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Referencias:

• Hudspeth, A., How hearing happens (1997) Neuron, 19, pp. 947-950
• Guinan, J.J., Physiology of olivocochlear efferents (1996) The cochlea, pp. 435-502. , Dallos, Popper, and Fay (Eds), Springer-Verlag, New York
• Guinan, J.J., Warr, W.B., Norris, B.E., Differential olivocochlear projections from lateral vs medial zones of the superior olivary complex (1983) J Comp Neurol, 221, pp. 358-370
• Rasmussen, G.L., The olivary peduncle and other fiber projections of the superior olivary complex (1946) J Comp Neurol, 84, pp. 141-219
• Warr, W., Organization of olivocochlear efferent systems in mammals (1992) The mammalian auditory pathway: neuroanatomy, pp. 410-448. , Douglas W., Popper A., and Fay R. (Eds), Springler-Verlag, New York
• Dallos, P., Cochlear amplification, outer hair cells and prestin (2008) Curr Opin Neurobiol, 18, pp. 370-376
• Hudspeth, A.J., Making an effort to listen: mechanical amplification in the ear (2008) Neuron, 59, pp. 530-545
• Chan, D.K., Hudspeth, A.J., Ca2+ current-driven nonlinear amplification by the mammalian cochlea in vitro (2005) Nat Neurosci, 8, pp. 149-155
• Jia, S., He, D.Z., Motility-associated hair-bundle motion in mammalian outer hair cells (2005) Nat Neurosci, 8, pp. 1028-1034
• Kennedy, H.J., Crawford, A.C., Fettiplace, R., Force generation by mammalian hair bundles supports a role in cochlear amplification (2005) Nature, 433, pp. 880-883
• Brownell, W., Bader, C., Bertrand, D., de Ribaupierre, Y., Evoked mechanical responses of isolated cochlear hair cells (1985) Science, 227, pp. 194-196
• Zheng, J., Shen, W., He, D.Z., Long, K.B., Madison, L.D., Dallos, P., Prestin is the motor protein of cochlear outer hair cells (2000) Nature, 405, pp. 149-155
• Mount, D.B., Romero, M.F., The SLC26 gene family of multifunctional anion exchangers (2004) Pflugers Arch, 447, pp. 710-721
• Franchini, L.F., Elgoyhen, A.B., Adaptive evolution in mammalian proteins involved in cochlear outer hair cell electromotility (2006) Mol Phylogenet Evol, 41, pp. 622-635
• Fuchs, P., Synaptic transmission at vertebrate hair cells (1996) Current Opinion in Neurobiol, 6, pp. 514-519
• Dolan, D.F., Nuttall, A.L., Masked cochlear whole-nerve response intensity functions altered by electrical stimulation of the crossed olivocochlear bundle (1988) J Acoust Soc Am, 83, pp. 1081-1086
• Kawase, T., Delgutte, B., Liberman, M.C., Antimasking effects of the olivocochlear reflex. II. Enhancement of auditory-nerve response to masked tones (1993) J Neurophysiol, 70, pp. 2533-2549
• Winslow, R.L., Sachs, M.B., Single-tone intensity discrimination based on auditory-nerve rate responses in backgrounds of quiet, noise, and with stimulation of the crossed olivocochlear bundle (1988) Hear Res, 35, pp. 165-189
• Delano, P.H., Elgueda, D., Hamame, C.M., Robles, L., Selective attention to visual stimuli reduces cochlear sensitivity in chinchillas (2007) J Neurosci, 27, pp. 4146-4153
• Oatman, L.C., Effects of visual attention on the intensity of auditory evoked potentials (1976) Exp Neurol, 51, pp. 41-53
• Liberman, M.C., The olivocochlear efferent bundle and susceptibility of the inner ear to acoustic injury (1991) J Neurophysiol, 65, pp. 123-132
• Maison, S.F., Liberman, M.C., Predicting vulnerability to acoustic injury with a noninvasive assay of olivocochlear reflex strength (2000) J Neurosci, 20, pp. 4701-4707
• Maison, S.F., Luebke, A.E., Liberman, M.C., Zuo, J., Efferent protection from acoustic injury is mediated via alpha9 nicotinic acetylcholine receptors on outer hair cells (2002) J Neurosci, 22, pp. 10838-10846
• Rajan, R., Electrical stimulation of the inferior colliculus at low rates protects the cochlea from auditory desensitization (1990) Brain Res, 506, pp. 192-204
• Taranda, J., Maison, S.F., Ballestero, J.A., Katz, E., Savino, J., Vetter, D.E., A point mutation in the hair cell nicotinic cholinergic receptor prolongs cochlear inhibition and enhances noise protection (2009) PLoS Biol, 7, pp. e18
• Blanchet, C., Erostegui, C., Sugasawa, M., Dulon, D., Acetylcholine-induced potassium current of guinea pig outer hair cells: its dependence on a calcium influx through nicotinic-like receptors (1996) J Neurosci, 16, pp. 2574-2584
• Chen, C., LeBlanc, C., Bobbin, R., Differences in cholinergic responses from outer hair cells of rat and guinea pig (1996) Hearing Research, 98, pp. 9-17
• Doi, T., Ohmori, H., Acetylcholine increases intracellular Ca2+ concentration and hyperpolarizes the guinea-pig outer hair cell (1993) Hearing Res, 67, pp. 179-188
• Dulon, D., Lenoir, M., Cholinergic responses in developing outer hair cells of the rat cochlea (1996) European J Neurosci, 8, pp. 1945-1952
• Erostegui, C., Norris, C.H., Bobbin, R.P., In vitro characterization of a cholinergic receptor on outer hair cells (1994) Hearing Res, 74, pp. 135-147
• Evans, M., Acetylcholine activates two currents in guinea-pig outer hair cells (1996) J Physiol, 491, pp. 563-578
• Fuchs, P.A., Murrow, B.W., A novel cholinergic receptor mediates inhibition of chick cochlear hair cells (1992) Proc R Soc Lond B, 248, pp. 35-40
• Fuchs, P.A., Murrow, B.W., Cholinergic inhibition of short (outer) hair cells of the chick's cochlea (1992) J Neurosci, 12, pp. 800-809
• Housley, G.D., Ashmore, J.F., Direct measurement of the action of acetylcholine on isolated outer hair cells of the guinea pig cochlea (1991) Proc R Soc Lond B, 244, pp. 161-167
• Dulon, D., Luo, L., Zhang, C., Ryan, A.F., Expression of small-conductance calcium-activated potassium channels (SK) in outer hair cells of the rat cochlea (1998) Eur J Neurosci, 10, pp. 907-915
• Oliver, D., Klocker, N., Schuck, J., Baukrowitz, T., Ruppersberg, J.P., Fakler, B., Gating of Ca2+-activated K+ channels controls fast inhibitory synaptic transmission at auditory outer hair cells (2000) Neuron, 26, pp. 595-601
• Elgoyhen, A.B., Johnson, D.S., Boulter, J., Vetter, D.E., Heinemann, S., α9: an acetylcholine receptor with novel pharmacological properties expressed in rat cochlear hair cells (1994) Cell, 79, pp. 705-715
• Vetter, D., Lieberman, M., Mann, J., Barhanin, J., Boulter, J., Brown, M., Role of α9 nicotinic ACh receptor subunits in the development and function of cochlear efferent innervation (1999) Neuron, 23, pp. 93-103
• Katz, E., Verbitsky, M., Rothlin, C., Vetter, D., Heinemann, S., Elgoyhen, A., High calcium permeability and calcium block of the α9 nicotinic acetylcholine receptor (2000) Hearing Res, 141, pp. 117-128
• Rothlin, C., Verbitsky, M., Katz, E., Elgoyhen, A., The α9 nicotinic acetylcholine receptor shares pharmacological properties with type A γ-aminobutyric acid, glycine and type 3 serotonin receptors (1999) Molec Pharmacol, 55, pp. 248-254
• Verbitsky, M., Rothlin, C., Katz, E., Elgoyhen, A.B., Mixed nicotinic-muscarinic properties of the a9 nicotinic cholinergic receptor (2000) Neuropharmacology, 39, pp. 2515-2524
• Glowatzki, E., Wild, K., Brandle, U., Fakler, G., Fakler, B., Zenner, H.P., Cell-specific expression of the alpha 9 n-ACh receptor subunit in auditory hair cells revealed by single-cell RT-PCR (1995) Proc R Soc Lond B, 262, pp. 141-147
• Morley, B., Li, H., Hiel, H., Drescher, D., Elgoyhen, A.B., Identification of the subunits of the nicotinic cholinergic receptors in the rat cochlea using RT-PCR and in situ hybridization (1998) Molec Brain Res, 53, pp. 78-87
• McNiven, A.I., Yuhas, W.A., Fuchs, P.A., Ionic dependence and agonist preference of an acetylcholine receptor in hair cells (1996) Auditory Neurosci, 2, pp. 63-77
• Le Novere, N., Changeux, J., Molecular evolution of the nicotinic acetylcholine receptor: an example of multigene family in excitable cells (1995) J Molec Evol, 40, pp. 155-172
• Le Novere, N., Corringer, P.J., Changeux, J.P., The diversity of subunit composition in nAChRs: evolutionary origins, physiologic and pharmacologic consequences (2002) J Neurobiol, 53, pp. 447-456
• Elgoyhen, A.B., Vetter, D., Katz, E., Rothlin, C., Heinemann, S., Boulter, J., Alpha 10: A determinant of nicotinic cholinergic receptor function in mammalian vestibular and cochlear mechanosensory hair cells (2001) Proc Natl Acad Sci, USA, 98, pp. 3501-3506
• Lustig, L.R., Peng, H., Hiel, H., Yamamoto, T., Fuchs, P., Molecular cloning and mapping of the human nicotinic acetylcholine receptor α10 (CHRNA10) (2001) Genomics, 73, pp. 272-283
• Sgard, F., Charpentier, E., Bertrand, S., Walker, N., Caput, D., Graham, D., A novel human nicotinic receptor subunit, α10, that confers functionality to the α9-subunit (2002) Molec Pharmacol, 61, pp. 150-159
• Vetter, D.E., Katz, E., Maison, S.F., Taranda, J., Turcan, S., Ballestero, J., The alpha10 nicotinic acetylcholine receptor subunit is required for normal synaptic function and integrity of the olivocochlear system (2007) Proc Natl Acad Sci USA, 104, pp. 20594-20599
• Plazas, P.V., Katz, E., Gomez-Casati, M.E., Bouzat, C., Elgoyhen, A.B., Stoichiometry of the α9α10 nicotinic cholinergic receptor (2005) J Neurosci, 25, pp. 10905-10912
• Vio, M.M., Holme, R.H., Hearing loss and tinnitus: 250 million people and a US$10 billion potential market (2005) Drug Discov Today, 10, pp. 1263-1265
• Cohen, S.M., Labadie, R.F., Haynes, D.S., Primary care approach to hearing loss: the hidden disability (2005) Ear Nose Throat J, 84 (26), pp. 9-31. , 44
• Mohr, P.E., Feldman, J.J., Dunbar, J.L., McConkey-Robbins, A., Niparko, J.K., Rittenhouse, R.K., The societal costs of severe to profound hearing loss in the United States (2000) Int J Technol Assess Health Care, 16, pp. 1120-1135
• Cryns, K., Van Camp, G., Deafness genes and their diagnostic applications (2004) Audiol Neurootol, 9, pp. 2-22
• Vrijens, K., Van Laer, L., Van Camp, G., Human hereditary hearing impairment: mouse models can help to solve the puzzle (2008) Hum Genet, 124, pp. 325-348
• Pujol, R., Carlier, E., Cochlear synaptogenesis after sectioning the efferent bundle (1982) Brain Res, 255, pp. 151-154
• Walsh, E., McGee, J., Does activity in the olivocochlear bundle affect development of the auditory periphery? (1997) Diversity in auditory mechanics, pp. 376-385. , Lewis E., Long G., Lyon R., Narins P., Steele C., and Hecht-Poinar E. (Eds), World Scientific, Singapore
• Walsh, E., McGee, J., McFadden, S., Liberman, M., Long-term effects of sectioning the olivocochlear bundle in neonatal cats (1998) J Neurosci, 18, pp. 3859-3869
• Simmons, D.D., Development of the inner ear efferent system across vertebrate species (2002) J Neurobiol, 53, pp. 228-250
• Glowatzki, E., Fuchs, P., Cholinergic synaptic inhibition of inner hair cells in the neonatal mammalian cochlea (2000) Science, 288, pp. 2366-2368
• Katz, E., Elgoyhen, A.B., Gomez-Casati, M.E., Knipper, M., Vetter, D.E., Fuchs, P.A., Developmental regulation of nicotinic synapses on cochlear inner hair cells (2004) J Neurosci, 24, pp. 7814-7820
• Lim, D.J., Effects of noise and ototoxic drugs at the cellular level in the cochlea: a review (1986) Am J Otolaryngol, 7, pp. 73-99
• Borg, E., Canlon, B., Engstrom, B., Noise-induced hearing loss. Literature review and experiments in rabbits. Morphological and electrophysiological features, exposure parameters and temporal factors, variability and interactions (1995) Scand Audiol Suppl, 40, pp. 1-147
• Barney, R., Bohnker, B.K., Hearing thresholds for U.S. Marines: comparison of aviation, combat arms, and other personnel (2006) Aviat Space Environ Med, 77, pp. 53-56
• Bohnker, B.K., Page, J.C., Rovig, G.W., Betts, L.S., Sack, D.M., Navy Hearing Conservation Program: 1995-1999 retrospective analysis of threshold shifts for age, sex, and officer/enlisted status (2004) Mil Med, 169, pp. 73-76
• Rovig, G.W., Bohnker, B.K., Page, J.C., Hearing health risk in a population of aircraft carrier flight deck personnel (2004) Mil Med, 169, pp. 429-432
• Neitzel, R., Meischke, H., Daniell, W.E., Trabeau, M., Somers, S., Seixas, N.S., Development and pilot test of hearing conservation training for construction workers (2008) Am J Ind Med, 51, pp. 120-129
• Tak, S., Davis, R.R., Calvert, G.M., Exposure to hazardous workplace noise and use of hearing protection devices among US workers-NHANES, 1999-2004 (2009) Am J Ind Med, 52, pp. 358-371
• Trabeau, M., Neitzel, R., Meischke, H., Daniell, W.E., Seixas, N.S., A comparison of "Train-the-Trainer" and expert training modalities for hearing protection use in construction (2008) Am J Ind Med, 51, pp. 130-137
• Landen, D., Wilkins, S., Stephenson, M., McWilliams, L., Noise exposure and hearing loss among sand and gravel miners (2004) J Occup Environ Hyg, 1, pp. 532-541
• Neitzel, R., Yost, M., Task-based assessment of occupational vibration and noise exposures in forestry workers (2002) AIHA J (Fairfax, Va), 63, pp. 617-627
• Beckett, W.S., Chamberlain, D., Hallman, E., May, J., Hwang, S.A., Gomez, M., Hearing conservation for farmers: source apportionment of occupational and environmental factors contributing to hearing loss (2000) J Occup Environ Med, 42, pp. 806-813
• Hong, O.S., Kim, M.J., Factors associated with hearing loss among workers of the airline industry in Korea (2001) ORL Head Neck Nurs, 19, pp. 7-13
• Jaruchinda, P., Thongdeetae, T., Panichkul, S., Hanchumpol, P., Prevalence and an analysis of noise-induced hearing loss in army helicopter pilots and aircraft mechanics (2005) J Med Assoc Thai, 88 (SUPPL. 3), pp. S232-S239
• Kim, J., Park, H., Ha, E., Jung, T., Paik, N., Yang, S., Combined effects of noise and mixed solvents exposure on the hearing function among workers in the aviation industry (2005) Ind Health, 43, pp. 567-573
• Landon, P., Breysse, P., Chen, Y., Noise exposures of rail workers at a North American chemical facility (2005) Am J Ind Med, 47, pp. 364-369
• Seshagiri, B., Exposure to noise on board locomotives (2003) AIHA J (Fairfax, Va), 64, pp. 699-707
• Kumar, A., Mathur, N.N., Varghese, M., Mohan, D., Singh, J.K., Mahajan, P., Effect of tractor driving on hearing loss in farmers in India (2005) Am J Ind Med, 47, pp. 341-348
• Solecki, L., Characteristics of annual exposure to noise among private farmers on family farms of mixed-production profile (2006) Ann Agric Environ Med, 13, pp. 113-118
• Biassoni, E.C., Serra, M.R., Richtert, U., Joekes, S., Yacci, M.R., Carignani, J.A., Recreational noise exposure and its effects on the hearing of adolescents. Part II. Development of hearing disorders (2005) Int J Audiol, 44, pp. 74-85
• Serra, M.R., Biassoni, E.C., Richter, U., Minoldo, G., Franco, G., Abraham, S., Recreational noise exposure and its effects on the hearing of adolescents. Part I. an Interdisciplinary long-term study (2005) Int J Audiol, 44, pp. 65-73
• Lynch, E.D., Kil, J., Compounds for the prevention and treatment of noise-induced hearing loss (2005) Drug Discov Today, 10, pp. 1291-1298
• Henderson, D., Bielefeld, E.C., Harris, K.C., Hu, B.H., The role of oxidative stress in noise-induced hearing loss (2006) Ear Hear, 27, pp. 1-19
• Kopke, R.D., Jackson, R.L., Coleman, J.K., Liu, J., Bielefeld, E.C., Balough, B.J., NAC for noise: from the bench top to the clinic (2007) Hear Res, 226, pp. 114-125
• Wang, J., Ruel, J., Ladrech, S., Bonny, C., van de Water, T.R., Puel, J.L., Inhibition of the c-Jun N-terminal kinase-mediated mitochondrial cell death pathway restores auditory function in sound-exposed animals (2007) Mol Pharmacol, 71, pp. 654-666
• Kil, J., Pierce, C., Tran, H., Gu, R., Lynch, E.D., Ebselen treatment reduces noise induced hearing loss via the mimicry and induction of glutathione peroxidase (2007) Hear Res, 226, pp. 44-51
• Chen, G.D., Kong, J., Reinhard, K., Fechter, L.D., NMDA receptor blockage protects against permanent noise-induced hearing loss but not its potentiation by carbon monoxide (2001) Hear Res, 154, pp. 108-115
• Duan, M., Chen, Z., Qiu, J., Ulfendahl, M., Laurell, G., Borg, E., Low-dose, long-term caroverine administration attenuates impulse noise-induced hearing loss in the rat (2006) Acta Otolaryngol, 126, pp. 1140-1147
• Reiter, E.R., Liberman, M.C., Efferent-mediated protection from acoustic overexposure: relation to slow effects of olivocochlear stimulation (1995) J Neurophysiol, 73, pp. 506-514
• Kujawa, S.G., Liberman, M.C., Conditioning-related protection from acoustic injury: effects of chronic deefferentation and sham surgery (1997) J Neurophysiol, 78, pp. 3095-3106
• Handrock, M., Zeisberg, J., The influence of the effect system on adaptation, temporary and permanent threshold shift (1982) Arch Otorhinolaryngol, 234, pp. 191-195
• Eggermont, J.J., Role of auditory cortex in noise- and drug-induced tinnitus (2008) Am J Audiol, 17, pp. S162-S169
• Moller, A.R., Tinnitus: presence and future (2007) Prog Brain Res, 166, pp. 3-16
• Tyler, R., Coelho, C., Tao, P., Ji, H., Noble, W., Gehringer, A., Identifying tinnitus subgroups with cluster analysis (2008) Am J Audiol, 17, pp. S176-S184
• Mount, C., Downton, C., Alzheimer disease: progress or profit? (2006) Nat Med, 12, pp. 780-784
• Rammes, G., Schierloh, A., Neramexane (merz pharmaceuticals/forest laboratories) (2006) IDrugs, 9, pp. 128-135
• Plazas, P.V., Savino, J., Kracun, S., Gomez-Casati, M.E., Katz, E., Parsons, C.G., Inhibition of the alpha9alpha10 nicotinic cholinergic receptor by neramexane, an open channel blocker of N-methyl-d-aspartate receptors (2007) Eur J Pharmacol, 566, pp. 11-19
• Eggermont, J.J., Tinnitus: neurobiological substrates (2005) Drug Discov Today, 10, pp. 1283-1290
• Van de Heyning, P., Vermeire, K., Diebl, M., Nopp, P., Anderson, I., De Ridder, D., Incapacitating unilateral tinnitus in single-sided deafness treated by cochlear implantation (2008) Ann Otol Rhinol Laryngol, 117, pp. 645-652
• Mody, M., Wehner, D.T., Ahlfors, S.P., Auditory word perception in sentence context in reading-disabled children (2008) Neuroreport, 19, pp. 1567-1571
• Demonet, J.F., Taylor, M.J., Chaix, Y., Developmental dyslexia (2004) Lancet, 363, pp. 1451-1460
• Ramirez, J., Mann, V., Using auditory-visual speech to probe the basis of noise-impaired consonant-vowel perception in dyslexia and auditory neuropathy (2005) J Acoust Soc Am, 118, pp. 1122-1133
• Sperling, A.J., Lu, Z.L., Manis, F.R., Seidenberg, M.S., Deficits in perceptual noise exclusion in developmental dyslexia (2005) Nat Neurosci, 8, pp. 862-863
• Kawase, T., Liberman, M.C., Antimasking effects of the olivocochlear reflex. I. Enhancement of compound action potentials to masked tones (1993) J Neurophysiol, 70, pp. 2519-2532
• Micheyl, C., Carbonnel, O., Collet, L., Medial olivocochlear system and loudness adaptation: differences between musicians and non-musicians (1995) Brain Cogn, 29, pp. 127-136
• Micheyl, C., Collet, L., Involvement of the olivocochlear bundle in the detection of tones in noise (1996) J Acoust Soc Am, 99, pp. 1604-1610
• Micheyl, C., Khalfa, S., Perrot, X., Collet, L., Difference in cochlear efferent activity between musicians and non-musicians (1997) Neuroreport, 8, pp. 1047-1050
• Micheyl, C., Perrot, X., Collet, L., Relationship between auditory intensity discrimination in noise and olivocochlear efferent system activity in humans (1997) Behav Neurosci, 111, pp. 801-807
• Giraud, A.L., Garnier, S., Micheyl, C., Lina, G., Chays, A., Chery-Croze, S., Auditory efferents involved in speech-in-noise intelligibility (1997) Neuroreport, 8, pp. 1779-1783
• Kumar, U.A., Vanaja, C.S., Functioning of olivocochlear bundle and speech perception in noise (2004) Ear Hear, 25, pp. 142-146
• Veuillet, E., Bazin, F., Collet, L., Objective evidence of peripheral auditory disorders in learning-impaired children (1999) J Audiol Med, 8, pp. 18-29
• Brashears, S.M., Morlet, T.G., Berlin, C.I., Hood, L.J., Olivocochlear efferent suppression in classical musicians (2003) J Am Acad Audiol, 14, pp. 314-324
• Veuillet, E., Magnan, A., Ecalle, J., Thai-Van, H., Collet, L., Auditory processing disorder in children with reading disabilities: effect of audiovisual training (2007) Brain, 130, pp. 2915-2928
• de Boer, J., Thornton, A.R., Neural correlates of perceptual learning in the auditory brainstem: efferent activity predicts and reflects improvement at a speech-in-noise discrimination task (2008) J Neurosci, 28, pp. 4929-4937
• Lindstrom, J.M., Nicotinic acetylcholine receptors of muscles and nerves: comparison of their structures, functional roles, and vulnerability to pathology (2003) Ann N Y Acad Sci, 998, pp. 41-52
• Gotti, C., Riganti, L., Vailati, S., Clementi, F., Brain neuronal nicotinic receptors as new targets for drug discovery (2006) Curr Pharm Des, 12, pp. 407-428
• Hogg, R.C., Buisson, B., Bertrand, D., Allosteric modulation of ligand-gated ion channels (2005) Biochem Pharmacol, 70, pp. 1267-1276
• White, H.K., Levin, E.D., Chronic transdermal nicotine patch treatment effects on cognitive performance in age-associated memory impairment (2004) Psychopharmacology (Berl), 171, pp. 465-471
• Smith, R.C., Singh, A., Infante, M., Khandat, A., Kloos, A., Effects of cigarette smoking and nicotine nasal spray on psychiatric symptoms and cognition in schizophrenia (2002) Neuropsychopharmacology, 27, pp. 479-497
• Albuquerque, E.X., Santos, M.D., Alkondon, M., Pereira, E.F., Maelicke, A., Modulation of nicotinic receptor activity in the central nervous system: a novel approach to the treatment of Alzheimer disease (2001) Alzheimer Dis Assoc Disord, 15 (SUPPL. 1), pp. S19-S25
• Bertrand, D., Gopalakrishnan, M., Allosteric modulation of nicotinic acetylcholine receptors (2007) Biochem Pharmacol, 74, pp. 1155-1163
• Hurst, R.S., Hajos, M., Raggenbass, M., Wall, T.M., Higdon, N.R., Lawson, J.A., A novel positive allosteric modulator of the alpha7 neuronal nicotinic acetylcholine receptor: in vitro and in vivo characterization (2005) J Neurosci, 25, pp. 4396-4405
• Zorrilla de San Martin, J., Ballestero, J., Katz, E., Elgoyhen, A.B., Fuchs, P.A., Ryanodine is a positive modulator of acetylcholine receptor gating in cochlear hair cells (2007) J Assoc Res Otolaryngol, 8, pp. 474-483
• Rothlin, C.V., Lioudyno, M.I., Silbering, A.F., Plazas, P.V., Casati, M.E., Katz, E., Direct interaction of serotonin type 3 receptor ligands with recombinant and native alpha 9 alpha 10-containing nicotinic cholinergic receptors (2003) Mol Pharmacol, 63, pp. 1067-1074

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