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LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to Microtubules
Proper lamination of the cerebral cortex requires the orchestrated motility of neurons from their place of birth to their final destination. Improper neuronal migration may result in a wide range of diseases, including brain malformations, such as lissencephaly, mental retardation, schizophrenia, an...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3820303/ https://www.ncbi.nlm.nih.gov/pubmed/24278775 http://dx.doi.org/10.1155/2013/393975 |
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author | Reiner, Orly |
author_facet | Reiner, Orly |
author_sort | Reiner, Orly |
collection | PubMed |
description | Proper lamination of the cerebral cortex requires the orchestrated motility of neurons from their place of birth to their final destination. Improper neuronal migration may result in a wide range of diseases, including brain malformations, such as lissencephaly, mental retardation, schizophrenia, and autism. Ours and other studies have implicated that microtubules and microtubule-associated proteins play an important role in the regulation of neuronal polarization and neuronal migration. Here, we will review normal processes of brain development and neuronal migration, describe neuronal migration diseases, and will focus on the microtubule-associated functions of LIS1 and DCX, which participate in the regulation of neuronal migration and are involved in the human developmental brain disease, lissencephaly. |
format | Online Article Text |
id | pubmed-3820303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-38203032013-11-25 LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to Microtubules Reiner, Orly Scientifica (Cairo) Review Article Proper lamination of the cerebral cortex requires the orchestrated motility of neurons from their place of birth to their final destination. Improper neuronal migration may result in a wide range of diseases, including brain malformations, such as lissencephaly, mental retardation, schizophrenia, and autism. Ours and other studies have implicated that microtubules and microtubule-associated proteins play an important role in the regulation of neuronal polarization and neuronal migration. Here, we will review normal processes of brain development and neuronal migration, describe neuronal migration diseases, and will focus on the microtubule-associated functions of LIS1 and DCX, which participate in the regulation of neuronal migration and are involved in the human developmental brain disease, lissencephaly. Hindawi Publishing Corporation 2013 2013-03-17 /pmc/articles/PMC3820303/ /pubmed/24278775 http://dx.doi.org/10.1155/2013/393975 Text en Copyright © 2013 Orly Reiner. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Reiner, Orly LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to Microtubules |
title | LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to Microtubules |
title_full | LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to Microtubules |
title_fullStr | LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to Microtubules |
title_full_unstemmed | LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to Microtubules |
title_short | LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to Microtubules |
title_sort | lis1 and dcx: implications for brain development and human disease in relation to microtubules |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3820303/ https://www.ncbi.nlm.nih.gov/pubmed/24278775 http://dx.doi.org/10.1155/2013/393975 |
work_keys_str_mv | AT reinerorly lis1anddcximplicationsforbraindevelopmentandhumandiseaseinrelationtomicrotubules |