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Mouse models of human disease: An evolutionary perspective

The use of mice as model organisms to study human biology is predicated on the genetic and physiological similarities between the species. Nonetheless, mice and humans have evolved in and become adapted to different environments and so, despite their phylogenetic relatedness, they have become very d...

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Autor principal: Perlman, Robert L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4875775/
https://www.ncbi.nlm.nih.gov/pubmed/27121451
http://dx.doi.org/10.1093/emph/eow014
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author Perlman, Robert L.
author_facet Perlman, Robert L.
author_sort Perlman, Robert L.
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description The use of mice as model organisms to study human biology is predicated on the genetic and physiological similarities between the species. Nonetheless, mice and humans have evolved in and become adapted to different environments and so, despite their phylogenetic relatedness, they have become very different organisms. Mice often respond to experimental interventions in ways that differ strikingly from humans. Mice are invaluable for studying biological processes that have been conserved during the evolution of the rodent and primate lineages and for investigating the developmental mechanisms by which the conserved mammalian genome gives rise to a variety of different species. Mice are less reliable as models of human disease, however, because the networks linking genes to disease are likely to differ between the two species. The use of mice in biomedical research needs to take account of the evolved differences as well as the similarities between mice and humans.
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spelling pubmed-48757752016-05-24 Mouse models of human disease: An evolutionary perspective Perlman, Robert L. Evol Med Public Health Commentary The use of mice as model organisms to study human biology is predicated on the genetic and physiological similarities between the species. Nonetheless, mice and humans have evolved in and become adapted to different environments and so, despite their phylogenetic relatedness, they have become very different organisms. Mice often respond to experimental interventions in ways that differ strikingly from humans. Mice are invaluable for studying biological processes that have been conserved during the evolution of the rodent and primate lineages and for investigating the developmental mechanisms by which the conserved mammalian genome gives rise to a variety of different species. Mice are less reliable as models of human disease, however, because the networks linking genes to disease are likely to differ between the two species. The use of mice in biomedical research needs to take account of the evolved differences as well as the similarities between mice and humans. Oxford University Press 2016-05-21 /pmc/articles/PMC4875775/ /pubmed/27121451 http://dx.doi.org/10.1093/emph/eow014 Text en © The Author(s) 2016. Published by Oxford University Press on behalf of the Foundation for Evolution, Medicine, and Public Health. 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 Commentary
Perlman, Robert L.
Mouse models of human disease: An evolutionary perspective
title Mouse models of human disease: An evolutionary perspective
title_full Mouse models of human disease: An evolutionary perspective
title_fullStr Mouse models of human disease: An evolutionary perspective
title_full_unstemmed Mouse models of human disease: An evolutionary perspective
title_short Mouse models of human disease: An evolutionary perspective
title_sort mouse models of human disease: an evolutionary perspective
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4875775/
https://www.ncbi.nlm.nih.gov/pubmed/27121451
http://dx.doi.org/10.1093/emph/eow014
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