Patterning of Central Synapses in Regeneration of the Optic Nerve in Teleosts

1948; University of Chicago Press; Volume: 21; Issue: 4 Linguagem: Inglês

10.1086/physzool.21.4.30152014

ISSN

1937-4267

Autores

R. W. Sperry,

Tópico(s)

Retinal Development and Disorders

Resumo

Previous articleNext article No AccessPatterning of Central Synapses in Regeneration of the Optic Nerve in TeleostsR. W. SperryR. W. Sperry Search for more articles by this author PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by Volume 21, Number 4Oct., 1948 Article DOIhttps://doi.org/10.1086/physzool.21.4.30152014 Views: 6Total views on this site Citations: 106Citations are reported from Crossref Journal History This article was published in Physiological Zoology (1928-1998), which is continued by Physiological and Biochemical Zoology (1999-present). PDF download Crossref reports the following articles citing this article:John T. Schmidt Early work supports chemoaffinity with one contradictory result, (Jan 2020): 15–35.https://doi.org/10.1016/B978-0-12-818579-7.00002-XYuqin Yin, Silmara De Lima, Hui-Ya Gilbert, Nicholas J. Hanovice, Sheri L. Peterson, Rheanna M. Sand, Elena G. Sergeeva, Kimberly A. Wong, Lili Xie, Larry I. Benowitz, Andrea Antal, Bernhard Sabel Optic nerve regeneration: A long view, Restorative Neurology and Neuroscience 37, no.66 (Dec 2019): 525–544.https://doi.org/10.3233/RNN-190960Kayo Sugitani, Kazuhiro Ogai, Haruka Muto, Keisuke Onodera, Ayaka Matsuoka, Takahira Sugita, Yoshiki Koriyama A novel activation mechanism of cellular Factor XIII in zebrafish retina after optic nerve injury, Biochemical and Biophysical Research Communications 517, no.11 (Sep 2019): 57–62.https://doi.org/10.1016/j.bbrc.2019.07.003Mayssa H. Mokalled, Kenneth D. Poss A Regeneration Toolkit, Developmental Cell 47, no.33 (Nov 2018): 267–280.https://doi.org/10.1016/j.devcel.2018.10.015Ilse Bollaerts, Lien Veys, Emiel Geeraerts, Lien Andries, Lies De Groef, Tom Buyens, Manuel Salinas-Navarro, Lieve Moons, Inge Van Hove Complementary research models and methods to study axonal regeneration in the vertebrate retinofugal system, Brain Structure and Function 223, no.22 (Nov 2017): 545–567.https://doi.org/10.1007/s00429-017-1571-3Kayo Sugitani, Yoshiki Koriyama, Mayuko Sera, Kunizo Arai, Kazuhiro Ogai, Keisuke Wakasugi A novel function of neuroglobin for neuroregeneration in mice after optic nerve injury, Biochemical and Biophysical Research Communications 493, no.33 (Nov 2017): 1254–1259.https://doi.org/10.1016/j.bbrc.2017.09.127G.B. Whitworth, B.C. Misaghi, D.M. Rosenthal, E.A. Mills, D.J. Heinen, A.H. Watson, C.W. Ives, S.H. Ali, K. Bezold, N. Marsh-Armstrong, F.L. Watson Translational profiling of retinal ganglion cell optic nerve regeneration in Xenopus laevis, Developmental Biology 426, no.22 (Jun 2017): 360–373.https://doi.org/10.1016/j.ydbio.2016.06.003Kevin K. Park, Xueting Luo, Skyler J. Mooney, Benjamin J. Yungher, Stephane Belin, Chen Wang, Melissa M. Holmes, Zhigang He Retinal ganglion cell survival and axon regeneration after optic nerve injury in naked mole-rats, Journal of Comparative Neurology 525, no.22 (Jul 2016): 380–388.https://doi.org/10.1002/cne.24070D L Williams Regenerating reptile retinas: a comparative approach to restoring retinal ganglion cell function, Eye 31, no.22 (Nov 2016): 167–172.https://doi.org/10.1038/eye.2016.224Ryne A. Gorsuch, David R. Hyde Regulation of Müller glial dependent neuronal regeneration in the damaged adult zebrafish retina, Experimental Eye Research 123 (Jun 2014): 131–140.https://doi.org/10.1016/j.exer.2013.07.012Satoru Kato, Toru Matsukawa, Yoshiki Koriyama, Kayo Sugitani, Kazuhiro Ogai A molecular mechanism of optic nerve regeneration in fish: The retinoid signaling pathway, Progress in Retinal and Eye Research 37 (Nov 2013): 13–30.https://doi.org/10.1016/j.preteyeres.2013.07.004Yuki Kamioka, Chieko Fujikawa, Kazuhiro Ogai, Kayo Sugitani, Seiji Watanabe, Satoru Kato, Keisuke Wakasugi Functional characterization of fish neuroglobin: Zebrafish neuroglobin is highly expressed in amacrine cells after optic nerve injury and can translocate into ZF4 cells, Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics 1834, no.99 (Sep 2013): 1779–1788.https://doi.org/10.1016/j.bbapap.2013.02.021Günther K. H. Zupanc, Ruxandra F. Sîrbulescu Teleost Fish as a Model System to Study Successful Regeneration of the Central Nervous System, (Dec 2012): 193–233.https://doi.org/10.1007/82_2012_297Chieko Fujikawa, Mikiko Nagashima, Kazuhiro Mawatari, Satoru Kato HSP70 Gene Expression in the Zebrafish Retina After Optic Nerve Injury: A Comparative Study Under Heat Shock Stresses, (Nov 2011): 663–668.https://doi.org/10.1007/978-1-4614-0631-0_84Mikiko Nagashima, Chieko Fujikawa, Kazuhiro Mawatari, Yusuke Mori, Satoru Kato HSP70, the earliest-induced gene in the zebrafish retina during optic nerve regeneration: Its role in cell survival, Neurochemistry International 58, no.88 (Jul 2011): 888–895.https://doi.org/10.1016/j.neuint.2011.02.017Kerry N. Veth, Jason R. Willer, Ross F. Collery, Matthew P. Gray, Gregory B. Willer, Daniel S. Wagner, Mary C. Mullins, Ava J. Udvadia, Richard S. Smith, Simon W. M. John, Ronald G. Gregg, Brian A. Link, Janey Wiggs Mutations in Zebrafish lrp2 Result in Adult-Onset Ocular Pathogenesis That Models Myopia and Other Risk Factors for Glaucoma, PLoS Genetics 7, no.22 (Feb 2011): e1001310.https://doi.org/10.1371/journal.pgen.1001310Manabu Kaneda, Mikiko Nagashima, Kazuhiro Mawatari, Tomoya Nunome, Kenichiro Muramoto, Kayo Sugitani, Satoru Kato Growth-Associated Protein43 (GAP43) Is a Biochemical Marker for the Whole Period of Fish Optic Nerve Regeneration, (Dec 2009): 97–104.https://doi.org/10.1007/978-1-4419-1399-9_12Amy T. Mccurley, Gloria V. Callard Time course Analysis of Gene expression patterns in ZebrafIsh Eye during Optic Nerve Regeneration, Journal of Experimental Neuroscience 4 (Jul 2010): JEN.S5006.https://doi.org/10.4137/JEN.S5006Yoshiki Koriyama, Rie Yasuda, Keiko Homma, Kazuhiro Mawatari, Mikiko Nagashima, Kayo Sugitani, Toru Matsukawa, Satoru Kato Nitric oxide-cGMP signaling regulates axonal elongation during optic nerve regeneration in the goldfish in vitro and in vivo, Journal of Neurochemistry 110, no.33 (Aug 2009): 890–901.https://doi.org/10.1111/j.1471-4159.2009.06182.xMarta Parrilla, Concepción Lillo, M. Javier Herrero-Turrion, Rosario Arévalo, Juan Manuel Lara, José Aijón, Almudena Velasco Pax2 in the optic nerve of the goldfish, a model of continuous growth, Brain Research 1255 (Feb 2009): 75–88.https://doi.org/10.1016/j.brainres.2008.12.010Manabu Kaneda, Mikiko Nagashima, Tomoya Nunome, Takanori Muramatsu, Yoichi Yamada, Mamoru Kubo, Kenichiro Muramoto, Toru Matsukawa, Yoshiki Koriyama, Kayo Sugitani, Ivan H. Vachkov, Kazuhiro Mawatari, Satoru Kato Changes of phospho-growth-associated protein 43 (phospho-GAP43) in the zebrafish retina after optic nerve injury: A long-term observation, Neuroscience Research 61, no.33 (Jul 2008): 281–288.https://doi.org/10.1016/j.neures.2008.03.008MICHAEL P. CALLAHAN, ALLEN F. MENSINGER Restoration of visual function following optic nerve regeneration in bluegill (Lepomis macrochirus) × pumpkinseed (Lepomis gibbosus) hybrid sunfish, Visual Neuroscience 24, no.0303 (May 2007): 309–317.https://doi.org/10.1017/S0952523807070289Christine Gervasi, Amar Thyagarajan, Ben G. Szaro Increased expression of multiple neurofilament mRNAs during regeneration of vertebrate central nervous system axons, The Journal of Comparative Neurology 461, no.22 (Apr 2003): 262–275.https://doi.org/10.1002/cne.10695D. Clemente, A. Porteros, J.R. Alonso, E. Weruaga, J. Aijón, R. Arévalo Effects of axotomy on the expression of NADPH-diaphorase in the visual pathway of the tench, Brain Research 925, no.22 (Jan 2002): 183–194.https://doi.org/10.1016/S0006-8993(01)03279-6Elena Vecino, Jesús Avila Distribution of the phosphorylated form of microtubule associated protein 1B in the fish visual system during optic nerve regeneration, Brain Research Bulletin 56, no.22 (Sep 2001): 131–137.https://doi.org/10.1016/S0361-9230(01)00618-9Almudena Velasco, Marı́a Julia Bragado, David Jimeno, Elena Caminos, Concepción Lillo, José Aijón, Juan M. Lara Growing and regenerating axons in the visual system of teleosts are recognized with the antibody RT97, Brain Research 883, no.11 (Nov 2000): 98–106.https://doi.org/10.1016/S0006-8993(00)02783-9Lukas W. A. Roth, Peter Bormann, Christa Wiederkehr, Eva Reinhard β-Thymosin, a modulator of the actin cytoskeleton is increased in regenerating retinal ganglion cells, European Journal of Neuroscience 11, no.1010 (Dec 2001): 3488–3498.https://doi.org/10.1046/j.1460-9568.1999.00715.xS Kato, M Devadas, K Okada, Y Shimada, M Ohkawa, K Muramoto, N Takizawa, T Matsukawa Fast and slow recovery phases of goldfish behavior after transection of the optic nerve revealed by a computer image processing system, Neuroscience 93, no.33 (Aug 1999): 907–914.https://doi.org/10.1016/S0306-4522(99)00202-XRafael P. Ballestero, Joseph A. Dybowski, Gallia Levy, Bernard W. Agranoff, Michael D. Uhler Cloning and Characterization of zRICH, a 2′,3′-Cyclic-Nucleotide 3′-Phosphodiesterase Induced During Zebrafish Optic Nerve Regeneration, Journal of Neurochemistry 72, no.44 (Dec 2001): 1362–1371.https://doi.org/10.1046/j.1471-4159.1999.721362.xPeter Bormann, Lukas W.A. Roth, David Andel, Manuel Ackermann, Eva Reinhard zfNLRR, a Novel Leucine-Rich Repeat Protein Is Preferentially Expressed during Regeneration in Zebrafish, Molecular and Cellular Neuroscience 13, no.33 (Mar 1999): 167–179.https://doi.org/10.1006/mcne.1999.0742Elena Caminos, Elena Becker, Dionisio Mart�n-Zanca, Elena Vecino Neurotrophins and their receptors in the tench retina during optic nerve regeneration, The Journal of Comparative Neurology 404, no.33 (Feb 1999): 321–331.https://doi.org/10.1002/(SICI)1096-9861(19990215)404:3<321::AID-CNE4>3.0.CO;2-YE Vecino, L Ulloa, J Avila The phosphorylated isoform of microtubule associated protein 1B (MAP1B) is expressed in the visual system of the tench (Tinca tinca, L) during optic nerve regeneration, Neuroscience Letters 245, no.22 (Apr 1998): 93–96.https://doi.org/10.1016/S0304-3940(98)00188-8W.Maxwell Cowan The Emergence of Modern Neuroanatomy and Developmental Neurobiology, Neuron 20, no.33 (Mar 1998): 413–426.https://doi.org/10.1016/S0896-6273(00)80985-XJuan M. Lara, Almudena Velasco, Concepción Lillo, David Jimeno, José Aijón Characterization of the Glial Cells in the Teleost Visual Pathway, (Jan 1998): 3–18.https://doi.org/10.1007/978-1-4615-5737-1_1Elena Vecino, Elena Caminos, Elena Becker, Dionisio Martín-Zanca, Neville N. Osborne Expression of Neurotrophins and their Receptors Within the Glial Cells of Retina and Optic Nerve, (Jan 1998): 149–166.https://doi.org/10.1007/978-1-4615-5737-1_8E. Vecino, A. Velasco, E. Caminos, J. Aijón Distribution of S100 immunoreactivity in the retina and optic nerve head of the teleostTinca tinca L., Microscopy Research and Technique 36, no.11 (Jan 1997): 17–25.https://doi.org/10.1002/(SICI)1097-0029(19970101)36:1<17::AID-JEMT2>3.0.CO;2-WAlmudena Velasco, Jesús G. Briñón, Elena Caminos, Juan M. Lara, José Aijón S-100-Positive Glial Cells are Involved in the Regeneration of the Visual Pathway of Teleosts, Brain Research Bulletin 43, no.33 (Jan 1997): 327–336.https://doi.org/10.1016/S0361-9230(97)00014-2David A. Cameron Asymmetric retinal growth: Evidence for regulation by a retinotopic mechanism, Visual Neuroscience 13, no.33 (Jun 2009): 493–500.https://doi.org/10.1017/S0952523800008166Almudena Velasco, Elena Caminos, Elena Vecino, Juan M. Lara, José Aijón Microglia in normal and regenerating visual pathways of the tench (Tinca tinca L., 1758; Teleost) : a study with tomato lectin, Brain Research 705, no.1-21-2 (Dec 1995): 315–324.https://doi.org/10.1016/0006-8993(95)01204-4Tomer Sivron, Michal Schwartz Glial cell types, lineages, and response to injury in rat and fish: Implications for regeneration, Glia 13, no.33 (Mar 1995): 157–165.https://doi.org/10.1002/glia.440130302Orly Eizenberg, Michael G. Kaplitt, Shoshana Eitan, Donald W. Pfaff, David L. Hirschberg, Michal Schwartz Linear dimeric interleukin-2 obtained by the use of a defective herpes simplex viral vector: conformation-activity relationship, Molecular Brain Research 26, no.1-21-2 (Oct 1994): 156–162.https://doi.org/10.1016/0169-328X(94)90086-8T. Sivron, M. E. Schwab, M. Schwartz Presence of growth inhibitors in fish optic nerve myelin: Postinjury changes, The Journal of Comparative Neurology 343, no.22 (May 1994): 237–246.https://doi.org/10.1002/cne.903430205Yangu Zhao, Ben G. Szaro The return of phosphorylated and nonphosphorylated epitopes of neurofilament proteins to the regenerating optic nerve ofXenopus laevis, The Journal of Comparative Neurology 343, no.11 (May 1994): 158–172.https://doi.org/10.1002/cne.903430112Tomer Sivron, Ilana Cohen, Michal Schwartz Intermediate filaments reminiscent of immature cells expressed by goldfish (Carassius auratus) astrocytes and oligodendrocytes in vitro, Cell & Tissue Research 275, no.22 (Feb 1994): 327–337.https://doi.org/10.1007/BF00319431Ilana Cohen, Tomer Sivron, Vered Lavie, Eran Blaugrund, Michal Schwartz Vimentin immunoreactive glial cells in the fish optic nerve: Implications for regeneration, Glia 10, no.11 (Jan 1994): 16–29.https://doi.org/10.1002/glia.440100104Michal Schwartz, Tomer Sivron, Shoshana Eitan, David L. Hirschberg, Mirit Lotan, Anat Elman-Faber Chapter 27 Cytokines and cytokine-related substances regulating glial cell response to injury of the central nervous system, (Jan 1994): 331–341.https://doi.org/10.1016/S0079-6123(08)61147-4Ilana Cohen, Yael Shani, Michal Schwartz Cloning and characteristics of fish glial fibrillary acidic protein: Implications for optic nerve regeneration, The Journal of Comparative Neurology 334, no.33 (Aug 1993): 431–443.https://doi.org/10.1002/cne.903340308Michal Schwartz New light on nerve regeneration in the mammalian nervous system, Endeavour 17, no.11 (Mar 1993): 38–40.https://doi.org/10.1016/0160-9327(93)90010-ZIlana Cohen, Michal Schwartz cDNA clones from fish optic nerve, Comparative Biochemistry and Physiology Part B: Comparative Biochemistry 104, no.33 (Mar 1993): 439–447.https://doi.org/10.1016/0305-0491(93)90265-7Raymond D. Lund, Jeffrey D. Radel, Kathleen T. Yee Experimental Manipulation of the Developing Rodent Visual System, (Jan 1993): 72–90.https://doi.org/10.1007/978-1-4899-6707-7_7D.P.M. Northmore, M.A. Celenza Recovery of contrast sensitivity during optic nerve regeneration in fish, Experimental Neurology 115, no.11 (Jan 1992): 69–72.https://doi.org/10.1016/0014-4886(92)90224-EGlenn H. Kageyama, Ronald L. Meyer Laminar histochemical and cytochemical localization of cytochrome oxidase in the goldfish retina and optic tectum in response to deafferentation and during regeneration, The Journal of Comparative Neurology 278, no.44 (Dec 1988): 521–542.https://doi.org/10.1002/cne.902780405L. R. Marotte, R. F. Mark Retinal projections to the superior colliculus and dorsal lateral geniculate nucleus in the tammar wallaby ( Macropus eugenii ): II. Topography after rotation of an eye prior to retinal innervation of the brain, Journal of Comparative Neurology 271, no.22 (Oct 2004): 274–292.https://doi.org/10.1002/cne.902710208Larry I. Benowitz, John T. Schmidt Activity-dependent sharpening of the regenerating retinotectal projection in goldfish: relationship to the expression of growth-associated proteins, Brain Research 417, no.11 (Aug 1987): 118–126.https://doi.org/10.1016/0006-8993(87)90185-5Nora I. Perrone-Bizzozero, Larry I. Benowitz Expression of a 48-Kilodalton Growth-Associated Protein in the Goldfish Retina, Journal of Neurochemistry 48, no.22 (Feb 1987): 644–652.https://doi.org/10.1111/j.1471-4159.1987.tb04141.xBernice Grafstein, Donald W. Burmeister, Charlotte M. McGuinness, Gary W. Perry, Janet R. Sparrow Chapter 10 Role of fast axonal transport in regeneration of goldfish optic axons, (Jan 1987): 113–120.https://doi.org/10.1016/S0079-6123(08)61818-XMyong G. Yoon, Larry I. Benowitz, Frank A. Baker The optic tectum regulates the transport of specific proteins in regenerating optic fibers of goldfish, Brain Research 382, no.22 (Sep 1986): 339–351.https://doi.org/10.1016/0006-8993(86)91343-0BERNICE GRAFSTEIN THE RETINA AS A REGENERATING ORGAN, (Jan 1986): 275–335.https://doi.org/10.1016/B978-0-12-044276-8.50013-8C. Stein-Izsak, A. Harel, A. Solomon, M. Belkin, M. Schwartz Alterations in mRNA Translation Products Associated with Regenerative Responses in the Retina, Journal of Neurochemistry 45, no.66 (Dec 1985): 1754–1760.https://doi.org/10.1111/j.1471-4159.1985.tb10531.xRodrigo O. Kuljis, Harvey J. Karten Regeneration of peptide-containing retinofugal axons into the optic tectum with reappearance of a substance P-containing lamina, The Journal of Comparative Neurology 240, no.11 (Oct 1985): 1–15.https://doi.org/10.1002/cne.902400102Peter H. Schiller The Superior Colliculus and Visual Function, (Jan 2011): 457–505.https://doi.org/10.1002/cphy.cp010311L. R. Marotte Optic axons ignore denervated foreign territory in goldfish tectum, The Journal of Comparative Neurology 225, no.33 (May 1984): 372–386.https://doi.org/10.1002/cne.902250305D.P.M. Northmore, Tom Masino Recovery of vision in fish after optic nerve crush: A behavioral and electrophysiological study, Experimental Neurology 84, no.11 (Apr 1984): 109–125.https://doi.org/10.1016/0014-4886(84)90009-8Larry I. Benowitz Target-Dependent and Target-Independent Changes in Rapid Axonal Transport During Regeneration of the Goldfish Retinotectal Pathway, (Jan 1984): 145–169.https://doi.org/10.1007/978-1-4684-1197-3_10Joseph E. Le Doux CEREBRAL ASYMMETRY AND THE INTEGRATED FUNCTION OF THE BRAIN, (Jan 1983): 203–216.https://doi.org/10.1016/B978-0-12-773250-3.50012-7Marion Murray A quantitative study of regenerative sprouting by optic axons in goldfish, The Journal of Comparative Neurology 209, no.44 (Aug 1982): 352–362.https://doi.org/10.1002/cne.902090405W. Maxwell Cowan, Thomas E. Finger Regeneration and Regulation in the Developing Central Nervous System, (Jan 1982): 377–415.https://doi.org/10.1007/978-1-4684-1131-7_11D. I. McCloskey Corollary Discharges: Motor Commands and Perception, (Jan 2011): 1415–1447.https://doi.org/10.1002/cphy.cp010232D. Louise Edwards, Roberta M. Alpert, Bernice Grafstein Recovery of vision in regeneration of goldfish optic axons: Enhancement of axonal outgrowth by a conditioning lesion, Experimental Neurology 72, no.33 (Jun 1981): 672–686.https://doi.org/10.1016/0014-4886(81)90016-9D.P.M. Northmore, L.C. Skeen, J.M. Pindzola Visuomotor perimetry in fish: A new approach to the functional analysis of altered visual pathways, Vision Research 21, no.66 (Jan 1981): 843–853.https://doi.org/10.1016/0042-6989(81)90184-XM. Romeskie, S.C. Sharma Retinal projection to a rotated tectal reimplant following long-term tectal denervation in adult goldfish, Brain Research 201, no.11 (Nov 1980): 202–205.https://doi.org/10.1016/0006-8993(80)90786-6Ronald L. Meyer Retinotectal Projection in Goldfish to an Inappropriate Region with a Reversal in Polarity, Science 205, no.44084408 (Aug 1979): 819–821.https://doi.org/10.1126/science.462191J. Wye-Dvorak, L.R. Marotte, R.F. Mark Retinotectal reorganization in goldfish—I. Effects of season, lighting conditions and size of fish, Neuroscience 4, no.66 (Jun 1979): 789–802.https://doi.org/10.1016/0306-4522(79)90007-1Martha Romeskie, S.C. Sharma The goldfish optic tectum: A golgi study, Neuroscience 4, no.55 (May 1979): 625–642.https://doi.org/10.1016/0306-4522(79)90139-8Nicholas A. Ingoglia, S.C. Sharma The effect of inhibition of axonal RNA transport on the restoration of retinotectal projections in regenerating optic nerves of goldfish, Brain Research 156, no.11 (Nov 1978): 141–145.https://doi.org/10.1016/0006-8993(78)90090-2Nicholas A. Ingoglia THE EFFECT OF INTRAOCULAR INJECTION OF CORDYCEPIN ON RETINAL RNA SYNTHESIS AND ON RNA AXONALLY TRANSPORTED DURING REGENERATION OF THE OPTIC NERVES OF GOLDFISH, Journal of Neurochemistry 30, no.55 (May 1978): 1029–1039.https://doi.org/10.1111/j.1471-4159.1978.tb12396.xJohn T. Schmidt Retinal fibers alter tectal positional markers during the expansion of the half retinal projection in goldfish, The Journal of Comparative Neurology 177, no.22 (Jan 1978): 279–299.https://doi.org/10.1002/cne.901770207Michael S. Gazzaniga, Joseph E. LeDoux The Nature of Interhemispheric Communication, (Jan 1978): 9–44.https://doi.org/10.1007/978-1-4899-2206-9_2Dean Yager Psychophysical Functions in Fish with Respecified Retinotectal Connections, (Jan 1978): 725–732.https://doi.org/10.1007/978-3-540-35397-3_64 References, (Jan 1978): 303–328.https://doi.org/10.1016/B978-0-12-741850-6.50019-7Alan D. Springer, Bernard W. Agranoff Effect of temperature on rate of goldfish optic nerve regeneration: A radioautographic and behavioral study, Brain Research 128, no.33 (Jun 1977): 405–415.https://doi.org/10.1016/0006-8993(77)90167-6L. Luckenbill-Edds, S. C. Sharma Retinotectal projection of the adult winter flounder (Pseudopleuronectes americanus), The Journal of Comparative Neurology 173, no.22 (May 1977): 307–318.https://doi.org/10.1002/cne.901730207Andrew Francis, C.Lynn Orndoff Bengston, M.S. Gazzaniga Interocular equivalence after optic nerve regeneration in goldfish, Experimental Neurology 53, no.11 (Oct 1976): 94–101.https://doi.org/10.1016/0014-4886(76)90284-3Marion Murray Regeneration of retinal axons into the goldfish optic tectum, The Journal of Comparative Neurology 168, no.22 (Jul 1976): 175–195.https://doi.org/10.1002/cne.901680202Stephen Goldberg Central nervous system regeneration and ophthalmology, Survey of Ophthalmology 20, no.44 (Jan 1976): 261–272.https://doi.org/10.1016/0039-6257(76)90225-3 Bibliography, (Jan 1976): 327–366.https://doi.org/10.1016/B978-0-12-257450-4.50015-XM.J. KEATING The Formation of Visual Neuronal Connections: An Appraisal of the Present Status of the Theory of “Neuronal Specificity”, (Jan 1976): 59–110.https://doi.org/10.1016/B978-0-12-609303-2.50010-8G.E. Landreth, E.A. Neale, J.H. Neale, R.S. Duff, M.R. Braford, R.G. Northcutt, B.W. Agranoff Evaluation of [3H]proline for radioautographic tracing of axonal projections in the teleost visual system, Brain Research 91, no.11 (Jun 1975): 25–42.https://doi.org/10.1016/0006-8993(75)90464-3Ronald L. Meyer, R.W. Sperry Tests for neuroplasticity in the anuran retinotectal system, Experimental Neurology 40, no.22 (Aug 1973): 525–539.https://doi.org/10.1016/0014-4886(73)90093-9Myong Geun Yoon Transposition of the visual projection from the nasal hemiretina onto the foreign rostral zone of the optic tectum in goldfish, Experimental Neurology 37, no.33 (Dec 1972): 451–462.https://doi.org/10.1016/0014-4886(72)90088-XJ. H. Neale, E. A. Neale, B. W. Agranoff Radioautography of the Optic Tectum of the Goldfish after Intraocular Injection of [3H]Proline, Science 176, no.40334033 (Apr 1972): 407–410.https://doi.org/10.1126/science.176.4033.407S.S. Easter Pursuit eye movements in goldfish (Carassius auratus), Vision Research 12, no.44 (Apr 1972): 673–IN8.https://doi.org/10.1016/0042-6989(72)90161-7Myonggeun Yoon Reorganization of retinotectal projection following surgical operations on the optic tectum in goldfish, Experimental Neurology 33, no.22 (Nov 1971): 395–411.https://doi.org/10.1016/0014-4886(71)90031-8Emerson Hibbard Visual recovery following regeneration of the optic nerve through the oculomotor nerve root in Xenopus, Experimental Neurology 19, no.33 (Nov 1967): 350–356.https://doi.org/10.1016/0014-4886(67)90031-3K. K. Tandon, Sansar Chand Sharma On the degeneration and regeneration of optic nerve fibres with return of vision inDanio rerio (Ham.), Proceedings / Indian Academy of Sciences 60, no.44 (Oct 1964): 287–292.https://doi.org/10.1007/BF03051994Carmine D. Clemente Regeneration in The Vertebrate Central Nervous System, (Jan 1964): 257–301.https://doi.org/10.1016/S0074-7742(08)60771-0H.L. Arora, R.W. Sperry Color discrimination after optic nerve regeneration in the fish Astronotus ocellatus, Developmental Biology 7 (Jan 1963): 234–243.https://doi.org/10.1016/0012-1606(63)90120-9Domenica G. Attardi, R.W. Sperry Preferential selection of central pathways by regenerating optic fibers, Experimental Neurology 7, no.11 (Jan 1963): 46–64.https://doi.org/10.1016/0014-4886(63)90093-1L. S. Stone Polarization of the retina and development of vision, Journal of Experimental Zoology 145, no.11 (Oct 1960): 85–95.https://doi.org/10.1002/jez.1401450108R.M. Gaze Regeneration of the Optic Nerve in Amphibia, (Jan 1960): 1–40.https://doi.org/10.1016/S0074-7742(08)60118-XEmerson Hibbard Central integration of developing nerve tracts from supernumerary grafted eyes and brain in the frog, Journal of Experimental Zoology 141, no.22 (Jul 1959): 323–351.https://doi.org/10.1002/jez.1401410207E.G. HEALEY THE NERVOUS SYSTEM, (Jan 1957): 1–119.https://doi.org/10.1016/B978-1-4832-2763-4.50005-5Virginia M. McMurray The development of the optic lobes in Xenopus laevis. The effect of repeated crushing of the optic nerve, Journal of Experimental Zoology 125, no.22 (Mar 1954): 247–263.https://doi.org/10.1002/jez.1401250205R. W. Sperry Myotypic specificity in teleost motoneurons, The Journal of Comparative Neurology 93, no.22 (Oct 1950): 277–287.https://doi.org/10.1002/cne.900930208R. W. Sperry, Nancy Miner Formation within sensory nucleus V of synaptic associations mediating cutaneous localization, The Journal of Comparative Neurology 90, no.33 (Jun 1949): 403–423.https://doi.org/10.1002/cne.900900306 Priscilla Rasquin Regeneration of the Optic Nerve after Section with Return of Vision in the Characin Astyanax mexicanus, Physiological Zoology 22, no.22 (Sep 2015): 131–135.https://doi.org/10.1086/physzool.22.2.30152035

Referência(s)
Altmetric
PlumX