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Thomas A. Wynn

Researcher at University of California, San Diego

Publications -  300
Citations -  61781

Thomas A. Wynn is an academic researcher from University of California, San Diego. The author has contributed to research in topics: Cytokine & Schistosoma mansoni. The author has an hindex of 111, co-authored 276 publications receiving 52854 citations. Previous affiliations of Thomas A. Wynn include Los Alamos National Laboratory & Urbana University.

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Journal ArticleDOI

Schistosoma mansoni arginase shares functional similarities with human orthologs but depends upon disulphide bridges for enzymatic activity.

TL;DR: It is demonstrated for the first time that several developmental stages of the human parasite Schistosoma mansoni express arginase, which is responsible for the hydrolysis of l-arginine to l-ornithine and urea, and it is discovered that S. mansoniArginase is well adapted to the physiological conditions that exist in the human host.
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Heat shock protein 70 is a positive regulator of airway inflammation and goblet cell hyperplasia in a mouse model of allergic airway inflammation.

TL;DR: A pathogenic role for HSp70 is identified in hematopoietic cells during allergic airway inflammation; this illustrates the potential utility of targeting Hsp70 to alleviate allergen-induced Th2 cytokines, goblet cell hyperplasia, and airwayinflammation.
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Local Structure of Glassy Lithium Phosphorus Oxynitride Thin Films: A Combined Experimental and Ab Initio Approach

TL;DR: In this paper, a structural model of RF-sputtered LiPON is provided, and the short-range structure results from 1D and 2D solid-state NMR experiments are compared with first principles chemical shielding calculations of Li-P-O/N crystals and ab initio molecular dynamics-generated amorphous LiPon models.
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Cytokines as determinants of disease and disease interactions.

TL;DR: The immune response to pathogens results in both host resistance and immunopathology, and Cytokines and in particular those lymphokines produced by Th1 and Th2 cells play a key role in determining the balance between these two immunologic outcomes.