The DOI matches its Crossref record; 31 of the 31 references it cites were found in a registry or an index.
Melanopsin and rod-cone photoreceptive systems account for all major accessory visual functions in mice
Open accessAbstract
In the mammalian retina, besides the conventional rod-cone system, a melanopsin-associated photoreceptive system exists that conveys photic information for accessory visual functions such as pupillary light reflex and circadian photo-entrainment. On ablation of the melanopsin gene, retinal ganglion cells that normally express melanopsin are no longer intrinsically photosensitive. Furthermore, pupil reflex, light-induced phase delays of the circadian clock and period lengthening of the circadian rhythm in constant light are all partially impaired. Here, we investigated whether additional photoreceptive systems participate in these responses. Using mice lacking rods and cones, we measured the action spectrum for phase-shifting the circadian rhythm of locomotor behaviour. This spectrum matches that for the pupillary light reflex in mice of the same genotype, and that for the intrinsic photosensitivity of the melanopsin-expressing retinal ganglion cells. We have also generated mice lacking melanopsin coupled with disabled rod and cone phototransduction mechanisms. These animals have an intact retina but fail to show any significant pupil reflex, to entrain to light/dark cycles, and to show any masking response to light. Thus, the rod-cone and melanopsin systems together seem to provide all of the photic input for these accessory visual functions.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Additionally, melanopsin (λmax ~480 nm) is expressed in intrinsically photosensitive retinal ganglion cells (ipRGCs) that mediate circadian entrainment, the pupillary light reflex, and light-regulated changes in mood (Panda et al., 2003; Hattar et al., 2003; Fernandez et al., 2018).”
From Ventral striatum dopamine release encodes unique properties of visual stimuli in mice (2023) · cites this paper as Hattar et al., 2003
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Phototransduction by retinal ganglion cells that set the circadian clock
Berson, D. M., Dunn, F. A., & Takao, M. (2002) · Science · doi:10.1126/science.1067262 · Cited by 3,629
Hattar, S., Liao, H.-W., Takao, M., Berson, D. M., & Yau, K.-W. (2002) · Science · doi:10.1126/science.1069609 · Cited by 2,734
Self-citationA Novel Human Opsin in the Inner Retina
Provencio, I., Rodriguez, I. R., Jiang, G., Hayes, W. P., Moreira, E. F., & Rollag, M. D. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-02-00600.2000 · Cited by 1,290
Melanopsin: An opsin in melanophores, brain, and eye
Provencio, I., Jiang, G., De Grip, W. J., Hayes, W. P., & Rollag, M. D. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.1.340 · Cited by 975
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
Melanopsin ( Opn4 ) Requirement for Normal Light-Induced Circadian Phase Shifting
Panda, S., Sato, T. K., Castrucci, A. M., Rollag, M. D., DeGrip, W. J., Hogenesch, J. B., Provencio, I., & Kay, S. A. (2002) · Science · doi:10.1126/science.1076848 · Cited by 861
Diminished Pupillary Light Reflex at High Irradiances in Melanopsin-Knockout Mice
Lucas, R. J., Hattar, S. S., Takao, M., Berson, D. M., Foster, F., & Yau, K. (2003) · Science · doi:10.1126/science.1077293 · Cited by 835
Self-citationRole of Melanopsin in Circadian Responses to Light
Ruby, N. F., Brennan, T. J., Xie, X., Cao, V. H., Franken, P., Heller, H. C., & O’Hara, B. F. (2002) · Science · doi:10.1126/science.1076701 · Cited by 647
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
Characterization of an ocular photopigment capable of driving pupillary constriction in mice
Lucas, R. J., Douglas, R. H., & Foster, R. G. (2001) · Nature Neuroscience · doi:10.1038/88443 · Cited by 614
Self-citation
Research works printed but not linked: 1
- Aschoff, J. in Trends in Chronobiology. Advances in the Biosciences Vol. 73 (eds Hekkens, W. T. J. M., Kerkhof, G. A. & Rietveld, W. J.) 149–161 (Pergamon, Oxford, 1988)
Cited by
Sorted by citations
Items 301–400 of 998
A behavioural characterisation of the FVB/N mouse strain
Pugh, P. L., Ahmed, S. F., Smith, M. I., Upton, N., & Hunter, A. J. (2004) · Behavioural Brain Research · doi:10.1016/j.bbr.2004.04.021 · Cited by 76
Semo, M., Gias, C., Ahmado, A., Sugano, E., Allen, A. E., Lawrence, J. M., Tomita, H., Coffey, P. J., & Vugler, A. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015009 · Cited by 80
Butler, M. P., & Silver, R. (2010) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2010.1509 · Cited by 78
Telling the Time with a Broken Clock: Quantifying Circadian Disruption in Animal Models
Brown, L. A., Fisk, A. S., Pothecary, C. A., & Peirson, S. N. (2019) · Biology · doi:10.3390/biology8010018 · Cited by 82
Circadian and photic modulation of daily rhythms in diurnal mammals
Yan, L., Smale, L., & Núñez, A. A. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14172 · Cited by 77
Semo, M., Lupi, D., Peirson, S. N., Butler, J. N., & Foster, F. (2003) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2003.03061.x · Cited by 75
Foster, F. (2005) · Nature · doi:10.1038/433698a · Cited by 75
Human phase response curve to intermittent blue light using a commercially available device
Revell, V. L., Molina, T. A., & Eastman, C. I. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.235416 · Cited by 78
Circadian regulation in the retina: From molecules to network
Ko, G. Y. ‐. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14185 · Cited by 74
Circadian Photoreception in VertebratesPreprint
Doyle, S. E., & Menaker, M. (2007) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2007.72.003 · Cited by 73
Hilaire, M. A. S., Ámundadóttir, M. L., Rahman, S. A., Rajaratnam, S. M. W., Rüger, M., Brainard, G. C., Czeisler, C. A., Andersen, M., Gooley, J. J., & Lockley, S. W. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2205301119 · Cited by 74
Circadian Photoreception: Spotlight on the Brain
Lockley, S. W., & Gooley, J. J. (2006) · Current Biology · doi:10.1016/j.cub.2006.08.039 · Cited by 89
Impaired light masking in dopamine D2 receptor–null mice
Doi, M., Yujnovsky, I., Hirayama, J., Malerba, M., Tirotta, E., Sassone‐Corsi, P., & Borrelli, E. (2006) · Nature Neuroscience · doi:10.1038/nn1711 · Cited by 71
Mouland, J. W., Martial, F. P., Watson, A. J., Lucas, R. J., & Brown, T. M. (2019) · Current Biology · doi:10.1016/j.cub.2019.10.028 · Cited by 70
Self-citationDiversity of zebrafish peripheral oscillators revealed by luciferase reporting
Kaneko, M. A. N., de Borsetti, N. H., & Cahill, G. M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0606563103 · Cited by 73
Using light to tell the time of day: sensory coding in the mammalian circadian visual network
Brown, T. M. (2016) · Journal of Experimental Biology · doi:10.1242/jeb.132167 · Cited by 72
Optogenetic Gene Therapy for the Degenerate Retina: Recent Advances
McClements, M. E., Staurenghi, F., MacLaren, R. E., & Cehajic‐Kapetanovic, J. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.570909 · Cited by 73
Alexander, I. H., Cuthbertson, F. M., Ratnarajan, G., Safa, R., Mellington, F. E., Foster, F., Downes, S. M., & Wulff, K. (2014) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.14-14054 · Cited by 69
Irradiance encoding in the suprachiasmatic nuclei by rod and cone photoreceptors
van Diepen, H. C., Ramkisoensing, A., Peirson, S. N., Foster, F., & Meijer, J. H. (2013) · The FASEB Journal · doi:10.1096/fj.13-233098 · Cited by 71
Photoreception for Circadian, Neuroendocrine, and Neurobehavioral Regulation
Hanifin, J. P., & Brainard, G. C. (2007) · Journal of PHYSIOLOGICAL ANTHROPOLOGY · doi:10.2114/jpa2.26.87 · Cited by 69
Barrionuevo, P. A., & Cao, D. (2016) · Journal of Vision · doi:10.1167/16.11.29 · Cited by 69
Evidence for Multiple Phototransduction Pathways in a Reef-Building Coral
Mason, B. M., Schmale, M. C., Gibbs, P., Miller, M. W., Wang, Q., Levay, K., Shestopalov, V. I., & Slepak, V. Z. (2012) · PLoS ONE · doi:10.1371/journal.pone.0050371 · Cited by 68
Evolution and diversity of opsins
Terakita, A., Kawano‐Yamashita, E., & Koyanagi, M. (2011) · Wiley Interdisciplinary Reviews Membrane Transport and Signalling · doi:10.1002/wmts.6 · Cited by 65
Masana, M. I., Sumaya, I. C., Becker-André, M., & Dubocovich, M. L. (2007) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00687.2006 · Cited by 68
Inner retinal photoreception independent of the visual retinoid cycle
Tu, D. C., Owens, L. A., Anderson, L. G., Golczak, M., Doyle, S. E., McCall, M. A., Menaker, M., Palczewski, K., & Gelder, R. N. V. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600917103 · Cited by 72
Light, Sleep and Circadian Rhythms in Older Adults With Alzheimer’s Disease and Related Dementias
Figueiro, M. G. (2017) · Neurodegenerative Disease Management · doi:10.2217/nmt-2016-0060 · Cited by 73
Douglas, R. H. (2018) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2018.04.005 · Cited by 69
Self-citationLi, M.-T., Cao, L.-H., Xiao, N., Tang, M., Deng, B., Tian, Y., Yoshii, T., & Luo, D.-G. (2018) · Nature Communications · doi:10.1038/s41467-018-06506-5 · Cited by 67
The Human Circadian Timing System and Sleep-Wake Regulation
Czeisler, C. A., Buxton, O. M., & Khalsa, S. B. S. (2005) · Principles and Practice of Sleep Medicine · doi:10.1016/b0-72-160797-7/50038-0 · Cited by 67
Ocular Autonomic Nervous System: An Update from Anatomy to Physiological Functions
Wu, F., Zhao, Y., & Zhang, H. (2022) · Vision · doi:10.3390/vision6010006 · Cited by 69
Changes in the Circadian Rhythm in Patients with Primary Glaucoma
Wang, H., Zhang, Y., Ding, J., & Wang, N. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062841 · Cited by 69
A Comprehensive Overview of the Neural Mechanisms of Light Therapy
Huang, X., Tao, Q., & Ren, C. (2023) · Neuroscience Bulletin · doi:10.1007/s12264-023-01089-8 · Cited by 73
Dauchy, R. T., Wren, M. A., Dauchy, E. M., Hoffman, A. E., Hanifin, J. P., Warfield, B., Jablonski, M., Brainard, G. C., Hill, S. M., Mao, L., et al. (2015) · PubMed Central · Cited by 65
The Involvement of the Oxidative Stress in Murine Blue LED Light-Induced Retinal Damage Model
Nakamura, M., Kuse, Y., Tsuruma, K., Shimazawa, M., & Hara, H. (2017) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b16-01008 · Cited by 65
Visual responses in mice lacking critical components of all known retinal phototransduction cascades
Allen, A. E., Cameron, M. A., Brown, T. M., Vugler, A. A., & Lucas, R. J. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015063 · Cited by 64
Self-citationDisruption of Circadian Rhythms by Light During Day and Night
Figueiro, M. G. (2017) · Current Sleep Medicine Reports · doi:10.1007/s40675-017-0069-0 · Cited by 70
Nagare, R., Rea, M. S., Plitnick, B., & Figueiro, M. G. (2019) · Journal of Biological Rhythms · doi:10.1177/0748730419828056 · Cited by 66
Modelling ‘non-visual’ effects of daylighting in a residential environment
Andersen, M., Gochenour, S. J., & Lockley, S. W. (2013) · Building and Environment · doi:10.1016/j.buildenv.2013.08.018 · Cited by 70
Rahman, S. A., Marcu, S., Shapiro, C. M., Brown, T. J., & Casper, R. F. (2010) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00597.2010 · Cited by 63
Circadian Effects of Light No Brighter Than Moonlight
Evans, J. A., Elliott, J. A., & Gorman, M. R. (2007) · Journal of Biological Rhythms · doi:10.1177/0748730407301988 · Cited by 66
Pupillary responses driven by ipRGCs and classical photoreceptors are impaired in glaucoma
Kelbsch, C., Maeda, F., Straßer, T., Blumenstock, G., Wilhelm, B., Wilhelm, H. M., & Peters, T. M. (2016) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/s00417-016-3351-9 · Cited by 65
Ganjawala, T. H., Lu, Q., Fenner, M., Abrams, G. W., & Pan, Z. (2019) · Molecular Therapy · doi:10.1016/j.ymthe.2019.04.002 · Cited by 64
Mien, I. H., Chua, E. C.-P., Lau, P., Tan, L.-C., Lee, I. T.-G., Yeo, S. C., Tan, S. S., & Gooley, J. J. (2014) · PLoS ONE · doi:10.1371/journal.pone.0096532 · Cited by 65
Do magnetic fields cause increased risk of childhood leukemia via melatonin disruption?
Henshaw, D. L., & Reiter, R. J. (2005) · Bioelectromagnetics · doi:10.1002/bem.20135 · Cited by 63
Neural mechanism for hypothalamic-mediated autonomic responses to light during migraine
Noseda, R., Lee, A. J., Nir, R., Bernstein, C. A., Kainz, V., Bertisch, S. M., Buettner, C., Borsook, D., & Burstein, R. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1708361114 · Cited by 66
Melanopsin and Cone Photoreceptor Inputs to the Afferent Pupil Light Response
Zele, A. J., Adhikari, P., Cao, D., & Feigl, B. (2019) · Frontiers in Neurology · doi:10.3389/fneur.2019.00529 · Cited by 67
Hughes, S., Pothecary, C. A., Jagannath, A., Foster, F., Hankins, M. W., & Peirson, S. N. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07944.x · Cited by 63
Self-citationEffects of blue-light irradiation during dental treatment
Yoshino, F., & Yoshida, A. (2018) · Japanese Dental Science Review · doi:10.1016/j.jdsr.2018.06.002 · Cited by 62
Nocturnal Activity in a Diurnal Rodent (Arvicanthis Niloticus): The Importance of Masking
Redlin, U., & Mrosovsky, N. (2004) · Journal of Biological Rhythms · doi:10.1177/0748730403260371 · Cited by 63
Self-citationOptogenetic Therapy for Visual Restoration
Sakai, D., Tomita, H., & Maeda, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232315041 · Cited by 62
Clinical implications of the melanopsin-based non–image-forming visual system
Ksendzovsky, A., Pomeraniec, I. J., Zaghloul, K. A., Provencio, J. J., & Provencio, I. (2017) · Neurology · doi:10.1212/wnl.0000000000003761 · Cited by 61
Peirson, S. N., Bovée‐Geurts, P. H. M., Lupi, D., Jeffery, G., DeGrip, W. J., & Foster, F. (2004) · Molecular Brain Research · doi:10.1016/j.molbrainres.2004.01.007 · Cited by 59
Loss of Circadian Photoentrainment and Abnormal Retinal Electrophysiology in Math5 Mutant Mice
Brzezinski, J. A., Brown, N. L., Tanikawa, A., Bush, R. A., Sieving, P. A., Vitaterna, M. H., Takahashi, J. S., & Glaser, T. (2005) · Investigative Opthalmology & Visual Science · doi:10.1167/iovs.04-1123 · Cited by 60
Understanding the dermal light sense in the context of integrative photoreceptor cell biology
Ramirez, M. D., Speiser, D. I., Pankey, M. S., & Oakley, T. H. (2011) · Visual Neuroscience · doi:10.1017/s0952523811000150 · Cited by 60
A Self-Regulating Gap Junction Network of Amacrine Cells Controls Nitric Oxide Release in the Retina
Jacoby, J., Nath, A., Jessen, Z. F., & Schwartz, G. W. (2018) · Neuron · doi:10.1016/j.neuron.2018.09.047 · Cited by 63
Circadian Modulation of Melanopsin-Driven Light Response in Rat Ganglion-Cell Photoreceptors
Weng, S.-J., Wong, K. Y., & Berson, D. M. (2009) · Journal of Biological Rhythms · doi:10.1177/0748730409343767 · Cited by 61
Doyle, S. E., Castrucci, A. M. D. L., McCall, M. A., Provencio, I., & Menaker, M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600934103 · Cited by 62
Impact of age and retinal degeneration on the light input to circadian brain structures
Lupi, D., Semo, M., & Foster, F. (2010) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2010.03.006 · Cited by 59
Melanopsin phototransduction: beyond canonical cascades
Contreras, E., Nobleman, A. P., Robinson, P. R., & Schmidt, T. M. (2021) · Journal of Experimental Biology · doi:10.1242/jeb.226522 · Cited by 62
Lorenz, B., Strohmayr, E., Zahn, S., Friedburg, C., Kramer, M., Preising, M. N., & Stieger, K. (2012) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.12-9974 · Cited by 59
Rüger, M., Gordijn, M. C. M., Beersma, D. G. M., de Vries, B., & Daan, S. (2005) · Journal of Biological Rhythms · doi:10.1177/0748730404270539 · Cited by 58
Light-Dependent Regulation of Sleep and Wake States by Prokineticin 2 in Zebrafish
Chen, S., Reichert, S., Singh, C., Oikonomou, G., Rihel, J., & Prober, D. A. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.001 · Cited by 62
Why a Fly? Using Drosophila to Understand the Genetics of Circadian Rhythms and Sleep
Hendricks, J. C., & Sehgal, A. (2004) · SLEEP · doi:10.1093/sleep/27.2.334 · Cited by 58
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
Revell, V. L., Barrett, D. C. G., Schlangen, L. J. M., & Skene, D. J. (2010) · Chronobiology International · doi:10.3109/07420528.2010.516048 · Cited by 57
Melanopsin Is Highly Resistant to Light and Chemical Bleaching in Vivo
Sexton, T. J., Golczak, M., Palczewski, K., & Gelder, R. N. V. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.325969 · Cited by 62
Light as a modulator of emotion and cognition: Lessons learned from studying a diurnal rodent
Yan, L., Lonstein, J. S., & Núñez, A. A. (2018) · Hormones and Behavior · doi:10.1016/j.yhbeh.2018.09.003 · Cited by 56
Role of Rhodopsins as Circadian Photoreceptors in the Drosophila melanogaster
Senthilan, P. R., Grebler, R., Reinhard, N., Rieger, D., & Helfrich‐Förster, C. (2019) · Biology · doi:10.3390/biology8010006 · Cited by 56
Melanopsin-Dependent Persistence and Photopotentiation of Murine Pupillary Light Responses
Zhu, Y., Tu, D. C., Denner, D., Shane, T. S., Fitzgerald, C. M., & Gelder, R. N. V. (2007) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.06-0925 · Cited by 58
Buhr, E. D., & Gelder, R. N. V. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1323350111 · Cited by 55
Saint‐Charles, A., Michard‐Vanhée, C., Alejevski, F., Chélot, E., Boivin, A., & Rouyer, F. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.23994 · Cited by 54
Brainard, G. C., Barger, L. K., Soler, R. R., & Hanifin, J. P. (2016) · Current Opinion in Pulmonary Medicine · doi:10.1097/mcp.0000000000000329 · Cited by 55
Role of a novel photopigment, melanopsin, in behavioral adaptation to light
Nayak, S. K., Jegla, T. J., & Panda, S. (2006) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-006-5581-1 · Cited by 57
Selective Stimulation of Penumbral Cones Reveals Perception in the Shadow of Retinal Blood Vessels
Spitschan, M., Aguirre, G. K., & Brainard, D. H. (2015) · PLoS ONE · doi:10.1371/journal.pone.0124328 · Cited by 53
Unified framework to evaluate non-visual spectral effectiveness of light for human health
Ámundadóttir, M. L., Lockley, S. W., & Andersen, M. (2016) · Lighting Research & Technology · doi:10.1177/1477153516655844 · Cited by 58
Mechanisms of circadian clock interactions with aryl hydrocarbon receptor signalling
Tischkau, S. A. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14361 · Cited by 56
Li, P., Temple, S. E., Gao, Y., Haimberger, T., Hawryshyn, C. W., & Li, L. (2005) · Journal of Experimental Biology · doi:10.1242/jeb.01424 · Cited by 54
Retinal pathways influence temporal niche
Doyle, S. E., Yoshikawa, T., Hillson, H., & Menaker, M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0801728105 · Cited by 57
Zhou, T.-H., Dang, W.-M., Ma, Y.-T., Hu, C.-Q., Wang, N., Zhang, G.-Y., Wang, G., Shi, C., Zhang, H., Guo, B., et al. (2018) · Journal of Affective Disorders · doi:10.1016/j.jad.2017.09.038 · Cited by 53
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
Mammalian circadian clock system: Molecular mechanisms for pharmaceutical and medical sciences
Okamura, H., Doi, M., Fustin, J., Yamaguchi, Y., & Matsuo, M. (2010) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2010.06.004 · Cited by 56
Lucas, R. J., Allen, A. E., Brainard, G. C., Brown, T. M., Dauchy, R. T., Didikoğlu, A., Do, M. T. H., Gaskill, B. N., Hattar, S. S., Hawkins, P., et al. (2024) · PLoS Biology · doi:10.1371/journal.pbio.3002535 · Cited by 55
Self-citationThe activation of directional stem cell motility by green light-emitting diode irradiation
Ong, W.-K., Chen, H.-F., Tsai, C.-T., Fu, Y.-J., Wong, Y.-S., Yen, T., Chang, T., Huang, H., Lee, O. K., Chien, S., et al. (2012) · Biomaterials · doi:10.1016/j.biomaterials.2012.11.065 · Cited by 52
Circadian clock components in the rat neocortex: daily dynamics, localization and regulation
Rath, M. F., Rohde, K., Fahrenkrug, J., & Møller, M. (2012) · Brain Structure and Function · doi:10.1007/s00429-012-0415-4 · Cited by 51
Light-dependent phosphorylation of the carboxy tail of mouse melanopsin
Blasic, J. R., Brown, R. L., & Robinson, P. R. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0891-3 · Cited by 52
Melanopsin—Shedding Light on the Elusive Circadian Photopigment
Brown, R. L., & Robinson, P. R. (2004) · Chronobiology International · doi:10.1081/cbi-120037816 · Cited by 51
Frigato, E., Vallone, D., Bertolucci, C., & Foulkes, N. S. (2006) · Die Naturwissenschaften · doi:10.1007/s00114-006-0119-9 · Cited by 52
Evidence for an impact of melanopsin activation on unique white perception
Cao, D., Chang, A., & Gai, S. (2018) · Journal of the Optical Society of America A · doi:10.1364/josaa.35.00b287 · Cited by 51
Evolutionary Constraint on Visual and Nonvisual Mammalian Opsins
Upton, B. A., Díaz, N. M., Gordon, S. A., Gelder, R. N. V., Buhr, E. D., & Lang, R. A. (2021) · Journal of Biological Rhythms · doi:10.1177/0748730421999870 · Cited by 54
Liu, Q., Wang, Z., Cao, J., Dong, Y., & Chen, Y. (2022) · Antioxidants · doi:10.3390/antiox11071218 · Cited by 51
Dauchy, R. T., Dauchy, E. M., Hanifin, J. P., Gauthreaux, S. L., Mao, L., Belancio, V. P., Ooms, T. G., Dupepe, L. M., Jablonski, M., Warfield, B., et al. (2013) · Europe PMC (PubMed Central) · Cited by 51
Grozdanić, S. D., Matic, M., Sakaguchi, D. S., & Kardon, R. H. (2007) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.07-0249 · Cited by 54
Thin-film optical notch filter spectacle coatings for the treatment of migraine and photophobia
Hoggan, R. N., Subhash, A., Blair, S., Digre, K. B., Baggaley, S. K., Gordon, J., Brennan, K. C., Warner, J. E. A., Crum, A. V., & Katz, B. J. (2016) · Journal of Clinical Neuroscience · doi:10.1016/j.jocn.2015.09.024 · Cited by 51
Biophysical Variation within the M1 Type of Ganglion Cell Photoreceptor
Emanuel, A. J., Kapur, K., & Do, M. T. H. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.09.095 · Cited by 48
(2017) · PubMed · Cited by 51
Guido, M. E., Marchese, N. A., Ríos, M. N., Morera, L. P., Díaz, N. M., Garbarino‐Pico, E., & Contin, M. A. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00997-x · Cited by 54
High‐intensity red light suppresses melatonin
Hanifin, J. P., Stewart, K. T., Smith, P. H., Tanner, R. D., Rollag, M. D., & Brainard, G. C. (2006) · Chronobiology International · doi:10.1080/07420520500521988 · Cited by 52
Rahman, M. S., Kim, B.-H., Takemura, A., Park, C.-B., & Lee, Y.-D. (2004) · Journal of Biological Rhythms · doi:10.1177/0748730404266712 · Cited by 50
Sundowning syndrome in aging and dementia: Research in mouse models
Bedrosian, T. A., & Nelson, R. J. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2012.05.005 · Cited by 50
In synch but not in step: Circadian clock circuits regulating plasticity in daily rhythms
Evans, J. A., & Gorman, M. R. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.01.072 · Cited by 49
Metadata
- Authors
- Hattar, S., Lucas, R. J., Mrosovsky, N., Thompson, S., Douglas, R. H., Hankins, M. W., Lem, J., Biel, M., Hofmann, F., Foster, R. G., & Yau, K.-W.
- Affiliations
- Howard Hughes Medical Institute (US)
- Imperial College London (GB)
- University of Toronto (CA)
- City, University of London (GB)
- Tufts University (US)
- Ludwig-Maximilians-Universität München (DE)
- Technical University of Munich (DE)
- Corresponding author
- Yau, K.-W.
- Venue
- Nature
- Published
- 2003-06-15
- Volume
- 424
- Issue
- 6944
- Pages
- 75-81
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC2885907
- OpenAlex
- W2014028088
- Cited by
- 1,245
- References
- 31
- Citations by year
- 2026: 19 · 2025: 32 · 2024: 49 · 2023: 44 · 2022: 50 · 2021: 43 · 2020: 65 · 2019: 76 · 2018: 58 · 2017: 64 · 2016: 64 · 2015: 50 · 2014: 67 · 2013: 61 · 2012: 53
- FWCI
- 20.12
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- mediaTUM – the media and publications repository of the Technical University Munich (Technical University Munich) (submittedVersion)
- Research Explorer (The University of Manchester) (submittedVersion)
- Funders
- Wellcome Trust
- National Eye Institute (R37EY006837, R01EY014596, R01EY006837)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Health Sciences › Medicine › Ophthalmology › Retinal Development and Disorders
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Photoreceptor and optogenetics research
- Keywords
- melanopsin, pupillary light reflex, circadian phase shifting, action spectrum, retinal ganglion cells, mice, light entrainment
- MeSH terms
- Melanopsin, Animals, Circadian Rhythm, Darkness, Female, Ion Channels, Light, Male, Mice, Inbred C3H, Motor Activity, Reflex, Pupillary, Retinal Ganglion Cells, Vision, Ocular, Visual Perception, Rod Opsins, Gene Deletion, Retinal Rod Photoreceptor Cells, Retinal Cone Photoreceptor Cells, Mice, Knockout, Mice, Cyclic Nucleotide-Gated Cation Channels
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