Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Paul Bischoff"'
Three cohorts of six pre-service Earth Science teachers (undergraduate majors in Earth Science Education) participated in summer research experiences focused on developing dynamic physical models of Earth processes to help middle and high school stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3b2ecbdda81c4437aabce6fb8305c42
Autor:
Yasuyoshi Iso, Shigeru Ando, Harrie J.M. Gijsen, Yasuto Kido, Shinji Suzuki, Herman Borghys, Kenji Morimoto, Vijay Urmaliya, Deborah Dhuyvetter, Takahiko Yamamoto, Ard Teisman, Gaku Sakaguchi, Naoki Kanegawa, Nigel Austin, Eriko Matsuoka, An Van Den Bergh, Hisanori Ito, Takuya Oguma, Francois Paul Bischoff, Tamio Fukushima, Peter Verboven, Tomoyuki Kawachi, Kenji Nakahara, Yoshinori Yamano, Kosuke Anan, Ken-ichi Kusakabe
Publikováno v:
ChemMedChem. 14:1894-1910
The β-site amyloid precursor protein cleaving enzyme 1 (BACE1, also known as β-secretase) is a promising target for the treatment of Alzheimer's disease. A pKa lowering approach over the initial leads was adopted to mitigate hERG inhibition and P-g
Autor:
Robert George Manley, Glenn Packard, Viraj Garg, Paul Bischoff, Karl D. Hirschman, Karthik Bhadrachalam, Adam Rosenfeld
Publikováno v:
ECS Transactions. 86:57-72
The development of low-temperature polycrystalline silicon (LTPS) based on excimer laser annealing (ELA) has realized CMOS TFTs with notable electrical performance. The flat-panel display industry is searching for alternative LTPS strategies which ar
Autor:
Manuel Hitzenberger, Francois Paul Bischoff, Marc Mercken, Sam Lismont, Katarzyna Marta Zoltowska, Natalie S. Ryan, Martin Zacharias, Dieter Petit, Lucía Chávez-Gutiérrez
Publikováno v:
The EMBO Journal
γ-Secretase complexes (GSECs) are multimeric membrane proteases involved in a variety of physiological processes and linked to Alzheimer's disease (AD). Presenilin (PSEN, catalytic subunit), Nicastrin (NCT), Presenilin Enhancer 2 (PEN-2), and Anteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60075822ea25a5936594d3aafd319d16
https://lirias.kuleuven.be/handle/123456789/654197
https://lirias.kuleuven.be/handle/123456789/654197
Autor:
Garrett Berlond Minne, Michel Surkyn, Harrie J.M. Gijsen, Francois Paul Bischoff, Nigel Austin, Marc Mercken, Didier Berthelot, Chiara Zavattaro, Ishtiyaque Ahmad, Gregor James Macdonald, Adriana Ingrid Velter, Michel Anna Jozef De Cleyn, Deborah Dhuyvetter, Sven Franciscus Anna Van Brandt, Serge Maria Aloysius Pieters, Yves Emiel Maria Van Roosbroeck, Swapan Kumar Samanta, Herman Borghys
Publikováno v:
Bioorganicmedicinal chemistry letters. 29(14)
The discovery, design and synthesis of a new series of GSMs is described. The classical imidazole heterocycle has been replaced by a cyano group attached to an indole nucleus. The exploration of this series has led to compound 26-S which combined hig
Publikováno v:
Geological Society of America Abstracts with Programs.
Autor:
Brian Lord, Jason C. Rech, Brian Scott, Kirsten L. Morton, Nicholas I. Carruthers, Victor Contreras, Natalie A. Hawryluk, Qi Wang, Xiaohui Jiang, Francois Paul Bischoff, Michael A. Letavic, Alan D. Wickenden, Pascal Bonaventure, Hong Ao, Serge Maria Aloysius Pieters, Zachary S. Sales, Anindya Bhattacharya, Adriana Ingrid Velter
Publikováno v:
ACS Medicinal Chemistry Letters. 4:419-422
The synthesis and preclinical characterization of two novel, brain penetrating P2X7 compounds will be described. Both compounds are shown to be high potency P2X7 antagonists in human, rat, and mouse cell lines and both were shown to have high brain c
Publikováno v:
Geological Society of America Abstracts with Programs.
Autor:
Josée E. Leysen, Margot H. Bakker, R. P. Klok, Albert D. Windhorst, François Paul Bischoff, Ludo Edmond Josephine Kennis, L. Heylen, Jacobus D. M. Herscheid, Xavier Langlois, Mirek Jurzak, M. Van der Mey
Publikováno v:
Bioorganic and Medicinal Chemistry, 14(13), 4526-4534. Elsevier Limited
Van der Mey, M, Windhorst, A D, Klok, R P, Herscheid, J D M, Kennis, L E, Bischoff, F, Bakker, M, Langlois, X, Heylen, L, Jurzak, M & Leysen, J E 2006, ' Synthesis and biodistribution of [ 11 C]R107474, a new radiolabeled α 2-adrenoceptor antagonist ', Bioorganic and Medicinal Chemistry, vol. 14, no. 13, pp. 4526-4534 . https://doi.org/10.1016/j.bmc.2006.02.029
Van der Mey, M, Windhorst, A D, Klok, R P, Herscheid, J D M, Kennis, L E, Bischoff, F, Bakker, M, Langlois, X, Heylen, L, Jurzak, M & Leysen, J E 2006, ' Synthesis and biodistribution of [ 11 C]R107474, a new radiolabeled α 2-adrenoceptor antagonist ', Bioorganic and Medicinal Chemistry, vol. 14, no. 13, pp. 4526-4534 . https://doi.org/10.1016/j.bmc.2006.02.029
R107474, 2-methyl-3-[2-(1,2,3,4-tetrahydrobenzo[4,5]furo[3,2-c]pyridin-2-yl)ethyl]-4H-pyrido[1,2-a]pyrimidin-4-one, was investigated using in vitro and in vivo receptor assays and proved to be a potent and relatively selective α2-adrenoceptor antago
Autor:
Dominique Jean-Pierre Mabire, Alain Philippe Poncelet, Anne Simone Josephine Lesage, Ludy van Beijsterveldt, François Paul Bischoff, Ria Wouters, Christophe Adelinet, Yvan Rene Simonnet, Sophie Coupa, Marc Venet
Publikováno v:
Journal of Medicinal Chemistry. 48:2134-2153
We describe the discovery and the structure-activity relationship of a new series of quinoline derivatives acting as selective and highly potent noncompetitive mGlu1 antagonists. We first identified cis-10 as a fairly potent mGlu1 antagonist (IC(50)