{"id":7,"date":"2012-05-18T18:09:06","date_gmt":"2012-05-18T18:09:06","guid":{"rendered":"http:\/\/as.vanderbilt.edu\/catanialab\/manage\/?page_id=7"},"modified":"2018-04-20T15:07:07","modified_gmt":"2018-04-20T15:07:07","slug":"publications","status":"publish","type":"page","link":"https:\/\/wp0.vanderbilt.edu\/catanialab\/publications\/","title":{"rendered":"Peer Reviewed Publications"},"content":{"rendered":"<h2 id=\"menuright\"><a title=\"Other Publications\" href=\"http:\/\/as.vanderbilt.edu\/catanialab\/other-publications\/\">Other Publications<\/a><\/h2>\n<h4>2017<\/h4>\n<p>Catania KC (2017) Power Transfer to a Human during an Electric Eel\u2019s Shocking Leap. Current Biology.\u00a0 27:2887-2891.e2. doi: 10.1016\/j.cub.2017.08.034 <a href=\"https:\/\/cdn.vanderbilt.edu\/vu-wordpress-0\/wp-content\/uploads\/sites\/182\/2018\/04\/19174939\/2017-Power-Transfer-to-a-Human-during-an-Electric-Eel%E2%80%99s-Shocking-Leap.pdf\">pdf<\/a><\/p>\n<p>Catania KC (2017) Behavioral pieces of neuroethological puzzles. Journal of Comparative Physiology A. 203:677-689. doi: 10.1007\/s00359-016-1143-7. <a href=\"https:\/\/cdn.vanderbilt.edu\/vu-wordpress-0\/wp-content\/uploads\/sites\/182\/2018\/04\/19174939\/2017-Behavioral-pieces-of-neuroethological-puzzles.pdf\">pdf<\/a><\/p>\n<p>Catania KC (2017) Electrical Potential of Leaping Eels. Brain, Behavior and Evolution. 89:262-273. doi: 10.1159\/000475743. <a href=\"https:\/\/cdn.vanderbilt.edu\/vu-wordpress-0\/wp-content\/uploads\/sites\/182\/2018\/04\/19174939\/2017-Electrical-Potential-of-Leaping-Eels.pdf\">pdf<\/a><\/p>\n<p>Sinclair, A. W., Glickman, S., Catania, K., Shinohara, A., Baskin, L., &amp; Cunha, G. R. (2017). Comparative Morphology of the Penis and Clitoris in Four Species of Moles (Talpidae). Journal of Experimental Zoology Part B: Molecular and Developmental Evolution, 328(3), 275-294. doi: 10.1002\/jez.b.22732. <a href=\"https:\/\/cdn.vanderbilt.edu\/vu-wordpress-0\/wp-content\/uploads\/sites\/182\/2018\/04\/19174939\/2017-Comparative-Morphology-of-the-Penis-and-Clitoris-in-Four-Species-of-Moles-Talpidae1.pdf\">pdf<\/a><\/p>\n<h4>2016<\/h4>\n<p>Catania KC (2016) Leaping eels electrify threats supporting Humboldt\u2019s account of a battle with horses. Proceedings of the National Academy of Sciences. 113 (25) 6979-6984 <a href=\"https:\/\/cdn.vanderbilt.edu\/vu-wordpress-0\/wp-content\/uploads\/sites\/182\/2018\/04\/19174939\/2016-Leaping-eels-electrify-threats-supporting-Humboldt%E2%80%99s-account-of-a-battle-with-horses.pdf\">pdf<\/a><\/p>\n<p>Sawyer EK and Catania KC. (2016) Somatosensory organ topography across the star of a star-nosed mole (Condylura cristata). Journal of Comparative Neurology. J Comp Neurol. 524:917-929. <a href=\"https:\/\/cdn.vanderbilt.edu\/vu-wordpress-0\/wp-content\/uploads\/sites\/182\/2018\/04\/19174939\/2016-Somatosensory-Organ-Topography-Across-the-Star-of-the-Star-Nosed-Mole-Condylura-cristata.pdf\">pdf<\/a><\/p>\n<h4>2015<\/h4>\n<p>Catania KC (2015) Electric eels concentrate their electric field to induce involuntary fatigue in struggling prey.\u00a0 Current Biology.\u00a0 25:2889-2898. <a href=\"https:\/\/cdn.vanderbilt.edu\/vu-wordpress-0\/wp-content\/uploads\/sites\/182\/2018\/04\/19174939\/2015-Electric-Eels-Concentrate-Their-Electric-Field-to-Induce-Involuntary-Fatigue-in-Struggling-Prey.pdf\">pdf<\/a><\/p>\n<p>Catania KC (2015) Electric Eels Use High-Voltage to Track Fast Moving Prey.\u00a0 Nature Communications.\u00a0 6:8638 doi:10.1038\/ncomms9638 <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2015\/11\/Nature-Com.pdf\">pdf<\/a><\/p>\n<p>Catania KC (2015) An optimized biological TASER: Electric eels remotely induce or arrest movement in nearby prey.\u00a0 Brain, Behavior, and Evolution. 86:38-47. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2015\/11\/Brain-Beh-Evol.pdf\">pdf<\/a><\/p>\n<p>Marzban H, Hoy N, Buchok M, Catania KC, Hawkes R. (2015) Compartmentation of the Cerebellar Cortex: Adaptation to Lifestyle in the Star-Nosed Mole Condylura cristata. Cerebellum. 14:106-118.<\/p>\n<h4>2014<\/h4>\n<p>Catania K (2014) The shocking predatory strike of the electric eel.\u00a0 Science 346:1231-1234. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2015\/11\/Science.pdf\">pdf<\/a><\/p>\n<p>Leitch DB, Sarko DK, Catania KC (2014) Brain mass and cranial nerve size in shrews and moles. Scientific Reports 4:6241.<\/p>\n<p>Ribeiro PF, Manger PR, Catania KC, Kaas JH, Herculano-Houzel S.\u00a0 (2014)\u00a0 Greater addition of neurons to the olfactory bulb than to the cerebral cortex of eulipotyphlans but not rodents, afrotherians or primates. Frontiers in Neuroanatomy 8:23. doi: 10.3389<\/p>\n<p>Sawyer EK, Leitch DB, Catania KC (2014) Organization of the spinal trigeminal nucleus in Star-Nosed Moles.\u00a0 Journal of Comparative Neurology. 522:3335-3350.<\/p>\n<h4><a name=\"2013\"><\/a>2013<\/h4>\n<p>Sarko DK, Leitch DB, Catania KC (2013) Cutaneous and periodontal inputs to the cerebellum of the naked mole-rat (Heterocephalus glaber).\u00a0 Frontiers in Neuroanatomy.\u00a0 7:39<\/p>\n<p>Catania KC, Catania EH, Sawyer EK, Leitch DB (2013) Barrelettes without Barrels in the American Water Shrew. PLoS ONE 8(6): e65975. doi:10.1371\/journal.pone.0065975 <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2013\/06\/Catania-2013-PLoS.pdf\">pdf<\/a><\/p>\n<p>Gerhold, K.A., Pellegrino, M., Tsunozaki, M., Morita, T., Leitch, D.B., Tsuruda, P.R., Brem, R.B., Catania, K.C., and Bautista, D.M. (2013). The star-nosed mole reveals clues to the molecular basis of Mammalian touch. PloS one 8, e55001. <a title=\"pdf\" href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2013\/03\/pone.0055001.pdf\">pdf<\/a><\/p>\n<p>Catania, K.C. (2013). Stereo and serial sniffing guide navigation to an odour source in a mammal. Nat Commun 4, 1441. <a title=\"pdf\" href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2013\/03\/ncomms2444.pdf\">pdf<\/a><\/p>\n<p>Catania, K.C. (2013). The neurobiology and behavior of the American water shrew (Sorex palustris). Journal of comparative physiology A, Neuroethology, sensory, neural, and behavioral physiology.\u00a0 DOI 10.1007\/s00359-012-0781-7<\/p>\n<h4><a name=\"2012\"><\/a>2012<\/h4>\n<p>Leitch DB and Catania KC (2012) Structure, innervation, and response properties of integumentary sensory organs in crocodilians.\u00a0 Journal of Experimental Biology. 215: 4217-4230<\/p>\n<p>Catania, K.C. (2012). Tactile sensing in specialized predators &#8211; from behavior to the brain. Current opinion in neurobiology 22, 251-258.<\/p>\n<p>Gillis AJ, Modrell MS, Northcutt RG, Catania KC, Luer CA, and Baker CV (2012) Electrosensory ampullary organs are derived from lateral line placodes in cartilaginous fishes. Development. 139:3142-3146.<\/p>\n<p>Catania, K.C. (2012) The evolution of brains and behavior for optimal foraging: a tale of two predators. Proceedings of the National Acadamy of Sciences.\u00a0 doi:10.1073\/pnas.1201885109. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/05\/Catania-2012-pnas.201201885.pdf\">PDF<\/a><\/p>\n<h4><a name=\"2011\"><\/a>2011<\/h4>\n<p>Koyabu, D., Endo, H., Mitgutsch, C., Suwa, G., Catania, K.C., Zollikofer, C.P., Oda, S., Koyasu, K., Ando, M., and Sanchez-Villagra, M.R. (2011). Heterochrony and developmental modularity of cranial osteogenesis in lipotyphlan mammals. EvoDevo 2, 21. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf30.pdf\">PDF<\/a><\/p>\n<p>Leitch, D.B., Gauthier, D., Sarko, D.K., and Catania, K.C. (2011). Chemoarchitecture of layer 4 isocortex in the American water shrew (Sorex palustris). Brain, behavior and evolution 78, 261-271.<\/p>\n<p>Herculano-Houzel, S., Ribeiro, P., Campos, L., Valotta da Silva, A., Torres, L.B., Catania, K.C., and Kaas, J.H. (2011). Updated neuronal scaling rules for the brains of Glires (rodents\/lagomorphs). Brain, behavior and evolution 78, 302-314.<\/p>\n<p>Catania, K.C. (2011). The sense of touch in the star-nosed mole: from mechanoreceptors to the brain. Philosophical transactions of the Royal Society of London Series B, Biological sciences 366, 3016-3025. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/05\/Phil.-Trans.-R.-Soc.-20111.pdf\">PDF<\/a><\/p>\n<p>Catania, K.C., Leitch, D.B., and Gauthier, D. (2011). A star in the brainstem reveals the first step of cortical magnification. PloS one 6, e22406. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf29.pdf\">PDF<\/a><\/p>\n<p>Catania, K.C. (2011). The brain and behavior of the tentacled snake. Annals of the New York Academy of Sciences 1225, 83-89.<\/p>\n<p>Marzban, H., Hoy, N., Aavani, T., Sarko, D.K., Catania, K.C., and Hawkes, R. (2011). Compartmentation of the cerebellar cortex in the naked mole-rat (Heterocephalus glaber). Cerebellum 10, 435-448.<\/p>\n<p>Sarko, D.K., Leitch, D.B., Girard, I., Sikes, R.S., and Catania, K.C. (2011). Organization of somatosensory cortex in the Northern grasshopper mouse (Onychomys leucogaster), a predatory rodent. The Journal of comparative neurology 519, 64-74. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf28.pdf\">PDF<\/a><\/p>\n<h4><a name=\"2010\"><\/a>2010<\/h4>\n<p>Campbell, K.L., Storz, J.F., Signore, A.V., Moriyama, H., Catania, K.C., Payson, A.P., Bonaventura, J., Stetefeld, J., and Weber, R.E. (2010). Molecular basis of a novel adaptation to hypoxic-hypercapnia in a strictly fossorial mole. BMC evolutionary biology 10, 214. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf27.pdf\">PDF<\/a><\/p>\n<p>Catania, K.C. (2010). Born knowing: tentacled snakes innately predict future prey behavior. PloS one 5, e10953. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf26.pdf\">PDF<\/a><\/p>\n<p>Catania, K.C., Leitch, D.B., and Gauthier, D. (2010). Function of the appendages in tentacled snakes (Erpeton tentaculatus). The Journal of experimental biology 213, 359-367. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf25.pdf\">PDF<\/a><\/p>\n<h4><a name=\"2009\"><\/a>2009<\/h4>\n<p>Seluanov, A., Hine, C., Azpurua, J., Feigenson, M., Bozzella, M., Mao, Z., Catania, K.C., and Gorbunova, V. (2009). Hypersensitivity to contact inhibition provides a clue to cancer resistance of naked mole-rat. Proceedings of the National Academy of Sciences of the United States of America 106, 19352-19357. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf24.pdf\">PDF<\/a><\/p>\n<p>Catania, K.C. (2009). Symposium overview: Underwater sniffing guides olfactory localization in semiaquatic mammals. Annals of the New York Academy of Sciences 1170, 407-412.\u00a0<a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/05\/2009d-2.pdf\">PDF<\/a><\/p>\n<p>Sarko, D.K., Catania, K.C., Leitch, D.B., Kaas, J.H., and Herculano-Houzel, S. (2009). Cellular scaling rules of insectivore brains. Frontiers in neuroanatomy 3, 8. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf23.pdf\">PDF<\/a><\/p>\n<p>Catania, K.C. (2009). Tentacled snakes turn C-starts to their advantage and predict future prey behavior. Proceedings of the National Academy of Sciences of the United States of America 106, 11183-11187. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf22.pdf\">PDF<\/a><\/p>\n<p>Dengler-Crish, C.M., and Catania, K.C. (2009). Cessation of reproduction-related spine elongation after multiple breeding cycles in female naked mole-rats. Anat Rec (Hoboken) 292, 131-137. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf21.pdf\">PDF<\/a><\/p>\n<h4><a name=\"2008\"><\/a>2008<\/h4>\n<p>Catania, K.C. (2008). Worm grunting, fiddling, and charming&#8211;humans unknowingly mimic a predator to harvest bait. PloS one 3, e3472. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf20.pdf\">PDF<\/a><\/p>\n<p>Seluanov, A., Hine, C., Bozzella, M., Hall, A., Sasahara, T.H., Ribeiro, A.A., Catania, K.C., Presgraves, D.C., and Gorbunova, V. (2008). Distinct tumor suppressor mechanisms evolve in rodent species that differ in size and lifespan. Aging cell 7, 813-823. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf19.pdf\">PDF<\/a><\/p>\n<p>Henry, E.C., Sarko, D.K., and Catania, K.C. (2008). Central projections of trigeminal afferents innervating the face in naked mole-rats (Heterocephalus glaber). Anat Rec (Hoboken) 291, 988-998. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf18.pdf\">PDF<\/a><\/p>\n<p>Catania, K.C., Hare, J.F., and Campbell, K.L. (2008). Water shrews detect movement, shape, and smell to find prey underwater. Proceedings of the National Academy of Sciences of the United States of America 105, 571-576. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf17.pdf\">PDF<\/a><\/p>\n<h4><a name=\"2007\"><\/a>2007<\/h4>\n<p>Dengler-Crish, C.M., and Catania, K.C. (2007). Phenotypic plasticity in female naked mole-rats after removal from reproductive suppression. The Journal of experimental biology 210, 4351-4358. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf16.pdf\">PDF<\/a><\/p>\n<p>Marasco, P.D., Tsuruda, P.R., Bautista, D.M., and Catania, K.C. (2007). Fine structure of Eimer&#8217;s organ in the coast mole (Scapanus orarius). Anat Rec (Hoboken) 290, 437-448. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf15.pdf\">PDF<\/a><\/p>\n<p>Marasco, P.D., and Catania, K.C. (2007). Response properties of primary afferents supplying Eimer&#8217;s organ. The Journal of experimental biology 210, 765-780. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf14.pdf\">PDF<\/a><\/p>\n<p>Henry, E.C., Dengler-Crish, C.M., and Catania, K.C. (2007). Growing out of a caste&#8211;reproduction and the making of the queen mole-rat. The Journal of experimental biology 210, 261-268. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf13.pdf\">PDF<\/a><\/p>\n<p>Seluanov, A., Chen, Z., Hine, C., Sasahara, T.H., Ribeiro, A.A., Catania, K.C., Presgraves, D.C., and Gorbunova, V. (2007). Telomerase activity coevolves with body mass not lifespan. Aging cell 6, 45-52. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf12.pdf\">PDF<\/a><\/p>\n<h4><a name=\"2006\"><\/a>2006<\/h4>\n<p>Catania, K.C. (2006). Olfaction: underwater &#8216;sniffing&#8217; by semi-aquatic mammals. Nature 444, 1024-1025. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/05\/2006g.pdf\">PDF<\/a><\/p>\n<p>Dengler-Crish, C.M., Crish, S.D., O&#8217;Riain, M.J., and Catania, K.C. (2006). Organization of the somatosensory cortex in elephant shrews (E. edwardii). The anatomical record Part A, Discoveries in molecular, cellular, and evolutionary biology 288, 859-866. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf11.pdf\">PDF<\/a><\/p>\n<p>Catania, K.C., and Henry, E.C. (2006). Touching on somatosensory specializations in mammals. Current opinion in neurobiology 16, 467-473.<\/p>\n<p>Marasco, P.D., Tsuruda, P.R., Bautista, D.M., Julius, D., and Catania, K.C. (2006). Neuroanatomical evidence for segregation of nerve fibers conveying light touch and pain sensation in Eimer&#8217;s organ of the mole. Proceedings of the National Academy of Sciences of the United States of America 103, 9339-9344. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf10.pdf\">PDF<\/a><\/p>\n<p>Henry, E.C., and Catania, K.C. (2006). Cortical, callosal, and thalamic connections from primary somatosensory cortex in the naked mole-rat (Heterocephalus glaber), with special emphasis on the connectivity of the incisor representation. The anatomical record Part A, Discoveries in molecular, cellular, and evolutionary biology 288, 626-645. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf9.pdf\">PDF<\/a><\/p>\n<p>Henry, E.C., Remple, M.S., O&#8217;Riain, M.J., and Catania, K.C. (2006). Organization of somatosensory cortical areas in the naked mole-rat (Heterocephalus glaber). The Journal of comparative neurology 495, 434-452.<\/p>\n<p>Crish, S.D., Dengler-Crish, C.M., and Catania, K.C. (2006). Central visual system of the naked mole-rat (Heterocephalus glaber). The anatomical record Part A, Discoveries in molecular, cellular, and evolutionary biology 288, 205-212. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf8.pdf\">PDF<\/a><\/p>\n<h4><a name=\"2005\"><\/a>2005<\/h4>\n<p>Catania, K.C. (2005). Star-nosed moles. Current biology : CB 15, R863-864.<\/p>\n<p>Catania, K.C. (2005). Evolution of sensory specializations in insectivores. The anatomical record Part A, Discoveries in molecular, cellular, and evolutionary biology 287, 1038-1050. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf7.pdf\">PDF<\/a><\/p>\n<p>Henry, E.C., Marasco, P.D., and Catania, K.C. (2005). Plasticity of the cortical dentition representation after tooth extraction in naked mole-rats. The Journal of comparative neurology 485, 64-74.<\/p>\n<p>Catania, K.C., and Remple, F.E. (2005). Asymptotic prey profitability drives star-nosed moles to the foraging speed limit. Nature 433, 519-522. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/05\/nature03250-1.pdf\">PDF<\/a><\/p>\n<h4><a name=\"2004\"><\/a>2004<\/h4>\n<p>Mills, S.L., and Catania, K.C. (2004). Identification of retinal neurons in a regressive rodent eye (the naked mole-rat). Visual neuroscience 21, 107-117. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf6.pdf\">PDF<\/a><\/p>\n<p>Catania, K.C., and Remple, F.E. (2004). Tactile foveation in the star-nosed mole. Brain, behavior and evolution 63, 1-12.<\/p>\n<p>Catania, K.C., and Kaas, J.H. (1996). The Unusual Nose and Brain of the Star-Nosed Mole. BioScience 46, 578-586.<\/p>\n<h4><a name=\"2003\"><\/a>2003<\/h4>\n<p>Rubenstein, N.M., Cunha, G.R., Wang, Y.Z., Campbell, K.L., Conley, A.J., Catania, K.C., Glickman, S.E., and Place, N.J. (2003). Variation in ovarian morphology in four species of New World moles with a peniform clitoris. Reproduction 126, 713-719. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf5.pdf\">PDF<\/a><\/p>\n<p>Remple, M.S., Henry, E.C., and Catania, K.C. (2003). Organization of somatosensory cortex in the laboratory rat (Rattus norvegicus): Evidence for two lateral areas joined at the representation of the teeth. The Journal of comparative neurology 467, 105-118.<\/p>\n<p>Crish, S.D., Comer, C.M., Marasco, P.D., and Catania, K.C. (2003). Somatosensation in the superior colliculus of the star-nosed mole. The Journal of comparative neurology 464, 415-425.<\/p>\n<h4><a name=\"2002\"><\/a>2002<\/h4>\n<p>Catania, K.C. (2002). Barrels, stripes, and fingerprints in the brain &#8211; implications for theories of cortical organization. Journal of neurocytology 31, 347-358.<\/p>\n<p>Sachdev, R.N., and Catania, K.C. (2002). Effects of stimulus duration on neuronal response properties in the somatosensory cortex of the star-nosed mole. Somatosensory &amp; motor research 19, 272-278. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf4.pdf\">PDF<\/a><\/p>\n<p>Sachdev, R.N., and Catania, K.C. (2002). Receptive fields and response properties of neurons in the star-nosed mole&#8217;s somatosensory fovea. Journal of neurophysiology 87, 2602-2611.<\/p>\n<p>Kaas, J.H., and Catania, K.C. (2002). How do features of sensory representations develop? BioEssays : news and reviews in molecular, cellular and developmental biology 24, 334-343.<\/p>\n<p>Catania, K.C., and Remple, M.S. (2002). Somatosensory cortex dominated by the representation of teeth in the naked mole-rat brain. Proceedings of the National Academy of Sciences of the United States of America 99, 5692-5697. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf3.pdf\">PDF<\/a><\/p>\n<h4><a name=\"2001\"><\/a>2001<\/h4>\n<p>Catania, K.C., and Kaas, J.H. (2001). Areal and callosal connections in the somatosensory cortex of the star-nosed mole. Somatosensory &amp; motor research 18, 303-311.<\/p>\n<p>Catania, K.C. (2001). Early development of a somatosensory fovea: a head start in the cortical space race? Nature neuroscience 4, 353-354.<\/p>\n<p>Jain, N., Qi, H.X., Catania, K.C., and Kaas, J.H. (2001). Anatomic correlates of the face and oral cavity representations in the somatosensory cortical area 3b of monkeys. The Journal of comparative neurology 429, 455-468.<\/p>\n<h4><a name=\"2000\"><\/a>2000<\/h4>\n<p>Catania, K.C. (2000). Cortical-organization in moles: evidence of new areas and a specialized S2. Somatosensory &amp; motor research 17, 335-347.<\/p>\n<p>Catania, K.C. (2000). Epidermal sensory organs of moles, shrew moles, and desmans: a study of the family talpidae with comments on the function and evolution of Eimer&#8217;s organ. Brain, behavior and evolution 56, 146-174.<\/p>\n<p>Northcutt, R.G., Barlow, L.A., Braun, C.B., and Catania, K.C. (2000). Distribution and innervation of taste buds in the axolotl. Brain, behavior and evolution 56, 123-145.<\/p>\n<p>Catania, K.C. (2000). Cortical organization in insectivora: the parallel evolution of the sensory periphery and the brain. Brain, behavior and evolution 55, 311-321.<\/p>\n<p>Catania, K.C., Jain, N., Franca, J.G., Volchan, E., and Kaas, J.H. (2000). The organization of somatosensory cortex in the short-tailed opossum (Monodelphis domestica). Somatosensory &amp; motor research 17, 39-51.<\/p>\n<p>Catania, K.C., Collins, C.E., and Kaas, J.H. (2000). Organization of sensory cortex in the East African hedgehog (Atelerix albiventris). The Journal of comparative neurology 421, 256-274.<\/p>\n<p>Franca, J.G., Volchan, E., Jain, N., Catania, K.C., Oliveira, R.L., Hess, F.F., Jablonka, M., Rocha-Miranda, C.E., and Kaas, J.H. (2000). Distribution of NADPH-diaphorase cells in visual and somatosensory cortex in four mammalian species. Brain research 864, 163-175.<\/p>\n<h4><a name=\"1999\"><\/a>1999<\/h4>\n<p>Catania, K.C. (1999). A nose that looks like a hand and acts like an eye: the unusual mechanosensory system of the star-nosed mole. Journal of comparative physiology A, Sensory, neural, and behavioral physiology 185, 367-372.<\/p>\n<p>Catania, K.C., Northcutt, R.G., and Kaas, J.H. (1999). The development of a biological novelty: a different way to make appendages as revealed in the snout of the star-nosed mole Condylura cristata. The Journal of experimental biology 202, 2719-2726. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf2.pdf\">PDF<\/a><\/p>\n<p>Catania, K.C., Lyon, D.C., Mock, O.B., and Kaas, J.H. (1999). Cortical organization in shrews: evidence from five species. The Journal of comparative neurology 410, 55-72.<\/p>\n<h4><a name=\"1998\"><\/a>1998<\/h4>\n<p>Jain, N., Catania, K.C., and Kaas, J.H. (1998). A histologically visible representation of the fingers and palm in primate area 3b and its immutability following long-term deafferentations. Cereb Cortex 8, 227-236. <a href=\"https:\/\/s3.amazonaws.com\/vu-wp0\/wp-content\/uploads\/sites\/182\/2012\/07\/pdf1.pdf\">PDF<\/a><\/p>\n<h4><a name=\"1997\"><\/a>1997<\/h4>\n<p>Catania, K.C., and Kaas, J.H. (1997). Somatosensory fovea in the star-nosed mole: behavioral use of the star in relation to innervation patterns and cortical representation. The Journal of comparative neurology 387, 215-233.<\/p>\n<p>Jain, N., Catania, K.C., and Kaas, J.H. (1997). Deactivation and reactivation of somatosensory cortex after dorsal spinal cord injury. Nature 386, 495-498.<\/p>\n<p>Catania, K.C., and Kaas, J.H. (1997). Organization of somatosensory cortex and distribution of corticospinal neurons in the eastern mole (Scalopus aquaticus). The Journal of comparative neurology 378, 337-353.<\/p>\n<p>Catania, K.C., and Kaas, J.H. (1997). The mole nose instructs the brain. Somatosensory &amp; motor research 14, 56-58.<\/p>\n<h4><a name=\"1996\"><\/a>1996<\/h4>\n<p>Catania, K.C. (1996). Ultrastructure of the Eimer&#8217;s organ of the star-nosed mole. The Journal of comparative neurology 365, 343-354.<\/p>\n<p>Catania, K.C., and Kaas, J.H. (1996). The Unusual Nose and Brain of the Star-Nosed Mole. BioScience 46, 578-586.<\/p>\n<h4><a name=\"1995\"><\/a>1995<\/h4>\n<p>Catania, K.C. (1995). Magnified cortex in star-nosed moles. Nature 375, 453-454.<\/p>\n<p>Catania, K.C. (1995). A comparison of the Eimer&#8217;s organs of three North American moles: the hairy-tailed mole (Parascalops breweri), the star-nosed mole (Condylura cristata), and the eastern mole (Scalopus aquaticus). The Journal of comparative neurology 354, 150-160.<\/p>\n<p>Catania, K.C., and Kaas, J.H. (1995). Organization of the somatosensory cortex of the star-nosed mole. The Journal of comparative neurology 351, 549-567.<\/p>\n<p>Catania, K.C. (1995). Structure and innervation of the sensory organs on the snout of the star-nosed mole. The Journal of comparative neurology 351, 536-548.<\/p>\n<h4><a name=\"1994\"><\/a>1994<\/h4>\n<p>Northcutt, R.G., Catania, K.C., and Criley, B.B. (1994). Development of lateral line organs in the axolotl. The Journal of comparative neurology 340, 480-514.<\/p>\n<h4><a name=\"1993\"><\/a>1993<\/h4>\n<p>Catania, K.C., Northcutt, R.G., Kaas, J.H., and Beck, P.D. (1993). Nose stars and brain stripes. Nature 364, 493.<\/p>\n<h4><a name=\"1992\"><\/a>1992<\/h4>\n<p>Williams, J.R., Catania, K.C., and Carter, C.S. (1992). Development of partner preferences in female prairie voles (Microtus ochrogaster): the role of social and sexual experience. Hormones and behavior 26, 339-349.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Other Publications 2017 Catania KC (2017) Power Transfer to a Human during an Electric Eel\u2019s Shocking Leap. Current Biology.\u00a0 27:2887-2891.e2. doi: 10.1016\/j.cub.2017.08.034 pdf Catania KC (2017) Behavioral pieces of neuroethological puzzles. Journal of Comparative Physiology A. 203:677-689. doi: 10.1007\/s00359-016-1143-7. pdf &hellip; <a href=\"https:\/\/wp0.vanderbilt.edu\/catanialab\/publications\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1040,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"spay_email":""},"_links":{"self":[{"href":"https:\/\/wp0.vanderbilt.edu\/catanialab\/wp-json\/wp\/v2\/pages\/7"}],"collection":[{"href":"https:\/\/wp0.vanderbilt.edu\/catanialab\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/wp0.vanderbilt.edu\/catanialab\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/wp0.vanderbilt.edu\/catanialab\/wp-json\/wp\/v2\/users\/1040"}],"replies":[{"embeddable":true,"href":"https:\/\/wp0.vanderbilt.edu\/catanialab\/wp-json\/wp\/v2\/comments?post=7"}],"version-history":[{"count":16,"href":"https:\/\/wp0.vanderbilt.edu\/catanialab\/wp-json\/wp\/v2\/pages\/7\/revisions"}],"predecessor-version":[{"id":829,"href":"https:\/\/wp0.vanderbilt.edu\/catanialab\/wp-json\/wp\/v2\/pages\/7\/revisions\/829"}],"wp:attachment":[{"href":"https:\/\/wp0.vanderbilt.edu\/catanialab\/wp-json\/wp\/v2\/media?parent=7"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}