Lunar phase-dependent expression of cryptochrome and a photoperiodic mechanism for lunar phase-recognition in a reef fish, goldlined spinefoot

The neighbor-joining method: a new method for reconstructing phylogenetic trees.

Saitou, N., & Nei, M. (1987) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a040454 · Cited by 59,962 · see citing works

The cryb mutation identifies cryptochrome as a circadian photoreceptor in Drosophila

Stanewsky, R., Kaneko, M., Emery, P., Beretta, B., Wager-Smith, K., Kay, S. A., Rosbash, M., & Hall, J. C. (1998) · Cell · doi:10.1016/s0092-8674(00)81638-4 · Cited by 968 · 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

Mass spawning in tropical reef corals

Harrison, P. L., Babcock, R. C., Bull, G. D., Oliver, J. K., Wallace, C. C., & Willis, B. L. (1984) · Science · doi:10.1126/science.223.4641.1186 · Cited by 763 · see citing works

Light-Independent Role of CRY1 and CRY2 in the Mammalian Circadian Clock

Griffin, E. A., Staknis, D., & Weitz, C. J. (1999) · Science · doi:10.1126/science.286.5440.768 · Cited by 646 · see citing works

Light-Dependent Sequestration of TIMELESS by CRYPTOCHROME

Ceriani, M. F., Darlington, T. K., Staknis, D., Más, P., Petti, A. A., Weitz, C. J., & Kay, S. A. (1999) · Science · doi:10.1126/science.285.5427.553 · Cited by 565 · see citing works

Pinopsin is a chicken pineal photoreceptive molecule

Okano, T., Yoshizawa, T., & Fukada, Y. (1994) · Nature · doi:10.1038/372094a0 · Cited by 352 · see citing works

A mammalian neural tissue opsin (Opsin 5) is a deep brain photoreceptor in birds

Nakane, Y., Ikegami, K., Ono, H., Yamamoto, N., Yoshida, S., Hirunagi, K., Ebihara, S., Kubo, Y., & Yoshimura, T. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1006393107 · Cited by 343 · see citing works

Roles of the Two Drosophila CRYPTOCHROME Structural Domains in Circadian Photoreception

Busza, A. C., Emery-Le, M., Rosbash, M., & Emery, P. (2004) · Science · doi:10.1126/science.1096973 · Cited by 292 · see citing works

Putative Human Blue-Light Photoreceptors hCRY1 and hCRY2 Are Flavoproteins

Hsu, D. S., Zhao, X., Zhao, S., Kazantsev, A., Wang, R.-P., Todo, T., Wei, Y.-F., & Sancar, A. (1996) · Biochemistry · doi:10.1021/bi962209o · Cited by 291 · see citing works

Encephalopsin: A Novel Mammalian Extraretinal Opsin Discretely Localized in the Brain

Blackshaw, S., & Snyder, S. H. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-10-03681.1999 · Cited by 283 · see citing works

Delay in Feedback Repression by Cryptochrome 1 Is Required for Circadian Clock Function

Ukai‐Tadenuma, M., Yamada, R. G., Xu, H., Ripperger, J. A., Liu, A. C., & Ueda, H. R. (2011) · Cell · doi:10.1016/j.cell.2010.12.019 · Cited by 264 · see citing works

Light-Responsive Cryptochromes from a Simple Multicellular Animal, the Coral <i>Acropora millepora</i>

Levy, O., Appelbaum, L., Leggat, W., Gothlif, Y., Hayward, D. C., Miller, D. J., & Hoegh-Guldberg, O. (2007) · Science · doi:10.1126/science.1145432 · Cited by 263 · see citing works

Molecular and phylogenetic analyses reveal mammalian-like clockwork in the honey bee (<i>Apis mellifera</i>) and shed new light on the molecular evolution of the circadian clock

Rubin, E. B., Shemesh, Y., Cohen, M., Elgavish, S., Robertson, H. M., & Bloch, G. (2006) · Genome Research · doi:10.1101/gr.5094806 · Cited by 257 · see citing works

Similarity Among the Drosophila (6-4)Photolyase, a Human Photolyase Homolog, and the DNA Photolyase-Blue-Light Photoreceptor Family

Todo, T., Ryo, H., Yamamoto, K., Toh, H., Inui, T., Ayaki, H., Nomura, T., & Ikenaga, M. (1996) · Science · doi:10.1126/science.272.5258.109 · Cited by 247 · see citing works

Human cryptochrome exhibits light-dependent magnetosensitivity

Foley, L. E., Gegear, R. J., & Reppert, S. M. (2011) · Nature Communications · doi:10.1038/ncomms1364 · Cited by 214 · see citing works

Biological rhythms in the marine environment

DeCoursey, P. J. (1976) · Medical Entomology and Zoology · Cited by 207 · see citing works

Lunar cycles and reproductive activity in reef fishes with particular attention to rabbitfishes

Takemura, A., Rahman, M. S., Nakamura, S., Park, Y. J., & Takano, K. (2004) · Fish and Fisheries · doi:10.1111/j.1467-2679.2004.00164.x · Cited by 180 · see citing works

Mammalian circadian signaling networks and therapeutic targets

Liu, A. C., Lewis, W. G., & Kay, S. A. (2007) · Nature Chemical Biology · doi:10.1038/nchembio.2007.37 · Cited by 177 · see citing works

Cryptochrome Signaling in Plants†

Li, Q., & Yang, H. (2007) · Photochemistry and Photobiology · doi:10.1562/2006-02-28-ir-826 · Cited by 162 · see citing works

Molecular Evolution of the Photolyase–Blue-Light Photoreceptor Family

Kanai, S., Kikuno, R., Toh, H., Ryo, H., & Todo, T. (1997) · Journal of Molecular Evolution · doi:10.1007/pl00006258 · Cited by 158 · see citing works

Parapinopsin, a Novel Catfish Opsin Localized to the Parapineal Organ, Defines a New Gene Family

Blackshaw, S., & Snyder, S. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-21-08083.1997 · Cited by 157 · see citing works

Exo-rhodopsin: a novel rhodopsin expressed in the zebrafish pineal gland

Mano, H., Kojima, D., & Fukada, Y. (1999) · Molecular Brain Research · doi:10.1016/s0169-328x(99)00242-9 · Cited by 155 · see citing works

Light-dependent interaction between Drosophila CRY and the clock protein PER mediated by the carboxy terminus of CRY

Rosato, E., Codd, V., Mazzotta, G. M., Piccin, A., Zordan, M. A., Costa, R., & Kyriacou, C. P. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00259-7 · Cited by 151 · see citing works

Night irradiance and synchronization of lunar release of planula larvae in the reef coral Pocillopora damicornis

Jokiel, P. L., Itô, R., & Liu, P. M. (1985) · Marine Biology · doi:10.1007/bf00397164 · Cited by 134 · see citing works

Correlation between plasma steroid hormones and vitellogenin profiles and lunar periodicity in the female golden rabbitfish, Siganus guttatus (Bloch)

Rahman, M. S., Takemura, A., & Takano, K. (2000) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/s0305-0491(00)00240-6 · Cited by 95 · see citing works

Perception and possible utilization of moonlight intensity for reproductive activities in a lunar-synchronized spawner, the golden rabbitfish

Takemura, A., Susilo, E. S., Rahman, M. D. S., & Morita, M. (2004) · Journal of Experimental Zoology Part A Comparative Experimental Biology · doi:10.1002/jez.a.105 · Cited by 91 · see citing works

Identification of rhodopsin in the pigeon deep brain

Wada, Y., Okano, T., Adachi, A. A., Ebihara, S., & Fukada, Y. (1998) · FEBS Letters · doi:10.1016/s0014-5793(98)00138-0 · Cited by 84 · see citing works

Comparative Photochemistry of Animal Type 1 and Type 4 Cryptochromes

Öztürk, N., Selby, C. P., Song, S.-H., Ye, R., Tan, C., Kao, Y., Zhong, D., & Sancar, A. (2009) · Biochemistry · doi:10.1021/bi901043s · Cited by 83 · see citing works

Lunar spawning in Siganus canaliculatus

Hoque, M. M., Takemura, A., Matsuyama, M., Matsuura, S., & Takano, K. (1999) · Journal of Fish Biology · doi:10.1111/j.1095-8649.1999.tb02071.x · Cited by 69 · see citing works

Short Photoperiod Accelerates Preoptic and Ventral Telencephalic Salmon GnRH Synthesis and Precocious Maturation in Underyearling Male Masu Salmon

Amano, M., Hyodo, S., Kitamura, S., Ikuta, K., Suzuki, Y., Urano, A., & Aida, K. (1995) · General and Comparative Endocrinology · doi:10.1006/gcen.1995.1080 · Cited by 59 · see citing works

Nonvisual Photoreception in the Chick Iris

Tu, D. C., Batten, M. L., Palczewski, K., & Gelder, R. N. V. (2004) · Science · doi:10.1126/science.1101484 · Cited by 58 · see citing works

Moonlight affects nocturnal Period2 transcript levels in the pineal gland of the reef fish Siganus guttatus

Sugama, N., Park, J., Park, Y., Takeuchi, Y., Kim, S., & Takemura, A. (2008) · Journal of Pineal Research · doi:10.1111/j.1600-079x.2008.00566.x · Cited by 54 · see citing works

Photoinducible Phase-Specific Light Induction ofCry1Gene in the Pars Tuberalis of Japanese Quail

Yasuo, S., Watanabe, M., Tsukada, A., Takagi, T., Iigo, M., Shimada, K., Ebihara, S., & Yoshimura, T. (2003) · Endocrinology · doi:10.1210/en.2003-1285 · Cited by 52 · see citing works

Molecular mechanism of the photoperiodic response of gonads in birds and mammals

Yoshimura, T. (2005) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2005.09.009 · Cited by 52 · see citing works

Tight Temporal Consistency of Coral Mass Spawning at the Flower Garden Banks, Gulf of Mexico, from 1997-2003

Vize, P. D., Embesi, J. A., Nickell, M., Brown, D. P., & Hagman, D. K. (2005) · Gulf of Mexico Science · doi:10.18785/goms.2301.08 · Cited by 48 · see citing works

Timing the tides: genetic control of diurnal and lunar emergence times is correlated in the marine midge Clunio marinus

Kaiser, T. S., Neumann, D., & Heckel, D. G. (2011) · BMC Genetics · doi:10.1186/1471-2156-12-49 · Cited by 47 · see citing works

Histological evidence of lunar-synchronized ovarian development and spawning in the spiny rabbitfish Siganus spinus (Linnaeus) around the Ryukyus

Harahap, A. P., Takemura, A., Nakamura, S., Rahman, S., & Takano, K. (2001) · Fisheries Science · doi:10.1046/j.1444-2906.2001.00337.x · Cited by 42 · see citing works

Light Synchronization of the Daily Spawning Rhythms of Gilthead Sea bream (Sparus aurataL) Kept under Different Photoperiod and after Shifting the LD Cycle

Meseguer, C., Ramos, J., Bayarri, M. J., Oliveira, C. C. V., & Sánchez‐Vázquez, F. J. (2008) · Chronobiology International · doi:10.1080/07420520802380018 · Cited by 39 · see citing works

Effects of Shortened Photoperiod on Gonadotropin-Releasing Hormone, Gonadotropin, and Vitellogenin Gene Expression Associated with Ovarian Maturation in Rainbow Trout

Choi, S.-C., Lee, C. H., Park, W., Kim, D., & Sohn, Y. C. (2010) · ZOOLOGICAL SCIENCE · doi:10.2108/zsj.27.24 · Cited by 29 · see citing works

Rhythmic changes in testicular activity with lunar cycle in the forktail rabbitfish

Rahman, M. S., Takemura, A., Nakamura, S., & Takano, K. (2003) · Journal of Fish Biology · doi:10.1046/j.1095-8649.2003.00036.x · Cited by 22 · see citing works

Cryptochrome Genes Are Highly Expressed in the Ovary of the African Clawed Frog, Xenopus tropicalis

Kubo, Y., Takeuchi, T., Okano, K., & Okano, T. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009273 · Cited by 12 · see citing works

Circadian and circalunar clock interactions in a marine annelid

Zantke, J., Ishikawa-Fujiwara, T., Arboleda, E., Lohs, C., Schipany, K., Hallay, N., Straw, A. D., Todo, T., & Tessmar-Raible, K. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.08.031 · Cited by 148 · see citing works

An Overview of Monthly Rhythms and Clocks

Raible, F., Takekata, H., & Tessmar-Raible, K. (2017) · Frontiers in Neurology · doi:10.3389/fneur.2017.00189 · Cited by 121 · see citing works

The Still Dark Side of the Moon: Molecular Mechanisms of Lunar-Controlled Rhythms and Clocks

Andreatta, G., & Tessmar-Raible, K. (2020) · Journal of Molecular Biology · doi:10.1016/j.jmb.2020.03.009 · Cited by 111 · see citing works

Solvent Driving Force Ensures Fast Formation of a Persistent and Well-Separated Radical Pair in Plant Cryptochrome

Lüdemann, G., Solov’yov, I. A., Kubař, T., & Elstner, M. (2014) · Journal of the American Chemical Society · doi:10.1021/ja510550g · Cited by 95 · see citing works

Separation of photo-induced radical pair in cryptochrome to a functionally critical distance

Solov’yov, I. A., Domratcheva, T. M., & Schulten, K. J. (2014) · Scientific Reports · doi:10.1038/srep03845 · Cited by 90 · see citing works

Impacts of moonlight on fish reproduction

Ikegami, T., Takeuchi, Y., Hur, S., & Takemura, A. (2014) · Marine Genomics · doi:10.1016/j.margen.2013.11.007 · Cited by 62 · see citing works

Lunar biological effects and the magnetosphere

Bevington, M. (2015) · Pathophysiology · doi:10.1016/j.pathophys.2015.08.005 · Cited by 50 · see citing works

A Cryptochrome adopts distinct moon- and sunlight states and functions as sun- versus moonlight interpreter in monthly oscillator entrainment

Poehn, B., Krishnan, S., Zurl, M., Ćorić, A., Rokvić, D., Häfker, N. S., Jaenicke, E., Arboleda, E., Orel, L., Raible, F., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-32562-z · Cited by 40 · see citing works

Transcriptome dynamics over a lunar month in a broadcast spawning acroporid coral

Oldach, M. J., Workentine, M., Matz, M. V., Fan, T., & Vize, P. D. (2017) · Molecular Ecology · doi:10.1111/mec.14043 · Cited by 39 · see citing works

Circalunar clocks—Old experiments for a new era

Kaiser, T. S., & Neumann, J. (2021) · BioEssays · doi:10.1002/bies.202100074 · Cited by 35 · see citing works

Moonlight controls lunar-phase-dependency and regular oscillation of clock gene expressions in a lunar-synchronized spawner fish, Goldlined spinefoot

Takeuchi, Y., Kabutomori, R., Yamauchi, C., Miyagi, H., Takemura, A., Okano, K., & Okano, T. (2018) · Scientific Reports · doi:10.1038/s41598-018-24538-1 · Cited by 30 · see citing works

Canonical and cellular pathways timing gamete release in Acropora digitifera, Okinawa, Japan

Rosenberg, Y., Doniger, T., Harii, S., Sinniger, F., & Levy, O. (2017) · Molecular Ecology · doi:10.1111/mec.14062 · Cited by 30 · see citing works

Influence of moonlight on mRNA expression patterns of melatonin receptor subtypes in the pineal organ of a tropical fish

Park, Y.-J., Park, J., Takeuchi, Y., Hur, S., Lee, Y.-D., Kim, S.-J., & Takemura, A. (2013) · Marine Genomics · doi:10.1016/j.margen.2013.10.006 · Cited by 28 · see citing works

Effects of different phases of the lunar month on living organisms

Chakraborty, U. (2018) · Biological Rhythm Research · doi:10.1080/09291016.2018.1526502 · Cited by 31 · see citing works

Impacts of “supermoon” events on the physiology of a wild bird

Portugal, S. J., White, C. R., Frappell, P. B., Green, J. A., & Butler, P. J. (2019) · Ecology and Evolution · doi:10.1002/ece3.5311 · Cited by 23 · see citing works

Hypothalamic expression and moonlight-independent changes of Cry3 and Per4 implicate their roles in lunar clock oscillators of the lunar-responsive goldlined spinefoot

Toda, R., Okano, K., Takeuchi, Y., Yamauchi, C., Fukushiro, M., Takemura, A., & Okano, T. (2014) · PLoS ONE · doi:10.1371/journal.pone.0109119 · Cited by 20 · see citing works

Lunar Clock in Fish Reproduction

Ikegami, T., Takeuchi, Y., & Takemura, A. (2014) · Springer eBooks · doi:10.1007/978-4-431-55261-1_9 · Cited by 21 · see citing works

Photoreception and Signal Transduction in Corals: Proteomic and Behavioral Evidence for Cytoplasmic Calcium as a Mediator of Light Responsivity

Hilton, J., Brady, A. K., Spaho, S. A., & Vize, P. D. (2012) · Biological Bulletin · doi:10.1086/bblv223n3p291 · Cited by 18 · see citing works

Involvement of melatonin in transducing moon-related signals into the reproductive network of the female honeycomb grouper Epinephelus merra

Fukunaga, K., Yamashina, F., Ohta, N., Mizuno, H., Takeuchi, Y., Yamauchi, C., & Takemura, A. (2019) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2019.113211 · Cited by 17 · see citing works

Mass-nesting events in olive ridley sea turtles: environmental predictors of timing and size

Bézy, V. S., Putman, N. F., Umbanhowar, J., Orrego, C. M., Fonseca, L. G., Quirós, W. M., Valverde, R. A., & Lohmann, K. J. (2020) · Animal Behaviour · doi:10.1016/j.anbehav.2020.03.002 · Cited by 17 · see citing works

Lunar cycle and psychiatric hospital admissions for schizophrenia: new findings from Henan province, China

Wang, R., Hao, Y., Guo, H., Wang, M., Han, L., Zheng, R.-Y., He, J., & Wang, Z. (2020) · Chronobiology International · doi:10.1080/07420528.2019.1625054 · Cited by 15 · see citing works

Demystifying Circalunar and Diel Rhythmicity in Acropora digitifera under Constant Dim Light

Rosenberg, Y., Doniger, T., Harii, S., Sinniger, F., & Levy, O. (2019) · iScience · doi:10.1016/j.isci.2019.11.040 · Cited by 14 · see citing works

Identification and Characterization of Cryptochrome4 in the Ovary of Western Clawed Frog Xenopus tropicalis

Takeuchi, T., Kubo, Y., Okano, K., & Okano, T. (2014) · ZOOLOGICAL SCIENCE · doi:10.2108/zsj.31.152 · Cited by 13 · see citing works

Circadian and Circalunar Clock Interactions and the Impact of Light in Platynereis dumerilii

Zantke, J., Oberlerchner, H., & Tessmar‐Raible, K. (2014) · Springer eBooks · doi:10.1007/978-4-431-55261-1_8 · Cited by 13 · see citing works

Light- and circadian-controlled genes respond to a broad light spectrum in Puffer Fish-derived Fugu eye cells

Okano, K., Ozawa, S., Sato, H., Kodachi, S., Ito, M., Miyadai, T., Takemura, A., & Okano, T. (2017) · Scientific Reports · doi:10.1038/srep46150 · Cited by 13 · see citing works

Existence of a photoinducible phase for ovarian development and photoperiod-related alteration of clock gene expression in a damselfish

Takeuchi, Y., Hada, N., Imamura, S., Hur, S., Bouchekioua, S., & Takemura, A. (2015) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2015.06.010 · Cited by 12 · see citing works

An Overview of Chemistry, Kinetics, Toxicity and Therapeutic Potential of Boldine in Neurological Disorders

Akotkar, L., Aswar, U. M., Ganeshpurkar, A., Raj, R., & Pawar, A. (2023) · Neurochemical Research · doi:10.1007/s11064-023-03992-y · Cited by 10 · see citing works

Daily expression of a clock gene in the brain and pituitary of the Malabar grouper (Epinephelus malabaricus)

Yamashina, F., Takeuchi, Y., Fukunaga, K., Udagawa, S., Tan, E. S., Byun, J., Yamauchi, C., & Takemura, A. (2019) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2019.03.019 · Cited by 10 · see citing works

Moonlight is a key entrainer of lunar clock in the brain of the tropical grouper with full moon preference

Fukunaga, K., Yamashina, F., Takeuchi, Y., Yamauchi, C., & Takemura, A. (2020) · BMC Zoology · doi:10.1186/s40850-020-00060-8 · Cited by 10 · see citing works

A photoperiodic time measurement served by the biphasic expression of Cryptochrome1ab in the zebrafish eye

Okano, K., Saratani, Y., Tamasawa, A., Shoji, Y., Riko, T., & Okano, T. (2020) · Scientific Reports · doi:10.1038/s41598-020-61877-4 · Cited by 9 · see citing works

Physiological effects of the lunar cycle on the spawning of a coral reef fish, Abudefduf Vaigiensis: in vivo and in vitro trait

Golmoradizadeh, A., Noori, A., & Amiri, B. M. (2021) · Coral Reefs · doi:10.1007/s00338-021-02183-x · Cited by 8 · see citing works

Transcriptome survey of phototransduction and clock genes in marine bivalves

Sun, X., Zhou, L., Tian, J., Liu, Z. H., Wu, B., Dong, Y. H., Yang, A., & Ma, W. (2016) · Genetics and Molecular Research · doi:10.4238/gmr15048726 · Cited by 7 · see citing works

Effect of Circadian Clock and Light–Dark Cycles in Onchidium reevesii: Possible Implications for Long-Term Memory

Xu, G., Yang, T., & Shen, H. (2019) · Genes · doi:10.3390/genes10070488 · Cited by 5 · see citing works

Role of Cytochromes P450 in Intestinal Barrier Function: Possible Involvement in the Pathogenesis of Leaky Gut Syndrome

Makaro, A., Kasprzak, Z., Jaczynska, M., Świerczyński, M., & Sałaga, M. (2025) · Digestive Diseases and Sciences · doi:10.1007/s10620-025-08873-8 · Cited by 4 · see citing works

Changes in circadian parameters of humbug damselfish,Dascyllus aruanusaccording to lunar phase shifts in Micronesia

Choi, J. Y., Kim, N. N., Choi, Y., & Choi, C. Y. (2017) · Biological Rhythm Research · doi:10.1080/09291016.2016.1275395 · Cited by 4 · see citing works

Biological rhythms: Hormones under moon control

Andreatta, G., Raible, F., & Tessmar‐Raible, K. (2022) · Current Biology · doi:10.1016/j.cub.2022.10.018 · Cited by 2 · see citing works

Darkness at night during the new moon period alters the expression levels of the clock genes in the brain of a moon-related spawner, the Malabar grouper Epinephelus malabaricus

Yamashina, F., Zhu, Y., Takeuchi, Y., Yamauchi, C., Fukunaga, K., Udagawa, S., & Takemura, A. (2023) · Biological Rhythm Research · doi:10.1080/09291016.2023.2247801 · Cited by 2 · see citing works

Lunar cycle-mediated behaviours in animals, including humans

Mandal, F. B. (2023) · Israel Journal of Ecology and Evolution · doi:10.1163/22244662-bja10060 · Cited by 3 · see citing works

Molecular and ecophysiological aspects of semilunar synchronized spawning migration in the grass puffer

Ando, H. (2018) · Hikaku seiri seikagaku(Comparative Physiology and Biochemistry) · doi:10.3330/hikakuseiriseika.35.45 · Cited by 2 · see citing works

Lunar Age-Dependent Oscillations in Expression of the Genes for Kisspeptin, GnIH, and Their Receptors in the Grass Puffer during the Spawning Season

Shahjahan, M., Rahman, M. L., Ohno, Y., Zahangir, M. M., & Ando, H. (2023) · ZOOLOGICAL SCIENCE · doi:10.2108/zs230061 · Cited by 2 · see citing works

Current knowledge of lunar synchronized spawning in fish

Fukunaga, K., & Takemura, A. (2025) · Chronobiology International · doi:10.1080/07420528.2025.2591924 · Cited by 1 · see citing works

Effects of nocturnal illumination on fitness-related traits of the New Zealand common triplefin (Forsterygion lapillum)

Barclay, J. (2023) · doi:10.26686/wgtn.23575260 · Cited by 1 · see citing works

Additional file 1 of Moonlight is a key entrainer of lunar clock in the brain of the tropical grouper with full moon preference

Fukunaga, K., Yamashina, F., Takeuchi, Y., Yamauchi, C., & Takemura, A. (2020) · Figshare · doi:10.6084/m9.figshare.12940543

Additional file 2 of Moonlight is a key entrainer of lunar clock in the brain of the tropical grouper with full moon preference

Fukunaga, K., Yamashina, F., Takeuchi, Y., Yamauchi, C., & Takemura, A. (2020) · Figshare · doi:10.6084/m9.figshare.12940546

Non-linear and switchable light preferences of nocturnal loach (Misgurnus anguillicaudatus)

Yoshikawa, Y., Okano, K., & Okano, T. (2026) · Scientific Reports · doi:10.1038/s41598-026-44631-0

Kobayashi Award 2024: Cyclic regulation of the reproductive neuroendocrine system in fish: Using migratory fish as a model

Ando, H. (2026) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2026.114916

Response to light stimuli in the marine diatom Phaeodactylum tricornutum : Involvement of bHLH-PAS proteins in the circadian clock and plastid physiology

Manzotti, A. (2022) · theses.fr (ABES) · doi:10.70675/f8143d4czab93z4250z91abz54432e53522f

Moonlight controls lunar-phase-dependency and regular oscillation of clock gene expressions in a lunar-synchronized spawner fish, Goldlined spinefoot

Takeuchi, Y., Kabutomori, R., Yamauchi, C., Miyagi, H., Takemura, A., Okano, K., & Okano, T. (2018) · Scientific Reports · doi:10.1038/s41598-018-24538-1 · Cited by 30 · see citing works

Hypothalamic expression and moonlight-independent changes of Cry3 and Per4 implicate their roles in lunar clock oscillators of the lunar-responsive goldlined spinefoot

Toda, R., Okano, K., Takeuchi, Y., Yamauchi, C., Fukushiro, M., Takemura, A., & Okano, T. (2014) · PLoS ONE · doi:10.1371/journal.pone.0109119 · Cited by 20 · see citing works

Lunar Clock in Fish Reproduction

Ikegami, T., Takeuchi, Y., & Takemura, A. (2014) · Springer eBooks · doi:10.1007/978-4-431-55261-1_9 · Cited by 21 · see citing works

Hypothalamic Expression and Moonlight-Independent Changes of Cry3 and Per4 Implicate Their Roles in Lunar Clock Oscillators of the Lunar-Responsive Goldlined

(2016)

Moonlight is a key entrainer of lunar clock in the brain of the tropical grouper with full moon preference

Fukunaga, K., Yamashina, F., Takeuchi, Y., Yamauchi, C., & Takemura, A. (2020) · BMC Zoology · doi:10.1186/s40850-020-00060-8 · Cited by 10 · see citing works