This program project outlines a group of studies investigating the basic mechanisms underlying neuronal signalling. A group of six core facilities and six individual projects propose a coordinated, multidisciplinary series of studies on diverse nervous sytems. The core will serve an overall administrative function as well as including centralized data management and analysis, biochemical and electron microscopic instrumentation and electronics and machine shop services. Project 1 will study the mechanisms underlying neuromodulatory control of a completely described neural circuit. Project 2 will study the regulation of mammalian neuronal nicotinic receptors. Project 3 will test the hypothesis that the membranes of radial glial cells upon which the growth cones of embryonic retinal axons travel on their way to the tectum contain factors that support neurite outgrowth. Project 4 will investigate the cellular mechanisms by which leech Retzius neurons change their identity after target contact. Project 5 will test two hypotheses about the molecular modifications of ion channels that occur during embryonic development in Xenopus and Project 6 will study the molecular mechanisms used for signal transduction in Drosophila.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
5P01NS025916-03
Application #
3100222
Study Section
Special Emphasis Panel (SRC (01))
Project Start
1988-03-01
Project End
1991-02-28
Budget Start
1990-03-01
Budget End
1991-02-28
Support Year
3
Fiscal Year
1990
Total Cost
Indirect Cost
Name
University of California San Diego
Department
Type
Schools of Arts and Sciences
DUNS #
077758407
City
La Jolla
State
CA
Country
United States
Zip Code
92093
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French, K A; Murphy, J A; Szczupak, L (1998) Target tissues affect cellular properties of cocultured leech Retzius neurons. J Neurobiol 34:55-68
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Ernsberger, U; Spitzer, N C (1995) Convertible modes of inactivation of potassium channels in Xenopus myocytes differentiating in vitro. J Physiol 484 ( Pt 2):313-29

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