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Scott A. Chasse

Researcher at University of North Carolina at Chapel Hill

Publications -  12
Citations -  780

Scott A. Chasse is an academic researcher from University of North Carolina at Chapel Hill. The author has contributed to research in topics: GTPase-activating protein & RGS Proteins. The author has an hindex of 9, co-authored 11 publications receiving 729 citations. Previous affiliations of Scott A. Chasse include Uniformed Services University of the Health Sciences & University of Virginia.

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Journal ArticleDOI

A Seven-Transmembrane RGS Protein That Modulates Plant Cell Proliferation

TL;DR: An RGS protein (AtRGS1) in Arabidopsis that has a predicted structure similar to a GPCR as well as an RGS box with GTPase accelerating activity is identified, suggesting that AtRGS 1 is a critical modulator of plant cell proliferation.
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Association of a single nucleotide polymorphism in neuronal acetylcholine receptor subunit alpha 5 (CHRNA5) with smoking status and with 'pleasurable buzz' during early experimentation with smoking

TL;DR: The polymorphism in the CHRNA5 subunit was shown to be associated significantly with enhanced pleasurable responses to initial cigarettes in regular smokers in an a priori test, suggesting that phenotypes related to subjective experiences upon smoking experimentation may mediate the development of nicotine dependence.
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Structural basis of RXR-DNA interactions

TL;DR: The structure shows how a gene-regulatory site can induce conformational changes in a transcription factor that promote homo-cooperative assembly and illustrates how site selection is achieved in this large eukaryotic transcription factor family through discrete protein-protein interactions and the use of tandem DNA binding sites with characteristic spacings.
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Genome-scale analysis reveals Sst2 as the principal regulator of mating pheromone signaling in the yeast Saccharomyces cerevisiae.

TL;DR: It is suggested that Sst2 is the principal regulator of Gpa1-mediated signaling in vivo but that other proteins also contribute in distinct ways to pathway regulation.