Funding Agency

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
5R29AA009212-06
Application #
2045432
Study Section
Biochemistry, Physiology and Medicine Subcommittee (ALCB)
Project Start
1995-08-01
Project End
1998-03-31
Budget Start
1996-04-01
Budget End
1998-03-31
Support Year
6
Fiscal Year
1996
Total Cost
Indirect Cost

  Institution

Name
University of Alabama Birmingham
Department
Physiology
Type
Schools of Dentistry
DUNS #
004514360
City
Birmingham
State
AL
Country
United States
Zip Code
35294

  Publications

Ueno, S; Bracamontes, J; Zorumski, C et al. (1997) Bicuculline and gabazine are allosteric inhibitors of channel opening of the GABAA receptor. J Neurosci 17:625-34
Williams, K L; Tucker, J B; White, G et al. (1997) Lactone modulation of the gamma-aminobutyric acid A receptor: evidence for a positive modulatory site. Mol Pharmacol 52:114-9
Amin, J; Brooks-Kayal, A; Weiss, D S (1997) Two tyrosine residues on the alpha subunit are crucial for benzodiazepine binding and allosteric modulation of gamma-aminobutyric acidA receptors. Mol Pharmacol 51:833-41
Chang, Y; Wang, R; Barot, S et al. (1996) Stoichiometry of a recombinant GABAA receptor. J Neurosci 16:5415-24