Literature DB >> 11884356

Architecture and callosal connections of visual areas 17, 18, 19 and 21 in the ferret (Mustela putorius).

Giorgio M Innocenti1, Paul R Manger, Italo Masiello, Isabelle Colin, Laurent Tettoni.   

Abstract

Visual areas 17, 18, 19 and 21 of the ferret can be distinguished on the grounds of cytoarchitecture, myeloarchitecture and cytochrome oxidase reactivity, and with transneuronal tract-tracing from the eye. Each visual area contains callosally connected, as well as acallosal, regions. The callosal connections originate mainly from layers 2 and 3 and, more widely, from layer 6. Callosally projecting neurons and callosal terminals are organized in three roughly medio-laterally oriented bands. The posterior and intermediate bands straddle the 17/18 and 19/21 border, respectively; the third band extends along the medial bank of the lateral suprasylvian sulcus. These bands are linked by a variable number of bridges of connections that demarcate acallosal islands. The distribution of callosal connections predicts the existence of vertical meridian representations corresponding to each of the bands and of non-isotropic representations of the visual field within the bridges and islands.

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Year:  2002        PMID: 11884356     DOI: 10.1093/cercor/12.4.411

Source DB:  PubMed          Journal:  Cereb Cortex        ISSN: 1047-3211            Impact factor:   5.357


  35 in total

1.  Functional biases in visual cortex neurons with identified projections to higher cortical targets.

Authors:  Beata Jarosiewicz; James Schummers; Wasim Q Malik; Emery N Brown; Mriganka Sur
Journal:  Curr Biol       Date:  2012-02-02       Impact factor: 10.834

2.  Retinal input influences the size and corticocortical connectivity of visual cortex during postnatal development in the ferret.

Authors:  A S Bock; C D Kroenke; E N Taber; J F Olavarria
Journal:  J Comp Neurol       Date:  2012-04-01       Impact factor: 3.215

3.  Cortical feedback depolarization waves: a mechanism of top-down influence on early visual areas.

Authors:  Per E Roland; Akitoshi Hanazawa; Calle Undeman; David Eriksson; Tamas Tompa; Hiroyuki Nakamura; Sonata Valentiniene; Bashir Ahmed
Journal:  Proc Natl Acad Sci U S A       Date:  2006-08-04       Impact factor: 11.205

4.  Do cross-modal projections always result in multisensory integration?

Authors:  Brian L Allman; Ruben E Bittencourt-Navarrete; Leslie P Keniston; Alexandre E Medina; Meng Y Wang; M Alex Meredith
Journal:  Cereb Cortex       Date:  2008-01-17       Impact factor: 5.357

5.  Role of retinal input on the development of striate-extrastriate patterns of connections in the rat.

Authors:  R J Laing; A S Bock; J Lasiene; J F Olavarria
Journal:  J Comp Neurol       Date:  2012-10-01       Impact factor: 3.215

6.  Zinc histochemistry reveals circuit refinement and distinguishes visual areas in the developing ferret cerebral cortex.

Authors:  Reem Khalil; Jonathan B Levitt
Journal:  Brain Struct Funct       Date:  2012-09-30       Impact factor: 3.270

7.  Use of Synaptic Zinc Histochemistry to Reveal Different Regions and Laminae in the Developing and Adult Brain.

Authors:  Reem Khalil; Jonathan B Levitt
Journal:  J Vis Exp       Date:  2017-10-29       Impact factor: 1.355

8.  Specificity of neuronal responses in primary visual cortex is modulated by interhemispheric corticocortical input.

Authors:  Kerstin E Schmidt; Stephen G Lomber; Giorgio M Innocenti
Journal:  Cereb Cortex       Date:  2010-03-08       Impact factor: 5.357

9.  Target-specific contrast agents for magnetic resonance microscopy.

Authors:  Megan L Blackwell; Christian T Farrar; Bruce Fischl; Bruce R Rosen
Journal:  Neuroimage       Date:  2009-06       Impact factor: 6.556

10.  Evolution amplified processing with temporally dispersed slow neuronal connectivity in primates.

Authors:  Roberto Caminiti; Hassan Ghaziri; Ralf Galuske; Patrick R Hof; Giorgio M Innocenti
Journal:  Proc Natl Acad Sci U S A       Date:  2009-10-29       Impact factor: 11.205

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