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Larry G. Moss

Researcher at Duke University

Publications -  45
Citations -  4595

Larry G. Moss is an academic researcher from Duke University. The author has contributed to research in topics: Islet & Zebrafish. The author has an hindex of 27, co-authored 44 publications receiving 4423 citations. Previous affiliations of Larry G. Moss include Tufts Medical Center & University of California, San Francisco.

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The molecular structure of green fluorescent protein

TL;DR: The crystal structure of recombinant wild-type green fluorescent protein (GFP) has been solved to a resolution of 1.9 Å by multiwavelength anomalous dispersion phasing methods and the identification of the dimer contacts may allow mutagenic control of the state of assembly of the protein.
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Identification of β-cell-specific insulin gene transcription factor RIPE3b1 as mammalian MafA

TL;DR: Cloning of the human mafA (hMafA) is reported and it is demonstrated that it can specifically bind the insulin enhancer element RIPE3b and activate insulin-gene expression, suggesting that mMafA has an essential role in the function and differentiation of β-cells and thus may be associated with the pathophysiological origins of diabetes.
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Overexpression of Perilipin A and B Blocks the Ability of Tumor Necrosis Factor α to Increase Lipolysis in 3T3-L1 Adipocytes

TL;DR: These results provide the first evidence of how perilipin functions and suggest that TNF-α regulates lipolysis, in part, by decreasing perilipIn protein levels at the lipid droplet surface.
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Regulation of insulin gene expression by glucose and calcium in transfected primary islet cultures.

TL;DR: Experiments showing a reduction in the response to glucose in the presence of the calcium channel blocker verapamil suggest that calcium plays a role in the glucose response, possibly via regulation of factors interacting with this limited portion of the insulin gene.
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The insulin and islet amyloid polypeptide genes contain similar cell-specific promoter elements that bind identical beta-cell nuclear complexes.

TL;DR: In this article, the functions of isolated portions of the insulin, IAPP, and beta GK promoters were studied by using transient expression and DNA binding assays, showing that the patterns of expression of the beta-cell-specific genes result in part from sharing the same transcriptional regulators.