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dc.contributor.authorTotenhagen, John W.
dc.contributor.authorBernstein, Adam
dc.contributor.authorYoshimaru, Eriko S.
dc.contributor.authorErickson, Robert P.
dc.contributor.authorTrouard, Theodore P.
dc.date.accessioned2017-06-28T20:34:20Z
dc.date.available2017-06-28T20:34:20Z
dc.date.issued2017-05-24
dc.identifier.citationQuantitative magnetic resonance imaging of brain atrophy in a mouse model of Niemann-Pick type C disease 2017, 12 (5):e0178179 PLOS ONEen
dc.identifier.issn1932-6203
dc.identifier.doi10.1371/journal.pone.0178179
dc.identifier.urihttp://hdl.handle.net/10150/624480
dc.description.abstractIn vivo magnetic resonance imaging (MRI) was used to investigate regional and global brain atrophy in the neurodegenerative Niemann Pick Type C1 (NPC1) disease mouse model. Imaging experiments were conducted with the most commonly studied mouse model of NPC1 disease at early and late disease states. High-resolution in vivo images were acquired at early and late stages of the disease and analyzed with atlas-based registration to obtain measurements of twenty brain region volumes. A two-way ANOVA analysis indicated eighteen of these regions were different due to genotype and thirteen showed a significant interaction with age and genotype. The ability to measure in vivo neurodegeneration evidenced by brain atrophy adds to the ability to monitor disease progression and treatment response in the mouse model.
dc.description.sponsorshipNIH NIBIB [R01EB000343]en
dc.language.isoenen
dc.publisherPUBLIC LIBRARY SCIENCEen
dc.relation.urlhttp://dx.plos.org/10.1371/journal.pone.0178179en
dc.rightsThis is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.en
dc.rights.urihttps://creativecommons.org/publicdomain/zero/1.0/
dc.titleQuantitative magnetic resonance imaging of brain atrophy in a mouse model of Niemann-Pick type C diseaseen
dc.typeArticleen
dc.contributor.departmentUniv Arizona, Biomed Engn Programen
dc.contributor.departmentUniv Arizona, Dept Pediaten
dc.contributor.departmentUniv Arizona, Dept Mol & Cellular Biolen
dc.contributor.departmentUniv Arizona, Inst B105en
dc.contributor.departmentUniv Arizona, Dept Med Imagingen
dc.contributor.departmentUniv Arizona, McKight Brain Insten
dc.identifier.journalPLOS ONEen
dc.description.noteOpen access journal.en
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.en
dc.eprint.versionFinal published versionen
refterms.dateFOA2018-09-11T20:36:17Z
html.description.abstractIn vivo magnetic resonance imaging (MRI) was used to investigate regional and global brain atrophy in the neurodegenerative Niemann Pick Type C1 (NPC1) disease mouse model. Imaging experiments were conducted with the most commonly studied mouse model of NPC1 disease at early and late disease states. High-resolution in vivo images were acquired at early and late stages of the disease and analyzed with atlas-based registration to obtain measurements of twenty brain region volumes. A two-way ANOVA analysis indicated eighteen of these regions were different due to genotype and thirteen showed a significant interaction with age and genotype. The ability to measure in vivo neurodegeneration evidenced by brain atrophy adds to the ability to monitor disease progression and treatment response in the mouse model.


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This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
Except where otherwise noted, this item's license is described as This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.