Growth and Reshaping of Axons in the Establishment of Visual Callosal Connections

Technical considerations on the use of horseradish peroxidase as a neuronal marker

Adams, J. C. (1977) · Neuroscience · doi:10.1016/0306-4522(77)90074-4 · Cited by 914

Two new fluorescent retrograde neuronal tracers which are transported over long distances

Bentivoglio, M., Kuypers, H. G. J. M., Catsman‐Berrevoets, C. E., Loewe, H., & Dann, O. (1980) · Neuroscience Letters · doi:10.1016/0304-3940(80)90208-6 · Cited by 442

Columnar distribution of cortico-cortical fibers in the frontal association, limbic, and motor cortex of the developing rhesus monkey

Goldman, P. S., & Nauta, W. J. H. (1977) · Brain Research · doi:10.1016/0006-8993(77)90453-x · Cited by 414

Double retrograde neuronal labeling through divergent axon collaterals, using two fluorescent tracers with the same excitation wavelength which label different features of the cell

Kuypers, H. G. J. M., Bentivoglio, M., Catsman‐Berrevoets, C. E., & Bharos, A. T. (1980) · Experimental Brain Research · doi:10.1007/bf00236147 · Cited by 406

Exuberant projection into the corpus callosum from the visual cortex of newborn cats

Innocenti, G. M., Fiore, L., & Caminiti, R. (1977) · Neuroscience Letters · doi:10.1016/0304-3940(77)90185-9 · Cited by 341

Effects of visual experience on the maturation of the efferent system to the corpus callosum

Innocenti, G. M., & Frost, D. O. (1979) · Nature · doi:10.1038/280231a0 · Cited by 250

Postnatal shaping of callosal connections from sensory areas

Innocenti, G. M., & Caminiti, R. (1980) · Experimental Brain Research · doi:10.1007/bf00237518 · Cited by 209

Fluorescent retrograde neuronal labeling in rat by means of substances binding specifically to adeninethymine rich DNA

Bentivoglio, M., Kuypers, H. G. J. M., Catsman‐Berrevoets, C. E., & Dann, O. (1979) · Neuroscience Letters · doi:10.1016/0304-3940(79)96068-3 · Cited by 206

Anatomy of interhemispheric connections in the visual system of Boston Siamese and ordinary cats

Shatz, C. J. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901730307 · Cited by 194

Differential distribution of callosal projection neurons in the neonatal and adult rat

Ivy, G. O., Akers, R. M., & Killackey, H. P. (1979) · Brain Research · doi:10.1016/0006-8993(79)90247-6 · Cited by 166

Evidence that selective collateral elimination during postnatal development results in a restriction in the distribution of locus coeruleus neurons which project to the spinal cord in rats

Chen, K. S., & Stanfield, B. B. (1987) · Brain Research · doi:10.1016/s0006-8993(87)80038-0 · Cited by 17

Neonatal hippocampal neurons, retrogradely labeled with granular blue, survive intracerebral grafting and explantation to tissue culture

T�nder, N., Gaarskjaer, F. B., Sunde, N. A., & Zimmer, J. (1986) · Experimental Brain Research · doi:10.1007/bf00243844 · Cited by 17

Reorganization of Visual Callosal Connections Following Alterations of Retinal Input and Brain Damage

Restani, L., & Caleo, M. (2016) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2016.00086 · Cited by 16

Development of functional innervation in the second and third order auditory nuclei of the chick

Pettigrew, A. G., Ansselin, A. D., & Bramley, J. R. (1988) · Development · doi:10.1242/dev.104.4.575 · Cited by 16

Modulatory Events in the Development and Evolution of Primate Neocortex

Jones, E. G. (1990) · Cerebral cortex · doi:10.1007/978-1-4757-9622-3_9 · Cited by 15

An exuberant retinocollicular pathway in siamese kittens: Effects of competition and abnormal activity on its maturation

Berman, N. E. J., & Payne, B. R. (1985) · Developmental Brain Research · doi:10.1016/0165-3806(85)90171-3 · Cited by 16

Postnatal development of GABA- and glycine-mediated inhibition of feline retinal ganglion cells in the area centralis

Ikeda, H., & Robbins, J. (1985) · Developmental Brain Research · doi:10.1016/0165-3806(85)90002-1 · Cited by 16

The fates of the callosal neurons in neocortex after bisection of the corpus callosum, using the technique of retrograde neuronal labeling with two fluorescent dyes

Orihara, Y. I., Kishikawa, M., & Ono, K. (1997) · Brain Research · doi:10.1016/s0006-8993(97)01023-8 · Cited by 16

Somatotopically organized transient projections from the primary somatosensory cortex to the cerebellar cortex

Tolbert, D. L. (1989) · Developmental Brain Research · doi:10.1016/0165-3806(89)90013-8 · Cited by 15

Numbers of Axons Innervating Mystacial Vibrissa Follicles in Newborn and Adult Rats

Crissman, R. S., Warden, R. J., Siciliano, D. A., Klein, B. G., Renehan, W. E., Jacquin, M. F., & Rhoades, R. W. (1991) · Somatosensory & Motor Research · doi:10.3109/08990229109144734 · Cited by 15

Development of projection neurons of the mammalian cerebral cortex

Koester, S. E., & O'Leary, D. D. M. (1994) · Progress in brain research · doi:10.1016/s0079-6123(08)60541-5 · Cited by 15

A modification of biotinylated dextran amine histochemistry for labeling the developing mammalian brain

Ding, S., & Elberger, A. J. (1995) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(94)00127-3 · Cited by 15

induces recurrent synchronized burst activity in immature hippocampal CA3 neurones in vitro

King, A. E., Cherubini, E., & Ben‐Ari, Y. (1989) · Developmental Brain Research · doi:10.1016/0165-3806(89)90138-7 · Cited by 15

Phospholipid scramblase Xkr8 is required for developmental axon pruning via phosphatidylserine exposure

Neniškytė, U., Kuliešiūtė, U., Vadišiūtė, A., Jevdokimenko, K., Coletta, L., Deivasigamani, S., Pamedytytė, D., Daugelaviciene, N., Dabkevičienė, D., Perlas, E., et al. (2023) · The EMBO Journal · doi:10.15252/embj.2022111790 · Cited by 13

Bihemispheric Axonal Bifurcation of the Afferents to the Visual Cortical Areas during Postnatal Development in the Rat

Bullier, J., Dehay, C., & Dreher, B. (1990) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1990.tb00425.x · Cited by 14

Transient projections from rat occipital cortex are able to respond to a spinal target derived diffusible factor in vitro

Joosten, E. A. J., Bär, P. R., Gispen, W. H., & Bregman, B. S. (1993) · Neuroscience Letters · doi:10.1016/0304-3940(93)90863-g · Cited by 14

The role of competition in the refinement of the projections of sympathetic neurons to the rat eye during development

Hill, C. E., & Vidovic, M. (1989) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(89)90013-0 · Cited by 14

Does axonal branching contribute to the overproduction of optic nerve fibers during early development of the cat's visual system?

Lia, B., Williams, R. W., & Chalupa, L. M. (1986) · Developmental Brain Research · doi:10.1016/0165-3806(86)90220-8 · Cited by 14

Effects of neonatal splitting of the optic chiasm on the development of feline visual callosal connections

Boire, D., Morris, R., Ptito, M., Leporé, F., & Frost, D. O. (1995) · Experimental Brain Research · doi:10.1007/bf00242013 · Cited by 13

Postnatal development of the corticotectal projection in cats

Plummer, K. L., & Behan, M. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903150206 · Cited by 13

DEVELOPMENT OF CORTICAL AFFERENTS AND CORTICO‐TECTAL EFFERENTS OF THE MAMMALIAN (RAT) PRIMARY VISUAL CORTEX

Dreher, B., Thong, I. G., Shameem, N., & McCall, M. J. (1985) · Australian and New Zealand Journal of Ophthalmology · doi:10.1111/j.1442-9071.1985.tb00432.x · Cited by 13

Somatosensory receptive field properties of corpus callosum fibres in the raccoon

Guillemot, J., Richer, L., Ptito, M., Guilbert, M., & Leporé, F. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903210111 · Cited by 13

Effect of Bcl-2 overexpression on establishment of ipsilateral retinocollicular projection in mice

Yakura, T., Fukuda, Y., & Sawai, H. (2002) · Neuroscience · doi:10.1016/s0306-4522(01)00610-8 · Cited by 13

Development of neural connections between visual cortex and transplanted lateral geniculate nucleus in rats

Kurotani, T., Yamamoto, N., & Toyama, K. (1993) · Developmental Brain Research · doi:10.1016/0165-3806(93)90168-a · Cited by 13

Initial disorder and secondary retinotopic refinement of regenerating axons in the optic tract of the goldfish: signs of a new role for axon collateral loss

Becker, D. L., & Cook, J. E. (1987) · Development · doi:10.1242/dev.101.2.323 · Cited by 13

Changes in density of brainstem afferents in ferret primary auditory cortex (AI) during postnatal development.

Harper, M. S., & Wallace, M. N. (1995) · Europe PMC (PubMed Central) · Cited by 13

The genuineness of isthmo-optic neuronal death in chick embryos

Clarke, P. G. H. (1982) · Anatomy and Embryology · doi:10.1007/bf00305575 · Cited by 13

An autoradiographic study of the postnatal development of pericruciate cortical projections to the neostriatum and the claustrum of the cat

Adinolfi, A. M., & Levine, M. S. (1986) · Developmental Brain Research · doi:10.1016/0165-3806(86)90177-x · Cited by 12

Postnatal development and specification of the cat's visual corticotectal projection: efferent from the posteromedial lateral suprasylvian area

Bruce, L. L. (1993) · Developmental Brain Research · doi:10.1016/0165-3806(93)90045-c · Cited by 12

Fetal MRI based brain atlas analysis detects initial in utero effects of prenatal alcohol exposure

Stuempflen, M., Schwartz, E., Diogo, M. C., Glatter, S., Pfeiler, B., Kienast, P., Taymourtash, A., Schmidbauer, V. U., Bartha, L., Krampl‐Bettelheim, E., et al. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad005 · Cited by 11

White Matter Structure

Edgar, J. M., & Griffiths, I. R. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-396460-1.00007-x · Cited by 13

Role of neuropeptide Y projection on the development of serotonergic innervation in the suprachiasmatic nucleus of the rat, shown by triple intraocular grafts

Ueda, S., Matsumoto, Y., Nisimura, A., Azmitia, E. C., & Kawata, M. (1995) · Brain Research · doi:10.1016/0006-8993(94)01454-p · Cited by 11

Evidence That the Lateral Geniculate Nucleus Regulates the Normal Development of Visual Corticocortical Projections in the Cat

Carić, D., & Price, D. J. (1999) · Experimental Neurology · doi:10.1006/exnr.1999.7031 · Cited by 11

Functional consequences of modification of callosal connections by perinatal enucleation in rat visual cortex

Toldi, J., Wolff, J. R., & Wiese, U. H. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90403-x · Cited by 11

Characterization of the retraction response of goldfish retinal ganglion cell axons induced by monoclonal antibody 8A2 in vitro

Finnegan, S. G., Lemmon, V., & KOENIG, E. C. (1992) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.970230407 · Cited by 11

The Controversial Nature of the Evidence for Neuroplasticity of Afferent Axons in the Spinal Cord

Micevych, P. E., Rodin, B. E., & Kruger, L. (1986) · Springer eBooks · doi:10.1007/978-1-4684-4994-5_17 · Cited by 11

Selective retinal reinnervation of a surgically created tectal island in goldfish. II. Electron microscopic analysis

Edwards, M. A., & Murray, M. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902320310 · Cited by 11

Proteome dynamics during postnatal mouse corpus callosum development

Son, A. I., Fu, X., Suto, F., Liu, J. S.-H., Hashimoto‐Torii, K., & Torii, M. (2017) · Scientific Reports · doi:10.1038/srep45359 · Cited by 11

Microglial cells in the retina ofCarassius auratus: Effects of optic nerve crush

Salvador‐Silva, M., Vidal‐Sanz, M., & Villegas-P�rez, M. P. (2000) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(20000221)417:4 · Cited by 55

Duplication of brain parts in evolution

Kaas, J. H. (1984) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00018525 · Cited by 9

Postnatal development of the visual corpus callosum: The influence of activity of the retinofugal projections

Murphy, E. H., & Grigonis, A. M. (1988) · Behavioural Brain Research · doi:10.1016/0166-4328(88)90145-3 · Cited by 10

The origin of projections from the medullary reticular formation to the spinal cord, the diencephalon and the cerebellum at different stages of development in the north american opossum: Studies using single and double labeling techniques

Martin, G. F., Cabana, T., & Waltzer, R. P. (1988) · Neuroscience · doi:10.1016/0306-4522(88)90008-5 · Cited by 10

The organization of visual corticocortical connections in early postnatal kittens

Carić, D., & Price, D. J. (1996) · Neuroscience · doi:10.1016/0306-4522(96)00059-0 · Cited by 10

Developmental Reorganization of the Human Association Cortex during Perinatal and Postnatal Life

Kostović, I., Petanjek, Z., Delalle, I., & Judáš, M. (1992) · Birkhäuser Boston eBooks · doi:10.1007/978-1-4684-6805-2_1 · Cited by 10

Regressive changes among corticocortical neurons projecting from the lateral suprasylvian cortex to area 18 of the kitten's visual cortex

Kato, N., Ferrer, J. M. R., & Price, D. J. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90294-x · Cited by 10

Anatomy, Development, and Physiology of the Corpus Callosum

Jones, E. G. (1985) · Springer eBooks · doi:10.1007/978-1-4613-2419-5_1 · Cited by 10

A combination of Golgi impregnation and fluorescent retrograde labeling

Catsicas, S., Berbel, P. J., & Innocenti, G. M. (1986) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(86)90020-8 · Cited by 10

Refinement of the Primate Corticospinal Pathway During Prenatal Development

Gomes, A. R. R., Olivier, E., Killackey, H. P., Giroud, P., Berland, M., Knoblauch, K., Dehay, C., & Kennedy, H. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz116 · Cited by 9

High Angular Resolution Diffusion MRI Reveals Conserved and Deviant Programs in the Paths that Guide Human Cortical Circuitry

Charvet, C. J., Das, A., Song, J. W., Tindal-Burgess, D. J., Kabaria, P., Dai, G., Kane, T., & Takahashi, E. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz178 · Cited by 9

Fluorometric comparisons of the retrograde axonal transport of true blue and diamidino yellow from the rat caudate-putamen

Payne, J. N., & Peace, J. M. (1989) · Experimental Brain Research · doi:10.1007/bf00248540 · Cited by 9

Postnatal Development of the Retinal Projection to the Nucleus of the Optic Tract and Accessory Optic Nuclei in the Hooded Rat.

Bai, W.-Z., Meguro, R., Kaiya, T., & Norita, M. (2001) · Archivum histologicum japonicum · doi:10.1679/aohc.64.69 · Cited by 9

Primary visual cortex projections to extrastriate cortices in enucleated and anophthalmic mice

Laramée, M., Bronchti, G., & Boire, D. (2013) · Brain Structure and Function · doi:10.1007/s00429-013-0623-6 · Cited by 9

The Target of Exuberant Projections in Development

Innocenti, G. M. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhz344 · Cited by 9

Confirmation of the existence of transitory corpus callosum axons in area 17 of neonatal cat: an anterograde tracing study using biotinylated dextran amine

Ding, S., & Elberger, A. J. (1994) · Neuroscience Letters · doi:10.1016/0304-3940(94)90046-9 · Cited by 9

Imaging of individual normal and regenerating optic fibers in the brain of living adult goldfish

Danks, A. M., Kim, P., Wang, Z., & Meyer, R. L. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903450207 · Cited by 9

The Incidence of Bifurcation Among Corticocortical Connections from Area 17 in the Developing Visual Cortex of the Cat

Price, D. J., & Ferrer, J. M. R. (1993) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1993.tb00488.x · Cited by 9

Organization of callosal connections in the visual cortex of the rabbit following neonatal enucleation, dark rearing, and strobe rearing

Grigonis, A. M., & Murphy, E. H. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903120407 · Cited by 9

Postnatal refinement of interareal feedforward projections in ferret visual cortex

Khalil, R., Contreras-Ramirez, V., & Levitt, J. B. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1632-2 · Cited by 8

Cortical Visual Connections via the Corpus Callosum are Asymmetrical in Human Infantile Esotropia

ten Tusscher, M. P. M., Houtman, A. C., Mey, J. D., & Schuerbeek, P. V. (2017) · Strabismus · doi:10.1080/09273972.2017.1418898 · Cited by 8

Corpus callosum development in preterm and term infants

Fujii, Y., Kuriyama, M., Konishi, Y., Saito, M., & Sudo, M. (1994) · Pediatric Neurology · doi:10.1016/0887-8994(94)90046-9 · Cited by 8

The corpus callosum provides a massive transitory input to the visual cortex of cat and rat during early postnatal development

Elberger, A. J. (1994) · Behavioural Brain Research · doi:10.1016/0166-4328(94)90115-5 · Cited by 8

Postnatal development of area 17 callosal connections in Tupaia

Kretz, R., & Rager, G. H. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903260205 · Cited by 8

Chick wing innervation. III. Formation of axon collaterals in developing peripheral nerves

Ferns, M., & Hollyday, M. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903570207 · Cited by 8

Unilateral visual cortex deafferentation induces changes in receptive field properties of cortical cells in the intact hemisphere of normal and of monocularly deprived cats

Yinon, U., & Podell, M. (1987) · Developmental Brain Research · doi:10.1016/0165-3806(87)90154-4 · Cited by 8

Selective retinal reinnervation of a surgically created tectal island in goldfish. I. Light microscopic analysis

Edwards, M. A., Sharma, S. C., & Murray, M. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902320309 · Cited by 8

Excess Neuronal Branching Allows for Local Innervation of Specific Dendritic Compartments in Mature Cortex

Bird, A. D., Deters, L. H., & Cuntz, H. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa271 · Cited by 7

Control of Cell Number and Type in the Developing and Evolving Neocortex

Finlay, B. L. (1991) · Springer eBooks · doi:10.1007/978-1-4899-0652-6_4 · Cited by 7

Quantitative ultrastructure of physiologically identified premotoneuron terminals in the trigeminal motor nucleus in the cat

Shigenaga, Y., Hirose, Y., Yoshida, A., Fukami, H., Honma, S., & Bae, Y. C. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20001009)426:1 · Cited by 36

A Model of Developmental Synapse Elimination in the Central Nervous System: Possible Mechanisms and Functional Consequences

Lohof, A. M., Bailly, Y. J. R., Delhaye‐Bouchaud, N., & Mariani, J. (1997) · Advances in organ biology · doi:10.1016/s1569-2590(08)60181-0 · Cited by 7

Regulation of neuronal growth cone filopodia by nitric oxide

Wagenen, S. V., & Rehder, V. (1999) · Journal of Neurobiology · doi:10.1002/(sici)1097-4695(199905)39:2 · Cited by 77

Death of transcallosal neurons after close axotomy

Fishman, P. S., & Parks, D. A. (1998) · Brain Research · doi:10.1016/s0006-8993(97)01125-6 · Cited by 7

Untitled work

(1991) · Cited by 7

Compensatory Innervation in Development and Evolution

Pallas, S. L. (2007) · Elsevier eBooks · doi:10.1016/b0-12-370878-8/00101-4 · Cited by 7

Axon number in oculomotor nerves in Xenopus: Removal of one eye primordium affects both sides

Schönenberger, N., Escher, G., & der Loos, H. V. (1983) · Neuroscience Letters · doi:10.1016/0304-3940(83)90457-3 · Cited by 7

The Dynamics of Axon Bifurcation Development in the Cerebral Cortex of Typical and Acallosal Mice

Rayêe, D., Iack, P. M., Christoff, R. R., Lourenço, M. R., Bonifácio, C., Boltz, J., Lent, R., & Garcez, P. P. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.09.020 · Cited by 6

Cortical connections and functional interactions between visual cortical areas

Bullier, J. (2003) · doi:10.1093/acprof:oso/9780198505822.003.0002 · Cited by 6

Physiology and Plasticity of Interhemispheric Connections

Caleo, M., Innocenti, G. M., & Ptito, M. (2013) · Neural Plasticity · doi:10.1155/2013/176183 · Cited by 7

Different Developmental Strategies of the Telencephalic Commissures: A Comparison between the Ontogeneses of Visual Callosal Connections and of Olfactory Commissural Connections in Rodents

Lent, R. (1992) · Birkhäuser Boston eBooks · doi:10.1007/978-1-4899-6726-8_10 · Cited by 6

Coherence Patterns of Infant Sleep EEG in Absence of the Corpus Callosum

Kuks, J. B. M., & Vos, J. E. (1994) · Advances in behavioral biology · doi:10.1007/978-1-4613-0487-6_12 · Cited by 6

Age-related Aspects of Experience Effects upon Brain Structure

Greenough, W. T., & Schwark, H. D. (1984) · Springer eBooks · doi:10.1007/978-1-4613-2725-7_4 · Cited by 6

Collateralization in the mammalian nervous system

Sarter, M. F., & Markowitsch, H. J. (1985) · International Journal of Neuroscience · doi:10.3109/00207458508985390 · Cited by 5

Terminal field volume of the glossopharyngeal nerve in adult rats reverts to prepruning size following microglia depletion with PLX5622

Riquier, A. J., & Sollars, S. I. (2022) · Developmental Neurobiology · doi:10.1002/dneu.22904 · Cited by 5

Disappearing developing cells

Guillery, R. W., & Killackey, H. P. (1987) · Nature · doi:10.1038/325578a0 · Cited by 5

Neuronal growth and target recognition: lessons from the leech

Baker, M. W., & Macagno, E. R. (2001) · Canadian Journal of Zoology · doi:10.1139/cjz-79-2-204 · Cited by 5

Neuropeptide Y immunoreactive axons in the corpus callosum of the cat during postnatal development

Ding, S., & Elberger, A. J. (1994) · Anatomy and Embryology · doi:10.1007/bf00185846 · Cited by 5

Postnatal development of the striate cortical projection onto the extrageniculate visual thalamus in the cat: an HRP study

Kato, N. (1987) · Experimental Brain Research · doi:10.1007/bf00269460 · Cited by 5

Steps in the formation of a bipolar outgrowth pattern by cultured neurons, and their substrate dependence

De‐Miguel, F. F., & Vargas, J. (2002) · Journal of Neurobiology · doi:10.1002/neu.10017 · Cited by 5

An immunohistochemical study of neurotransmitter profiles in developing human visual cortex

Masood, F., Wadhwa, S., & Bijlani, V. (1993) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(93)90010-b · Cited by 5

Developmental interactions between the corpus callosum and the visual system in cats

Elberger, A. J. (1988) · Behavioural Brain Research · doi:10.1016/0166-4328(88)90142-8 · Cited by 5

Cross-Modal Plasticity in Sensory Cortex

Pallas, S. L. (1991) · Springer eBooks · doi:10.1007/978-1-4899-0652-6_19 · Cited by 5

The Plasticity of the Nervous System

Hundert, E. M. (1990) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198248965.003.0011 · Cited by 5

Transitory Neuronal Connections in Normal Development and Disease

Frost, D. O. (1989) · doi:10.1007/978-1-349-10732-2_2 · Cited by 5

Intrinsic threshold plasticity: cholinergic activation and role in the neuronal recognition of incomplete input patterns

Pham, T. D., & Hansel, C. (2022) · The Journal of Physiology · doi:10.1113/jp283473 · Cited by 6

Absence of impulse activity in cortical neurons with transient projections to the cerebellum

Tolbert, D. L. (1989) · Developmental Brain Research · doi:10.1016/0165-3806(89)90200-9 · Cited by 4

Neonatal depletion of serotonin increases the numbers of callosally projecting neurons in cat visual areas 17 and 18

Djavadian, R. L., Wielkopolska, E., & Turlejski, K. (2003) · Neuroscience Letters · doi:10.1016/j.neulet.2003.07.008 · Cited by 4

Model-based diagnosis of brain disorders: a prototype framework

Siregar, P., & Toulouse, P. (1995) · Artificial Intelligence in Medicine · doi:10.1016/0933-3657(95)00008-t · Cited by 4

Evidence that dorsal locus coeruleus neurons can maintain their spinal cord projection following neonatal transection of the dorsal adrenergic bundle in rats

Stanfield, B. B. (1989) · Experimental Brain Research · doi:10.1007/bf00230240 · Cited by 4

Development of the visual callosal cell distribution in the rat: Mature features are present at birth

Hernit, C. S., Murphy, K. M., & Sluyters, R. C. V. (1996) · Visual Neuroscience · doi:10.1017/s0952523800009160 · Cited by 4

A return to the Bauplan

Alberch, P. (1984) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00018380 · Cited by 4

The Normal and Abnormal Development of the Mammalian Visual System

Lund, R. D., & Chang, F. (1986) · Elsevier eBooks · doi:10.1016/b978-0-12-300271-6.50010-x · Cited by 4

Juvenile Visual Callosal Axons in Kittens Display Origin‐and Fate‐related Morphology and Distribution of Arbors

Zouaoui, D., & Innocenti, G. M. (1994) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1994.tb00577.x · Cited by 37

Postnatal shaping of callosal connections from sensory areas

Innocenti, G. M., & Caminiti, R. (1980) · Experimental Brain Research · doi:10.1007/bf00237518 · Cited by 209

Effects of visual experience on the maturation of the efferent system to the corpus callosum

Innocenti, G. M., & Frost, D. O. (1979) · Nature · doi:10.1038/280231a0 · Cited by 250

The corpus callosum provides a massive transitory input to the visual cortex of cat and rat during early postnatal development

Elberger, A. J. (1994) · Behavioural Brain Research · doi:10.1016/0166-4328(94)90115-5 · Cited by 8

Organization and postnatal development of callosal connections in the visual cortex of the rat

Olavarría, J. F., & Sluyters, R. C. V. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902390102 · Cited by 213