V. Arshavsky, Like Night and Day, Neuron, vol.36, issue.1, pp.1-3, 2002.
DOI : 10.1016/S0896-6273(02)00937-6

M. Belenky, C. Smeraski, I. Provencio, P. Sollars, and G. Pickard, Melanopsin retinal ganglion cells receive bipolar and amacrine cell synapses, The Journal of Comparative Neurology, vol.460, issue.3, pp.380-393, 2003.
DOI : 10.1002/cne.10652

D. Berson, F. Dunn, and M. Takao, Phototransduction by Retinal Ganglion Cells That Set the Circadian Clock, Science, vol.295, issue.5557, pp.1070-1073, 2002.
DOI : 10.1126/science.1067262

G. Brainard, B. Richardson, T. King, and R. Reiter, The influence of different light spectra on the suppression of pineal melatonin content in the syrian hamster, Brain Research, vol.294, issue.2, pp.333-339, 1984.
DOI : 10.1016/0006-8993(84)91045-X

P. Chen, W. Hao, L. Rife, X. Wang, D. Shen et al., A photic visual cycle of rhodopsin regeneration is dependent on RGR, Nature Genetics, vol.28, issue.3, pp.256-260, 2001.
DOI : 10.1038/90089

M. Contin, D. Verra, and M. Guido, An invertebrate-like phototransduction cascade mediates light detection in the chicken retinal ganglion cells, The FASEB Journal, vol.20, issue.14, pp.2648-2650, 2006.
DOI : 10.1096/fj.06-6133fje

D. Dacey, H. Liao, B. Peterson, F. Robinson, V. Smith et al., Melanopsin-expressing ganglion cells in primate retina signal colour and irradiance and project to the LGN, Nature, vol.341, issue.36, pp.749-754, 2005.
DOI : 10.1523/JNEUROSCI.3828-03.2004

O. Dkhissi-benyahya, B. Sicard, and H. Cooper, Effects of irradiance and stimulus duration on early gene expression (Fos) in the suprachiasmatic nucleus: temporal summation and reciprocity, J Neurosci, vol.20, pp.7790-7797, 2000.
URL : https://hal.archives-ouvertes.fr/inserm-00131432

S. Doyle, A. Castrucci, M. Mccall, I. Provencio, and M. Menaker, Nonvisual light responses in the Rpe65 knockout mouse: Rod loss restores sensitivity to the melanopsin system, Proceedings of the National Academy of Sciences, vol.103, issue.27, pp.10432-10437, 2006.
DOI : 10.1073/pnas.0600934103

E. Drouyer, C. Rieux, R. Hut, and H. Cooper, Responses of SCN neurons to light and dark adaptation: relative contributions of melanopsin and rod-cone inputs, J Neuroscience, 2007.
URL : https://hal.archives-ouvertes.fr/inserm-00174270

G. Fain, H. Matthews, M. Cornwall, and Y. Koutalos, Adaptation in vertebrate photoreceptors, Physiol Rev, vol.81, pp.117-151, 2001.

Y. Fu, H. Zhong, M. Wang, D. Luo, H. Liao et al., Intrinsically photosensitive retinal ganglion cells detect light with a vitamin A-based photopigment, melanopsin, Proceedings of the National Academy of Sciences, vol.102, issue.29, pp.10339-10344, 2005.
DOI : 10.1073/pnas.0501866102

P. Gamlin, D. Mcdougal, J. Pokorny, V. Smith, K. Yau et al., Human and macaque pupil responses driven by melanopsin-containing retinal ganglion cells, Vision Research, vol.47, issue.7, pp.946-954, 2007.
DOI : 10.1016/j.visres.2006.12.015

URL : http://doi.org/10.1016/j.visres.2006.12.015

J. Gooley, J. Lu, D. Fischer, and C. Saper, A broad role for melanopsin in nonvisual photoreception, J Neurosci, vol.23, issue.18, pp.7093-106, 2003.

. Gronfier, K. Wright, . Jr, R. Kronauer, and C. Czeisler, Entrainment of the human circadian pacemaker to longer-than-24-h days, Proceedings of the National Academy of Sciences, vol.104, issue.21, pp.9081-9086, 2007.
DOI : 10.1073/pnas.0702835104

URL : https://hal.archives-ouvertes.fr/inserm-00149594

S. Hattar, M. Kumar, A. Park, P. Tong, J. Tung et al., Central projections of melanopsin-expressing retinal ganglion cells in the mouse, The Journal of Comparative Neurology, vol.132, issue.3, pp.326-349, 2006.
DOI : 10.1002/cne.20970

S. Hattar, R. Lucas, N. Mrosovsky, S. Thompson, R. Douglas et al., Melanopsin and rod???cone photoreceptive systems account for all major accessory visual functions in mice, Nature, vol.424, issue.6944, pp.76-81, 2003.
DOI : 10.1038/nature01761

P. Hillman, S. Hochstein, and B. Minke, Transduction in invertebrate photoreceptors: role of pigment bistability, Physiol Rev, vol.63, pp.668-772, 1983.

M. Isoldi, M. Rollag, A. Castrucci, and I. Provencio, Rhabdomeric phototransduction initiated by the vertebrate photopigment melanopsin, Proceedings of the National Academy of Sciences, vol.102, issue.4, pp.1217-1221, 2005.
DOI : 10.1073/pnas.0409252102

A. Kiselev and S. Subramaniam, Activation and regeneration of rhodopsin in the insect visual cycle, Science, vol.266, issue.5189, pp.1369-1373, 1994.
DOI : 10.1126/science.7973725

M. Koyanagi, A. Terakita, K. Kubokawa, and Y. Shichida, -retinals as their chromophores, FEBS Letters, vol.288, issue.3, pp.525-528, 2002.
DOI : 10.1016/S0014-5793(02)03616-5

URL : https://hal.archives-ouvertes.fr/jpa-00253096

M. Koyanagi, K. Kubokawa, H. Tsukamoto, Y. Shichida, and A. Terakita, Cephalochordate Melanopsin: Evolutionary Linkage between Invertebrate Visual Cells and Vertebrate Photosensitive Retinal Ganglion Cells, Current Biology, vol.15, issue.11, pp.1065-1069, 2005.
DOI : 10.1016/j.cub.2005.04.063

URL : http://doi.org/10.1016/j.cub.2005.04.063

T. Kumbalasiri and I. Provencio, Melanopsin and other novel mammalian opsins, Experimental Eye Research, vol.81, issue.4, pp.368-375, 2005.
DOI : 10.1016/j.exer.2005.05.004

J. Lisman and Y. Sheline, Analysis of the rhodopsin cycle in limulus ventral photoreceptors using the early receptor potential, The Journal of General Physiology, vol.68, issue.5, pp.487-501, 1976.
DOI : 10.1085/jgp.68.5.487

R. Lucas, Chromophore regeneration: Melanopsin does its own thing, Proceedings of the National Academy of Sciences, vol.103, issue.27, pp.10153-10154, 2006.
DOI : 10.1073/pnas.0603955103

R. Lucas, R. Douglas, and R. Foster, Characterization of an ocular photopigment capable of driving pupillary constriction in mice, Nature Neuroscience, vol.4, issue.6, pp.621-626, 2001.
DOI : 10.1038/88443

R. Lucas, S. Hattar, M. Takao, D. Berson, R. Foster et al., Diminished Pupillary Light Reflex at High Irradiances in Melanopsin-Knockout Mice, Science, vol.299, issue.5604, pp.245-247, 2003.
DOI : 10.1126/science.1077293

T. Maeda, V. Hooser, J. Driessen, C. Filipek, S. Janssen et al., Evaluation of the role of the retinal G protein-coupled receptor (RGR) in the vertebrate retina in vivo, Journal of Neurochemistry, vol.43, issue.4, pp.944-956, 2003.
DOI : 10.1046/j.1471-4159.2003.01741.x

N. Mata, R. Radu, R. Clemmons, and G. Travis, Isomerization and Oxidation of Vitamin A in Cone-Dominant Retinas, Neuron, vol.36, issue.1, pp.69-80, 2002.
DOI : 10.1016/S0896-6273(02)00912-1

J. Mcbee, K. Palczewski, W. Baehr, and D. Pepperberg, Confronting Complexity: the Interlink of Phototransduction and Retinoid Metabolism in the Vertebrate Retina, Progress in Retinal and Eye Research, vol.20, issue.4, pp.469-529, 2001.
DOI : 10.1016/S1350-9462(01)00002-7

J. Meijer, K. Watanabe, J. Schaap, H. Albus, and L. Detari, Light responsiveness of the suprachiasmatic nucleus: long-term multiunit and single-unit recordings in freely moving rats, J Neurosci, vol.18, issue.21, pp.9078-9087, 1998.

Z. Melyan, E. Tarttelin, J. Bellingham, R. Lucas, and M. Hankins, Addition of human melanopsin renders mammalian cells photoresponsive, Nature, vol.29, issue.7027, pp.741-745, 2005.
DOI : 10.1126/science.1105121

S. Nayak, T. Jegla, and S. Panda, Role of a novel photopigment, melanopsin, in behavioral adaptation to light, Cellular and Molecular Life Sciences, vol.64, issue.2, pp.144-154, 2007.
DOI : 10.1007/s00018-006-5581-1

S. Panda, S. Nayak, B. Campo, J. Walker, J. Hogenesch et al., Illumination of the Melanopsin Signaling Pathway, Science, vol.307, issue.5709, pp.600-604, 2005.
DOI : 10.1126/science.1105121