Zobrazeno 1 - 10
of 11
pro vyhledávání: '"H. J. M. Gijsen"'
Autor:
A. Nash, H. J. M. Gijsen, B. J. Hrupka, K. S.-L. Teng, S. F. Lichtenthaler, H. Takeshima, J. M. Gunnersen, K. M. Munro
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract BACE inhibitors, which decrease BACE1 (β-secretase 1) cleavage of the amyloid precursor protein, are a potential treatment for Alzheimer’s disease. Clinical trials using BACE inhibitors have reported a lack of positive effect on patient s
Externí odkaz:
https://doaj.org/article/30fc73a123fe4f83943a0c12121c8a83
Autor:
Stefan F. Lichtenthaler, Brian Joel Hrupka, H. J. M. Gijsen, Hiroshi Takeshima, Kathleen Sue Lyn Teng, Jenny M. Gunnersen, Kathryn M. Munro, Amelia Nash
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Scientific reports 11(1), 15084 (2021). doi:10.1038/s41598-021-94369-0
Scientific Reports
Scientific reports 11(1), 15084 (2021). doi:10.1038/s41598-021-94369-0
Scientific Reports
BACE inhibitors, which decrease BACE1 (β-secretase 1) cleavage of the amyloid precursor protein, are a potential treatment for Alzheimer’s disease. Clinical trials using BACE inhibitors have reported a lack of positive effect on patient symptoms a
Autor:
Brian Joel Hrupka, H. J. M. Gijsen, Hiroshi Takeshima, Amelia Nash, Kathryn M. Munro, K. S-L. Teng, Jenny M. Gunnersen, Stefan F. Lichtenthaler
BackgroundBACE inhibitors, which decrease BACE1 (β-secretase 1) cleavage of the amyloid precursor protein, are a potential treatment for Alzheimer’s disease. Clinical trials using BACE inhibitors have reported a lack of positive effect on patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee73d7f53e2f0fe3a2f62895a01a9612
https://doi.org/10.21203/rs.3.rs-396650/v1
https://doi.org/10.21203/rs.3.rs-396650/v1
Autor:
R. V. A. Orru, J. B. P. A. Wijnberg, C. G. J. M. Seelen, Gerrit A. Stork, K. Kanai, H. J. M. Gijsen, A. De Groot, S.M. van der Kerk
Publikováno v:
ChemInform. 22
Publikováno v:
ChemInform. 22
Publikováno v:
ChemInform. 25
Publikováno v:
ChemInform. 25
Publikováno v:
Tetrahedron. 47:4409-4416
Starting from the readily available chiral synthon 5 the sesquiterpene ether (−)-kessane (1) can be synthesized in a 9 steps reaction sequence in an overall yield of 43%.
Autor:
F. G. Moers, Ae. de Groot, Jan M. M. Smits, H. J. M. Gijsen, J. B. P. A. Wijnberg, P.T. Beuskens
Publikováno v:
Journal of Crystallographic and Spectroscopic Research. 23:833-835
Autor:
J. Bermejo Barrera, H. J. M. Gijsen, A. G. González, Ae. de Groot, G. Prota, J. B. P. A. Wijnberg
Publikováno v:
Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products ISBN: 9783709193396
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d279f798ef55f694531deb72b90fe57
https://doi.org/10.1007/978-3-7091-9337-2
https://doi.org/10.1007/978-3-7091-9337-2