H. Aazh, A. El-refaie, and R. Humphriss, Gabapentin for Tinnitus: A Systematic Review, American Journal of Audiology, vol.20, issue.2, pp.151-158, 2011.
DOI : 10.1044/1059-0889(2011/10-0041)

D. R. Alessi, J. Zhang, A. Khanna, T. Hochdörfer, Y. Shang et al., The WNK-SPAK/OSR1 pathway: Master regulator of cation-chloride cotransporters, Science Signaling, vol.7, issue.334, 2014.
DOI : 10.1126/scisignal.2005365

M. Argence, I. Saez, R. Sassu, I. Vassias, P. P. Vidal et al., Modulation of inhibitory and excitatory synaptic transmission in rat inferior colliculus after unilateral cochleectomy: An in situ and immunofluorescence study, Neuroscience, vol.141, issue.3, pp.1193-1207, 2006.
DOI : 10.1016/j.neuroscience.2006.04.058
URL : https://hal.archives-ouvertes.fr/hal-00092469

D. M. Baguley and M. D. Atlas, Cochlear implants and tinnitus, Prog. Brain Res, vol.166, issue.07, pp.347-355, 2007.
DOI : 10.1016/S0079-6123(07)66033-6

D. M. Baguley, J. Phillips, R. L. Humphriss, S. Jones, P. R. Axon et al., The Prevalence and Onset of Gaze Modulation of Tinnitus and Increased Sensitivity to Noise After Translabyrinthine Vestibular Schwannoma Excision, Otology & Neurotology, vol.27, issue.2, pp.220-224, 2006.
DOI : 10.1097/01.mao.0000172412.87778.28

J. S. Baizer, K. M. Wong, S. Manohar, S. H. Hayes, D. Ding et al., Effects of acoustic trauma on the auditory system of the rat: The role of microglia, Neuroscience, vol.303, pp.299-311, 2015.
DOI : 10.1016/j.neuroscience.2015.07.004

A. L. Berman, The Brain Stem of the Cat: A Cytoarchitectonic Atlas with Stereotaxic Coordinates, 1968.

R. Bos, K. Sadlaoud, P. Boulenguez, D. Buttigieg, S. Liabeuf et al., Activation of 5-HT2A receptors upregulates the function of the neuronal K-Cl cotransporter KCC2, Proceedings of the National Academy of Sciences, vol.110, issue.1, pp.348-353, 2013.
DOI : 10.1073/pnas.1213680110

P. Boulenguez, S. Liabeuf, R. Bos, H. Bras, C. Jean-xavier et al., Down-regulation of the potassium-chloride cotransporter KCC2 contributes to spasticity after spinal cord injury, Nature Medicine, vol.26, issue.3, pp.302-307, 2010.
DOI : 10.1038/nm.2107

J. Burrone and V. N. Murthy, Synaptic gain control and homeostasis, Current Opinion in Neurobiology, vol.13, issue.5, pp.560-567, 2003.
DOI : 10.1016/j.conb.2003.09.007

S. Cai, W. D. Ma, Y. , and E. D. , Encoding Intensity in Ventral Cochlear Nucleus Following Acoustic Trauma: Implications for Loudness Recruitment, Journal of the Association for Research in Otolaryngology, vol.43, issue.217, pp.5-22, 2001.
DOI : 10.1007/s10162-008-0142-y

I. Chamma, M. Heubl, Q. Chevy, M. Renner, I. Moutkine et al., Activity-Dependent Regulation of the K/Cl Transporter KCC2 Membrane Diffusion, Clustering, and Function in Hippocampal Neurons, Journal of Neuroscience, vol.33, issue.39, pp.15488-15503, 2013.
DOI : 10.1523/JNEUROSCI.5889-12.2013

J. R. Christensen, K. B. Larsen, S. H. Lisanby, J. Scalia, V. Arango et al., Neocortical and hippocampal neuron and glial cell numbers in the rhesus monkey, The Anatomical Record: Advances in Integrative Anatomy and Evolutionary Biology, vol.344, issue.3, pp.330-340, 2007.
DOI : 10.1002/ar.20504

I. Cohen, V. Navarro, S. Clemenceau, M. Baulac, M. et al., On the Origin of Interictal Activity in Human Temporal Lobe Epilepsy in Vitro, Science, vol.298, issue.5597, pp.1418-1421, 2002.
DOI : 10.1126/science.1076510

J. A. Coull, S. Beggs, D. Boudreau, D. Boivin, M. Tsuda et al., BDNF from microglia causes the shift in neuronal anion gradient underlying neuropathic pain, Nature, vol.59, issue.7070, pp.1017-1021, 1038.
DOI : 10.1038/nature04223

G. W. Davis, HOMEOSTATIC CONTROL OF NEURAL ACTIVITY: From Phenomenology to Molecular Design, Annual Review of Neuroscience, vol.29, issue.1, pp.307-323, 2006.
DOI : 10.1146/annurev.neuro.28.061604.135751

G. W. Davis and C. S. Goodman, Synapse-specific control of synaptic efficacy at the terminals of a single neuron, Nature, vol.392, issue.6671, pp.82-86, 1998.
DOI : 10.1038/32176

D. Koninck and Y. , Altered chloride homeostasis in neurological disorders: a new target, Current Opinion in Pharmacology, vol.7, issue.1, pp.93-99, 2007.
DOI : 10.1016/j.coph.2006.11.005

N. Doyon, F. Ferrini, M. Gagnon, D. Koninck, and Y. , Treating pathological pain: is KCC2 the key to the gate?, Expert Review of Neurotherapeutics, vol.13, issue.5, pp.469-471, 2013.
DOI : 10.1586/ern.13.40

S. Dutheil, J. Brezun, J. Léonard, M. Lacour, and B. Tighilet, Neurogenesis and astrogenesis contribution to recovery of vestibular functions in the adult cat following unilateral vestibular neurectomy: cellular and behavioral evidence, Neuroscience, vol.164, issue.4, pp.1444-1456, 2009.
DOI : 10.1016/j.neuroscience.2009.09.048

S. Dutheil, G. Escoffier, A. Gharbi, I. Watabe, and B. Tighilet, GABAA Receptor Agonist and Antagonist Alter Vestibular Compensation and Different Steps of Reactive Neurogenesis in Deafferented Vestibular Nuclei of Adult Cats, Journal of Neuroscience, vol.33, issue.39, pp.15555-15566, 2013.
DOI : 10.1523/JNEUROSCI.5691-12.2013

S. Dutheil, M. Lacour, and B. Tighilet, Neurogenic Potential of the Vestibular Nuclei and Behavioural Recovery Time Course in the Adult Cat Are Governed by the Nature of the Vestibular Damage, PLoS ONE, vol.14, issue.8, 2011.
DOI : 10.1371/journal.pone.0022262.s003

S. Dutheil, I. Watabe, K. Sadlaoud, A. Tonetto, and B. Tighilet, BDNF Signaling Promotes Vestibular Compensation by Increasing Neurogenesis and Remodeling the Expression of Potassium-Chloride Cotransporter KCC2 and GABAA Receptor in the Vestibular Nuclei, Journal of Neuroscience, vol.36, issue.23, pp.6199-6212, 2016.
DOI : 10.1523/JNEUROSCI.0945-16.2016

F. Ferrini, D. Koninck, and Y. , Microglia Control Neuronal Network Excitability via BDNF Signalling, Neural Plasticity, vol.18, issue.5, p.429815, 2013.
DOI : 10.1126/science.1094925
URL : http://doi.org/10.1155/2013/429815

Y. Furukawa, M. Okada, N. Akaike, T. Hayashi, and J. Nabekura, Reduction of voltage-dependent magnesium block of N-methyl-d-aspartate receptor-mediated current by in vivo axonal injury, Neuroscience, vol.96, issue.2, pp.385-392, 2000.
DOI : 10.1016/S0306-4522(99)00553-9

M. Gagnon, M. J. Bergeron, G. Lavertu, A. Castonguay, S. Tripathy et al., Chloride extrusion enhancers as novel therapeutics for neurological diseases, Nature Medicine, vol.53, issue.11, pp.1524-1528, 2013.
DOI : 10.1038/nm.3356
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4005788

A. D. Gaudet, P. G. Popovich, and M. S. Ramer, Wallerian degeneration: gaining perspective on inflammatory events after peripheral nerve injury, Journal of Neuroinflammation, vol.8, issue.1, pp.110-120, 2011.
DOI : 10.1523/JNEUROSCI.2269-10.2010
URL : http://doi.org/10.1186/1742-2094-8-110

C. M. Gliddon, C. L. Darlington, and P. F. Smith, Effects of Chronic Infusion of a GABAA Receptor Agonist or Antagonist into the Vestibular Nuclear Complex on Vestibular Compensation in the Guinea Pig, Journal of Pharmacology and Experimental Therapeutics, vol.313, issue.3, pp.1126-1135, 2005.
DOI : 10.1124/jpet.104.082172

M. S. Grubb, J. Burrone, G. E. Hardingham, and H. Bading, Activity-dependent relocation of the axon initial segment fine-tunes neuronal excitability The Yin and Yang of NMDA receptor signalling, Nature Trends Neurosci, vol.465, issue.2602, pp.1070-1074, 2003.

N. Jaenisch, O. W. Witte, and C. Frahm, Downregulation of Potassium Chloride Cotransporter KCC2 After Transient Focal Cerebral Ischemia, Stroke, vol.41, issue.3, pp.151-159, 2010.
DOI : 10.1161/STROKEAHA.109.570424

M. M. Jalali, A. Kousha, S. E. Naghavi, R. Soleimani, and R. Banan, The effects of alprazolam on tinnitus: a cross-over randomized clinical trial, Med. Sci. Monit, vol.15, pp.55-60, 2009.

R. M. Johnson, R. Brummett, and A. Schleuning, Use of Alprazolam for Relief of Tinnitus: A Double-blind Study, Archives of Otolaryngology - Head and Neck Surgery, vol.119, issue.8, pp.842-84501880200042006, 1993.
DOI : 10.1001/archotol.1993.01880200042006

K. T. Kahle and E. Delpire, rheostasis, disease susceptibility, therapeutic target, Journal of Neurophysiology, vol.115, issue.1, pp.8-18, 2016.
DOI : 10.1152/jn.00865.2015
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4760510

K. Kaila, T. J. Price, J. A. Payne, M. Puskarjov, and J. Voipio, Cation-chloride cotransporters in neuronal development, plasticity and disease, Nature Reviews Neuroscience, vol.345, issue.10, pp.637-654, 1038.
DOI : 10.1038/nature04404

B. I. Kalappa, T. J. Brozoski, J. G. Turner, C. , and D. M. , Single unit hyperactivity and bursting in the auditory thalamus of awake rats directly correlates with behavioural evidence of tinnitus, The Journal of Physiology, vol.84, issue.22, pp.5065-5078, 2014.
DOI : 10.1113/jphysiol.2014.278572

J. A. Kaltenbach, J. Zhang, and C. E. Afman, Plasticity of spontaneous neural activity in the dorsal cochlear nucleus after intense sound exposure, Hearing Research, vol.147, issue.1-2, pp.282-292, 2000.
DOI : 10.1016/S0378-5955(00)00138-6

V. Kilman, M. C. Van-rossum, and G. G. Turrigiano, Activity deprivation reduces miniature IPSC amplitude by decreasing the number of postsynaptic GABA(A) receptors clustered at neocortical synapses, J. Neurosci, vol.22, pp.1328-1337, 2002.

K. C. Koerber, R. R. Pfeiffer, W. B. Warr, and N. Y. Kiang, Spontaneous spike discharges from single units in the cochlear nucleus after destruction of the cochlea, Experimental Neurology, vol.16, issue.2, pp.119-130, 1966.
DOI : 10.1016/0014-4886(66)90091-4

M. E. Kotas and R. Medzhitov, Homeostasis, Inflammation, and Disease Susceptibility, Cell, vol.160, issue.5, pp.816-827, 2015.
DOI : 10.1016/j.cell.2015.02.010
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4369762

H. Kuba, Y. Oichi, and H. Ohmori, Presynaptic activity regulates Na+ channel distribution at the axon initial segment, Nature, vol.277, issue.7301, pp.1075-1078, 2010.
DOI : 10.1038/nature09087

H. H. Lee, J. A. Walker, J. R. Williams, R. J. Goodier, J. A. Payne et al., Direct Protein Kinase C-dependent Phosphorylation Regulates the Cell Surface Stability and Activity of the Potassium Chloride Cotransporter KCC2, Journal of Biological Chemistry, vol.282, issue.41, pp.29777-29784, 2007.
DOI : 10.1074/jbc.M705053200

M. Liberge, C. Manrique, L. Bernard-demanze, and M. Lacour, Changes in TNF??, NF??B and MnSOD protein in the vestibular nuclei after unilateral vestibular deafferentation, Journal of Neuroinflammation, vol.7, issue.1, pp.91-101, 2010.
DOI : 10.1186/1742-2094-7-91

M. Lippmann, A. Bress, C. B. Nemeroff, P. M. Plotsky, and L. M. Monteggia, Long-term behavioural and molecular alterations associated with maternal separation in rats, European Journal of Neuroscience, vol.896, issue.Suppl. 2, pp.3091-3098, 2007.
DOI : 10.1111/j.1460-9568.2007.05522.x

S. Manohar, N. A. Paolone, M. Bleichfeld, S. H. Hayes, R. J. Salvi et al., Expression of doublecortin, a neuronal migration protein, in unipolar brush cells of the vestibulocerebellum and dorsal cochlear nucleus of the adult rat, Neuroscience, vol.202, pp.169-183, 2012.
DOI : 10.1016/j.neuroscience.2011.12.013

A. Mccormack, M. Edmondson-jones, H. Fortnum, P. Dawes, H. Middleton et al., The prevalence of tinnitus and the relationship with neuroticism in a middle-aged UK population, Journal of Psychosomatic Research, vol.76, issue.1, pp.56-60, 2014.
DOI : 10.1016/j.jpsychores.2013.08.018

J. C. Milbrandt, T. M. Holder, M. C. Wilson, R. J. Salvi, C. et al., GAD levels and muscimol binding in rat inferior colliculus following acoustic trauma, Hearing Research, vol.147, issue.1-2, pp.251-260, 2000.
DOI : 10.1016/S0378-5955(00)00135-0

A. R. Møller, Tinnitus and pain, Prog. Brain Res. Neuroscience, vol.166, issue.164, pp.47-53, 2007.
DOI : 10.1016/S0079-6123(07)66004-X

J. Nabekura, T. Ueno, A. Okabe, A. Furuta, T. Iwaki et al., Reduction of KCC2 expression and GABAA receptor-mediated excitation after in vivo axonal injury, J. Neurosci, vol.22, pp.4412-4417, 2002.

A. J. Noreña, An integrative model of tinnitus based on a central gain controlling neural sensitivity, Neuroscience & Biobehavioral Reviews, vol.35, issue.5, 2011.
DOI : 10.1016/j.neubiorev.2010.11.003

A. J. Noreña and J. J. Eggermont, Changes in spontaneous neural activity immediately after an acoustic trauma: implications for neural correlates of tinnitus, Hearing Research, vol.183, issue.1-2, pp.137-153, 2003.
DOI : 10.1016/S0378-5955(03)00225-9

A. J. Noreña and B. J. Farley, Tinnitus-related neural activity: Theories of generation, propagation, and centralization, Hearing Research, vol.295, pp.161-171, 2012.
DOI : 10.1016/j.heares.2012.09.010

A. J. Noreña, B. Gourévitch, N. Aizawa, and J. J. Eggermont, Spectrally enhanced acoustic environment disrupts frequency representation in cat auditory cortex, Nature Neuroscience, vol.110, issue.7, pp.932-939, 1038.
DOI : 10.1038/nn1720

A. J. Noreña, M. Tomita, and J. J. Eggermont, Neural Changes in Cat Auditory Cortex After a Transient Pure-Tone Trauma, Journal of Neurophysiology, vol.90, issue.4, pp.2387-2401, 2003.
DOI : 10.1152/jn.00139.2003

J. A. Payne, C. Rivera, J. Voipio, K. , and K. , Cation???chloride co-transporters in neuronal communication, development and trauma, Trends in Neurosciences, vol.26, issue.4, pp.199-206, 2003.
DOI : 10.1016/S0166-2236(03)00068-7

M. Pienkowski, R. Munguia, and J. J. Eggermont, Passive exposure of adult cats to bandlimited tone pip ensembles or noise leads to long-term response suppression in auditory cortex, Hearing Research, vol.277, issue.1-2, pp.117-126, 2011.
DOI : 10.1016/j.heares.2011.02.002

M. Pienkowski, R. Munguia, and J. J. Eggermont, Effects of passive, moderate-level sound exposure on the mature auditory cortex: Spectral edges, spectrotemporal density, and real-world noise, Hearing Research, vol.296, pp.121-130, 2013.
DOI : 10.1016/j.heares.2012.11.006

N. Quaranta, S. Wagstaff, and D. M. Baguley, Tinnitus and cochlear implantation, International Journal of Audiology, vol.103, issue.6, pp.245-251, 2004.
DOI : 10.1016/0168-0102(90)90031-9

J. Rinehart, Y. D. Maksimova, J. E. Tanis, K. L. Stone, C. A. Hodson et al., Sites of Regulated Phosphorylation that Control K-Cl Cotransporter Activity, Cell, vol.138, issue.3, pp.525-536, 2009.
DOI : 10.1016/j.cell.2009.05.031

L. Ris, C. De-waele, M. Serafin, P. P. Vidal, and E. Godaux, Neuronal activity in the ipsilateral vestibular nucleus following unilateral labyrinthectomy in the alert guinea pig, J. Neurophysiol, vol.74, pp.2087-2099, 1995.

C. Rivera, J. Voipio, J. Thomas-crusells, H. Li, Z. Emri et al., Mechanism of Activity-Dependent Downregulation of the Neuron-Specific K-Cl Cotransporter KCC2, Journal of Neuroscience, vol.24, issue.19, pp.4683-4691, 2004.
DOI : 10.1523/JNEUROSCI.5265-03.2004

L. C. Rutherford, S. B. Nelson, and G. G. Turrigiano, BDNF Has Opposite Effects on the Quantal Amplitude of Pyramidal Neuron and Interneuron Excitatory Synapses, Neuron, vol.21, issue.3, pp.521-530, 1998.
DOI : 10.1016/S0896-6273(00)80563-2

C. T. Sasaki, J. S. Kauer, and L. Babitz, Differential [14C]2-deoxyglucose uptake after deafferentation of the mammalian auditory pathway ??? a model for examining tinnitus, Brain Research, vol.194, issue.2, pp.511-516, 1980.
DOI : 10.1016/0006-8993(80)91233-0

R. Schaette and R. Kempter, Development of tinnitus-related neuronal hyperactivity through homeostatic plasticity after hearing loss: a computational model, European Journal of Neuroscience, vol.78, issue.11, pp.3124-3138, 2006.
DOI : 10.1111/j.1460-9568.2006.04774.x

S. E. Shore and J. Zhou, Somatosensory influence on the cochlear nucleus and beyond, Hearing Research, vol.216, issue.217, pp.90-99, 2006.
DOI : 10.1016/j.heares.2006.01.006

S. Sivakumaran, R. A. Cardarelli, J. Maguire, M. R. Kelley, L. Silayeva et al., Selective Inhibition of KCC2 Leads to Hyperexcitability and Epileptiform Discharges in Hippocampal Slices and In Vivo, Journal of Neuroscience, vol.35, issue.21, pp.8291-8296, 2015.
DOI : 10.1523/JNEUROSCI.5205-14.2015

C. J. Sumner, D. L. Tucci, and S. E. Shore, Responses of Ventral Cochlear Nucleus Neurons to Contralateral Sound After Conductive Hearing Loss, Journal of Neurophysiology, vol.94, issue.6, pp.4234-4243, 2005.
DOI : 10.1152/jn.00401.2005

S. K. Suneja, S. J. Potashner, and C. G. Benson, Plastic Changes in Glycine and GABA Release and Uptake in Adult Brain Stem Auditory Nuclei after Unilateral Middle Ear Ossicle Removal and Cochlear Ablation, Experimental Neurology, vol.151, issue.2, pp.273-2886812, 1998.
DOI : 10.1006/exnr.1998.6812

A. Tashiro, V. M. Sandler, N. Toni, C. Zhao, and F. H. Gage, NMDA-receptor-mediated, cell-specific integration of new neurons in adult dentate gyrus, Nature, vol.26, issue.7105, pp.929-933, 1038.
DOI : 10.1038/nature05028

P. Taupin, Protocols for studying adult neurogenesis: insights and recent developments, Regenerative Medicine, vol.2, issue.1, pp.51-62, 2007.
DOI : 10.2217/17460751.2.1.51

B. Tighilet, J. M. Brezun, G. D. Sylvie, C. Gaubert, and M. Lacour, New neurons in the vestibular nuclei complex after unilateral vestibular neurectomy in the adult cat, European Journal of Neuroscience, vol.509, issue.1, pp.47-58, 2007.
DOI : 10.1111/j.1460-9568.2006.05267.x

B. Tighilet, C. Manrique, and M. Lacour, Stress axis plasticity during vestibular compensation in the adult cat, Neuroscience, vol.160, issue.4, 2009.
DOI : 10.1016/j.neuroscience.2009.02.070

T. Toda, K. Ishida, H. Kiyama, T. Yamashita, L. et al., Downregulation of KCC2 expression and phosphorylation in motoneurons, and increases the number of in primary afferent projections to motoneurons in mice with post-stroke spasticity, PLoS ONE, vol.9, 2014.

M. Tsuda, T. Masuda, J. Kitano, H. Shimoyama, H. Tozaki-saitoh et al., IFN-?? receptor signaling mediates spinal microglia activation driving neuropathic pain, Proceedings of the National Academy of Sciences, vol.106, issue.19, pp.8032-8037, 2009.
DOI : 10.1073/pnas.0810420106
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2683100

G. 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

G. G. Turrigiano, The Self-Tuning Neuron: Synaptic Scaling of Excitatory Synapses, Cell, vol.135, issue.3, pp.422-435, 2008.
DOI : 10.1016/j.cell.2008.10.008

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

G. G. Turrigiano, N. , and S. B. , Thinking Globally, Acting Locally, Neuron, vol.21, issue.5, pp.933-935, 1998.
DOI : 10.1016/S0896-6273(00)80607-8

G. G. Turrigiano, N. , and S. B. , Homeostatic plasticity in the developing nervous system, Nature Reviews Neuroscience, vol.5, issue.2, pp.97-107, 2004.
DOI : 10.1038/nrn1327

C. Vale, J. Schoorlemmer, and D. H. Sanes, Deafness disrupts chloride transporter function and inhibitory synaptic transmission, J. Neurosci, vol.23, pp.7516-7524, 2003.

A. J. Watt and N. S. Desai, Homeostatic plasticity and STDP: keeping a neuron's cool in a fluctuating world, Frontiers in Synaptic Neuroscience, vol.2, 2010.
DOI : 10.3389/fnsyn.2010.00005

M. J. West, M. J. West, L. Slomianka, and H. J. Gundersen, New stereological methods for counting neurons, Neurobiology of Aging, vol.14, issue.4, pp.275-285, 1991.
DOI : 10.1016/0197-4580(93)90112-O

J. Wondolowski and D. Dickman, Emerging links between homeostatic synaptic plasticity and neurological disease, Frontiers in Cellular Neuroscience, vol.7, 2013.
DOI : 10.3389/fncel.2013.00223
URL : http://doi.org/10.3389/fncel.2013.00223

Y. Zennou-azogui, L. Borel, M. Lacour, L. Ez-zaher, and M. Ouaknine, Recovery of Head Postural Control Following Unilateral Vestibular Neurectomy in the Cat: Neck Muscle Activity and Neuronal Correlates in Deiters' Nuclei, Acta Oto-Laryngologica, vol.45, issue.sup509, pp.1-19, 1993.
DOI : 10.3109/00016489309130556

Y. Zheng, S. Begum, C. Zhang, K. Fleming, C. Masumura et al., Increased BrdU incorporation reflecting DNA repair, neuronal de-differentiation or possible neurogenesis in the adult cochlear nucleus following bilateral cochlear lesions in the rat, Experimental Brain Research, vol.100, issue.11, pp.477-487, 2011.
DOI : 10.1007/s00221-010-2491-0

Y. Zheng, H. Smithies, P. Aitken, C. Gliddon, L. Stiles et al., Cell proliferation in the cochlear nucleus following acoustic trauma in rat, Neuroscience, vol.303, pp.524-534, 2015.
DOI : 10.1016/j.neuroscience.2015.07.033

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