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dc.contributor.authorCallejas Marín, Antuca-
dc.contributor.authorMoreno Bravo, Juan Antonio-
dc.contributor.authorCompany Devesa, Verónica-
dc.contributor.authorMadrigal Verdú, María del Pilar-
dc.contributor.authorAlmagro García, Francisca de Paula-
dc.contributor.authorMartínez Pérez, Salvador-
dc.contributor.authorde Puelles Martínez de La Torre, Eduardo-
dc.contributor.otherInstituto de Neurocienciases_ES
dc.contributor.otherDepartamentos de la UMH::Patología y Cirugíaes_ES
dc.contributor.otherDepartamentos de la UMH::Histología y Anatomíaes_ES
dc.date.accessioned2024-02-06T17:17:57Z-
dc.date.available2024-02-06T17:17:57Z-
dc.date.created2022-02-
dc.identifier.citationFrontiers in Neuroanatomy 2022 Feb 10:16:830758es_ES
dc.identifier.issn1662-5129-
dc.identifier.urihttps://hdl.handle.net/11000/31170-
dc.description.abstractThe thalamocortical projections are part of the most important higher level processing connections in the vertebrates and follow a highly ordered pathway from their origin in the thalamus to the cerebral cortex. Their functional complexities are not only due to an extremely elaborate axon guidance process but also due to activity-dependent mechanisms. Gli2 is an intermediary transcription factor in the Sonic hedgehog (Shh) pathway. During neural early development, Shh has an important role in dorsoventral patterning, diencephalic anteroposterior patterning, and many later developmental processes, such as axon guidance and cell migration. Using a Gli2 knockout mouse line, we have studied the role of Shh signaling mediated by Gli2 in the development of the thalamocortical projections during embryonic development. In wild-type brains, we have described the normal trajectory of the thalamocortical axons into the context of the prosomeric model. Then, we have compared it with the altered thalamocortical axons course in Gli2 homozygous embryos. The thalamocortical axons followed different trajectories and were misdirected to other territories probably due to alterations in the Robo/Slit signaling mechanism. In conclusion, the alteration of Gli2-mediated Shh signaling produces an erroneous specification of several territories related with the thalamocortical axons. This is translated into a huge modification in the pathfinding signaling mechanisms needed for the correct wiring of the thalamocortical axonses_ES
dc.formatapplication/pdfes_ES
dc.format.extent13es_ES
dc.language.isoenges_ES
dc.publisherFrontiers Media [Commercial Publisher]es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectGli2es_ES
dc.subjectSlit1es_ES
dc.subjectSlit2es_ES
dc.subjectguidancees_ES
dc.subjectthalamocortical axonses_ES
dc.titleGli2-Mediated Shh Signaling Is Required for Thalamocortical Projection Guidancees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttps://doi.org/10.3389/fnana.2022.830758es_ES
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Artículos Patología y Cirugía


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