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Metallothionein genes: no association with Crohn's disease in a New Zealand population

Metallothioneins (MTs) are excellent candidate genes for Inflammatory Bowel Disease (IBD) and have previously been shown to have altered expression in both animal and human studies of IBD. This is the first study to examine genetic variants within the MT genes and aims to determine whether such gene...

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Detalles Bibliográficos
Autores principales: Morgan, Angharad R, Fraser, Alan G, Ferguson, Lynnette R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3280932/
https://www.ncbi.nlm.nih.gov/pubmed/22284420
http://dx.doi.org/10.1186/1477-5751-11-8
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author Morgan, Angharad R
Fraser, Alan G
Ferguson, Lynnette R
author_facet Morgan, Angharad R
Fraser, Alan G
Ferguson, Lynnette R
author_sort Morgan, Angharad R
collection PubMed
description Metallothioneins (MTs) are excellent candidate genes for Inflammatory Bowel Disease (IBD) and have previously been shown to have altered expression in both animal and human studies of IBD. This is the first study to examine genetic variants within the MT genes and aims to determine whether such genetic variants have an important role in this disease. 28 tag SNPs in genes MT1 (subtypes A, B, E, F, G, H, M, X), MT2, MT3 and MT4 were selected for genotyping in a well-characterized New Zealand dataset consisting of 406 patients with Crohn's Disease and 638 controls. We did not find any evidence of association for MT genetic variation with CD. The lack of association indicates that genetic variants in the MT genes do not play a significant role in predisposing to CD in the New Zealand population.
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spelling pubmed-32809322012-02-17 Metallothionein genes: no association with Crohn's disease in a New Zealand population Morgan, Angharad R Fraser, Alan G Ferguson, Lynnette R J Negat Results Biomed Brief Report Metallothioneins (MTs) are excellent candidate genes for Inflammatory Bowel Disease (IBD) and have previously been shown to have altered expression in both animal and human studies of IBD. This is the first study to examine genetic variants within the MT genes and aims to determine whether such genetic variants have an important role in this disease. 28 tag SNPs in genes MT1 (subtypes A, B, E, F, G, H, M, X), MT2, MT3 and MT4 were selected for genotyping in a well-characterized New Zealand dataset consisting of 406 patients with Crohn's Disease and 638 controls. We did not find any evidence of association for MT genetic variation with CD. The lack of association indicates that genetic variants in the MT genes do not play a significant role in predisposing to CD in the New Zealand population. BioMed Central 2012-01-28 /pmc/articles/PMC3280932/ /pubmed/22284420 http://dx.doi.org/10.1186/1477-5751-11-8 Text en Copyright ©2012 Morgan et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Report
Morgan, Angharad R
Fraser, Alan G
Ferguson, Lynnette R
Metallothionein genes: no association with Crohn's disease in a New Zealand population
title Metallothionein genes: no association with Crohn's disease in a New Zealand population
title_full Metallothionein genes: no association with Crohn's disease in a New Zealand population
title_fullStr Metallothionein genes: no association with Crohn's disease in a New Zealand population
title_full_unstemmed Metallothionein genes: no association with Crohn's disease in a New Zealand population
title_short Metallothionein genes: no association with Crohn's disease in a New Zealand population
title_sort metallothionein genes: no association with crohn's disease in a new zealand population
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3280932/
https://www.ncbi.nlm.nih.gov/pubmed/22284420
http://dx.doi.org/10.1186/1477-5751-11-8
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