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Scott Barbee photo

Scott Barbee

Professor

scott.barbee@du.edu

303-871-3582 (Office)

http://mysite.du.edu/~sbarbee/

Personal

Seeley G. Mudd Building, 2101 E. Wesley Ave. Denver, CO 80208

What I do

The Barbee lab focuses on understanding roles for RNA/protein interactions in Drosophila models for neurodevelopment and neurodegeneration.

Specialization(s)

Neurodevelopment, neurodegeneration, RNA biology

Degree(s)

  • Ph.D., Cell and Developmental Biology, University of Colorado Health Sciences Center, 2004
  • MS, Zoology and Physiology, University of Wyoming, 1998

Professional Affiliations

  • Front Range Neuroscience Group
  • RNA Society

Research

The Barbee lab uses Drosophila melanogaster and a model to understand the role of RNA/protein granules in neurons.

Areas of Research

Neurodevelopment
neurodegeneration

Key Projects

  • Exploring roles for FMR/P-bodies in presynaptic development

Featured Publications

Nesler, K. R., Starke, E. L., Boin, N. G., Ritz, M., & Barbee, S. A. (2016). Presynaptic CamKII regulates activity-dependent axon terminal growth. Molecular and cellular neurosciences, 76, 33-41.
Nesler, K. R., Sand, R. I., Symmes, B., Boin, N., Laun, A. E., & Barbee, S. A. (2013). The miRNA Pathway Controls Rapid Changes in Activity-Dependent Synaptic Structure at the Drosophila melanogaster Neuromuscular Junction. PLoS ONE, 8(7), e68385.
Pradhan, S. J., Nesler, K. R., Rosen, S. F., Kato, Y., Nakamura, A., Ramaswami, M., & Barbee, S. A. (2012). The conserved P body component HPat/Pat1 negatively regulates synaptic terminal growth at the larval Drosophila neuromuscular junction. Journal of Cell Science, 125(24), 6105-6116.
Barbee, S. A., Extes, P. S., Cziko, A. -M., Hillebrand, J., Luedeman, R. A., Coller, J. M., et al. (2006). Staufen- and FMRP-containing neuronal RNPs are structurally and functionally related to somatic P-bodies. Neuron, 52(6), 997-1009.