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Mouse polyQ database: a new online resource for research using mouse models of neurodegenerative diseases
BACKGROUND: The polyglutamine (polyQ) family of disorders comprises 9 genetic diseases, including several types of ataxia and Huntington disease. Approximately two decades of investigation and the creation of more than 130 mouse models of polyQ disorders have revealed many similarities between these...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625465/ https://www.ncbi.nlm.nih.gov/pubmed/26515641 http://dx.doi.org/10.1186/s13041-015-0160-8 |
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author | Szlachcic, Wojciech J. Switonski, Pawel M. Kurkowiak, Małgorzata Wiatr, Kalina Figiel, Maciej |
author_facet | Szlachcic, Wojciech J. Switonski, Pawel M. Kurkowiak, Małgorzata Wiatr, Kalina Figiel, Maciej |
author_sort | Szlachcic, Wojciech J. |
collection | PubMed |
description | BACKGROUND: The polyglutamine (polyQ) family of disorders comprises 9 genetic diseases, including several types of ataxia and Huntington disease. Approximately two decades of investigation and the creation of more than 130 mouse models of polyQ disorders have revealed many similarities between these diseases. The disorders share common mutation types, neurological characteristics and certain aspects of pathogenesis, including morphological and physiological neuronal alterations. All of the diseases still remain incurable. DESCRIPTION: The large volume of information collected as a result of the investigation of polyQ models currently represents a great potential for searching, comparing and translating pathogenesis and therapeutic information between diseases. Therefore, we generated a public database comprising the polyQ mouse models, phenotypes and therapeutic interventions tested in vivo. The database is available at http://conyza.man.poznan.pl/. CONCLUSION: The use of the database in the field of polyQ diseases may accelerate research on these and other neurodegenerative diseases and provide new perspectives for future investigation. |
format | Online Article Text |
id | pubmed-4625465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46254652015-10-30 Mouse polyQ database: a new online resource for research using mouse models of neurodegenerative diseases Szlachcic, Wojciech J. Switonski, Pawel M. Kurkowiak, Małgorzata Wiatr, Kalina Figiel, Maciej Mol Brain Research BACKGROUND: The polyglutamine (polyQ) family of disorders comprises 9 genetic diseases, including several types of ataxia and Huntington disease. Approximately two decades of investigation and the creation of more than 130 mouse models of polyQ disorders have revealed many similarities between these diseases. The disorders share common mutation types, neurological characteristics and certain aspects of pathogenesis, including morphological and physiological neuronal alterations. All of the diseases still remain incurable. DESCRIPTION: The large volume of information collected as a result of the investigation of polyQ models currently represents a great potential for searching, comparing and translating pathogenesis and therapeutic information between diseases. Therefore, we generated a public database comprising the polyQ mouse models, phenotypes and therapeutic interventions tested in vivo. The database is available at http://conyza.man.poznan.pl/. CONCLUSION: The use of the database in the field of polyQ diseases may accelerate research on these and other neurodegenerative diseases and provide new perspectives for future investigation. BioMed Central 2015-10-29 /pmc/articles/PMC4625465/ /pubmed/26515641 http://dx.doi.org/10.1186/s13041-015-0160-8 Text en © Szlachcic et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Szlachcic, Wojciech J. Switonski, Pawel M. Kurkowiak, Małgorzata Wiatr, Kalina Figiel, Maciej Mouse polyQ database: a new online resource for research using mouse models of neurodegenerative diseases |
title | Mouse polyQ database: a new online resource for research using mouse models of neurodegenerative diseases |
title_full | Mouse polyQ database: a new online resource for research using mouse models of neurodegenerative diseases |
title_fullStr | Mouse polyQ database: a new online resource for research using mouse models of neurodegenerative diseases |
title_full_unstemmed | Mouse polyQ database: a new online resource for research using mouse models of neurodegenerative diseases |
title_short | Mouse polyQ database: a new online resource for research using mouse models of neurodegenerative diseases |
title_sort | mouse polyq database: a new online resource for research using mouse models of neurodegenerative diseases |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625465/ https://www.ncbi.nlm.nih.gov/pubmed/26515641 http://dx.doi.org/10.1186/s13041-015-0160-8 |
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