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Axon pathology as a therapeutic target in Huntingdon's disease

ReferenceBBS/E/B/0000F252
Principal Investigator / Supervisor Professor Michael Philip Coleman
Co-Investigators /
Co-Supervisors
Professor Laura Conforti
Institution Babraham Institute
DepartmentBabraham Institute Department
Funding typeResearch
Value (£) 71,167
StatusCompleted
TypeInstitute Project
Start date 15/01/2010
End date 14/07/2011
Duration18 months

Abstract

Huntington's disease is a devastating, progressive deterioration in movement control accompanied by serious psychiatric defects that is strictly inherited. Each generation tends to develop the disease earlier than the last. The gene has been identified and a range of animal models have been generated. The disease mechanism is partially understood but much more needs to be done to move towards therapy. One of the major remaining questions involves the roles of axons, the long wire-like strands connecting each nerve cell with the next. Without these wires, nerve cells cannot function and parts of the nervous system stop working. One problem with studying axons is that they are so long, so it is not easy to see them microscopically in their entirety. We have developed new imaging methods to overcome these problems that we have already applied to mouse models of Alzheimer's disease. Here we will apply these same methods to Huntington's disease to determine where axon pathology fits into the sequence of events leading to this disease.

Summary

unavailable
Committee Not funded via Committee
Research TopicsNeuroscience and Behaviour
Research PriorityX – Research Priority information not available
Research Initiative X - not in an Initiative
Funding SchemeX – not Funded via a specific Funding Scheme
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