Since 1998, the Training Program in Neural Repair at UCLA has enabled a collaborative effort of Faculty with broad expertise in neural repair to provide in depth training in this expanding area of Neuroscience. This application requests support to pursue this program with expanded emphasis on training in skills that are made necessary by the evolution of our field. Our trainees will be schooled not only in the basic principles of neural development and response to injury but also in teamwork, innovative technical approaches, and the challenges of translating this basic understanding into benefits for patients. The training program will continue to draw on the unique strength of a group of faculty actively engaged in basic and clinical research on various aspects of Neural Repair at UCLA. Mentors for the program include established and junior investigators with expertise in stem cell differentiation, cell death and neuroprotection, neural development, plasticity and restoration of function after injury to the central nervous system. They include basic and clinical scientists, many of whom bridge the gap between the laboratory and advances in therapies for neurodegenerative diseases and brain injury. All have vigorous research programs and an active commitment to graduate and post-doctoral education. Graduate students in the training program obtain their degree in the Interdepartmental Graduate Program in Neuroscience or one of the ACCESS biomedical graduate programs at UCLA. The curriculum includes training in broad areas of cellular, molecular and system neuroscience, specialized courses in Neural Repair, weekly meetings with other trainees and faculty, seminars from renowned investigators in the field, and exposure to clinical research linked to advances in the field of neural repair. The trainees are encouraged to explore areas at the junction of multiple fields, to use multiple technical approaches, and to engage in collaborations between laboratories. Our goal is to train a cadre of young investigators that are fully prepared for the changing culture of science while retaining a solid background in their main area of expertise. This training approach will benefit from a history of fruitful collaborations and interactions among the mentors in the program and will continue to produce a cadre of young investigators with the ability to respond to the challenges of reducing the burden of disability resulting from degeneration and disruption of the central nervous system.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Institutional National Research Service Award (T32)
Project #
5T32NS007449-15
Application #
8261395
Study Section
Special Emphasis Panel (ZNS1-SRB-S (16))
Program Officer
Korn, Stephen J
Project Start
1998-07-01
Project End
2014-06-30
Budget Start
2012-07-01
Budget End
2014-06-30
Support Year
15
Fiscal Year
2012
Total Cost
$46,012
Indirect Cost
$12,063
Name
University of California Los Angeles
Department
Neurology
Type
Schools of Medicine
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Linares, Anthony J; Lin, Chia-Ho; Damianov, Andrey et al. (2015) The splicing regulator PTBP1 controls the activity of the transcription factor Pbx1 during neuronal differentiation. Elife 4:e09268
McDowell, Kimberly A; Shin, David; Roos, Kenneth P et al. (2014) Sleep dysfunction and EEG alterations in mice overexpressing alpha-synuclein. J Parkinsons Dis 4:531-539
O'Donnell, Kelley C; Lulla, Aaron; Stahl, Mark C et al. (2014) Axon degeneration and PGC-1?-mediated protection in a zebrafish model of ?-synuclein toxicity. Dis Model Mech 7:571-82
O'Donnell, Kelley C; Vargas, Mauricio E; Sagasti, Alvaro (2013) WldS and PGC-1? regulate mitochondrial transport and oxidation state after axonal injury. J Neurosci 33:14778-90
Watson, M B; Nobuta, H; Abad, C et al. (2013) PACAP deficiency sensitizes nigrostriatal dopaminergic neurons to paraquat-induced damage and modulates central and peripheral inflammatory activation in mice. Neuroscience 240:277-86
Villegas, Rosario; Martin, Seanna M; O'Donnell, Kelley C et al. (2012) Dynamics of degeneration and regeneration in developing zebrafish peripheral axons reveals a requirement for extrinsic cell types. Neural Dev 7:19
Rousso, David L; Pearson, Caroline Alayne; Gaber, Zachary B et al. (2012) Foxp-mediated suppression of N-cadherin regulates neuroepithelial character and progenitor maintenance in the CNS. Neuron 74:314-30
Minassian, Natali A; Lin, Meng-Chin A; Papazian, Diane M (2012) Altered Kv3.3 channel gating in early-onset spinocerebellar ataxia type 13. J Physiol 590:1599-614
Meer, Elliott J; Wang, Dan Ohtan; Kim, Sangmok et al. (2012) Identification of a cis-acting element that localizes mRNA to synapses. Proc Natl Acad Sci U S A 109:4639-44
Hayden, Eric Yale; Teplow, David B (2012) Continuous flow reactor for the production of stable amyloid protein oligomers. Biochemistry 51:6342-9

Showing the most recent 10 out of 31 publications