Andrew C. Terentis

Affiliations: 
Chemistry and Biochemistry Florida Atlantic University, Boca Raton, FL, United States 
Area:
Biochemistry
Website:
http://chemistry.fau.edu/directory/terentis.php
Google:
"Andrew Charles Terentis"
Bio:

http://www.worldcat.org/oclc/222702360

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Publications

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Lim YJ, Foo TC, Yeung A, et al. (2018) Human Indoleamine 2,3-Dioxygenase 1 is an Efficient Mammalian Nitrite Reductase. Biochemistry
Cosme PJ, Ye J, Sears S, et al. (2018) Label-Free Confocal Raman Mapping of Transportan in Melanoma Cells. Molecular Pharmaceutics
Corcoran CJ, Tang CC, Lykourinou V, et al. (2018) To be structurally well-defined or not to be, that is not the question for iron(III)–poly(4-Vinylpyridine-co-acrylamide) to exhibit catechol dioxygenase activity! Catalysis Communications. 106: 87-91
Yeung AW, Lim YJ, Hastad M, et al. (2016) Redox Control of the Critical Immune Regulatory Enzyme Indoleamine 2,3-Dioxygenase by NADPH Oxidase 2-Derived Reactive Oxygen Species in Human Monocytes Free Radical Biology and Medicine. 100
Lim YJ, Yeung AW, Ma Y, et al. (2016) Indoleamine 2,3-Dioxygenase Is a Novel Mammalian Nitrite Reductase Free Radical Biology and Medicine. 100
Yeung AW, Terentis AC, King NJ, et al. (2015) Role of indoleamine 2,3-dioxygenase in health and disease. Clinical Science (London, England : 1979). 129: 601-72
Terentis AC, Ye J. (2013) Peptide detection and structure determination in live cells using confocal Raman microscopy. Methods in Molecular Biology (Clifton, N.J.). 1081: 211-36
Freewan M, Rees MD, Plaza TS, et al. (2013) Human indoleamine 2,3-dioxygenase is a catalyst of physiological heme peroxidase reactions: implications for the inhibition of dioxygenase activity by hydrogen peroxide. The Journal of Biological Chemistry. 288: 1548-67
Ye J, Fox SA, Cudic M, et al. (2010) Determination of penetratin secondary structure in live cells with Raman microscopy. Journal of the American Chemical Society. 132: 980-8
Terentis AC, Freewan M, Sempértegui Plaza TS, et al. (2010) The selenazal drug ebselen potently inhibits indoleamine 2,3-dioxygenase by targeting enzyme cysteine residues. Biochemistry. 49: 591-600
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