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1. N. Sadato, A. Pascual-Leone, J. Grafman et al., “Activation of the primary visual cortex by Braille reading in blind subjects,” Nature, vol. 380, no. 6574, pp. 526–528, 1996. View at Publisher · View at Google Scholar · View at Scopus
2. D. Bavelier and H. J. Neville, “Cross-modal plasticity: where and how?” Nature Reviews Neuroscience, vol. 3, no. 6, pp. 443–452, 2002. View at Scopus
3. K. Sathian and R. Stilla, “Cross-modal plasticity of tactile perception in blindness,” Restorative Neurology and Neuroscience, vol. 28, no. 2, pp. 271–281, 2010. View at Publisher · View at Google Scholar · View at Scopus
4. H. Nishimura, K. Hashikawa, K. Doi et al., “Sign language “heard” in the auditory cortex,” Nature, vol. 397, no. 6715, article 116, 1999. View at Scopus
5. L. A. Petitto, R. J. Zatorre, K. Gauna, E. J. Nikelski, D. Dostie, and A. C. Evans, “Speech-like cerebral activity in profoundly deaf people processing signed languages: implications for the neural basis of human language,” Proceedings of the National Academy of Sciences of the United States of America, vol. 97, no. 25, pp. 13961–13966, 2000. View at Publisher · View at Google Scholar · View at Scopus
6. E. M. Finney, I. Fine, and K. R. Dobkins, “Visual stimuli activate auditory cortex in the deaf,” Nature Neuroscience, vol. 4, no. 12, pp. 1171–1173, 2001. View at Publisher · View at Google Scholar · View at Scopus
7. N. Lambertz, E. R. Gizewski, A. De Greiff, and M. Forsting, “Cross-modal plasticity in deaf subjects dependent on the extent of hearing loss,” Cognitive Brain Research, vol. 25, no. 3, pp. 884–890, 2005. View at Publisher · View at Google Scholar · View at Scopus
8. D. Bavelier, M. W. G. Dye, and P. C. Hauser, “Do deaf individuals see better?” Trends in Cognitive Sciences, vol. 10, no. 11, pp. 512–518, 2006. View at Publisher · View at Google Scholar · View at Scopus
9. P. Voss, F. Gougoux, R. J. Zatorre, M. Lassonde, and F. Lepore, “Differential occipital responses in early- and late-blind individuals during a sound-source discrimination task,” NeuroImage, vol. 40, no. 2, pp. 746–758, 2008. View at Publisher · View at Google Scholar · View at Scopus
10. S. G. Lomber, M. A. Meredith, and A. Kral, “Cross-modal plasticity in specific auditory cortices underlies visual compensations in the deaf,” Nature Neuroscience, vol. 13, no. 11, pp. 1421–1427, 2010. View at Publisher · View at Google Scholar · View at Scopus
11. M. A. Meredith, J. Kryklywy, A. J. McMillan, S. Malhotra, R. Lum-Tai, and S. G. Lomber, “Crossmodal reorganization in the early deaf switches sensory, but not behavioral roles of auditory cortex,” Proceedings of the National Academy of Sciences of the United States of America, vol. 108, no. 21, pp. 8856–8861, 2011. View at Publisher · View at Google Scholar · View at Scopus
12. A. Kral, J. H. Schröder, R. Klinke, and A. K. Engel, “Absence of cross-modal reorganization in the primary auditory cortex of congenitally deaf cats,” Experimental Brain Research, vol. 153, no. 4, pp. 605–613, 2003. View at Publisher · View at Google Scholar · View at Scopus
13. B. L. Allman, L. P. Keniston, and M. A. Meredith, “Adult deafness induces somatosensory conversion of ferret auditory cortex,” Proceedings of the National Academy of Sciences of the United States of America, vol. 106, no. 14, pp. 5925–5930, 2009. View at Publisher · View at Google Scholar · View at Scopus
14. L. P. Keniston, B. L. Allman, and M. A. Meredith, “Hearing impairment in adult ferrets induces partial crossmodal conversion of core auditory cortex,” Society for Neuroscience, vol. 41, article 476.13.
15. M. A. Meredith, L. P. Keniston, and B. L. Allman, “Multisensory dysfunction accompanies crossmodal plasticity following adult hearing impairment,” Neuroscience, vol. 214, pp. 136–148, 2012.
16. T. D. Mrsic-Flogel, H. Versnel, and A. J. King, “Development of contralateral and ipsilateral frequency representations in ferret primary auditory cortex,” European Journal of Neuroscience, vol. 23, no. 3, pp. 780–792, 2006. View at Publisher · View at Google Scholar · View at Scopus
17. D. R. Moore and J. E. Hine, “Rapid development of the auditory brainstem response threshold in individual ferrets,” Developmental Brain Research, vol. 66, no. 2, pp. 229–235, 1992. View at Publisher · View at Google Scholar · View at Scopus
18. R. K. Shepherd and R. L. Martin, “Onset of ototoxicity in the cat is related to onset of auditory function,” Hearing Research, vol. 92, no. 1-2, pp. 131–142, 1995. View at Publisher · View at Google Scholar · View at Scopus
19. S. A. Xu, R. K. Shepherd, Y. Chen, and G. M. Clark, “Profound hearing loss in the cat following the single co-administration of kanamycin and ethacrynic acid,” Hearing Research, vol. 70, no. 2, pp. 205–215, 1993. View at Publisher · View at Google Scholar · View at Scopus
20. J. K. Bizley, F. R. Nodal, I. Nelken, and A. J. King, “Functional organization of ferret auditory cortex,” Cerebral Cortex, vol. 15, no. 10, pp. 1637–1653, 2005. View at Publisher · View at Google Scholar · View at Scopus
21. P. R. Manger, G. Engler, C. K. E. Moll, and A. K. Engel, “Location, architecture, and retinotopy of the anteromedial lateral suprasylvian visual area (AMLS) of the ferret (Mustela putorius),” Visual Neuroscience, vol. 25, no. 1, pp. 27–37, 2008. View at Publisher · View at Google Scholar · View at Scopus
22. A. M. Ramsay and M. A. Meredith, “Multiple sensory afferents to ferret pseudosylvian sulcal cortex,” NeuroReport, vol. 15, no. 3, pp. 461–465, 2004. View at Publisher · View at Google Scholar · View at Scopus
23. C. L. Veenman, A. Reiner, and M. G. Honig, “Biotinylated dextran amine as an anterograde tracer for single- and double-labeling studies,” Journal of Neuroscience Methods, vol. 41, no. 3, pp. 239–254, 1992. View at Publisher · View at Google Scholar · View at Scopus
24. F. L. Rice, C. M. Gomez, S. S. Leclerc, R. W. Dykes, J. S. Moon, and K. Pourmoghadam, “Cytoarchitecture of the ferret suprasylvian gyrus correlated with areas containing multiunit responses elicited by stimulation of the face,” Somatosensory and Motor Research, vol. 10, no. 2, pp. 161–188, 1993. View at Scopus
25. S. S. Leclerc, F. L. Rice, R. W. Dykes, K. Pourmoghadam, and C. M. Gomez, “Electrophysiological examination of the representation of the face in the suprasylvian gyrus of the ferret: a correlative study with cytoarchitecture,” Somatosensory and Motor Research, vol. 10, no. 2, pp. 133–159, 1993. View at Scopus
26. P. R. Manger, G. Engler, C. K. E. Moll, and A. K. Engel, “The anterior ectosylvian visual area of the ferret: a homologue for an enigmatic visual cortical area of the cat?” European Journal of Neuroscience, vol. 22, no. 3, pp. 706–714, 2005. View at Publisher · View at Google Scholar · View at Scopus
27. P. R. Manger, I. Masiello, and G. M. Innocenti, “Areal organization of the posterior parietal cortex of the ferret (Mustela putorius),” Cerebral Cortex, vol. 12, no. 12, pp. 1280–1297, 2002. View at Scopus
28. J. Homman-Ludiye, P. R. Manger, and J. A. Bourne, “Immunohistochemical parcellation of the ferret (Mustela putorius) visual cortex reveals substantial homology with the cat (Felis catus),” Journal of Comparative Neurology, vol. 518, no. 21, pp. 4439–4462, 2010. View at Publisher · View at Google Scholar · View at Scopus
29. E. T. Auer, L. E. Bernstein, W. Sungkarat, and M. Singh, “Vibrotactile activation of the auditory cortices in deaf versus hearing adults,” NeuroReport, vol. 18, no. 7, pp. 645–648, 2007. View at Publisher · View at Google Scholar · View at Scopus
30. W. A. Foxworthy and M. A. Meredith, “An examination of somatosensory area SIII in ferret cortex,” Somatosensory and Motor Research, vol. 28, no. 1-2, pp. 1–10, 2011. View at Publisher · View at Google Scholar
31. L. P. Keniston, B. L. Allman, M. A. Meredith, and H. R. Clemo, “Somatosensory and multisensory properties of the medial bank of the ferret rostral suprasylvian sulcus,” Experimental Brain Research, vol. 196, no. 2, pp. 239–251, 2009. View at Publisher · View at Google Scholar · View at Scopus
32. S. E. Shore, “Plasticity of somatosensory inputs to the cochlear nucleus—implications for tinnitus,” Hearing Research, vol. 281, no. 1-2, pp. 38–46, 2011. View at Publisher · View at Google Scholar · View at Scopus
33. J. P. Rauschecker, “Compensatory plasticity and sensory substitution in the cerebral cortex,” Trends in Neurosciences, vol. 18, no. 1, pp. 36–43, 1995. View at Publisher · View at Google Scholar · View at Scopus
34. J. P. Rauschecker and U. Kniepert, “Auditory localization behaviour in visually deprived cats,” European Journal of Neuroscience, vol. 6, no. 1, pp. 149–160, 1994. View at Publisher · View at Google Scholar · View at Scopus
35. B. Röder, W. Teder-Sälejärvi, A. Sterr, F. Rösler, S. A. Hillyard, and H. J. Neville, “Improved auditory spatial tuning in blind humans,” Nature, vol. 400, no. 6740, pp. 162–166, 1999. View at Publisher · View at Google Scholar · View at Scopus
36. A. Fieger, B. Röder, W. Teder-Sälejärvi, S. A. Hillyard, and H. J. Neville, “Auditory spatial tuning in late-onset blindness in humans,” Journal of Cognitive Neuroscience, vol. 18, no. 2, pp. 149–157, 2006. View at Publisher · View at Google Scholar · View at Scopus
37. C. C. Lee and J. A. Winer, “Connections of cat auditory cortex: I. Thalamocortical system,” Journal of Comparative Neurology, vol. 507, no. 6, pp. 1879–1900, 2008. View at Publisher · View at Google Scholar · View at Scopus
38. C. C. Lee and J. A. Winer, “Connections of cat auditory cortex: II. Commissural system,” Journal of Comparative Neurology, vol. 507, no. 6, pp. 1901–1919, 2008. View at Publisher · View at Google Scholar · View at Scopus
39. C. C. Lee and J. A. Winer, “Connections of cat auditory cortex: III. Corticocortical system,” Journal of Comparative Neurology, vol. 507, no. 6, pp. 1920–1943, 2008. View at Publisher · View at Google Scholar · View at Scopus
40. E. Budinger, P. Heil, A. Hess, and H. Scheich, “Multisensory processing via early cortical stages: connections of the primary auditory cortical field with other sensory systems,” Neuroscience, vol. 143, no. 4, pp. 1065–1083, 2006. View at Publisher · View at Google Scholar · View at Scopus
41. D. L. Hunt, E. N. Yamoah, and L. Krubitzer, “Multisensory plasticity in congenitally deaf mice: how are cortical areas functionally specified?” Neuroscience, vol. 139, no. 4, pp. 1507–1524, 2006. View at Publisher · View at Google Scholar · View at Scopus
42. S. E. Shore and J. Zhou, “Somatosensory influence on the cochlear nucleus and beyond,” Hearing Research, vol. 216–217, no. 1-2, pp. 90–99, 2006. View at Publisher · View at Google Scholar · View at Scopus
43. S. E. Shore, Z. Vass, N. L. Wys, and R. A. Altschuler, “Trigeminal ganglion innervates the auditory brainstem,” Journal of Comparative Neurology, vol. 419, no. 3, pp. 271–285, 2000. View at Publisher · View at Google Scholar · View at Scopus
44. P. O. Kanold and E. D. Young, “Proprioceptive information from the pinna provides somatosensory input to cat dorsal cochlear nucleus,” The Journal of Neuroscience, vol. 21, no. 19, pp. 7848–7858, 2001. View at Scopus
45. L. M. Aitkin, C. E. Kenyon, and P. Philpott, “The representation of the auditory and somatosensory systems in the external nucleus of the cat inferior colliculus,” Journal of Comparative Neurology, vol. 196, no. 1, pp. 25–40, 1981. View at Scopus
46. S. E. Shore, S. Koehler, M. Oldakowski, L. F. Hughes, and S. Syed, “Dorsal cochlear nucleus responses to somatosensory stimulation are enhanced after noise-induced hearing loss,” European Journal of Neuroscience, vol. 27, no. 1, pp. 155–168, 2008. View at Publisher · View at Google Scholar · View at Scopus