L. Bennetto, N. Patel, and G. Fuller, Trigeminal neuralgia and its management, BMJ, vol.334, issue.7586, p.17255614, 2007.
DOI : 10.1136/bmj.39085.614792.BE

J. Zakrzewska and R. Mcmillan, Trigeminal neuralgia: the diagnosis and management of this excruciating and poorly understood facial pain, Postgraduate Medical Journal, vol.87, issue.1028, pp.410-416, 2011.
DOI : 10.1136/pgmj.2009.080473

M. Costigan, J. Scholz, and C. Woolf, Neuropathic Pain: A Maladaptive Response of the Nervous System to Damage, Annual Review of Neuroscience, vol.32, issue.1, pp.1-32, 2009.
DOI : 10.1146/annurev.neuro.051508.135531

D. Guo and J. Hu, Spinal presynaptic inhibition in pain control, Neuroscience, vol.283
DOI : 10.1016/j.neuroscience.2014.09.032

URL : http://doi.org/10.1016/j.neuroscience.2014.09.032

T. Pirttimaki, S. Hall, and H. Parri, Sustained Neuronal Activity Generated by Glial Plasticity, Journal of Neuroscience, vol.31, issue.21, pp.7637-7684, 2011.
DOI : 10.1523/JNEUROSCI.5783-10.2011

URL : http://www.jneurosci.org/content/jneuro/31/21/7637.full.pdf

C. Abbadie, S. Bhangoo, D. Koninck, Y. Malcangio, M. Melik-parsadaniantz et al., Chemokines and pain mechanisms, Brain Research Reviews, vol.60, issue.1, pp.125-134, 2009.
DOI : 10.1016/j.brainresrev.2008.12.002

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2691997

J. Scholz and C. Woolf, The neuropathic pain triad: neurons, immune cells and glia, Nature Neuroscience, vol.74, issue.11, pp.1361-1368, 2007.
DOI : 10.1152/physrev.00011.2002

F. Marchand, M. Perretti, and S. Mcmahon, Role of the Immune system in chronic pain, Nature Reviews Neuroscience, vol.21, issue.7, pp.521-553, 2005.
DOI : 10.1038/sj.bjp.0702423

H. Flor, T. Elbert, S. Knecht, C. Wienbruch, C. Pantev et al., Phantom-limb pain as a perceptual correlate of cortical reorganization following arm amputation, Nature, vol.375, issue.6531, pp.482-484, 1995.
DOI : 10.1038/375482a0

H. Flor, C. Braun, T. Elbert, N. Birbaumer, S. Knecht et al., Extensive reorganization of primary somatosensory cortex in chronic back pain patients\rPhantom-limb pain as a perceptual correlate of cortical reorganization following arm amputation, Neurosci Lett, pp.5-8, 1997.

R. Gracely, M. Geisser, T. Giesecke, M. Grant, F. Petzke et al., Pain catastrophizing and neural responses to pain among persons with fibromyalgia, Brain, vol.127, issue.4, pp.835-843, 2004.
DOI : 10.1093/brain/awh098

URL : https://academic.oup.com/brain/article-pdf/127/4/835/1116139/awh098.pdf

K. Juottonen, M. Gockel, T. Sil-?-?-n, H. Hurri, R. Hari et al., Altered central sensorimotor processing in patients with complex regional pain syndrome, Pain, vol.98, issue.3, pp.315-323, 2002.
DOI : 10.1016/S0304-3959(02)00119-7

B. Pleger, P. Ragert, P. Schwenkreis, A. Förster, C. Wilimzig et al., Patterns of cortical reorganization parallel impaired tactile discrimination and pain intensity in complex regional pain syndrome, NeuroImage, vol.32, issue.2, p.16753306, 2006.
DOI : 10.1016/j.neuroimage.2006.03.045

C. Maihofner, H. Handwerker, B. Neundorfer, and F. Birklein, Cortical reorganization during recovery from complex regional pain syndrome, Neurology, vol.63, issue.4, pp.693-701, 2004.
DOI : 10.1212/01.WNL.0000134661.46658.B0

N. Vartiainen, E. Kirveskari, K. Kallio-laine, E. Kalso, and N. Forss, Cortical Reorganization in Primary Somatosensory Cortex in Patients With Unilateral Chronic Pain, The Journal of Pain, vol.10, issue.8, pp.854-859, 2009.
DOI : 10.1016/j.jpain.2009.02.006

V. Apkarian-a, Y. Sosa, S. Sonty, R. Levy, R. Harden et al., Chronic Back Pain Is Associated with Decreased Prefrontal and Thalamic Gray Matter Density, Journal of Neuroscience, vol.24, issue.46, pp.10410-10415, 2004.
DOI : 10.1523/JNEUROSCI.2541-04.2004

C. M. Karin-)-swart, . Cma, J. Stins, and P. Beek, Cortical changes in complex regional pain syndrome (CRPS) European Journal of Pain, pp.902-907, 2009.

M. Baliki, T. Schnitzer, W. Bauer, and A. Apkarian, Brain Morphological Signatures for Chronic Pain, PLoS ONE, vol.6, issue.10, 2011.
DOI : 10.1371/journal.pone.0026010.s004

URL : http://doi.org/10.1371/journal.pone.0026010

C. Lin, Brain Signature of Chronic Orofacial Pain: A Systematic Review and Meta-Analysis on Neuroimaging Research of Trigeminal Neuropathic Pain and Temporomandibular Joint Disorders, PLoS ONE, vol.44, issue.4
DOI : 10.1371/journal.pone.0094300.s002

L. Becerra, S. Morris, S. Bazes, R. Gostic, S. Sherman et al., Trigeminal Neuropathic Pain Alters Responses in CNS Circuits to Mechanical (Brush) and Thermal (Cold and Heat) Stimuli, Journal of Neuroscience, vol.26, issue.42, pp.10646-10657, 2006.
DOI : 10.1523/JNEUROSCI.2305-06.2006

S. Gustin, C. Peck, S. Wilcox, P. Nash, G. Murray et al., Different Pain, Different Brain: Thalamic Anatomy in Neuropathic and Non-Neuropathic Chronic Pain Syndromes, Journal of Neuroscience, vol.31, issue.16, pp.5956-5964, 2011.
DOI : 10.1523/JNEUROSCI.5980-10.2011

URL : http://www.jneurosci.org/content/jneuro/31/16/5956.full.pdf

D. Desouza, M. Hodaie, and K. Davis, Abnormal trigeminal nerve microstructure and brain white matter in idiopathic trigeminal neuralgia, Pain, vol.155, issue.1, pp.37-44, 2014.
DOI : 10.1016/j.pain.2013.08.029

S. Gustin, C. Peck, L. Cheney, P. Macey, G. Murray et al., Pain and Plasticity: Is Chronic Pain Always Associated with Somatosensory Cortex Activity and Reorganization?, Journal of Neuroscience, vol.32, issue.43, pp.14874-14884, 2012.
DOI : 10.1523/JNEUROSCI.1733-12.2012

URL : http://www.jneurosci.org/content/jneuro/32/43/14874.full.pdf

A. Dasilva, L. Becerra, G. Pendse, B. Chizh, S. Tully et al., Colocalized Structural and Functional Changes in the Cortex of Patients with Trigeminal Neuropathic Pain, PLoS ONE, vol.109, issue.3, 2008.
DOI : 10.1371/journal.pone.0003396.s002

S. Gustin, C. Peck, P. Macey, G. Murray, and L. Henderson, Unraveling the Effects of Plasticity and Pain on Personality, The Journal of Pain, vol.14, issue.12, pp.1642-1652, 2013.
DOI : 10.1016/j.jpain.2013.08.005

S. Gustin, J. Mckay, E. Petersen, C. Peck, G. Murray et al., Subtle Alterations in Brain Anatomy May Change an Individual???s Personality in Chronic Pain, PLoS ONE, vol.16, issue.10
DOI : 10.1371/journal.pone.0109664.t002

URL : http://doi.org/10.1371/journal.pone.0109664

G. Bennett and Y. Xie, A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man, Pain, vol.33, issue.1, pp.87-107, 1988.
DOI : 10.1016/0304-3959(88)90209-6

B. Vos, A. Strassman, and R. Maciewicz, Behavioral evidence of trigeminal neuropathic pain following chronic constriction injury to the rat's infraorbital nerve, J Neurosci. Available, vol.14, pp.2708-2723, 1994.

D. Lam, B. Sessle, B. Cairns, and J. Hu, Neural Mechanisms of Temporomandibular Joint and Masticatory Muscle Pain: A Possible Role for Peripheral Glutamate Receptor Mechanisms, Pain Research and Management, vol.10, issue.3, pp.145-52, 2005.
DOI : 10.1155/2005/860354

Y. Imamura, H. Kawamoto, and O. Nakanishi, Characterization of heat-hyperalgesia in an experimental trigeminal neuropathy in rats, Experimental Brain Research, vol.116, issue.1, pp.97-103, 1997.
DOI : 10.1007/PL00005748

J. Kitagawa, M. Takeda, I. Suzuki, J. Kadoi, Y. Tsuboi et al., Mechanisms involved in modulation of trigeminal primary afferent activity in rats with peripheral mononeuropathy, European Journal of Neuroscience, vol.16, issue.7, pp.1976-1986, 2006.
DOI : 10.1113/jphysiol.1983.sp014747

J. Staiger, S. Bisler, A. Schleicher, P. Gass, J. Stehle et al., Exploration of a novel environment leads to the expression of inducible transcription factors in barrel-related columns, Neuroscience, vol.99, issue.1, pp.7-16, 2000.
DOI : 10.1016/S0306-4522(00)00166-4

L. Frangeul, C. Porrero, M. Garcia-amado, B. Maimone, M. Maniglier et al., Specific activation of the paralemniscal pathway during nociception, European Journal of Neuroscience, vol.518, issue.9, pp.1455-1464, 2014.
DOI : 10.1002/cne.22483

S. Pezet, Noxious Stimulation Induces Trk Receptor and Downstream ERK Phosphorylation in Spinal Dorsal Horn, Molecular and Cellular Neuroscience, vol.21, issue.4, pp.684-695, 2002.
DOI : 10.1006/mcne.2002.1205

H. Tsujino, E. Kondo, T. Fukuoka, Y. Dai, . Tokunaga-a et al., Activating Transcription Factor 3 (ATF3) Induction by Axotomy in Sensory and Motoneurons: A Novel Neuronal Marker of Nerve Injury, Molecular and Cellular Neuroscience, vol.15, issue.2, pp.170-182, 2000.
DOI : 10.1006/mcne.1999.0814

G. Paxinos, K. Franklin, and F. Paxinos, Available: https://www.elsevier.com/books/paxinos-and- franklins-the-mouse-brain-in-stereotaxic-coordinates, Stereotaxic Coordinates [Internet] . São Paulo, pp.978-978, 2012.

B. Vogt and G. Paxinos, Cytoarchitecture of mouse and rat cingulate cortex with human homologies. doi: 10, pp.429-441

R. Frostig, E. Lieke, and D. Ts-'o, Cortical functional architecture and local coupling between neuronal activity and the microcirculation revealed by in vivo high-resolution optical imaging of intrinsic signals., Proceedings of the National Academy of Sciences, vol.87, issue.16, pp.6082-6086, 1990.
DOI : 10.1073/pnas.87.16.6082

S. Sheth, M. Nemoto, M. Guiou, M. Walker, N. Pouratian et al., Evaluation of coupling between optical intrinsic signals and neuronal activity in rat somatosensory cortex, NeuroImage, vol.19, issue.3, pp.884-894, 2003.
DOI : 10.1016/S1053-8119(03)00086-7

M. Nemoto, S. Sheth, M. Guiou, N. Pouratian, and C. J. , Functional Signal-and Paradigm-Dependent Linear Relationships between Synaptic Activity and, J Neurosci, vol.Available, 2004.
DOI : 10.1523/jneurosci.4870-03.2004

URL : http://www.jneurosci.org/content/jneuro/24/15/3850.full.pdf

M. Cha, D. Kim, Z. Cho, J. Sohn, M. Chung et al., Modification of cortical excitability in neuropathic rats: A voltage-sensitive dye study, Neuroscience Letters, vol.464, issue.2, pp.117-121, 2009.
DOI : 10.1016/j.neulet.2009.08.024

C. Hubbard, S. Khan, S. Xu, M. Cha, R. Masri et al., Behavioral, metabolic and functional brain changes in a rat model of chronic neuropathic pain: A longitudinal MRI study, NeuroImage, vol.107, pp.333-344, 2015.
DOI : 10.1016/j.neuroimage.2014.12.024

R. Ji, H. Baba, G. Brenner, and C. Woolf, Nociceptive-specific activation of ERK in spinal neurons contributes to pain hypersensitivity, Nature Neuroscience, vol.2, issue.12, pp.1114-1119, 1999.
DOI : 10.1038/16040

R. Treede, D. Kenshalo, R. Gracely, and A. Jones, The cortical representation of pain, Pain, vol.79, issue.2, pp.105-116, 1999.
DOI : 10.1016/S0304-3959(98)00184-5

I. Tracey, Nociceptive processing in the human brain, Current Opinion in Neurobiology, vol.15, issue.4, pp.478-87, 2005.
DOI : 10.1016/j.conb.2005.06.010

D. Hayes and G. Northoff, Common brain activations for painful and non-painful aversive stimuli, BMC Neuroscience, vol.13, issue.1, p.22676259, 2012.
DOI : 10.1006/nimg.2002.1115

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464596

A. Apkarian, M. Bushnell, R. Treede, and J. Zubieta, Human brain mechanisms of pain perception and regulation in health and disease, European Journal of Pain, vol.22, issue.Pt 5, pp.463-84, 2005.
DOI : 10.1126/science.1060952

K. Thibault, W. Lin, A. Rancillac, M. Fan, T. Snollaerts et al., BDNF-Dependent Plasticity Induced by Peripheral Inflammation in the Primary Sensory and the Cingulate Cortex Triggers Cold Allodynia and Reveals a Major Role

H. Kawai, L. M. Kang, H. Hashimoto, Y. Liang, K. Lazar et al., Convergence of nicotine-induced and auditory-evoked neural activity activates ERK in auditory cortex, Synapse, vol.110, issue.8, pp.455-468, 2013.
DOI : 10.1016/S0092-8674(02)00897-8

K. Pozo and Y. Goda, Unraveling Mechanisms of Homeostatic Synaptic Plasticity, Neuron, vol.66, issue.3, p.20471348
DOI : 10.1016/j.neuron.2010.04.028

S. Fenster, W. Chung, R. Zhai, C. Cases-langhoff, B. Voss et al., Piccolo, a Presynaptic Zinc Finger Protein Structurally Related to Bassoon, Neuron, vol.25, issue.1, pp.203-214, 2000.
DOI : 10.1016/S0896-6273(00)80883-1

URL : http://doi.org/10.1016/s0896-6273(00)80883-1

V. Lazarevic, C. Schöne, M. Heine, E. Gundelfinger, and A. Fejtova, Extensive Remodeling of the Presynaptic Cytomatrix upon Homeostatic Adaptation to Network Activity Silencing, Journal of Neuroscience, vol.31, issue.28, p.21752995, 2011.
DOI : 10.1523/JNEUROSCI.2088-11.2011

C. Pontrello, M. Sun, A. Lin, T. Fiacco, K. Defea et al., Cofilin under control of ??-arrestin-2 in NMDA-dependent dendritic spine plasticity, long-term depression (LTD), and learning, Proceedings of the National Academy of Sciences, vol.26, issue.6, pp.442-51, 2012.
DOI : 10.1523/JNEUROSCI.4091-05.2006

J. Bamburg, A. Mcgough, and S. Ono, Putting a new twist on actin: ADF/cofilins modulate actin dynamics. Trends in Cell Biology, pp.364-370, 1999.
DOI : 10.1016/s0962-8924(99)01619-0

P. Clavelou, R. Dallel, T. Orliaguet, . Woda-a, and P. Raboisson, The orofacial formalin test in rats: effects of different formalin concentrations, Pain, vol.62, issue.3, pp.295-301, 1995.
DOI : 10.1016/0304-3959(94)00273-H

A. Krzyzanowska, S. Pittolo, M. Cabrerizo, S. Pez, J. Krishnasamy et al., Assessing nociceptive sensitivity in mouse models of inflammatory and neuropathic trigeminal pain, Journal of Neuroscience Methods, vol.201, issue.1, pp.46-54, 2011.
DOI : 10.1016/j.jneumeth.2011.07.006

T. Pelissier, J. Pajot, and R. Dallel, The orofacial capsaicin test in rats: effects of different capsaicin concentrations and morphine, Pain, vol.96, issue.1, pp.81-87, 2002.
DOI : 10.1016/S0304-3959(01)00432-8

H. Rossi, A. Jenkins, J. Kaufman, I. Bhattacharyya, R. Caudle et al., Characterization of bilateral trigeminal constriction injury using an operant facial pain assay, Neuroscience, vol.224, pp.294-306, 2012.
DOI : 10.1016/j.neuroscience.2012.08.015

M. Cha, K. Kohan, X. Zuo, J. Ling, and J. Gu, Assessment of chronic trigeminal neuropathic pain by the orofacial operant test in rats, Behavioural Brain Research, vol.234, issue.1, pp.82-90, 2012.
DOI : 10.1016/j.bbr.2012.06.020

J. Neubert, C. Widmer, W. Malphurs, H. Rossi, C. Vierck et al., Use of a novel thermal operant behavioral assay for characterization of orofacial pain sensitivity, Pain, vol.116, issue.3, pp.386-395, 2005.
DOI : 10.1016/j.pain.2005.05.011

T. Nolan, J. Hester, Y. Bokrand-donatelli, R. Caudle, and J. Neubert, Adaptation of a novel operant orofacial testing system to characterize both mechanical and thermal pain, Behavioural Brain Research, vol.217, issue.2, pp.477-480, 2011.
DOI : 10.1016/j.bbr.2010.10.022

E. Anderson, R. Mills, T. Nolan, A. Jenkins, G. Mustafa et al., Use of the Operant Orofacial Pain Assessment Device (OPAD) to Measure Changes in Nociceptive Behavior, Journal of Visualized Experiments, vol.76, issue.76, pp.1-6, 2013.
DOI : 10.3791/50336

J. Braz and A. Basbaum, Differential ATF3 expression in dorsal root ganglion neurons reveals the profile of primary afferents engaged by diverse noxious chemical stimuli, Pain, vol.150, issue.2, pp.290-301, 2010.
DOI : 10.1016/j.pain.2010.05.005

M. Xu, M. Aita, and C. Chavkin, Partial Infraorbital Nerve Ligation as a Model of Trigeminal Nerve Injury in the Mouse: Behavioral, Neural, and Glial Reactions, The Journal of Pain, vol.9, issue.11, p.18708302, 2008.
DOI : 10.1016/j.jpain.2008.06.006

F. Ma, L. Zhang, D. Lyons, and K. Westlund, Orofacial neuropathic pain mouse model induced by Trigeminal Inflammatory Compression (TIC) of the infraorbital nerve, Molecular Brain, vol.5, issue.1, p.23270529, 2012.
DOI : 10.1016/j.jpain.2012.03.008

Y. Lamour, G. Guilbaud, and J. C. , Rat somatosensory cortex II-Laminar and columnar organisation of noxious and non noxious inputs, Exp Brain Res, vol.49, pp.46-54, 1983.
DOI : 10.1007/bf00235540

S. Lee, B. Kang, M. Shin, M. J. Heo, C. Lee et al., Chronic Stress Decreases Cerebrovascular Responses During Rat Hindlimb Electrical Stimulation, Frontiers in Neuroscience, vol.225, issue.53, p.26778944, 2015.
DOI : 10.1016/j.bbr.2011.07.006

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4688360

J. Benoist, M. Gautron, and G. Guilbaud, Experimental model of trigeminal pain in the rat by constriction of one infraorbital nerve: changes in neuronal activities in the somatosensory cortices corresponding to the infraorbital nerve, Experimental Brain Research, vol.126, issue.3, pp.383-398, 1999.
DOI : 10.1007/s002210050745

C. Abbadie, J. Besson, and . Pmid, c-fos Expression in rat lumbar spinal cord during the development of adjuvant-induced arthritis, Neuroscience, vol.48, issue.4, pp.985-993, 1992.
DOI : 10.1016/0306-4522(92)90287-C

K. Kajander and G. Bennett, Onset of a painful peripheral neuropathy in rat: a partial and differential deafferentation and spontaneous discharge in A beta and A delta primary afferent neurons Available, J Neurophysiol, vol.68, pp.734-744, 1992.

J. Mao, D. Mayer, and D. Price, Patterns of increased brain activity indicative of pain in a rat model of peripheral mononeuropathy, J Neurosci. Available, vol.13, pp.2689-702, 1993.

P. Paulson, K. Casey, and T. Morrow, Long-term changes in behavior and regional cerebral blood flow associated with painful peripheral mononeuropathy in the rat, Pain, vol.95, issue.1, pp.31-40, 2002.
DOI : 10.1016/S0304-3959(01)00370-0

F. Karim, C. Wang, and R. Gereau, Metabotropic glutamate receptor subtypes 1 and 5 are activators of extracellular signal-regulated kinase signaling required for inflammatory pain in mice, J Neurosci, vol.21, issue.2111, pp.3771-37793771, 2001.

S. Pezet, Noxious Stimulation Induces Trk Receptor and Downstream ERK Phosphorylation in Spinal Dorsal Horn, Molecular and Cellular Neuroscience, vol.21, issue.4, pp.684-695, 2002.
DOI : 10.1006/mcne.2002.1205

H. Hu, B. Alter, Y. Carrasquillo, C. Qiu, and R. V. Gereau, Metabotropic Glutamate Receptor 5 Modulates Nociceptive Plasticity via Extracellular Signal-Regulated Kinase Kv4.2 Signaling in Spinal Cord Dorsal Horn Neurons, Journal of Neuroscience, vol.27, issue.48, pp.13181-13191, 2007.
DOI : 10.1523/JNEUROSCI.0269-07.2007

K. Moulder, J. Meeks, A. Shute, C. Hamilton, D. Erausquin et al., Plastic Elimination of Functional Glutamate Release Sites by Depolarization, Neuron, vol.42, issue.3, pp.423-435, 2004.
DOI : 10.1016/S0896-6273(04)00184-9

D. Gois, S. Schafer, M. Defamie, N. Chen, C. Ricci et al., Homeostatic Scaling of Vesicular Glutamate and GABA Transporter Expression in Rat Neocortical Circuits, Journal of Neuroscience, vol.25, issue.31, pp.7121-7133, 2005.
DOI : 10.1523/JNEUROSCI.5221-04.2005

O. Brien, R. Kamboj, S. Ehlers, M. Rosen, K. Fischbach et al., Activity-dependent modulation of synaptic AMPA receptor accumulation, Neuron, vol.21, issue.00, pp.1067-1078, 1998.

T. Thiagarajan, M. Lindskog, and R. Tsien, Adaptation to Synaptic Inactivity in Hippocampal Neurons, Neuron, vol.47, issue.5, pp.725-737, 2005.
DOI : 10.1016/j.neuron.2005.06.037

URL : http://doi.org/10.1016/j.neuron.2005.06.037

C. Wierenga, K. Ibata, and G. Turrigiano, Postsynaptic Expression of Homeostatic Plasticity at Neocortical Synapses, Journal of Neuroscience, vol.25, issue.11, pp.2895-2905, 2005.
DOI : 10.1523/JNEUROSCI.5217-04.2005

URL : http://www.jneurosci.org/content/jneuro/25/11/2895.full.pdf

R. Ji, T. Kohno, K. Moore, and C. Woolf, Central sensitization and LTP: do pain and memory share similar mechanisms?, Trends in Neurosciences, vol.26, issue.12, pp.696-705, 2003.
DOI : 10.1016/j.tins.2003.09.017

J. Gu, C. Lee, Y. Fan, D. Komlos, X. Tang et al., ADF/cofilin-mediated actin dynamics regulate AMPA receptor trafficking during synaptic plasticity, Nature Neuroscience, vol.143, issue.10, pp.1208-1215, 2010.
DOI : 10.1038/nn.2634

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2947576

L. Chen, C. Rex, M. Casale, C. Gall, and G. Lynch, Changes in Synaptic Morphology Accompany Actin Signaling during LTP, Journal of Neuroscience, vol.27, issue.20, pp.5363-5372, 2007.
DOI : 10.1523/JNEUROSCI.0164-07.2007

URL : http://www.jneurosci.org/content/jneuro/27/20/5363.full.pdf

C. Rex, C. Lin, E. Kramar, L. Chen, C. Gall et al., Brain-Derived Neurotrophic Factor Promotes Long-Term Potentiation-Related Cytoskeletal Changes in Adult Hippocampus, Journal of Neuroscience, vol.27, issue.11, pp.3017-3029, 2007.
DOI : 10.1523/JNEUROSCI.4037-06.2007

URL : http://www.jneurosci.org/content/jneuro/27/11/3017.full.pdf

T. Tsubota, R. Okubo-suzuki, Y. Ohashi, K. Tamura, and K. Ogata, Cofilin1 Controls Transcolumnar Plasticity in Dendritic Spines in Adult Barrel Cortex, PLOS Biology, vol.116, issue.2, 2015.
DOI : 10.1371/journal.pbio.1002070.s008

URL : http://doi.org/10.1371/journal.pbio.1002070

S. Kim and J. Nabekura, Rapid Synaptic Remodeling in the Adult Somatosensory Cortex following Peripheral Nerve Injury and Its Association with Neuropathic Pain, Journal of Neuroscience, vol.31, issue.14, pp.5477-5482, 2011.
DOI : 10.1523/JNEUROSCI.0328-11.2011

Z. Zhang and M. Deschênes, Intracortical axonal projections of lamina VI cells of the primary somatosensory cortex in the rat: a single-cell labeling study, J Neurosci, vol.17, pp.6365-6379, 1997.

E. Jones, Synchrony in the Interconnected Circuitry of the Thalamus and Cerebral Cortex, Annals of the New York Academy of Sciences, vol.282, issue.1, pp.10-23, 2009.
DOI : 10.1113/jphysiol.1984.sp015154

R. Gustin, T. Bichell, M. Bubser, J. Daily, I. Filonova et al., Tissue-specific variation of Ube3a protein expression in rodents and in a mouse model of Angelman syndrome, Neurobiology of Disease, vol.39, issue.3, pp.283-291, 2010.
DOI : 10.1016/j.nbd.2010.04.012

P. Pattany, R. Yezierski, E. Widerstrom-noga, B. Bowen, A. Martinez-arizala et al., Proton Magnetic Resonance Spectroscopy of the Thalamus in Patients with Chronic Neuropathic Pain after Spinal Cord Injury, AJNR Am J Neuroradiol, vol.23, pp.901-905, 2002.