R. H. Masland, Maturation of function in the developing rabbit retina, The Journal of Comparative Neurology, vol.175, issue.3, pp.275-86, 1977.
DOI : 10.1002/cne.901750303

J. S. Tootle, Early postnatal development of visual function in ganglion cells of the cat retina

E. Sernagor and N. M. Grzywacz, Emergence of complex receptive field properties of ganglion cells in the developing turtle retina, J. Neurophysiol, vol.73, pp.1355-64, 1995.

N. Tian, Developmental mechanisms that regulate retinal ganglion cell dendritic morphology, Developmental Neurobiology, vol.9, issue.12
DOI : 10.1002/dneu.20900
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923654

N. Tian and D. R. Copenhagen, Visual Stimulation Is Required for Refinement of ON and OFF Pathways in Postnatal Retina, Neuron, vol.39, issue.1, pp.85-96, 2003.
DOI : 10.1016/S0896-6273(03)00389-1

N. Tian and D. R. Copenhagen, Visual Deprivation Alters Development of Synaptic Function in Inner Retina after Eye Opening, Neuron, vol.32, issue.3, pp.439-449, 2001.
DOI : 10.1016/S0896-6273(01)00470-6

D. R. Cantrell, J. Cang, J. B. Troy, and X. Liu, Non-Centered Spike-Triggered Covariance Analysis Reveals Neurotrophin-3 as a Developmental Regulator of Receptive Field Properties of ON-OFF Retinal Ganglion Cells, PLoS Computational Biology, vol.7, issue.10, p.1000967, 2010.
DOI : 10.1371/journal.pcbi.1000967.s007

C. L. Koehler, N. P. Akimov, and R. C. Rentería, Receptive field center size decreases and firing properties mature in ON and OFF retinal ganglion cells after eye opening in the mouse, Journal of Neurophysiology, vol.106, issue.2
DOI : 10.1152/jn.01046.2010

J. Elstrott, Direction Selectivity in the Retina Is Established Independent of Visual Experience and Cholinergic Retinal Waves, Neuron, vol.58, issue.4, pp.499-506, 2008.
DOI : 10.1016/j.neuron.2008.03.013

H. Chen, X. Liu, and N. Tian, Subtype-dependent postnatal development of direction-and not peer-reviewed) is the author/funder. All rights reserved

. Szel, Unique topographic separation of two spectral classes of cones in the mouse retina, Journal of Comparative Neurology, vol.33, issue.3, pp.327-342, 1992.
DOI : 10.1002/cne.903250302

Á. Szél, P. Röhlich, A. R. Caffé, and T. Van-veen, Distribution of cone photoreceptors in the mammalian retina, Microscopy Research and Technique, vol.18, issue.6, pp.445-462, 1996.
DOI : 10.1002/(SICI)1097-0029(19961215)35:6<445::AID-JEMT4>3.0.CO;2-H

M. L. Applebury, The Murine Cone Photoreceptor, Neuron, vol.27, issue.3, pp.513-523, 2000.
DOI : 10.1016/S0896-6273(00)00062-3

P. Röhlich, T. Van-veen, and Á. Szél, Two different visual pigments in one retinal cone cell, Neuron, vol.13, issue.5, pp.1159-1166, 1994.
DOI : 10.1016/0896-6273(94)90053-1

Á. Lukáts, . Szabó, P. Röhlich, B. Vígh, and Á. Szél, Photopigment coexpression in mammals: Comparative and developmental aspects, Histol. Histopathol, vol.20, pp.551-574, 2005.

L. Chang, T. Breuninger, and T. Euler, Chromatic Coding from Cone-type Unselective Circuits in the Mouse Retina, Neuron, vol.77, issue.3, pp.559-571, 2013.
DOI : 10.1016/j.neuron.2012.12.012

B. Ekesten and P. Gouras, Cone and rod inputs to murine retinal ganglion cells: Evidence of cone opsin specific channels, Visual Neuroscience, vol.211, issue.06, pp.893-903, 2005.
DOI : 10.1016/S0896-6273(02)01046-2

Y. V. Wang, M. Weick, and J. Demb, Spectral and Temporal Sensitivity of Cone-Mediated Responses in Mouse Retinal Ganglion Cells, Journal of Neuroscience, vol.31, issue.21, pp.7670-7681, 2011.
DOI : 10.1523/JNEUROSCI.0629-11.2011

T. Baden, A Tale of Two Retinal Domains: Near-Optimal Sampling of Achromatic Contrasts in Natural Scenes through Asymmetric Photoreceptor Distribution, Neuron, vol.80, issue.5, pp.1206-1217, 2013.
DOI : 10.1016/j.neuron.2013.09.030

L. Yin, R. G. Smith, P. Sterling, and D. H. Brainard, Physiology and Morphology of Color-Opponent Ganglion Cells in a Retina Expressing a Dual Gradient of S and M Opsins, Journal of Neuroscience, vol.29, issue.9, pp.2706-2724, 2009.
DOI : 10.1523/JNEUROSCI.5471-08.2009

L. Peichl, Diversity of mammalian photoreceptor properties: Adaptations to habitat and lifestyle? Anat. Rec. -Part A Discov, Mol. Cell. Evol. Biol, vol.287, pp.1001-1012, 2005.

Y. Zhang, I. Kim, J. R. Sanes, and M. Meister, The most numerous ganglion cell type of the mouse retina is a selective feature detector, Proc. Natl. Acad. Sci, pp.2391-2398, 2012.
DOI : 10.1073/pnas.1211547109

A. Bleckert, G. W. Schwartz, M. H. Turner, F. Rieke, and R. O. Wong, Visual space is not peer-reviewed) is the author/funder. All rights reserved

L. Berdondini, Active pixel sensor array for high spatio-temporal resolution electrophysiological recordings from single cell to large scale neuronal networks, Lab on a Chip, vol.3, issue.18, p.2644, 2009.
DOI : 10.1002/acs.1077

A. Maccione, Following the ontogeny of retinal waves: pan-retinal recordings of population dynamics in the neonatal mouse, The Journal of Physiology, vol.20, issue.7, pp.1545-63, 2014.
DOI : 10.1113/jphysiol.2013.262840

G. Portelli, Rank order coding: a retinal information decoding strategy revealed by largescale multielectrode array retinal recordings. eneuro (2016). at <http://eneuro.org/content A super-resolution approach for receptive fields estimation of neuronal ensembles, BMC Neurosci, vol.12, issue.16, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01316105

Q. He, P. Wang, and N. Tian, Light-evoked synaptic activity of retinal ganglion and amacrine cells is regulated in developing mouse retina, European Journal of Neuroscience, vol.484, issue.Pt 1, pp.36-48, 2011.
DOI : 10.1111/j.1460-9568.2010.07484.x

J. Zhang and J. S. Diamond, Subunit- and Pathway-Specific Localization of NMDA Receptors and Scaffolding Proteins at Ganglion Cell Synapses in Rat Retina, Journal of Neuroscience, vol.29, issue.13, pp.4274-4286, 2009.
DOI : 10.1523/JNEUROSCI.5602-08.2009

B. K. Stafford, S. J. Park, K. Y. Wong, and J. B. Demb, Developmental Changes in NMDA Receptor Subunit Composition at ON and OFF Bipolar Cell Synapses onto Direction-Selective Retinal Ganglion Cells, Journal of Neuroscience, vol.34, issue.5, pp.1942-1948, 2014.
DOI : 10.1523/JNEUROSCI.4461-13.2014

P. D. Lukasiewicz and C. R. Shields, A diversity of GABA receptors in the retina, Seminars in Cell & Developmental Biology, vol.9, issue.3, pp.293-302, 1998.
DOI : 10.1006/scdb.1998.0238

P. D. Lukasiewicz, E. D. Eggers, B. T. Sagdullaev, and M. A. Mccall, GABAC receptor-mediated inhibition in the retina, Vision Research, vol.44, issue.28, pp.3289-3296, 2004.
DOI : 10.1016/j.visres.2004.07.023

B. T. Sagdullaev, M. A. Mccall, and P. Lukasiewicz, Presynaptic Inhibition Modulates Spillover, Creating Distinct Dynamic Response Ranges of Sensory Output, Neuron, vol.50, issue.6, pp.923-935, 2006.
DOI : 10.1016/j.neuron.2006.05.015

T. Schubert, Development of Presynaptic Inhibition Onto Retinal Bipolar Cell Axon not peer-reviewed) is the author/funder. All rights reserved

A. Greka, S. Lipton, and D. Zhang, Expression of GABA C receptor r1 and r2 subunits during development of the mouse retina, pp.3575-3582, 2000.

G. Y. Wang, L. C. Liets, and L. M. Chalupa, Unique functional properties of on and off pathways in the developing mammalian retina, J. Neurosci, vol.21, pp.4310-4317, 2001.

K. L. Myhr, P. D. Lukasiewicz, and R. O. Wong, Mechanisms underlying developmental changes in the firing patterns of ON and OFF retinal ganglion cells during refinement of their central projections, J. Neurosci, vol.21, pp.8664-71, 2001.

G. H. Jacobs, J. Neitz, and J. Deegan, Retinal receptors in rodents maximally sensitive to ultraviolet light, Nature, vol.353, issue.6345, pp.655-656, 1991.
DOI : 10.1038/353655a0

F. Naarendorp, Dark Light, Rod Saturation, and the Absolute and Incremental Sensitivity of Mouse Cone Vision, Journal of Neuroscience, vol.30, issue.37, pp.12495-12507, 2010.
DOI : 10.1523/JNEUROSCI.2186-10.2010

C. Jeon, E. Strettoi, and R. H. Masland, The Major Cell Populations of the Mouse Retina, J. Neurosci, vol.18, pp.8936-8946, 1998.

E. J. Chichilnisky, A simple white noise analysis of neuronal light responses, Network: Computation in Neural Systems, vol.12, issue.2, pp.199-213, 2001.
DOI : 10.1080/713663221

O. Schwartz, J. W. Pillow, N. C. Rust, and E. P. Simoncelli, Spike-triggered neural characterization, Journal of Vision, vol.6, issue.4, pp.484-507, 2006.
DOI : 10.1167/6.4.13

R. W. Young and R. W. Young, Cell death during differentiation of the retina in the mouse, The Journal of Comparative Neurology, vol.81, issue.3
DOI : 10.1002/cne.902290307

W. Wei, J. Elstrott, and M. B. Feller, Two-photon targeted recording of GFP-expressing neurons for light responses and live-cell imaging in the mouse retina, Nature Protocols, vol.154, issue.7, pp.1347-52, 2010.
DOI : 10.1038/nprot.2010.106

A. Maccione, Microelectronics, bioinformatics and neurocomputation for massive neuronal recordings in brain circuits with large scale multielectrode array probes, Brain Research Bulletin, vol.119
DOI : 10.1016/j.brainresbull.2015.07.008

. Bull, doi:10.1016/j.brainresbull.2015.07.008 not peer-reviewed) is the author/funder. All rights reserved, 2015.