Literature DB >> 12849185

Disruption of cellular transport: a common cause of neurodegeneration?

Andrew H Crosby1.   

Abstract

In many cases, the clinical manifestations of inherited neurodegenerative disorders appear after decades of normal function, which suggests that neurons may die through cumulative damage. Several genes that cause these diseases have been identified in recent years, but no common pathogenetic mechanism has been found. However, the most recent studies have begun to implicate the same mechanism in a range of neurodegenerative diseases, particularly those that involve motor neurons. The results of these studies suggest that the morphology and energy requirements of neurons make them particularly susceptible to the disruption of cellular transport systems.

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Year:  2003        PMID: 12849185     DOI: 10.1016/s1474-4422(03)00383-1

Source DB:  PubMed          Journal:  Lancet Neurol        ISSN: 1474-4422            Impact factor:   44.182


  5 in total

1.  Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementia.

Authors:  Michael A Simpson; Harold Cross; Christos Proukakis; Anna Pryde; Ruth Hershberger; Arnaud Chatonnet; Michael A Patton; Andrew H Crosby
Journal:  Am J Hum Genet       Date:  2003-10-16       Impact factor: 11.025

2.  The Roc domain of leucine-rich repeat kinase 2 is sufficient for interaction with microtubules.

Authors:  Payal N Gandhi; Xinglong Wang; Xiongwei Zhu; Shu G Chen; Amy L Wilson-Delfosse
Journal:  J Neurosci Res       Date:  2008-06       Impact factor: 4.164

3.  A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia.

Authors:  Johanna A Reed; Phillip A Wilkinson; Heema Patel; Michael A Simpson; Arnaud Chatonnet; Dimitri Robay; Michael A Patton; Andrew H Crosby; Thomas T Warner
Journal:  Neurogenetics       Date:  2005-02-12       Impact factor: 2.660

4.  Mutation in the AP4M1 gene provides a model for neuroaxonal injury in cerebral palsy.

Authors:  Annemieke J M H Verkerk; Rachel Schot; Belinda Dumee; Karlijn Schellekens; Sigrid Swagemakers; Aida M Bertoli-Avella; Maarten H Lequin; Jeroen Dudink; Paul Govaert; A L van Zwol; Jennifer Hirst; Marja W Wessels; Coriene Catsman-Berrevoets; Frans W Verheijen; Esther de Graaff; Irenaeus F M de Coo; Johan M Kros; Rob Willemsen; Patrick J Willems; Peter J van der Spek; Grazia M S Mancini
Journal:  Am J Hum Genet       Date:  2009-06-25       Impact factor: 11.025

5.  Normalization and expression changes in predefined sets of proteins using 2D gel electrophoresis: a proteomic study of L-DOPA induced dyskinesia in an animal model of Parkinson's disease using DIGE.

Authors:  Kim Kultima; Birger Scholz; Henrik Alm; Karl Sköld; Marcus Svensson; Alan R Crossman; Erwan Bezard; Per E Andrén; Ingrid Lönnstedt
Journal:  BMC Bioinformatics       Date:  2006-10-26       Impact factor: 3.169

  5 in total

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