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IMA New Directions Short Course - Preliminary Schedule


Typical Daily schedule

8:30-10 General Lecture
10-10:30 Break
10:30-12 General Lecture
12-1 Lunch
1-2 Topical Lecture
2-2:30 Break
2:30-4:30 Problem/Brainstorming Session


Suggested Topics

Day Lecture 1 Lecture 2 Topical Lecture Problem Ideas
#1 Introductions Bacterial Jim Keener quorum sensing
16 Enzyme kinetics chemotaxis biochemical switches in V.fisheri
      lac operon  
#2 Cellular homeostasis molecular Kathryn Tosney homeostasis of
17   motors I growth cone T. californicus
      motility  
#3 Channels, Gates molecular Alex Mogilner survival mechanism
18 Transporters motors II model of cell crawling: of h. pylori
      nematode sperm cell  
#4 Excitability muscle TBA iron metabolism in
19 HH Theory contraction   T. ferroxidans
         
#5 Calcium physics of Lihsia Chen (no problem
20 EC Coupling biological gels cell adhesion session today)
         
#6 Cell Cycle cell Robert Sheaff regul.&differ.
23   migration cell cycle control of urothelial cells
         
#7 Axons and Waves neutrofil Clifton Ragsdale calcium waves
24   chemotaxis neural connection in C. elegans
         
#8 Intercellular large gen&biochem Ron Siegel action poten. propag.
25 communication networks gel drug delivery in frog myocytes
         
#9 Bursting modeling Bob Tranquillo genetic basis of
26 Biochem. oscill. morphogenesis chemotaxis circadian rhythms
  circadian cycles      
#10 Biochemical signalling morphogenesis TBA: (no problem
27 cAMP, E. coli in Drosophila participant talk session today)

Titles:

Ron Siegel

MODELS OF AN AUTONOMOUS RHYTHMIC HORMONE DELIVERY SYSTEM

Certain disorders in sexual development and reproductive function are traced to disorders in the rhythmic, pulsatile secretion of gonadotropin releasing hormone (GnRH) from the hypothalamus. These disorders may require long-term hormone replacement therapy, and rhythmic delivery of GnRH is essential. Since GnRH is exceptionally potent, implantable hormone delivery systems may be considered. We are developing such a system, in which autonomous modulation of permeability of a hydrogel membrane to GnRH is driven by endogenous glucose, via a chemomechanical limit cycle established by feedback between the membrane and an enzyme. Several mathematical models of this system have been developed, with different levels of complexity. We will present results of a lumped, ODE-based model, for which the bifurcation structure has been worked out, and will also progress towards a more detailed, distributed (PDE-based) model.




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Jim Keener 2003-06-02