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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Company of Biologists Limited
2012
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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. |
format | Online Article Text |
id | pubmed-3339824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Company of Biologists Limited |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT norrisdominicp mousemodelsofciliopathiesthestateoftheart AT grimesdanielt mousemodelsofciliopathiesthestateoftheart |