Topographic organization of V1 projections through the corpus callosum in humans.

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2010

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Périmètre
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info:eu-repo/semantics/altIdentifier/doi/10.1016/j.neuroimage.2010.05.060

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info:eu-repo/semantics/altIdentifier/pmid/20553894

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info:eu-repo/semantics/altIdentifier/pissn/1095-9572[electronic], 1053-8119[linking]

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info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_70B415A7F8FF5

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M. Saenz et al., « Topographic organization of V1 projections through the corpus callosum in humans. », Serveur académique Lausannois, ID : 10.1016/j.neuroimage.2010.05.060


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The visual cortex in each hemisphere is linked to the opposite hemisphere by axonal projections that pass through the splenium of the corpus callosum. Visual-callosal connections in humans and macaques are found along the V1/V2 border where the vertical meridian is represented. Here we identify the topography of V1 vertical midline projections through the splenium within six human subjects with normal vision using diffusion-weighted MR imaging and probabilistic diffusion tractography. Tractography seed points within the splenium were classified according to their estimated connectivity profiles to topographic subregions of V1, as defined by functional retinotopic mapping. First, we report a ventral-dorsal mapping within the splenium with fibers from ventral V1 (representing the upper visual field) projecting to the inferior-anterior corner of the splenium and fibers from dorsal V1 (representing the lower visual field) projecting to the superior-posterior end. Second, we also report an eccentricity gradient of projections from foveal-to-peripheral V1 subregions running in the anterior-superior to posterior-inferior direction, orthogonal to the dorsal-ventral mapping. These results confirm and add to a previous diffusion MRI study (Dougherty et al., 2005) which identified a dorsal/ventral mapping of human splenial fibers. These findings yield a more detailed view of the structural organization of the splenium than previously reported and offer new opportunities to study structural plasticity in the visual system.

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