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dc.contributor.authorSundberg, John P.
dc.contributor.authorMcElwee, Kevin
dc.contributor.authorBrehm, Michael A.
dc.contributor.authorSu, Lishan
dc.contributor.authorKing, Lloyd E. Jr
dc.date2022-08-11T08:09:44.000
dc.date.accessioned2022-08-23T16:41:23Z
dc.date.available2022-08-23T16:41:23Z
dc.date.issued2015-11-01
dc.date.submitted2016-01-15
dc.identifier.citationJ Investig Dermatol Symp Proc. 2015 Nov;17(2):23-6. doi: 10.1038/jidsymp.2015.35. <a href="http://dx.doi.org/10.1038/jidsymp.2015.35">Link to article on publisher's site</a>
dc.identifier.issn1087-0024 (Linking)
dc.identifier.doi10.1038/jidsymp.2015.35
dc.identifier.pmid26551940
dc.identifier.urihttp://hdl.handle.net/20.500.14038/39874
dc.description.abstractDisease is not limited to humans. Rather, humans are but another mammal in a continuum, and as such, often share similar if not identical diseases with other mammalian species. Alopecia areata (AA) is such a disease. Natural disease occurs in humans, nonhuman primates, many domestic animals, and laboratory rodents. However, to be useful as models of human disease, affected animals need to be readily available to the research community, closely resemble the human disease, be easy to work with, and provide reproducible data. To date, the laboratory mouse (most if not all of the C3H substrains) and the Dundee experimental bald rat fit these criteria. Manipulations using full-thickness skin grafts or specific immune cell transfers have improved the models. New mouse models that carry a variety of genetic-based immunodeficiencies can now be used to recapitulate the human immune system and allow for human full-thickness skin grafts onto mice to investigate human-specific mechanistic and therapeutic questions. These models are summarized here including where they can currently be obtained from public access repositories.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=26551940&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC4722955/
dc.subjectAnimal Diseases
dc.subjectDermatology
dc.subjectInvestigative Techniques
dc.subjectLaboratory and Basic Science Research
dc.subjectSkin and Connective Tissue Diseases
dc.titleAnimal Models for Alopecia Areata: What and Where
dc.typeJournal Article
dc.source.journaltitleThe journal of investigative dermatology. Symposium proceedings / the Society for Investigative Dermatology, Inc. [and] European Society for Dermatological Research
dc.source.volume17
dc.source.issue2
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/2677
dc.identifier.contextkey8015329
html.description.abstract<p>Disease is not limited to humans. Rather, humans are but another mammal in a continuum, and as such, often share similar if not identical diseases with other mammalian species. Alopecia areata (AA) is such a disease. Natural disease occurs in humans, nonhuman primates, many domestic animals, and laboratory rodents. However, to be useful as models of human disease, affected animals need to be readily available to the research community, closely resemble the human disease, be easy to work with, and provide reproducible data. To date, the laboratory mouse (most if not all of the C3H substrains) and the Dundee experimental bald rat fit these criteria. Manipulations using full-thickness skin grafts or specific immune cell transfers have improved the models. New mouse models that carry a variety of genetic-based immunodeficiencies can now be used to recapitulate the human immune system and allow for human full-thickness skin grafts onto mice to investigate human-specific mechanistic and therapeutic questions. These models are summarized here including where they can currently be obtained from public access repositories.</p>
dc.identifier.submissionpathoapubs/2677
dc.contributor.departmentDiabetes Center of Excellence
dc.contributor.departmentProgram in Molecular Medicine
dc.source.pages23-6


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