dc.creatorVillarroel Campos, David Leonardo
dc.creatorGonzález Billault, Christian
dc.date.accessioned2019-03-15T16:09:09Z
dc.date.available2019-03-15T16:09:09Z
dc.date.created2019-03-15T16:09:09Z
dc.date.issued2014
dc.identifierDev Neurobiol . 2014 Oct;74(10):953-71
dc.identifier1932846X
dc.identifier19328451
dc.identifier10.1002/dneu.22178
dc.identifierhttps://repositorio.uchile.cl/handle/2250/166428
dc.description.abstractThe functions of microtubule-associated protein 1B (MAP1B) have historically been linked to the development of the nervous system, based on its very early expression in neurons and glial cells. Moreover, mice in which MAP1B is genetically inactivated have been used extensively to show its role in axonal elongation, neuronal migration, and axonal guidance. In the last few years, it has become apparent that MAP1B has other cellular and molecular functions that are not related to its microtubule-stabilizing properties in the embryonic and adult brain. In this review, we present a systematic review of the canonical and novel functions of MAP1B and propose that, in addition to regulating the polymerization of microtubule and actin microfilaments, MAP1B also acts as a signaling protein involved in normal physiology and pathological conditions in the nervous system.
dc.languageen
dc.publisherJohn Wiley
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceDevelopmental Neurobiology
dc.subjectCytoskeleton
dc.subjectFMRP
dc.subjectNeuronal differentiation
dc.subjectNeuronal signaling
dc.subjectNeurotransmitter receptors
dc.titleThe MAP1B case: An old MAP that is new again
dc.typeArtículo de revista


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