Amanda M. Barkley‐Levenson

This study investigates the effects of Slc39a8 genotype on ethanol consumption and related behaviors in mice, finding reduced alcohol intake in heterozygous knockout mice without changes in locomotion or affective behaviors.

This study shows that Dpp6 knockout mice exhibit sex-dependent changes in ethanol-related behaviors, including increased conditioned place preference and anxiolytic effects.

This study examines the effects of binge-like ethanol drinking on nest building behavior in mice, finding reduced nest scores at 7 days post-drinking but not at 48 hours.

This study examines the neurometabolomic effects of wood smoke exposure in aged mice and evaluates the protective effects of anti-aging therapies.

This study investigates whether GLO1 inhibition affects cocaine or oxycodone-induced locomotor activity and conditioned place preference, finding no significant effects.

This study identifies indirect genetic effects (IGE) from peers in mice using igeGWAS and confirms IGE genes through knockout experiments.

This study shows that genetic and pharmacological manipulations of GLO1 affect ethanol withdrawal seizure severity in mice.

This study uses a discrete-trial current-intensity intracranial self-stimulation procedure to assess both reward-enhancing and aversive effects of ethanol in mice, finding dose-dependent changes in response thresholds.

This study investigates whether GLO1 inhibition or overexpression affects ethanol's locomotor effects, finding no such alteration despite previous effects on ethanol consumption.

This study shows that inhibiting glyoxalase 1 with pBBG reduces alcohol self-administration in both dependent and nondependent rats, with greater effect in dependent animals.