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Mouse models of ciliopathies: the state of the art

The ciliopathies are an apparently disparate group of human diseases that all result from defects in the formation and/or function of cilia. They include disorders such as Meckel-Grüber syndrome (MKS), Joubert syndrome (JBTS), Bardet-Biedl syndrome (BBS) and Alström syndrome (ALS). Reflecting the ma...

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Detalles Bibliográficos
Autores principales: Norris, Dominic P., Grimes, Daniel T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Limited 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3339824/
https://www.ncbi.nlm.nih.gov/pubmed/22566558
http://dx.doi.org/10.1242/dmm.009340
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author Norris, Dominic P.
Grimes, Daniel T.
author_facet Norris, Dominic P.
Grimes, Daniel T.
author_sort Norris, Dominic P.
collection PubMed
description The ciliopathies are an apparently disparate group of human diseases that all result from defects in the formation and/or function of cilia. They include disorders such as Meckel-Grüber syndrome (MKS), Joubert syndrome (JBTS), Bardet-Biedl syndrome (BBS) and Alström syndrome (ALS). Reflecting the manifold requirements for cilia in signalling, sensation and motility, different ciliopathies exhibit common elements. The mouse has been used widely as a model organism for the study of ciliopathies. Although many mutant alleles have proved lethal, continued investigations have led to the development of better models. Here, we review current mouse models of a core set of ciliopathies, their utility and future prospects.
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spelling pubmed-33398242012-05-02 Mouse models of ciliopathies: the state of the art Norris, Dominic P. Grimes, Daniel T. Dis Model Mech Perspective The ciliopathies are an apparently disparate group of human diseases that all result from defects in the formation and/or function of cilia. They include disorders such as Meckel-Grüber syndrome (MKS), Joubert syndrome (JBTS), Bardet-Biedl syndrome (BBS) and Alström syndrome (ALS). Reflecting the manifold requirements for cilia in signalling, sensation and motility, different ciliopathies exhibit common elements. The mouse has been used widely as a model organism for the study of ciliopathies. Although many mutant alleles have proved lethal, continued investigations have led to the development of better models. Here, we review current mouse models of a core set of ciliopathies, their utility and future prospects. The Company of Biologists Limited 2012-05 /pmc/articles/PMC3339824/ /pubmed/22566558 http://dx.doi.org/10.1242/dmm.009340 Text en © 2012. Published by The Company of Biologists Ltd This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial Share Alike License (http://creativecommons.org/licenses/by-nc-sa/3.0), which permits unrestricted non-commercial use, distribution and reproduction in any medium provided that the original work is properly cited and all further distributions of the work or adaptation are subject to the same Creative Commons License terms
spellingShingle Perspective
Norris, Dominic P.
Grimes, Daniel T.
Mouse models of ciliopathies: the state of the art
title Mouse models of ciliopathies: the state of the art
title_full Mouse models of ciliopathies: the state of the art
title_fullStr Mouse models of ciliopathies: the state of the art
title_full_unstemmed Mouse models of ciliopathies: the state of the art
title_short Mouse models of ciliopathies: the state of the art
title_sort mouse models of ciliopathies: the state of the art
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3339824/
https://www.ncbi.nlm.nih.gov/pubmed/22566558
http://dx.doi.org/10.1242/dmm.009340
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