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Ami Graham

Researcher at University of Texas Southwestern Medical Center

Publications -  12
Citations -  4263

Ami Graham is an academic researcher from University of Texas Southwestern Medical Center. The author has contributed to research in topics: Nucleus accumbens & Ventral tegmental area. The author has an hindex of 11, co-authored 12 publications receiving 3811 citations. Previous affiliations of Ami Graham include University of Texas at Dallas.

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Molecular Adaptations Underlying Susceptibility and Resistance to Social Defeat in Brain Reward Regions

TL;DR: It is shown that molecular recapitulations of three prototypical adaptations associated with the unsusceptible phenotype are each sufficient to promote resistant behavior and validate a multidisciplinary approach to examine the neurobiological mechanisms of variations in stress resistance.
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Mania-like behavior induced by disruption of CLOCK.

TL;DR: It is shown that mice carrying a mutation in the Clock gene display an overall behavioral profile that is strikingly similar to human mania, including hyperactivity, decreased sleep, lowered depression-like behavior, lower anxiety, and an increase in the reward value for cocaine, sucrose, and medial forebrain bundle stimulation.
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Histone Deacetylase 5 Epigenetically Controls Behavioral Adaptations to Chronic Emotional Stimuli

TL;DR: It is suggested that proper balance of histone acetylation is a crucial factor in the saliency of a given stimulus and that disruption of this balance is involved in the transition from an acute adaptive response to a chronic psychiatric illness.
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Knockdown of Clock in the Ventral Tegmental Area Through RNA Interference Results in a Mixed State of Mania and Depression-Like Behavior

TL;DR: In this paper, the authors used RNA interference and viral-mediated gene transfer to knock down Clock expression specifically in the ventral tegmental area (VTA) of mice, and found that knockdown of Clock, particularly in the VTA, results in hyperactivity and a reduction in anxiety-related behavior, which is similar to the phenotype of the Clock Δ19 mice.