Zobrazeno 1 - 7
of 7
pro vyhledávání: '"V M, Gehle"'
Publikováno v:
Alcoholism, clinical and experimental research. 25(12)
In previous studies, genetic correlations were observed between hypnotic sensitivity to ethanol and high-affinity neurotensin receptor (NTS1) binding. Provisional quantitative trait loci (QTLs) were identified for these traits, and some of these QTLs
Autor:
V M, Gehle, V G, Erwin
Publikováno v:
Alcoholism, clinical and experimental research. 24(5)
It has been proposed that development of tolerance to the behavioral effects of ethanol depends on the degree of impairment produced by the drug; that is, more sensitive individuals should develop greater tolerance. Tests of this hypothesis with resp
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 293(1)
Genetic regulation of acute tolerance to ethanol may be associated with ethanol consumption and other ethanol-related behaviors in rodents. We have used lines of mice, selectively bred for high and low acute functional tolerance (HAFT and LAFT, respe
Publikováno v:
Alcoholism, clinical and experimental research. 23(11)
Low doses of the N-methyl-D-aspartate receptor (NMDAR) antagonist MK-801 (dizocilpine) or ethanol increase locomotor activity to a lesser extent in long-sleep (LS), than in short-sleep (SS), mice. LS mice also have fewer brain [3H]MK-801 binding site
Autor:
V M, Gehle, V G, Erwin
Publikováno v:
Alcoholism, clinical and experimental research. 22(2)
The C57BL/6, DBA/2, and recombinant inbred (RI) strains derived from them (BxD RIs) are the most frequently studied mouse strains with regard to genetic regulation of voluntary ethanol consumption (YEC). We have studied VEC in an alternate genetic mo
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 280(2)
We have analyzed LSXSS recumbinant inbred for ethanol-induced activity using 2.0 g/kg ethanol and a new method we call ethanol activation slope. The ethanol activation slope provides a robust dose-response measure of ethanol activation, independent o
Autor:
K, Sumikawa, V M, Gehle
Publikováno v:
The Journal of biological chemistry. 267(9)
Each subunit of the nicotinic acetylcholine receptor (AChR) contains two conserved cysteine residues, which are known to form a disulfide bond, in the N-terminal extracellular domain. The role of this retained structural feature in the biogenesis of