Quantitative magnetic resonance imaging of brain atrophy in a mouse model of Niemann-Pick type C disease
| dc.contributor.author | Totenhagen, John W. | |
| dc.contributor.author | Bernstein, Adam | |
| dc.contributor.author | Yoshimaru, Eriko S. | |
| dc.contributor.author | Erickson, Robert P. | |
| dc.contributor.author | Trouard, Theodore P. | |
| dc.date.accessioned | 2017-06-28T20:34:20Z | |
| dc.date.available | 2017-06-28T20:34:20Z | |
| dc.date.issued | 2017-05-24 | |
| dc.identifier.citation | Quantitative magnetic resonance imaging of brain atrophy in a mouse model of Niemann-Pick type C disease 2017, 12 (5):e0178179 PLOS ONE | en |
| dc.identifier.issn | 1932-6203 | |
| dc.identifier.doi | 10.1371/journal.pone.0178179 | |
| dc.identifier.uri | http://hdl.handle.net/10150/624480 | |
| dc.description.abstract | In 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.sponsorship | NIH NIBIB [R01EB000343] | en |
| dc.language.iso | en | en |
| dc.publisher | PUBLIC LIBRARY SCIENCE | en |
| dc.relation.url | http://dx.plos.org/10.1371/journal.pone.0178179 | en |
| dc.rights | 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. | en |
| dc.rights.uri | https://creativecommons.org/publicdomain/zero/1.0/ | |
| dc.title | Quantitative magnetic resonance imaging of brain atrophy in a mouse model of Niemann-Pick type C disease | en |
| dc.type | Article | en |
| dc.contributor.department | Univ Arizona, Biomed Engn Program | en |
| dc.contributor.department | Univ Arizona, Dept Pediat | en |
| dc.contributor.department | Univ Arizona, Dept Mol & Cellular Biol | en |
| dc.contributor.department | Univ Arizona, Inst B105 | en |
| dc.contributor.department | Univ Arizona, Dept Med Imaging | en |
| dc.contributor.department | Univ Arizona, McKight Brain Inst | en |
| dc.identifier.journal | PLOS ONE | en |
| dc.description.note | Open access journal. | en |
| dc.description.collectioninformation | This 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.version | Final published version | en |
| refterms.dateFOA | 2018-09-11T20:36:17Z | |
| html.description.abstract | In 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. |

