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Linking the Primary Cilium to Cell Migration in Tissue Repair and Brain Development

Primary cilia are unique sensory organelles that coordinate cellular signaling networks in vertebrates. Inevitably, defects in the formation or function of primary cilia lead to imbalanced regulation of cellular processes that causes multisystemic disorders and diseases, commonly known as ciliopathi...

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Detalles Bibliográficos
Autores principales: Veland, Iben Rønn, Lindbæk, Louise, Christensen, Søren Tvorup
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776690/
https://www.ncbi.nlm.nih.gov/pubmed/26955067
http://dx.doi.org/10.1093/biosci/biu179
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author Veland, Iben Rønn
Lindbæk, Louise
Christensen, Søren Tvorup
author_facet Veland, Iben Rønn
Lindbæk, Louise
Christensen, Søren Tvorup
author_sort Veland, Iben Rønn
collection PubMed
description Primary cilia are unique sensory organelles that coordinate cellular signaling networks in vertebrates. Inevitably, defects in the formation or function of primary cilia lead to imbalanced regulation of cellular processes that causes multisystemic disorders and diseases, commonly known as ciliopathies. Mounting evidence has demonstrated that primary cilia coordinate multiple activities that are required for cell migration, which, when they are aberrantly regulated, lead to defects in organogenesis and tissue repair, as well as metastasis of tumors. Here, we present an overview on how primary cilia may contribute to the regulation of the cellular signaling pathways that control cyclic processes in directional cell migration.
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spelling pubmed-47766902016-03-07 Linking the Primary Cilium to Cell Migration in Tissue Repair and Brain Development Veland, Iben Rønn Lindbæk, Louise Christensen, Søren Tvorup Bioscience Overview Articles Primary cilia are unique sensory organelles that coordinate cellular signaling networks in vertebrates. Inevitably, defects in the formation or function of primary cilia lead to imbalanced regulation of cellular processes that causes multisystemic disorders and diseases, commonly known as ciliopathies. Mounting evidence has demonstrated that primary cilia coordinate multiple activities that are required for cell migration, which, when they are aberrantly regulated, lead to defects in organogenesis and tissue repair, as well as metastasis of tumors. Here, we present an overview on how primary cilia may contribute to the regulation of the cellular signaling pathways that control cyclic processes in directional cell migration. Oxford University Press 2014-11-25 2014-12-01 /pmc/articles/PMC4776690/ /pubmed/26955067 http://dx.doi.org/10.1093/biosci/biu179 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of the American Institute of Biological Sciences. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Overview Articles
Veland, Iben Rønn
Lindbæk, Louise
Christensen, Søren Tvorup
Linking the Primary Cilium to Cell Migration in Tissue Repair and Brain Development
title Linking the Primary Cilium to Cell Migration in Tissue Repair and Brain Development
title_full Linking the Primary Cilium to Cell Migration in Tissue Repair and Brain Development
title_fullStr Linking the Primary Cilium to Cell Migration in Tissue Repair and Brain Development
title_full_unstemmed Linking the Primary Cilium to Cell Migration in Tissue Repair and Brain Development
title_short Linking the Primary Cilium to Cell Migration in Tissue Repair and Brain Development
title_sort linking the primary cilium to cell migration in tissue repair and brain development
topic Overview Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776690/
https://www.ncbi.nlm.nih.gov/pubmed/26955067
http://dx.doi.org/10.1093/biosci/biu179
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