physiology · doi:10.1146/annurev.physiol.63.1.647 · Cited by 1,444 · see citing works

Interacting molecular loops in the mammalian circadian clock

Shearman, L. P., Sriram, S., Weaver, D. R., Maywood, E. S., Chaves, I., Zheng, B., Kume, K., Lee, C. C., van der, G. T. J., Horst, et al. (2000) · Science · doi:10.1126/science.288.5468.1013 · Cited by 1,367 · see citing works

Suprachiasmatic Nucleus: Cell Autonomy and Network Properties

Welsh, D. K., Takahashi, J. S., & Kay, S. A. (2010) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021909-135919 · Cited by 1,216 · see citing works

Circadian rhythm disruption and mental health

Walker, W. H., Walton, J. C., DeVries, A. C., & Nelson, R. J. (2020) · Translational Psychiatry · doi:10.1038/s41398-020-0694-0 · Cited by 1,030 · see citing works

CRY, a Drosophila clock and light-regulated cryptochrome, is a major contributor to circadian rhythm resetting and photosensitivity

Emery, P., So, W. V., Kaneko, M., Hall, J. C., & Rosbash, M. (1998) · Cell · doi:10.1016/s0092-8674(00)81637-2 · Cited by 912 · see citing works

Molecular components of the mammalian circadian clock

Buhr, E. D., & Takahashi, J. S. (2013) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-25950-0_1 · Cited by 738 · see citing works

The mPer2 gene encodes a functional component of the mammalian circadian clock

Zheng, B., Larkin, D. W., Albrecht, U., Sun, Z. S., Sage, M., Eichele, G., Lee, C. C., & Bradley, A. (1999) · Nature · doi:10.1038/22118 · Cited by 718 · see citing works

Differential regulation of mammalian <i>Period</i> genes and circadian rhythmicity by cryptochromes 1 and 2

Vitaterna, M. H., Selby, C. P., Todo, T., Niwa, H., Thompson, C., Fruechte, E. M., Hitomi, K., Thresher, R. J., Ishikawa, T., Miyazaki, J., et al. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.21.12114 · Cited by 690 · 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

The circadian clock: pacemaker and tumour suppressor

Fu, L., & Lee, C. C. (2003) · Nature reviews. Cancer · doi:10.1038/nrc1072 · Cited by 678 · see citing works

Metabolism and cancer: the circadian clock connection

Sahar, S., & Sassone-Corsi, P. (2009) · Nature Reviews Cancer · doi:10.1038/nrc2747 · Cited by 551 · see citing works

Linking neural activity and molecular oscillations in the SCN

Colwell, C. S. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn3086 · Cited by 474 · see citing works

<i>mPer1</i> and <i>mPer2</i> Are Essential for Normal Resetting of the Circadian Clock

Albrecht, U., Zheng, B., Larkin, D., Sun, Z. S., & Lee, C. C. (2001) · Journal of Biological Rhythms · doi:10.1177/074873001129001791 · Cited by 375 · see citing works

Timing of light exposure affects mood and brain circuits

Bedrosian, T. A., & Nelson, R. J. (2017) · Translational Psychiatry · doi:10.1038/tp.2016.262 · Cited by 356 · see citing works

The mammalian clock component PERIOD2 coordinates circadian output by interaction with nuclear receptors

Schmutz, I., Ripperger, J. A., Baeriswyl-Aebischer, S., & Albrecht, U. (2010) · Genes &amp; Development · doi:10.1101/gad.564110 · Cited by 361 · see citing works

Mammalian Per-Arnt-Sim Proteins in Environmental Adaptation

McIntosh, B. E., Hogenesch, J. B., & Bradfield, C. A. (2010) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021909-135922 · Cited by 352 · see citing works

Analysis of clock proteins in mouse SCN demonstrates phylogenetic divergence of the circadian clockwork and resetting mechanisms

Field, M. D., Maywood, E. S., O'Brien, J. A., Weaver, D. R., Reppert, S. M., & Hastings, M. H. (2000) · Neuron · doi:10.1016/s0896-6273(00)80906-x · Cited by 343 · see citing works

Restricted‐feeding‐induced anticipatory activity rhythm is associated with a phase‐shift of the expression of <i>mPer1</i> and <i>mPer2</i> mRNA in the cerebral cortex and hippocampus but not in the suprachiasmatic nucleus of mice

Wakamatsu, H., Yoshinobu, Y., Aida, R., Moriya, T., Akiyama, M., & Shibata, S. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01483.x · Cited by 308 · see citing works

Molecular insights into human daily behavior

Brown, S. A., Kunz, D., Dumas, A., Westermark, P. O., Vanselow, K., Tilmann-Wahnschaffe, A., Herzel, H., & Kramer, A. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0707772105 · Cited by 270 · see citing works

Clock genes, oscillators, and cellular networks in the suprachiasmatic nuclei

Hastings, M. H., & Herzog, E. D. (2004) · Journal of Biological Rhythms · doi:10.1177/0748730404268786 · Cited by 246 · see citing works

Shift Work, Jet Lag, and Female Reproduction

Mahoney, M. M. (2010) · International Journal of Endocrinology · doi:10.1155/2010/813764 · Cited by 209 · see citing works

Differential regulation of mPER1 and mTIM proteins in the mouse suprachiasmatic nuclei: new insights into a core clock mechanism

Hastings, M. H., Field, M. D., Maywood, E. S., Weaver, D. R., & Reppert, S. M. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-12-j0001.1999 · Cited by 166 · see citing works

Estrogen differentially regulates expression of <i>Per1</i> and <i>Per2</i> genes between central and peripheral clocks and between reproductive and nonreproductive tissues in female rats

Nakamura, T. J., Moriya, T., Inoue, S., Shimazoe, T., Watanabe, S., Ebihara, S., & Shinohara, K. (2005) · Journal of Neuroscience Research · doi:10.1002/jnr.20677 · Cited by 165 · 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

Photic Entrainment of the Circadian System

Ashton, A., Foster, R., & Jagannath, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23020729 · Cited by 106 · see citing works

The biological clock of very premature primate infants is responsive to light

Hao, H., & Rivkees, S. A. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.5.2426 · Cited by 93 · see citing works

Differential daily expression of <i>Per1</i> and <i>Per2</i> mRNA in the suprachiasmatic nucleus of fetal and early postnatal mice

Shimomura, H., Moriya, T., Sudo, M., Wakamatsu, H., Akiyama, M., Miyake, Y., & Shibata, S. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2000.01438.x · Cited by 87 · see citing works

The clock gene PER2 and sleep problems: Association with alcohol consumption among Swedish adolescents

Comasco, E., Nordquist, N., Göktürk, C., Åslund, C., Hallman, J., Oreland, L., & Nilsson, K. W. (2010) · Upsala Journal of Medical Sciences · doi:10.3109/03009731003597127 · Cited by 76 · see citing works

Select cognitive deficits in vasoactive intestinal peptide deficient mice

Chaudhury, D., Loh, D. H., Dragich, J. M., Hagopian, A., & Colwell, C. S. (2008) · BMC Neuroscience · doi:10.1186/1471-2202-9-63 · Cited by 73 · see citing works

Strong resetting of the mammalian clock by constant light followed by constant darkness

Chen, R., Seo, D.-O., Bell, E., von Gall, C., & Lee, C. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2191-08.2008 · Cited by 53 · see citing works

Age-related change and its sex differences in histoarchitecture of the hypothalamic suprachiasmatic nucleus of F344/N rats

Tsukahara, S., Tanaka, S., Ishida, K., Hoshi, N., & Kitagawa, H. (2005) · Experimental Gerontology · doi:10.1016/j.exger.2004.10.003 · Cited by 40 · see citing works

Genetics of circadian rhythms

Vitaterna, M. H., Shimomura, K., & Jiang, P. (2019) · Neurologic Clinics · doi:10.1016/j.ncl.2019.05.002 · Cited by 36 · see citing works

Central Circadian Clock Regulates Energy Metabolism

Ding, G., Gong, Y., Eckel-Mahan, K. L., & Sun, Z. (2018) · Advances in Experimental Medicine and Biology · doi:10.1007/978-981-13-1286-1_5 · Cited by 33 · see citing works

Insight into molecular core clock mechanism of embryonic and early postnatal rat suprachiasmatic nucleus

Sládek, M., Sumová, A., Kovačíková, Z., Bendová, Z., Laurinová, K., & Illnerová, H. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401149101 · Cited by 145 · see citing works

Real-Time Recording of Circadian Per1 and Per2 Expression in the Suprachiasmatic Nucleus of Freely Moving Rats

Yamaguchi, Y., Okada, K., Mizuno, T., Ota, T., Yamada, H., Doi, M., Kobayashi, M., Tei, H., Shigeyoshi, Y., & Okamura, H. (2015) · Journal of Biological Rhythms · doi:10.1177/0748730415621412 · Cited by 20 · see citing works

Antibodies for assessing circadian clock proteins in the rodent suprachiasmatic nucleus

LeSauter, J., Lambert, C. M., Robotham, M. R., Model, Z., Silver, R., & Weaver, D. R. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035938 · Cited by 31 · see citing works

Differential daily expression of <i>Per1</i> and <i>Per2</i> mRNA in the suprachiasmatic nucleus of fetal and early postnatal mice

Shimomura, H., Moriya, T., Sudo, M., Wakamatsu, H., Akiyama, M., Miyake, Y., & Shibata, S. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2000.01438.x · Cited by 87 · see citing works

Vasoactive intestinal polypeptide induces per1 and per2 gene expression in the rat suprachiasmatic nucleus late at night

Nielsen, H. S., Hannibal, J., & Fahrenkrug, J. (2002) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01882.x · Cited by 90 · see citing works