D. Choquet and A. Triller, The Dynamic Synapse, Neuron, vol.80, issue.3, pp.691-703, 2013.
DOI : 10.1016/j.neuron.2013.10.013

URL : http://doi.org/10.1016/j.neuron.2013.10.013

F. Crick and . Neurobiology, Neurobiology: Memory and molecular turnover, Nature, vol.312, issue.5990, p.101, 1984.
DOI : 10.1038/312101a0

M. Rosenberg, J. Meier, A. Triller, and C. Vannier, Dynamics of glycine receptor insertion in the neuronal plasma membrane, Journal of Neuroscience, vol.21, issue.14, pp.5036-5044, 2001.

P. Thomas, M. Mortensen, A. Hosie, and T. Smart, Dynamic mobility of functional GABAA receptors at inhibitory synapses, Nature Neuroscience, vol.557, issue.7, pp.889-897, 2005.
DOI : 10.1073/pnas.90.16.7819

Y. Bogdanov, G. Michels, C. Armstrong-gold, P. Haydon, J. Lindstrom et al., Synaptic GABAA receptors are directly recruited from their extrasynaptic counterparts, The EMBO Journal, vol.20, issue.18, pp.4381-4389, 2006.
DOI : 10.1074/jbc.273.2.964

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1570424

C. Specht, I. Izeddin, P. Rodriguez, E. Beheiry, M. Rostaing et al., Quantitative Nanoscopy of Inhibitory Synapses: Counting Gephyrin Molecules and Receptor Binding Sites, Neuron, vol.79, issue.2, pp.308-321, 2013.
DOI : 10.1016/j.neuron.2013.05.013

URL : http://doi.org/10.1016/j.neuron.2013.05.013

E. Kim, N. Schrader, B. Smolinsky, C. Bedet, C. Vannier et al., Deciphering the structural framework of glycine receptor anchoring by gephyrin, The EMBO Journal, vol.9, issue.6, pp.1385-1395, 2006.
DOI : 10.1007/PL00006390

S. Tyagarajan and J. Fritschy, Gephyrin: a master regulator of neuronal function?, Nature Reviews Neuroscience, vol.29, issue.3, pp.141-156, 2014.
DOI : 10.1038/nrn3670

M. Calamai, C. Specht, J. Heller, D. Alcor, P. Machado et al., Gephyrin Oligomerization Controls GlyR Mobility and Synaptic Clustering, Journal of Neuroscience, vol.29, issue.24, pp.7639-7648, 2009.
DOI : 10.1523/JNEUROSCI.5711-08.2009

A. Vlachos, S. Reddy-alla, T. Papadopoulos, T. Deller, and H. Betz, Homeostatic Regulation of Gephyrin Scaffolds and Synaptic Strength at Mature Hippocampal GABAergic Postsynapses?, Cerebral Cortex, vol.23, issue.11, pp.2700-2711, 2013.
DOI : 10.1093/cercor/bhs260

S. Okabe, Fluorescence imaging of synapse formation and remodeling, Microscopy, vol.62, issue.1, pp.51-62, 2013.
DOI : 10.1093/jmicro/dfs083

N. Schrader, E. Kim, J. Winking, J. Paulukat, H. Schindelin et al., Biochemical Characterization of the High Affinity Binding between the Glycine Receptor and Gephyrin, Journal of Biological Chemistry, vol.279, issue.18, pp.18733-18741, 2004.
DOI : 10.1074/jbc.M311245200

M. Sola, V. Bavro, J. Timmins, T. Franz, R. -. Blum et al., Structural basis of dynamic glycine receptor clustering by gephyrin, The EMBO Journal, vol.26, issue.13, pp.2510-2519, 2004.
DOI : 10.1016/S0969-2126(01)00588-3

URL : https://hal.archives-ouvertes.fr/hal-00313935

A. Belaidi and G. Schwarz, Metal insertion into the molybdenum cofactor: product???substrate channelling demonstrates the functional origin of domain fusion in gephyrin, Biochemical Journal, vol.74, issue.1, pp.149-157, 2013.
DOI : 10.1074/jbc.M112.341826

J. Herweg and G. Schwarz, Splice-specific Glycine Receptor Binding, Folding, and Phosphorylation of the Scaffolding Protein Gephyrin, Journal of Biological Chemistry, vol.287, issue.16, pp.12645-12656, 2012.
DOI : 10.1074/jbc.M112.341826

M. Ehrensperger, C. Hanus, C. Vannier, A. Triller, and M. Dahan, Multiple Association States between Glycine Receptors and Gephyrin Identified by SPT Analysis, Biophysical Journal, vol.92, issue.10, pp.3706-3718, 2007.
DOI : 10.1529/biophysj.106.095596

URL : http://doi.org/10.1529/biophysj.106.095596

C. Ribrault, K. Sekimoto, and A. Triller, From the stochasticity of molecular processes to the variability of synaptic transmission, Nature Reviews Neuroscience, vol.30, issue.7, pp.375-387, 2011.
DOI : 10.1038/nrn3025

C. Haselwandter, M. Calamai, M. Kardar, A. Triller, and R. Da-silveira, Formation and Stability of Synaptic Receptor Domains, Physical Review Letters, vol.113, issue.23, pp.238104-21770547, 2011.
DOI : 10.1016/j.tins.2005.11.003

C. Haselwandter, M. Kardar, A. Triller, and R. Da-silveira, Self-assembly and plasticity of synaptic domains through a reaction-diffusion mechanism, Physical Review E, vol.302, issue.3, p.32705, 2015.
DOI : 10.1021/j100540a008

V. Burlakov, N. Emptage, A. Goriely, and P. Bressloff, Synaptic Bistability Due to Nucleation and Evaporation of Receptor Clusters, Physical Review Letters, vol.65, issue.2, pp.28101-22324711, 2012.
DOI : 10.1073/pnas.0502332102

M. Turner, P. Sens, and N. Socci, Nonequilibrium raftlike membrane domains under continuous recycling. Physical review letters, pp.168301-16241845, 2005.
DOI : 10.1103/physrevlett.95.168301

URL : https://hal.archives-ouvertes.fr/hal-00108206

J. Gómez, F. Sagués, and R. Reigada, Actively maintained lipid nanodomains in biomembranes, Physical Review E, vol.5, issue.2, p.21907, 2008.
DOI : 10.1083/jcb.141.4.929

B. Quang, M. Mani, O. Markova, T. Lecuit, and P. Lenne, Principles of E-cadherin supramolecular organization in vivo, Current Biology, vol.23, issue.22, pp.2197-2207, 2013.

H. Shouval, Clusters of interacting receptors can stabilize synaptic efficacies, Proceedings of the National Academy of Sciences, vol.28, issue.2, pp.14440-14445, 2005.
DOI : 10.1016/S0896-6273(00)00129-X

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1242325

W. White, On the form of steady-state solutions to the coagulation equations, Journal of Colloid and Interface Science, vol.87, issue.1, pp.204-2080021, 1982.
DOI : 10.1016/0021-9797(82)90382-4

Z. Rácz, Aggregation in the presence of sources and sinks: A scaling theory, Physical Review A, vol.17, issue.2, pp.1129-1133, 1985.
DOI : 10.1088/0305-4470/17/2/009

Z. Nusser, J. Roberts, A. Baude, J. Richards, and P. Somogyi, Relative densities of synaptic and extrasynaptic GABAA receptors on cerebellar granule cells as determined by a quantitative immunogold method, The Journal of Neuroscience, vol.15, issue.4, pp.2948-2960, 1995.

P. Saffman and M. Delbrück, Brownian motion in biological membranes., Proceedings of the National Academy of Sciences, pp.3111-3113, 1975.
DOI : 10.1073/pnas.72.8.3111

URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC432930/pdf

Y. Gambin, R. Lopez-esparza, M. Reffay, E. Sierecki, N. Gov et al., Lateral mobility of proteins in liquid membranes revisited, Proceedings of the National Academy of Sciences, vol.1, issue.10, pp.2098-2102, 2006.
DOI : 10.1039/FT9959104269

P. Meakin, Formation of Fractal Clusters and Networks by Irreversible Diffusion-Limited Aggregation, Physical Review Letters, vol.50, issue.13, pp.1119-1122, 1983.
DOI : 10.1103/PhysRevLett.50.1062

S. Mv, Grundriß der Koagulationskinetik kolloider Lösungen, Colloid & Polymer Science, vol.21, issue.3, pp.98-104, 1917.

R. Ziff, E. Mcgrady, and P. Meakin, On the validity of Smoluchowski???s equation for cluster???cluster aggregation kinetics, The Journal of Chemical Physics, vol.82, issue.11, pp.5269-5274, 1985.
DOI : 10.1088/0305-4470/16/10/026

A. Dumoulin, S. Levi, B. Riveau, B. Gasnier, and A. Triller, Formation of mixed glycine and GABAergic synapses in cultured spinal cord neurons, European Journal of Neuroscience, vol.749, issue.11, pp.3883-3892, 2000.
DOI : 10.1016/S0006-8993(96)01326-1

Y. Pomeau, Sym?trie des fluctuations dans le renversement du temps, Journal de Physique, vol.43, issue.6, pp.859-86701982004306085900, 1982.
DOI : 10.1051/jphys:01982004306085900

URL : https://hal.archives-ouvertes.fr/jpa-00209463/document

Y. Pomeau, L. Berre, M. Ginibre, and J. , Ultimate statistical physics: fluorescence of a single atom, Journal of Statistical Mechanics: Theory and Experiment, vol.2016, issue.10, pp.1040021742-5468, 2016.
DOI : 10.1088/1742-5468/2016/10/104002

A. Hyman, C. Weber, and F. Jülicher, Liquid-Liquid Phase Separation in Biology, Annual Review of Cell and Developmental Biology, vol.30, issue.1, pp.39-58, 2014.
DOI : 10.1146/annurev-cellbio-100913-013325

M. Zeng, Y. Shang, Y. Araki, T. Guo, R. Huganir et al., Phase Transition in Postsynaptic Densities Underlies Formation of Synaptic Complexes and Synaptic Plasticity, Cell, vol.166, issue.5, pp.1163-1175, 2016.
DOI : 10.1016/j.cell.2016.07.008

C. Brangwynne, Phase transitions and size scaling of membrane-less organelles, The Journal of Cell Biology, vol.203, issue.6, pp.875-881, 2013.
DOI : 10.1093/jb/mvt001

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871435

J. Singer and A. Berger, Contribution of single-channel properties to the time course and amplitude variance of quantal glycine currents recorded in rat motoneurons, Journal of Neurophysiology, vol.81, issue.4, pp.1608-1616, 1999.

J. Rigo, C. Badiu, and P. Legendre, Heterogeneity of Postsynaptic Receptor Occupancy Fluctuations among Glycinergic Inhibitory Synapses in the Zebrafish Hindbrain, The Journal of Physiology, vol.12, issue.3, pp.819-832, 2003.
DOI : 10.1046/j.1460-9568.2000.00282.x

URL : https://hal.archives-ouvertes.fr/hal-00080136

T. Witten and L. Sander, Diffusion-Limited Aggregation, a Kinetic Critical Phenomenon, Physical Review Letters, vol.80, issue.19, pp.1400-1403, 1981.
DOI : 10.1016/0375-9601(80)90023-7

D. Kessler, J. Koplik, and H. Levine, Pattern selection in fingered growth phenomena Advances in Physics, pp.255-339, 1988.
DOI : 10.1080/00018738800101379

A. Minerbi, R. Kahana, L. Goldfeld, M. Kaufman, S. Marom et al., Long-term relationships between synaptic tenacity, synaptic remodeling, and network activity):e1000136. https, PLoS Biol, vol.7, issue.6, 2009.
DOI : 10.1371/journal.pbio.1000136

URL : http://doi.org/10.1371/journal.pbio.1000136

H. Kesten, Random difference equations and Renewal theory for products of random matrices, Acta Mathematica, vol.131, issue.0, pp.207-248, 1973.
DOI : 10.1007/BF02392040

A. Statman, M. Kaufman, A. Minerbi, N. Ziv, and N. Brenner, Synaptic Size Dynamics as an Effectively Stochastic Process, PLoS Computational Biology, vol.33, issue.10, p.25275505, 2014.
DOI : 10.1371/journal.pcbi.1003846.s006

URL : http://doi.org/10.1371/journal.pcbi.1003846

A. Rubinski and N. Ziv, Remodeling and Tenacity of Inhibitory Synapses: Relationships with Network Activity and Neighboring Excitatory Synapses, PLOS Computational Biology, vol.295, issue.9, pp.1004632-26599330, 2015.
DOI : 10.1371/journal.pcbi.1004632.s006

V. Tatavarty, Q. Sun, and G. Turrigiano, How to Scale Down Postsynaptic Strength, Journal of Neuroscience, vol.33, issue.32, pp.13179-13189, 2013.
DOI : 10.1523/JNEUROSCI.1676-13.2013

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3735890

M. Zita, I. Marchionni, E. Bottos, M. Righi, D. Sal et al., Post-phosphorylation prolyl isomerisation of gephyrin represents a mechanism to modulate glycine receptors function, The EMBO Journal, vol.56, issue.7, pp.1761-1771, 2007.
DOI : 10.1016/j.bbadis.2004.10.003

A. Sergé, N. Bertaux, H. Rigneault, and D. Marguet, Dynamic multiple-target tracing to probe spatiotemporal cartography of cell membranes, Nature Methods, vol.84, issue.8, pp.687-694, 2008.
DOI : 10.1038/nmeth.1176

I. Izeddin, C. Specht, M. Lelek, X. Darzacq, A. Triller et al., Super-resolution dynamic imaging of dendritic spines using a low-affinity photoconvertible actin probe):e15611. https, PloS one, vol.6, issue.1, p.21264214, 2011.