the goal of this project is to define the mechanisms by which input from the retina and LGN directs the postnatal development of orientation selectivity in the ferret. This will be accomplished by (1) blocking retinal output with tetrodotoxin during development and (2) preventing axons from the LGN from reaching the cortex by destroying the cortical subplate. Following recovery from these manipulations,their effetcts will be assessed by optical and single unit recordings in the adult accompanied by an assessment of alterations in the cortical anatomy. The goal will be to describe disruptions in the normal corresponding physiological changes in neural response properties.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32EY006880-01
Application #
2535990
Study Section
Visual Sciences B Study Section (VISB)
Project Start
1998-03-30
Project End
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
1
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Physiology
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Frank, M G; Issa, N P; Stryker, M P (2001) Sleep enhances plasticity in the developing visual cortex. Neuron 30:275-87