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Bernard Masereel

Researcher at Université de Namur

Publications -  186
Citations -  6688

Bernard Masereel is an academic researcher from Université de Namur. The author has contributed to research in topics: Thromboxane-A synthase & Thromboxane. The author has an hindex of 42, co-authored 185 publications receiving 6181 citations. Previous affiliations of Bernard Masereel include Université libre de Bruxelles & University of Liège.

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Reversal of tumoral immune resistance by inhibition of tryptophan 2,3-dioxygenase

TL;DR: A TDO inhibitor was developed, which, upon systemic treatment, restored the ability of mice to reject TDO-expressing tumors and established proof-of-concept for the use of TDO inhibitors in cancer therapy.
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An overview of inhibitors of Na(+)/H(+) exchanger.

TL;DR: Extensive pre-clinical studies indicated that NHE inhibitors afford substantial protection in different animal models of myocardial ischemia (MI) and reperfusion, but the results of clinical trials involving eniporide and cariporides were mixed.
Journal Article

Reversal of Tumoral Immune Resistance by Inhibition of Tryptophan 2,3-Dioxygenase (TDO): Design, Synthesis and Preclinical Evaluation of a Novel TDO Inhibitor.

TL;DR: In this paper, the authors showed that enzymatically active Tryptophan 2,3-dioxygenase (TDO) is expressed in a significant proportion of human tumors and developed a TDO inhibitor which, upon systemic treatment, restored the ability of mice to reject TDO-expressing tumors.
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Targeting tumor-associated carbonic anhydrase IX in cancer therapy

TL;DR: Selective CA IX inhibitors could prove useful for elucidating the role of CA IX in hypoxic cancers, for controlling the pH imbalance in tumor cells and for developing diagnostic or therapeutic applications for tumor management.
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Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins.

TL;DR: A new series of variously substituted coumarins and a thiocoumarin for their interaction with 13 mammalian CA isoforms, detecting low nanomolar and isoform selective inhibitors, afford isoform-selective CAIs with various biomedical applications, which render these classes of compounds superior to the clinically used sulfonamides.