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Proteomics of neurodegenerative diseases: analysis of human post‐mortem brain
Dementias are prevalent brain disorders in the aged population. Dementias pose major socio‐medical burden, but currently there is no cure available. Novel proteomics approaches hold promise to identify alterations of the brain proteome that could provide clues on disease etiology, and identify candi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899881/ https://www.ncbi.nlm.nih.gov/pubmed/30289976 http://dx.doi.org/10.1111/jnc.14603 |
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author | Li, K. W. Ganz, Andrea B. Smit, August B. |
author_facet | Li, K. W. Ganz, Andrea B. Smit, August B. |
author_sort | Li, K. W. |
collection | PubMed |
description | Dementias are prevalent brain disorders in the aged population. Dementias pose major socio‐medical burden, but currently there is no cure available. Novel proteomics approaches hold promise to identify alterations of the brain proteome that could provide clues on disease etiology, and identify candidate proteins to develop further as a biomarker. In this review, we focus on recent proteomics findings from brains affected with Alzheimer's Disease, Parkinson Disease Dementia, Frontotemporal Dementia, and Amyotrophic Lateral Sclerosis. These studies confirmed known cellular changes, and in addition identified novel proteins that may underlie distinct aspects of the diseases. [Image: see text] https://onlinelibrary.wiley.com/page/journal/14714159/homepage/virtual_issues.htm. |
format | Online Article Text |
id | pubmed-6899881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68998812019-12-19 Proteomics of neurodegenerative diseases: analysis of human post‐mortem brain Li, K. W. Ganz, Andrea B. Smit, August B. J Neurochem Reviews Dementias are prevalent brain disorders in the aged population. Dementias pose major socio‐medical burden, but currently there is no cure available. Novel proteomics approaches hold promise to identify alterations of the brain proteome that could provide clues on disease etiology, and identify candidate proteins to develop further as a biomarker. In this review, we focus on recent proteomics findings from brains affected with Alzheimer's Disease, Parkinson Disease Dementia, Frontotemporal Dementia, and Amyotrophic Lateral Sclerosis. These studies confirmed known cellular changes, and in addition identified novel proteins that may underlie distinct aspects of the diseases. [Image: see text] https://onlinelibrary.wiley.com/page/journal/14714159/homepage/virtual_issues.htm. John Wiley and Sons Inc. 2018-11-22 2019-11 /pmc/articles/PMC6899881/ /pubmed/30289976 http://dx.doi.org/10.1111/jnc.14603 Text en © 2018 The Authors. Journal of Neurochemistry published by John Wiley & Sons Ltd on behalf of International Society for Neurochemistry This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Reviews Li, K. W. Ganz, Andrea B. Smit, August B. Proteomics of neurodegenerative diseases: analysis of human post‐mortem brain |
title | Proteomics of neurodegenerative diseases: analysis of human post‐mortem brain |
title_full | Proteomics of neurodegenerative diseases: analysis of human post‐mortem brain |
title_fullStr | Proteomics of neurodegenerative diseases: analysis of human post‐mortem brain |
title_full_unstemmed | Proteomics of neurodegenerative diseases: analysis of human post‐mortem brain |
title_short | Proteomics of neurodegenerative diseases: analysis of human post‐mortem brain |
title_sort | proteomics of neurodegenerative diseases: analysis of human post‐mortem brain |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899881/ https://www.ncbi.nlm.nih.gov/pubmed/30289976 http://dx.doi.org/10.1111/jnc.14603 |
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