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Nora D. Volkow

Researcher at National Institute on Drug Abuse

Publications -  1038
Citations -  121498

Nora D. Volkow is an academic researcher from National Institute on Drug Abuse. The author has contributed to research in topics: Dopamine & Addiction. The author has an hindex of 165, co-authored 958 publications receiving 107463 citations. Previous affiliations of Nora D. Volkow include National Institutes of Health & North Shore University Hospital.

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Binding of the non-classical cannabinoid CP 55,940, and the diarylpyrazole AM251 to rodent brain cannabinoid receptors.

TL;DR: In vitro autoradiography demonstrated that the distribution of binding sites for [123I]AM251 in rat brain was very similar to published distributions of binding Sites for [3H]CP 55,940, suggesting that AM251 binds to the same site (the cannabinoid CB1 receptor) in rodent brains as CP55,940.
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Laterality Patterns of Brain Functional Connectivity: Gender Effects

TL;DR: The laterality patterns of short-range and long-range functional connectivity and the gender effects on theseLaterality patterns are studied and it is found that males had greater rightward lateralization of brain connectivity in superior temporal, inferior frontal, and inferior occipital cortices (short-range), whereas females had greater leftward lateralized of long- range connectivity in the inferior frontal cortex.
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Ethanol self-administration and ethanol conditioned place preference are reduced in mice lacking cannabinoid CB1 receptors.

TL;DR: The results demonstrate that the cannabinoid CB1 receptor is an essential component of the molecular pathways underlying the reinforcing effects of alcohol, and medications targeting the CB1 receptors may be beneficial for the treatment of alcoholism.
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Measuring age-related changes in dopamine D2 receptors with 11C-raclopride and 18F-N-methylspiroperidol.

TL;DR: Findings of correlational analysis between age and dopamine D2 receptor availability were significant for both ligand and both ligands documented significant age-related decreases in dopamine D 2 receptors that occurred relatively early in life.