The DOI matches its Crossref record; 44 of the 46 references it cites were found in a registry or an index.
A Differential Response of Two Putative Mammalian Circadian Regulators, mper1and mper2, to Light
Open accessAbstract
A mouse gene, mper1, having all the properties expected of a circadian clock gene, was reported recently. This gene is expressed in a circadian pattern in the suprachiasmatic nucleus (SCN). mper1 maintains this pattern of circadian expression in constant darkness and can be entrained to a new light/dark cycle. Here we report the isolation of a second mammalian gene, mper2, which also has these properties and greater homology to Drosophila period. Expression of mper1 and mper2 is overlapping but asynchronous by 4 hr. mper1, unlike period and mper2, is expressed rapidly after exposure to light at CT22. It appears that mper1 is the pacemaker component which responds to light and thus mediates photic entrainment.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Light exposure during the night phase shifts the clock transcription-translations cycle by rapidly inducing expression of Per1 or Per2, depending on whether the light occurs during the early or late night42–44.”
From Circadian rhythm disruption and mental health (2020) · cites this paper as [42]
Citations
Cites
Molecular Cloning: A Laboratory Manual
Sambrook, J., Fritsch, E., & Maniatis, T. (1989) · UCLA - Biblioteca de Ciencias de la Salud · Cited by 133,589
Basic local alignment search tool
Altschul, S. F., Gish, W., Miller, W., Myers, E. W., & Lipman, D. J. (1990) · Journal of Molecular Biology · doi:10.1006/jmbi.1990.9999 · Cited by 98,669
Clock Mutants of Drosophila melanogaster
Konopka, R. J., & Benzer, S. (1971) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.68.9.2112 · Cited by 2,287
Transplanted Suprachiasmatic Nucleus Determines Circadian Period
Ralph, M. R., Foster, R. G., Davis, F. C., & Menaker, M. (1990) · Science · doi:10.1126/science.2305266 · Cited by 1,853
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
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
Feedback of the Drosophila period gene product on circadian cycling of its messenger RNA levels
Hardin, P. E., Hall, J. C., & Rosbash, M. (1990) · Nature · doi:10.1038/343536a0 · Cited by 1,156
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
Nagase, T. (1998) · DNA Research · doi:10.1093/dnares/5.1.31 · Cited by 844
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
Research works printed but not linked: 1
- Card, J.P., and Moore, R.Y. (1991). The organization of visual circuits influencing the circadian activity of the suprachiasmatic nucleus. In Suprachiasmatic Nucleus: The Mind's Clock, D.C. Klein, R.Y. Moore, and S.M. Reppert, eds. (New York, Oxford University Press) 51–76.
Cited by
Sorted by citations
Items 601–700 of 877
Modeling Reveals a Key Mechanism for Light-Dependent Phase Shifts of Neurospora Circadian Rhythms
Bellman, J., Kim, J. K., Lim, S., & Hong, C. I. (2018) · Biophysical Journal · doi:10.1016/j.bpj.2018.07.029 · Cited by 16
Expression of Tgfα in the suprachiasmatic nuclei of nocturnal and diurnal rodents
Tournier, B. B., Dardente, H., Vuillez, P., Pévet, P., & Challet, É. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2006.12.026 · Cited by 16
Kovačíková, Z., Sládek, M., Laurinová, K., Bendová, Z., Illnerová, H., & Sumová, A. (2005) · Brain Research · doi:10.1016/j.brainres.2005.10.022 · Cited by 17
A novel protein interacts with a clock-related protein, rPer1
Matsuki, T., Kiyama, A., Kawabuchi, M., Okada, M., & Nagai, K. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02857-8 · Cited by 18
5-HT3 receptor-mediated photic-like responses of the circadian clock in the rat
Graff, C., Challet, É., Pévet, P., & Wollnik, F. (2006) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.09.016 · Cited by 16
Light‐Induced Tyrosine Phosphorylation of BIT in the Rat Suprachiasmatic Nucleus
Nakahata, Y., Okumura, N., Shima, T., Okada, M., & Nagai, K. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.0742436.x · Cited by 16
REGγ regulates circadian clock by modulating BMAL1 protein stability
Kubra, S., Zhang, H., Si, Y., Gao, X. C., Wang, T., Pan, L., Li, L., Zhong, N., Fu, J., Zhang, B., et al. (2021) · Cell Death Discovery · doi:10.1038/s41420-021-00704-9 · Cited by 15
Korf, H. (2024) · Cell and Tissue Research · doi:10.1007/s00441-024-03913-7 · Cited by 16
Positive Autoregulation Delays the Expression Phase of Mammalian Clock Gene Per2
Ogawa, Y., Koike, N., Kurosawa, G., Soga, T., Tomita, M., & Tei, H. (2011) · PLoS ONE · doi:10.1371/journal.pone.0018663 · Cited by 15
Time-dependent glucocorticoid administration differently affects peripheral circadian rhythm in rats
Wu, T., & Fu, Z. (2017) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmx115 · Cited by 15
Light Has Diverse Spatiotemporal Molecular Changes in the Mouse Suprachiasmatic Nucleus
Duy, P. Q., Komal, R., Richardson, M. E. S., Hahm, K. S., Fernandez, D. C., & Hattar, S. S. (2020) · Journal of Biological Rhythms · doi:10.1177/0748730420961214 · Cited by 15
Zhu, H., Vadigepalli, R., Rafferty, R., Gonye, G. E., Weaver, D. R., & Schwaber, J. S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037833 · Cited by 15
Lemmer, B. (2006) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/iembs.2006.260857 · Cited by 15
Mechanisms by which circadian rhythm disruption may lead to cancer
Beckett, M., & Roden, L. C. (2010) · South African Journal of Science · doi:10.4102/sajs.v105i11/12.125 · Cited by 14
Sterina, E., Michopoulos, V., Linnstaedt, S. D., Neylan, T. C., Clifford, G. D., Ethun, K. F., Lori, A., Wingo, A. P., ROTHBAUM, B. O., Ressler, K. J., et al. (2022) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2022.105729 · Cited by 14
Rigid Cooperation of Per1 and Per2 proteins
Tamiya, H., Ogawa, S., Ouchi, Y., & Akishita, M. (2016) · Scientific Reports · doi:10.1038/srep32769 · Cited by 16
Period 2: A Regulator of Multiple Tissue-Specific Circadian Functions
Ruggiero, G., Livne, Z. B.-M., Wexler, Y., Geyer, N., Vallone, D., Gothilf, Y., & Foulkes, N. S. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.718387 · Cited by 15
Araki, R., Nakahara, M., Fukumura, R., Takahashi, H., Mori, K., Umeda, N., Sujino, M., Inouye, S. T., & Abe, M. (2006) · Brain Research · doi:10.1016/j.brainres.2006.04.096 · Cited by 14
Caldelas, I., Chimal‐Monroy, J., Martı́nez–Gómez, M., & Hudson, R. (2005) · Biological Rhythm Research · doi:10.1080/09291010400028500 · Cited by 14
A Negative Regulatory Element Required for Light-Dependentpinopsin Gene Expression
Takanaka, Y., Okano, T., Yamamoto, K., & Fukada, Y. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-11-04357.2002 · Cited by 14
Bulla gouldiana period Exhibits Unique Regulation at the mRNA and Protein Levels
Constance, C. M., Green, C. B., Tei, H., & Block, G. D. (2002) · Journal of Biological Rhythms · doi:10.1177/074873002237136 · Cited by 14
Molecular Genetic Basis for Mammalian Circadian Rhythms
Vitaterna, M. H., Pinto, L. H., & Turek, F. W. (2005) · Elsevier eBooks · doi:10.1016/b0-72-160797-7/50037-9 · Cited by 15
Different levels of circadian (de)synchrony – where does it hurt?
Galinde, A. A., Al‐Μughales, F., Oster, H., & Heyde, I. (2022) · F1000Research · doi:10.12688/f1000research.127234.2 · Cited by 13
Circadian Gene Variants in Diseases
Gršković, P., & Korać, P. (2023) · Genes · doi:10.3390/genes14091703 · Cited by 15
Vitaterna, M. H., & Turek, F. W. (2011) · Elsevier eBooks · doi:10.1016/b978-1-4160-6645-3.00012-8 · Cited by 16
Light Input to the Mammalian Circadian Clock
Dannerfjord, A. A., Brown, L. A., Foster, F., & Peirson, S. N. (2020) · Methods in molecular biology · doi:10.1007/978-1-0716-0381-9_18 · Cited by 12
Light-induced changes in the suprachiasmatic nucleus transcriptome regulated by the ERK/MAPK pathway
Alzate‐Correa, D., Aten, S., Campbell, M. J., Hoyt, K. R., & Obrietan, K. H. (2021) · PLoS ONE · doi:10.1371/journal.pone.0249430 · Cited by 14
Wu, T., Dong, Y., Yang, Z., Kato, H., Ni, Y., & Fu, Z. (2009) · Chronobiology International · doi:10.1080/07420520903044208 · Cited by 13
Bering, T., Carstensen, M. B., & Rath, M. F. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.14128 · Cited by 13
Kolker, D. E., Olson, S. L., Dutton-Boilek, J., Bennett, K. M., Wallen, E. P., Horton, T. H., & Turek, F. W. (2002) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00362.2001 · Cited by 13
SCN-AVP release of mPer1/mPer2 double-mutant mice in vitro
van der Veen, D. R., Mulder, G., Oster, H., Gerkema, M. P., & Hut, R. A. (2008) · Journal of Circadian Rhythms · doi:10.1186/1740-3391-6-5 · Cited by 13
Short-term propofol anaesthesia down-regulates clock genes expression in the master clock
Ben‐Hamouda, N., Poirel, V., Dispersyn, G., Pévet, P., Challet, É., & Pain, L. (2018) · Chronobiology International · doi:10.1080/07420528.2018.1499107 · Cited by 13
The circadian gene Clock is required for the correct early expression of the head specific gene Otx2
Morgan, R. (2002) · The International Journal of Developmental Biology · doi:10.1387/ijdb.12533023 · Cited by 13
Meijer, J. H. (2001) · Handbook of behavioral neurobiology · doi:10.1007/978-1-4615-1201-1_8 · Cited by 13
Synchronisation mechanisms of circadian rhythms in the suprachiasmatic nucleus
Li, Y., Liu, Z., Zhang, J., Wang, R., & Chen, L. (2009) · IET Systems Biology · doi:10.1049/iet-syb.2007.0057 · Cited by 12
MAP kinase additively activates the mouse Per1 gene promoter with CaM kinase II
Nomura, K., Takeuchi, Y., & Fukunaga, K. (2006) · Brain Research · doi:10.1016/j.brainres.2006.08.087 · Cited by 12
Dardente, H., Wyse, C. A., Lincoln, G. A., Wagner, G., & Hazlerigg, D. G. (2016) · PLoS ONE · doi:10.1371/journal.pone.0159201 · Cited by 12
Effects of 50 Hz magnetic fields on circadian rhythm control in mice
Lundberg, L., Sienkiewicz, Z. J., Anthony, D. C., & Broom, K. A. (2019) · Bioelectromagnetics · doi:10.1002/bem.22188 · Cited by 12
mPER1‐mediated nuclear export of mCRY1/2 is an important element in establishing circadian rhythm
Loop, S., Katzer, M., & Pieler, T. (2005) · EMBO Reports · doi:10.1038/sj.embor.7400372 · Cited by 12
Making Time: Conservation of Biological Clocks from Fungi to Animals
Dunlap, J., & Loros, J. (2017) · ASM Press eBooks · doi:10.1128/9781555819583.ch24 · Cited by 12
Molecular genetic response to varied wavelengths of light in Xiphophorus maculatus skin
Chang, J. T., Lü, Y., Boswell, W. T., Boswell, M., Caballero, K. L., & Walter, R. B. (2015) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2015.10.002 · Cited by 11
Mood phenotypes in rodent models with circadian disturbances
Imamura, K., & Takumi, T. (2022) · Neurobiology of Sleep and Circadian Rhythms · doi:10.1016/j.nbscr.2022.100083 · Cited by 11
Tamaru, T., Okada, M., Nagai, K., Nakagawa, H., & Takamatsu, K. (1999) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1999.0722191.x · Cited by 11
Ramanathan, C., Campbell, A., Tomczak, A., Nunez, A. A., Smale, L., & Yan, L. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.04.040 · Cited by 11
Epigenetics, Brain and Behavior
Sassone‐Corsi, P., & Christen, Y. (2012) · Research and perspectives in neurosciences · doi:10.1007/978-3-642-27913-3 · Cited by 11
Circadian clock genes in mammalian clockwork, metabolism and behaviour
Kaasik, K. (2005) · DSpace repository (University of Tartu) · Cited by 11
Book Review: Molecular Regulation of Circadian Rhythms in Drosophila and Mammals
Meyer-Bernstein, E. L., & Sehgal, A. (2001) · The Neuroscientist · doi:10.1177/107385840100700606 · Cited by 12
Effect of Brefeldin A on Melatonin Secretion of Chick Pineal Cells
Hirota, T., Kagiwada, S., Kasahara, T., Okano, T., Murata, M., & Fukada, Y. (2001) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a002836 · Cited by 11
Touitou, Y., Cermakian, N., & Touitou, C. (2024) · Chronobiology International · doi:10.1080/07420528.2024.2353857 · Cited by 12
Chakir, I., Dumont, S., Pévet, P., Ouarour, A., Challet, É., & Vuillez, P. (2014) · Brain Research · doi:10.1016/j.brainres.2014.10.063 · Cited by 10
Liška, K., Sládek, M., Houdek, P., Shrestha, N., Lužná, V., Ralph, M. R., & Sumová, A. (2021) · Neuroendocrinology · doi:10.1159/000517689 · Cited by 10
Oligodeoxynucleotide Methods for Analyzing the Circadian Clock in the Suprachiasmatic Nucleus
Tischkau, S. A., & Gillette, M. U. (2005) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(05)93031-0 · Cited by 10
Hepatic gene expression profiling of 5′-AMP-induced hypometabolism in mice
Zhao, Z., Miki, T., Oort-Jansen, A. V., Matsumoto, T., Loose, D. S., & Lee, C. C. (2011) · Physiological Genomics · doi:10.1152/physiolgenomics.00174.2010 · Cited by 11
Self-citationIntroduction to the Clock System
Cox, K. H., & Takahashi, J. S. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-81147-1_1 · Cited by 11
Phase shifts and Per gene expression in mouse suprachiasmatic nucleus
Yan, L., Hochstetler, K. J., Silver, R., & Bult‐Ito, A. (2003) · Neuroreport · doi:10.1097/00001756-200307010-00012 · Cited by 10
Chromatin remodeling and neuronal function: exciting links
Santos, M., Coelho, P. A., & Maciel, P. (2006) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2006.00227.x · Cited by 10
Ouk, K., Aungier, J., Ware, M., & Morton, A. J. (2019) · eNeuro · doi:10.1523/eneuro.0088-19.2019 · Cited by 11
Watanabe, K., Deboer, T., & Meijer, J. H. (2001) · Journal of Biological Rhythms · doi:10.1177/074873001129002259 · Cited by 10
Schibler, U., & Lavery, D. J. (1999) · Springer eBooks · doi:10.1007/978-3-642-59828-9_31 · Cited by 10
Haraguchi, A., Du, Y., Shiraishi, R., Takahashi, Y., Nakamura, T. J., & Shibata, S. (2022) · Sleep and Biological Rhythms · doi:10.1007/s41105-021-00365-2 · Cited by 9
Simultaneous Electrophysiological Recording and Calcium Imaging of Suprachiasmatic Nucleus Neurons
Irwin, R. P., & Allen, C. N. (2013) · Journal of Visualized Experiments · doi:10.3791/50794 · Cited by 9
Tanoue, S., Fujimoto, K., Myung, J., Hatanaka, F., Kato, Y., & Takumi, T. (2015) · Frontiers in Neurology · doi:10.3389/fneur.2015.00166 · Cited by 9
Kernek, K. L., Trofatter, J. A., Mayeda, A. R., Lahiri, D. K., & Hofstetter, J. R. (2006) · Behavior Genetics · doi:10.1007/s10519-005-9032-9 · Cited by 9
Forward genetic approach for behavioral neuroscience using animal models
Funato, H. (2020) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.96.002 · Cited by 9
Dong, Y., Goguen, D., Robertson, H. A., & Rusak, B. (2002) · Neuroscience · doi:10.1016/s0306-4522(01)00609-1 · Cited by 9
Landry, G. J., & Mistlberger, R. E. (2005) · Brain Research · doi:10.1016/j.brainres.2005.08.013 · Cited by 9
Keeping pace with Neurospora circadian rhythms
Bell‐Pedersen, D. (1998) · Microbiology · doi:10.1099/00221287-144-7-1699 · Cited by 8
Depriving Mice of Sleep also Deprives of Food
Đukanović, N., Spada, F. L., Emmenegger, Y., Niederhäuser, G., Preitner, F., & Franken, P. (2022) · Clocks & Sleep · doi:10.3390/clockssleep4010006 · Cited by 9
Bode, B., Rossner, M. J., & Oster, H. (2011) · Chronobiology International · doi:10.3109/07420528.2011.607374 · Cited by 8
Light-dependent effects on mood: Mechanistic insights from animal models
Copenhaver, A. E., Roberts, R. C., & LeGates, T. A. (2022) · Progress in brain research · doi:10.1016/bs.pbr.2022.02.016 · Cited by 8
Nuclear import of mPER3 in Xenopus oocytes and HeLa cells requires complex formation with mPER1
Loop, S., & Pieler, T. (2005) · FEBS Journal · doi:10.1111/j.1742-4658.2005.04798.x · Cited by 8
Zhu, Y. L., Fu, A., Hoffman, A. E., Figueiro, M. G., Carskadon, M. A., Sharkey, K. M., & Rea, M. S. (2013) · Sleep Medicine · doi:10.1016/j.sleep.2012.12.006 · Cited by 8
Circadian-Time Sickness: Time-of-Day Cue-Conflicts Directly Affect Health
van Ee, R., de Cruys, S. V., Schlangen, L. J. M., & Vlaskamp, B. N. S. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2016.09.004 · Cited by 9
Koinuma, S., Kori, H., Tokuda, I. T., Yagita, K., & Shigeyoshi, Y. (2017) · PLoS ONE · doi:10.1371/journal.pone.0181223 · Cited by 8
Cholecystokinin‐2 receptor mediated gene expression in neuronal PC12 cells
Hansen, T. V. O., Borup, R., Marstrand, T. T., Rehfeld, J. F., & Nielsen, F. C. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.05076.x · Cited by 8
High Amplitude Phase Resetting in Rev-Erbα/Per1 Double Mutant Mice
Jud, C., Hayoz, A., & Albrecht, U. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012540 · Cited by 8
Self-citationGènes d'horloge, rythmes circadiens et prise alimentaire
Challet, É. (2007) · Pathologie Biologie · doi:10.1016/j.patbio.2006.12.005 · Cited by 8
Valencia-Sánchez, S., Davis, M., Martensen, J., Hoeffer, C. A., Link, C. D., & Opp, M. R. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.07.027 · Cited by 7
Lu, T., Sun, Y., Ma, Q., Zhu, M., Liu, D., Ma, J., Ma, Y., Chen, H., & Guan, W. (2016) · Molecular Genetics and Genomics · doi:10.1007/s00438-016-1246-4 · Cited by 7
Lalpekhlui, R., Renthlei, Z., & Trivedi, A. K. (2022) · Chronobiology International · doi:10.1080/07420528.2022.2062374 · Cited by 7
Kim, N. N., Shin, H. S., Lee, J., & Choi, C. Y. (2011) · Animal Cells and Systems · doi:10.1080/19768354.2011.611536 · Cited by 7
Turek, F. W., & Kolker, D. E. (2001) · European Neuropsychopharmacology · doi:10.1016/s0924-977x(01)00124-9 · Cited by 7
Rovirosa, L., Ramos-Morales, A., & Javierre, B. M. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.592087 · Cited by 5
Phase and period responses to short light pulses in a wild diurnal rodent,Funambulus pennanti
Kumar, D., & Singaravel, M. (2013) · Chronobiology International · doi:10.3109/07420528.2013.851084 · Cited by 7
The Biological Clock and Its Resetting by Light
Johnsson, A., & Engelmann, W. (2007) · Springer eBooks · doi:10.1007/978-0-387-72655-7_14 · Cited by 7
Álvarez-López, C., Cernuda‐Cernuda, R., Alcorta, E., Álvarez‐Viejo, M., & García-Fernández, J. M. (2004) · Brain Research · doi:10.1016/j.brainres.2004.07.057 · Cited by 7
Overview of Chronopharmaceutics
Youan, B.-B. C. (2009) · Wiley eBooks · doi:10.1002/9780470498392.ch1 · Cited by 7
Yeh, P., Jhan, K.-C., Chua, E.-P., Chen, W.-C., Chu, S., Wu, S., & Chen, S. (2025) · Nature Communications · doi:10.1038/s41467-025-58661-1 · Cited by 6
Diurnal and seasonal molecular rhythms in the human brain and their relation to Alzheimer disease
Lim, A. S. P. (2021) · Handbook of clinical neurology · doi:10.1016/b978-0-12-819975-6.00017-0 · Cited by 6
Zhou, Q., Wang, K., Qiu, J., Zhu, D., Tian, T., Zhang, Y., & Qin, X. (2021) · Open Biology · doi:10.1098/rsob.210140 · Cited by 5
Wendrich, K. S., Azimi, H., Ripperger, J. A., Ravussin, Y., Rainer, G., & Albrecht, U. (2023) · Clocks & Sleep · doi:10.3390/clockssleep5020017 · Cited by 6
Self-citationPačesová, D., Spišská, V., Novotný, J., & Bendová, Z. (2023) · Journal of Neuroscience Research · doi:10.1002/jnr.25236 · Cited by 6
Light, blindness and endocrine secretions
Bellastella, A., Amato, G., Bizzarro, A., Carella, C., Criscuolo, T., Iorio, S., Muccitelli, V. I., Pisano, G., Sinisi, A. A., & Bellis, A. D. (1999) · Journal of Endocrinological Investigation · doi:10.1007/bf03343663 · Cited by 6
Interactive Organization of the Circadian Core Regulators PER2, BMAL1, CLOCK and PML
Miki, T., Zhao, Z., & Lee, C. C. (2016) · Scientific Reports · doi:10.1038/srep29174 · Cited by 6
Self-citationRodent models in translational circadian photobiology
Tir, S., Steel, L. C. E., Tam, S. K. E., Semo, M., Pothecary, C. A., Vyazovskiy, V. V., Foster, F., & Peirson, S. N. (2022) · Progress in brain research · doi:10.1016/bs.pbr.2022.02.015 · Cited by 6
The cell adhesion molecule EphA4 is involved in circadian clock functions
Kießling, S., O’Callaghan, E. K., Freyburger, M., Cermakian, N., & Mongrain, V. (2017) · Genes Brain & Behavior · doi:10.1111/gbb.12387 · Cited by 7
Green, C., & Liu, X. (2002) · Investigative Ophthalmology & Visual Science · Cited by 6
(Too Many) Mathematical Models of Circadian Clocks (?)
Lema, M. A., Echave, J., & Golombek, D. A. (2001) · Biological Rhythm Research · doi:10.1076/brhm.32.2.285.1350 · Cited by 6
Pretzmann, C. P., Fahrenkrug, J., & Georg, B. (2008) · Journal of Molecular Neuroscience · doi:10.1007/s12031-008-9063-9 · Cited by 6
Brenna, A., Borsa, M., Sarò, G., Ripperger, J. A., Glauser, D. A., Yang, Z., Adamantidis, A., & Albrecht, U. (2024) · eLife · doi:10.7554/elife.97029 · Cited by 6
Self-citation
Metadata
- Authors
- Albrecht, U., Sun, Z. S., Eichele, G., & Lee, C. C.
- Affiliations
- Baylor College of Medicine (US)
- Corresponding author
- Lee, Cheng Chi
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 1997-12
- Volume
- 91
- Issue
- 7
- Pages
- 1055-1064
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2151468131
- Cited by
- 879
- References
- 46
- Citations by year
- 2026: 6 · 2025: 7 · 2024: 15 · 2023: 14 · 2022: 16 · 2021: 27 · 2020: 17 · 2019: 20 · 2018: 16 · 2017: 27 · 2016: 27 · 2015: 22 · 2014: 29 · 2013: 28 · 2012: 26
- FWCI
- 15.79
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Light effects on plants
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and Work-Related Fatigue
- Keywords
- mPer1, mPer2, clock genes, light entrainment, suprachiasmatic nucleus, light response, circadian pacemaker
- MeSH terms
- Amino Acid Sequence, Animals, Circadian Rhythm, Light, Male, Mice, Inbred C57BL, Molecular Sequence Data, Nuclear Proteins, Transcription Factors, Gene Expression, DNA, Complementary, Cell Cycle Proteins, Mice, Period Circadian Proteins
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review