S. Martin, P. Grimwood, and R. Morris, Synaptic Plasticity and Memory: An Evaluation of the Hypothesis, Annual Review of Neuroscience, vol.23, issue.1, pp.649-711, 2000.
DOI : 10.1146/annurev.neuro.23.1.649

U. Bhalla and R. Iyengar, Emergent Properties of Networks of Biological Signaling Pathways, Science, vol.283, issue.5400, pp.381-387, 1999.
DOI : 10.1126/science.283.5400.381

E. Kandel, The Molecular Biology of Memory Storage: A Dialogue Between Genes and Synapses, Science, vol.294, issue.5544, pp.1030-1038, 2001.
DOI : 10.1126/science.1067020

A. Routtenberg and J. Rekart, Post-translational protein modification as the substrate for long-lasting memory, Trends in Neurosciences, vol.28, issue.1, pp.12-19, 2005.
DOI : 10.1016/j.tins.2004.11.006

T. Soderling and V. Derkach, Postsynaptic protein phosphorylation and LTP, Trends in Neurosciences, vol.23, issue.2, pp.75-80, 2000.
DOI : 10.1016/S0166-2236(99)01490-3

K. Ganguly, L. Kiss, and M. Poo, Enhancement of presynaptic neuronal excitability by correlated presynaptic and postsynaptic spiking, Nat Neurosci, vol.3, pp.1018-1026, 2000.

D. Winder and J. Sweatt, Roles of serine/threonine phosphatases in hippocampel synaptic plasticity, Nature Reviews Neuroscience, vol.18, issue.7, pp.461-474, 2001.
DOI : 10.1038/35081514

G. Malleret, U. Haditsch, D. Genoux, M. Jones, and T. Bliss, Inducible and Reversible Enhancement of Learning, Memory, and Long-Term Potentiation by Genetic Inhibition of Calcineurin, Cell, vol.104, issue.5, pp.675-686, 2001.
DOI : 10.1016/S0092-8674(01)00264-1

Y. Huang, C. Pittenger, and E. Kandel, A form of long-lasting, learning-related synaptic plasticity in the hippocampus induced by heterosynaptic low-frequency pairing, Proceedings of the National Academy of Sciences, vol.101, issue.3, pp.859-864, 2004.
DOI : 10.1073/pnas.2237201100

J. Lisman, A mechanism for memory storage insensitive to molecular turnover: a bistable autophosphorylating kinase., Proceedings of the National Academy of Sciences, vol.82, issue.9, pp.3055-3057, 1985.
DOI : 10.1073/pnas.82.9.3055

D. 'alcantara, P. Schiffmann, S. Swillens, and S. , -controlled phosphorylation and dephosphorylation pathways, European Journal of Neuroscience, vol.81, issue.12, pp.2521-2528, 2003.
DOI : 10.1046/j.1460-9568.2003.02693.x

URL : https://hal.archives-ouvertes.fr/in2p3-00159393

G. Castellani, E. Quinlan, L. Cooper, and H. Shouval, A biophysical model of bidirectional synaptic plasticity: Dependence on AMPA and NMDA receptors, Proceedings of the National Academy of Sciences, vol.98, issue.22, pp.12772-12777, 2001.
DOI : 10.1073/pnas.201404598

P. Smolen, D. Baxter, and J. Byrne, A Model of the Roles of Essential Kinases in the Induction and Expression of Late Long-Term Potentiation, Biophysical Journal, vol.90, issue.8, pp.2309-2325, 2006.
DOI : 10.1529/biophysj.105.072470

H. Abarbanel, L. Gibb, R. Huerta, and M. Rabinovich, Biophysical model of synaptic plasticity dynamics, Biological Cybernetics, vol.89, issue.3, pp.214-226, 2003.
DOI : 10.1007/s00422-003-0422-x

H. Shouval, M. Bear, and L. Cooper, A unified model of NMDA receptor-dependent bidirectional synaptic plasticity, Proceedings of the National Academy of Sciences, vol.99, issue.16, pp.10831-10836, 2002.
DOI : 10.1073/pnas.152343099

M. Bear, A synaptic basis for memory storage in the cerebral cortex, Proceedings of the National Academy of Sciences, vol.93, issue.24, pp.13453-13459, 1996.
DOI : 10.1073/pnas.93.24.13453

I. Ismailov, D. Kalikulov, T. Inoue, and M. Friedlander, The Kinetic Profile of Intracellular Calcium Predicts Long-Term Potentiation and Long-Term Depression, Journal of Neuroscience, vol.24, issue.44, pp.9847-9861, 2004.
DOI : 10.1523/JNEUROSCI.0738-04.2004

P. Sjostrom, G. Turrigiano, and S. Nelson, Rate, Timing, and Cooperativity Jointly Determine Cortical Synaptic Plasticity, Neuron, vol.32, issue.6, pp.1149-1164, 2001.
DOI : 10.1016/S0896-6273(01)00542-6

M. Nishiyama, K. Hong, K. Mikoshiba, M. Poo, and K. Kato, Calcium stores regulate the polarity and input specificity of synaptic modification, Nature, vol.408, pp.584-588, 2000.

D. Angeli, J. Ferrell, . Jr, and E. Sontag, Detection of multistability, bifurcations, and hysteresis in a large class of biological positive-feedback systems, Proceedings of the National Academy of Sciences, vol.101, issue.7, pp.1822-1827, 2004.
DOI : 10.1073/pnas.0308265100

A. Zhabotinsky, Bistability in the Ca2+/Calmodulin-Dependent Protein Kinase-Phosphatase System, Biophysical Journal, vol.79, issue.5, pp.2211-2221, 2000.
DOI : 10.1016/S0006-3495(00)76469-1

P. Miller, A. Zhabotinsky, J. Lisman, and X. Wang, The Stability of a Stochastic CaMKII Switch: Dependence on the Number of Enzyme Molecules and Protein Turnover, PLoS Biology, vol.35, issue.4, p.107, 2005.
DOI : 10.1371/journal.pbio.0030107.t001

A. Hayer and U. Bhalla, Molecular Switches at the Synapse Emerge from Receptor and Kinase Traffic, PLoS Computational Biology, vol.8, issue.2, pp.137-154, 2005.
DOI : 10.1371/journal.pcbi.0010020.sg002

H. Song, P. Smolen, E. Av-ron, D. Baxter, and J. Byrne, Bifurcation and Singularity Analysis of a Molecular Network for the Induction of Long-Term Memory, Biophysical Journal, vol.90, issue.7, pp.2309-2325, 2006.
DOI : 10.1529/biophysj.105.074500

C. Petersen, R. Malenka, R. Nicoll, and J. Hopfield, All-or-none potentiation at CA3-CA1 synapses, Proceedings of the National Academy of Sciences, vol.95, issue.8, pp.4732-4737, 1998.
DOI : 10.1073/pnas.95.8.4732

O. Connor, D. Wittenberg, G. Wang, and S. , Graded bidirectional synaptic plasticity is composed of switch-like unitary events, Proceedings of the National Academy of Sciences, vol.102, issue.27, pp.9679-9684, 2005.
DOI : 10.1073/pnas.0502332102

J. Montgomery and D. Madison, State-Dependent Heterogeneity in Synaptic Depression between Pyramidal Cell Pairs, Neuron, vol.33, issue.5, pp.765-777, 2002.
DOI : 10.1016/S0896-6273(02)00606-2

S. Shi, Y. Hayashi, R. Petralia, S. Zaman, and R. Wenthold, Rapid Spine Delivery and Redistribution of AMPA Receptors After Synaptic NMDA Receptor Activation, Science, vol.284, issue.5421, pp.1811-1816, 1999.
DOI : 10.1126/science.284.5421.1811

A. Heynen, E. Quinlan, D. Bae, and M. Bear, Bidirectional, Activity-Dependent Regulation of Glutamate Receptors in the Adult Hippocampus In Vivo, Neuron, vol.28, issue.2, pp.527-536, 2000.
DOI : 10.1016/S0896-6273(00)00130-6

A. Luthi, M. Wikstrom, M. Palmer, P. Matthews, and T. Benke, Bidirectional modulation of AMPA receptor unitary conductance by synaptic activity, BMC Neuroscience, vol.5, issue.1, p.44, 2004.
DOI : 10.1186/1471-2202-5-44

S. Tomita, V. Stein, T. Stocker, R. Nicoll, and D. Bredt, Bidirectional Synaptic Plasticity Regulated by Phosphorylation of Stargazin-like TARPs, Neuron, vol.45, issue.2, pp.269-277, 2005.
DOI : 10.1016/j.neuron.2005.01.009

J. Esteban, S. Shi, C. Wilson, M. Nuriya, and R. Huganir, PKA phosphorylation of AMPA receptor subunits controls synaptic trafficking underlying plasticity, Nature Neuroscience, vol.6, issue.2, pp.136-143, 2003.
DOI : 10.1038/nn997

G. Turrigiano, K. Leslie, N. Desai, L. Rutherford, and S. Nelson, Activity-dependent scaling of quantal amplitude in neocortical neurons, Nature, vol.391, issue.6670, pp.892-896, 1998.
DOI : 10.1038/36103

A. Watt, M. Van-rossum, K. Macleod, S. Nelson, and G. Turrigiano, Activity Coregulates Quantal AMPA and NMDA Currents at Neocortical Synapses, Neuron, vol.26, issue.3, pp.659-670, 2000.
DOI : 10.1016/S0896-6273(00)81202-7

J. Magee and E. Cook, Somatic EPSP amplitude is independent of synapse location in hippocampal pyramidal neurons, Nature Neuroscience, vol.3, issue.9, pp.895-903, 2000.
DOI : 10.1038/78800

M. Smith, G. Ellis-davies, and J. Magee, Mechanism of the distance-dependent scaling of Schaffer collateral synapses in rat CA1 pyramidal neurons, The Journal of Physiology, vol.548, issue.1, pp.245-258, 2003.
DOI : 10.1113/jphysiol.2002.036376

S. Royer and D. Pare, Conservation of total synaptic weight through balanced synaptic depression and potentiation, Nature, vol.382, issue.6931, pp.518-522, 2003.
DOI : 10.1016/S0166-2236(97)01124-7

G. Turrigiano, L. Abbott, and E. Marder, Activity-dependent changes in the intrinsic properties of cultured neurons, Science, vol.264, issue.5161, pp.974-977, 1994.
DOI : 10.1126/science.8178157

A. Egorov, B. Hamam, E. Fransen, M. Hasselmo, and A. Alonso, Graded persistent activity in entorhinal cortex neurons, Nature, vol.17, issue.6912, pp.173-178, 2002.
DOI : 10.1073/pnas.93.24.13481

G. Daoudal, Y. Hanada, and D. Debanne, Bidirectional plasticity of excitatory postsynaptic potential (EPSP)-spike coupling in CA1 hippocampal pyramidal neurons, Proceedings of the National Academy of Sciences, vol.99, issue.22, pp.14512-14517, 2002.
DOI : 10.1073/pnas.222546399

J. Oestreich, N. Dembrow, A. George, and H. Zakon, A ???Sample-and-Hold??? Pulse-Counting Integrator as a Mechanism for Graded Memory Underlying Sensorimotor Adaptation, Neuron, vol.49, issue.4, pp.577-588, 2006.
DOI : 10.1016/j.neuron.2006.01.027

J. Lisman and A. Zhabotinsky, A Model of Synaptic Memory, Neuron, vol.31, issue.2, pp.191-201, 2001.
DOI : 10.1016/S0896-6273(01)00364-6

R. Malenka, B. Lancaster, and R. Zucker, Temporal limits on the rise in postsynaptic calcium required for the induction of long-term potentiation, Neuron, vol.9, issue.1, pp.121-128, 1992.
DOI : 10.1016/0896-6273(92)90227-5

H. Chen, N. Otmakhov, S. Strack, R. Colbran, and J. Lisman, Is persistent activity of calcium/calmodulin-dependent kinase required for the maintenance of LTP?, J Neurophysiol, vol.85, pp.1368-1376, 2001.

I. Lengyel, K. Voss, M. Cammarota, K. Bradshaw, and V. Brent, Autonomous activity of CaMKII is only transiently increased following the induction of long-term potentiation in the rat hippocampus, European Journal of Neuroscience, vol.446, issue.11, pp.3063-3072, 2004.
DOI : 10.1111/j.1460-9568.2004.03748.x

S. Cooke, J. Wu, F. Plattner, M. Errington, and M. Rowan, Autophosphorylation of ??CaMKII is not a general requirement for NMDA receptor-dependent LTP in the adult mouse, The Journal of Physiology, vol.25, issue.3, pp.805-818, 2006.
DOI : 10.1113/jphysiol.2006.111559

M. Ito, Cerebellar long-term depression: Characterization, signal transduction, and functional roles, Physiol Rev, vol.81, pp.1143-1195, 2001.

G. Castellani, E. Quinlan, F. Bersani, L. Cooper, and H. Shouval, A model of bidirectional synaptic plasticity: From signaling network to channel conductance, Learning & Memory, vol.12, issue.4, pp.423-432, 2005.
DOI : 10.1101/lm.80705

H. Shouval, G. Castellani, B. Blais, L. Yeung, and L. Cooper, Converging evidence for a simplified biophysical model of synaptic plasticity, Biological Cybernetics, vol.87, issue.5-6, pp.383-391, 2002.
DOI : 10.1007/s00422-002-0362-x

B. Droz, H. Koenig, L. Biamberardino, D. Giamberardino, and L. , Axonal migration of protein and glycoprotein to nerve endings. I. Radioautographic analysis of the renewal of protein in nerve endings of chicken ciliary ganglion after intracerebral injection of [3H]lysine, Brain Research, vol.60, issue.1, pp.93-127, 1973.
DOI : 10.1016/0006-8993(73)90852-4

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

E. Fransen, B. Tahvildari, A. Egorov, M. Hasselmo, and A. Alonso, Mechanism of Graded Persistent Cellular Activity of Entorhinal Cortex Layer V Neurons, Neuron, vol.49, issue.5, pp.735-746, 2006.
DOI : 10.1016/j.neuron.2006.01.036

A. Kirkwood, M. Rioult, and M. Bear, Experience-dependent modification of synaptic plasticity in visual cortex, Nature, vol.381, issue.6582, pp.526-528, 1996.
DOI : 10.1038/381526a0

D. Brager, X. Cai, and S. Thompson, Activity-dependent activation of presynaptic protein kinase C mediates post-tetanic potentiation, Nature Neuroscience, vol.6, issue.6, pp.551-552, 2003.
DOI : 10.1038/nn1067

A. Volianskis and M. Jensen, Transient and sustained types of long-term potentiation in the CA1 area of the rat hippocampus, The Journal of Physiology, vol.9, issue.2, pp.459-492, 2003.
DOI : 10.1113/jphysiol.2003.044214

M. Rioult-pedotti, D. Friedman, and J. Donoghue, Learning-Induced LTP in Neocortex, Science, vol.290, issue.5491, pp.533-536, 2000.
DOI : 10.1126/science.290.5491.533

R. Racine, N. Milgram, and S. Hafner, Long-term potentiation phenomena in the rat limbic forebrain, Brain Research, vol.260, issue.2, pp.217-231, 1983.
DOI : 10.1016/0006-8993(83)90676-5

W. Abraham, S. Mason, J. Demmer, J. Williams, and C. Richardson, Correlations between immediate early gene induction and the persistence of long-term potentiation, Neuroscience, vol.56, issue.3, pp.717-727, 1993.
DOI : 10.1016/0306-4522(93)90369-Q

W. Abraham, B. Christie, B. Logan, P. Lawlor, and M. Dragunow, Immediate early gene expression associated with the persistence of heterosynaptic long-term depression in the hippocampus., Proceedings of the National Academy of Sciences, vol.91, issue.21, pp.10049-10053, 1994.
DOI : 10.1073/pnas.91.21.10049

W. Abraham, B. Logan, J. Greenwood, and M. Dragunow, Induction and experience-dependent consolidation of stable long-term potentiation lasting months in the hippocampus, J Neurosci, vol.22, pp.9626-9634, 2002.

C. Trepel and R. Racine, Long-term potentiation in the neocortex of the adult, freely moving rat, Cerebral Cortex, vol.8, issue.8, pp.719-729, 1998.
DOI : 10.1093/cercor/8.8.719

V. Doyere, M. Errington, S. Laroche, and T. Bliss, Low???frequency trains of paired stimuli induce long???term depression in area CA1 but not in dentate gyrus of the intact rat, Hippocampus, vol.6, issue.1, pp.52-57, 1996.
DOI : 10.1002/(SICI)1098-1063(1996)6:1<52::AID-HIPO9>3.3.CO;2-Q

W. Abraham, How long will long-term potentiation last?, Philosophical Transactions of the Royal Society B: Biological Sciences, vol.358, issue.1432, pp.735-744, 2003.
DOI : 10.1098/rstb.2002.1222

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1693170

E. Bienenstock, L. Cooper, and P. Munro, THEORY FOR THE DEVELOPMENT OF NEURON SELECTIVITY: ORIENTATION SPECIFICITY AND BINOCULAR INTERACTION IN VISUAL CORTEX, J Neurosci, vol.2, pp.32-48, 1982.
DOI : 10.1142/9789812795885_0006

G. Turrigiano, Homeostatic plasticity in neuronal networks: the more things change, the more they stay the same, Trends in Neurosciences, vol.22, issue.5, pp.221-227, 1999.
DOI : 10.1016/S0166-2236(98)01341-1

M. Coesmans, J. Weber, D. Zeeuw, C. Hansel, and C. , Bidirectional Parallel Fiber Plasticity in the Cerebellum under Climbing Fiber Control, Neuron, vol.44, issue.4, pp.691-700, 2004.
DOI : 10.1016/j.neuron.2004.10.031

J. Sanes and J. Lichtman, Can molecules explain long-term potentiation?, Nature Neuroscience, vol.2, issue.7, pp.597-604, 1999.
DOI : 10.1038/10154

C. Brody, R. Romo, and A. Kepecs, Basic mechanisms for graded persistent activity: discrete attractors, continuous attractors, and dynamic representations, Current Opinion in Neurobiology, vol.13, issue.2, pp.204-211, 2003.
DOI : 10.1016/S0959-4388(03)00050-3

Y. Loewenstein and H. Sompolinsky, Temporal integration by calcium dynamics in a model neuron, Nature Neuroscience, vol.6, issue.9, pp.961-967, 2003.
DOI : 10.1038/nn1109

S. Sajikumar, S. Navakkode, and J. Frey, Protein synthesis-dependent long-term functional plasticity: methods and techniques, Current Opinion in Neurobiology, vol.15, issue.5, pp.607-613, 2005.
DOI : 10.1016/j.conb.2005.08.009

T. Whittingham, W. Lust, D. Christakis, and J. Passonneau, Metabolic Stability of Hippocampal Slice Preparations During Prolonged Incubation, Journal of Neurochemistry, vol.11, issue.3, pp.689-696, 1984.
DOI : 10.1007/BF00234729

O. Ho, J. Delgado, O. Dell, and T. , Phosphorylation of proteins involved in activity-dependent forms of synaptic plasticity is altered in hippocampal slices maintained in???vitro, Journal of Neurochemistry, vol.23, issue.6, pp.1344-1357, 2004.
DOI : 10.1111/j.1471-4159.2004.02815.x

K. Micheva and S. Smith, Strong Effects of Subphysiological Temperature on the Function and Plasticity of Mammalian Presynaptic Terminals, Journal of Neuroscience, vol.25, issue.33, pp.7481-7488, 2005.
DOI : 10.1523/JNEUROSCI.1801-05.2005

J. Lisman, A mechanism for the Hebb and the anti-Hebb processes underlying learning and memory., Proceedings of the National Academy of Sciences, vol.86, issue.23, pp.9574-9578, 1989.
DOI : 10.1073/pnas.86.23.9574

H. Shouval, Clusters of interacting receptors can stabilize synaptic efficacies, Proceedings of the National Academy of Sciences, vol.102, issue.40, pp.14440-14445, 2005.
DOI : 10.1073/pnas.0506934102

G. Bi and M. Poo, Synaptic modifications in cultured hippocampal neurons: Dependence on spike timing, synaptic strength, and postsynaptic cell type, J Neurosci, vol.18, pp.10464-10472, 1998.

P. Frankland and B. Bontempi, The organization of recent and remote memories, Nature Reviews Neuroscience, vol.75, issue.2, pp.119-130, 2005.
DOI : 10.1523/JNEUROSCI.4100-03.2004

S. Fusi, P. Drew, and L. Abbott, Cascade Models of Synaptically Stored Memories, Neuron, vol.45, issue.4, pp.599-611, 2005.
DOI : 10.1016/j.neuron.2005.02.001

S. Roth, J. Denu, and C. Allis, Histone Acetyltransferases, Annual Review of Biochemistry, vol.70, issue.1, pp.81-120, 2001.
DOI : 10.1146/annurev.biochem.70.1.81

J. Mannick and C. Schonhoff, Nitrosylation: the next phosphorylation?, Archives of Biochemistry and Biophysics, vol.408, issue.1, pp.1-6, 2002.
DOI : 10.1016/S0003-9861(02)00490-3

Y. Nishizuka, The molecular heterogeneity of protein kinase C and its implications for cellular regulation, Nature, vol.334, issue.6184, pp.661-665, 1988.
DOI : 10.1038/334661a0

C. Huang, J. Ferrell, and . Jr, Ultrasensitivity in the mitogen-activated protein kinase cascade., Proceedings of the National Academy of Sciences, vol.93, issue.19, pp.10078-10083, 1996.
DOI : 10.1073/pnas.93.19.10078

L. Huang and S. Taylor, Dissecting cAMP Binding Domain A in the RI?? Subunit of cAMP-dependent Protein Kinase: DISTINCT SUBSITES FOR RECOGNITION OF cAMP AND THE CATALYTIC SUBUNIT, Journal of Biological Chemistry, vol.273, issue.41, pp.26739-26746, 1998.
DOI : 10.1074/jbc.273.41.26739

A. Gerlach, N. Gangopadhyay, and D. Devor, Kinase-dependent Regulation of the Intermediate Conductance, Calcium-dependent Potassium Channel, hIK1, Journal of Biological Chemistry, vol.275, issue.1, pp.585-598, 2000.
DOI : 10.1074/jbc.275.1.585

A. Stewart, T. Ingebritsen, and P. Cohen, The Protein Phosphatases Involved in Cellular Regulation. 5. Purification and Properties of a Ca2+ /Calmodulin-Dependent Protein Phosphatase (2B) from Rabbit Skeletal Muscle, European Journal of Biochemistry, vol.157, issue.2, pp.289-295, 1983.
DOI : 10.1038/296613a0

P. Stemmer and C. Klee, Dual Calcium Ion Regulation of Calcineurin by Calmodulin and Calcineurin B, Biochemistry, vol.33, issue.22, pp.6859-6866, 1994.
DOI : 10.1021/bi00188a015

J. Schaechter and L. Benowitz, Activation of protein kinase C by arachidonic acid selectively enhances the phosphorylation of GAP-43 in nerve terminal membranes, J Neurosci, vol.13, pp.4361-4371, 1993.

Y. Takai, A. Kishimoto, Y. Iwasa, Y. Kawahara, and T. Mori, Calciumdependent activation of a multifunctional protein kinase by membrane phospholipids, J Biol Chem, vol.254, pp.3692-3695, 1979.

G. Long, J. Rosen, and F. Schanne, Lead activation of protein kinase C from rat brain. Determination of free calcium, lead, and zinc by 19F NMR, J Biol Chem, vol.269, pp.834-837, 1994.

K. Smith, E. Gibson, and M. Dell-'acqua, cAMP-Dependent Protein Kinase Postsynaptic Localization Regulated by NMDA Receptor Activation through Translocation of an A-Kinase Anchoring Protein Scaffold Protein, Journal of Neuroscience, vol.26, issue.9, pp.2391-2402, 2006.
DOI : 10.1523/JNEUROSCI.3092-05.2006

Y. Yoshimura, Y. Sogawa, and T. Yamauchi, /calmodulin-dependent protein kinase II from postsynaptic densities, FEBS Letters, vol.279, issue.2-3, pp.239-242, 1999.
DOI : 10.1016/S0014-5793(99)00226-4

P. Poisbeau, M. Cheney, M. Browning, and I. Mody, Modulation of synaptic GABAA receptor function by PKA and PKC in adult hippocampal neurons, J Neurosci, vol.19, pp.674-683, 1999.

G. Snyder, S. Galdi, A. Fienberg, P. Allen, and A. Nairn, Regulation of AMPA receptor dephosphorylation by glutamate receptor agonists, Neuropharmacology, vol.45, issue.6, pp.703-713, 2003.
DOI : 10.1016/S0028-3908(03)00319-8

K. Roche, O. Brien, R. Mammen, A. Bernhardt, J. Huganir et al., Characterization of Multiple Phosphorylation Sites on the AMPA Receptor GluR1 Subunit, Neuron, vol.16, issue.6, pp.1179-1188, 1996.
DOI : 10.1016/S0896-6273(00)80144-0

R. Hourez, K. Azdad, G. Vanwalleghem, C. Roussel, and D. Gall, Activation of protein kinase C and inositol 1,4,5-triphosphate receptors antagonistically modulate voltage-gated sodium channels in striatal neurons, Brain Research, vol.1059, issue.2, pp.189-196, 2005.
DOI : 10.1016/j.brainres.2005.08.031

H. Misonou, M. Menegola, D. Mohapatra, L. Guy, and K. Park, Bidirectional Activity-Dependent Regulation of Neuronal Ion Channel Phosphorylation, Journal of Neuroscience, vol.26, issue.52, pp.13505-13514, 2006.
DOI : 10.1523/JNEUROSCI.3970-06.2006

U. Bhalla, Signaling in Small Subcellular Volumes. II. Stochastic and Diffusion Effects on Synaptic Network Properties, Biophysical Journal, vol.87, issue.2, pp.745-753, 2004.
DOI : 10.1529/biophysj.104.040501

D. Gillespie, Exact stochastic simulation of coupled chemical reactions, The Journal of Physical Chemistry, vol.81, issue.25, p.2340, 1977.
DOI : 10.1021/j100540a008

G. Adam and M. Delbrü-ck, Reduction of dimensionality in biological diffusion processes, Structural chemistry and molecular biology, 1968.

O. Berg, J. Paulsson, and M. Ehrenberg, Fluctuations and Quality of Control in Biological Cells: Zero-Order Ultrasensitivity Reinvestigated, Biophysical Journal, vol.79, issue.3, pp.1228-1236, 2000.
DOI : 10.1016/S0006-3495(00)76377-6

B. Smith, H. Roy, D. Koninck, P. Grutter, P. et al., Dendritic Spine Viscoelasticity and Soft-Glassy Nature: Balancing Dynamic Remodeling with Structural Stability, Biophysical Journal, vol.92, issue.4, pp.1419-1430, 2007.
DOI : 10.1529/biophysj.106.092361

URL : http://doi.org/10.1529/biophysj.106.092361

K. Bielefeldt and M. Jackson, Intramolecular and intermolecular enzymatic modulation of ion channels in excised membrane patches, Biophysical Journal, vol.66, issue.6, pp.1904-1914, 1994.
DOI : 10.1016/S0006-3495(94)80984-1

B. Hille, Ionic channels of excitable membranes, 1992.