Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Anusch Peyman"'
Autor:
Susan Kühnast, José W.A. van der Hoorn, Elsbet J. Pieterman, Anita M. van den Hoek, William J. Sasiela, Viktoria Gusarova, Anusch Peyman, Hans-Ludwig Schäfer, Uwe Schwahn, J. Wouter Jukema, Hans M.G. Princen
Publikováno v:
Journal of Lipid Research, Vol 55, Iss 10, Pp 2103-2112 (2014)
Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibition is a potential novel strategy for treatment of CVD. Alirocumab is a fully human PCSK9 monoclonal antibody in phase 3 clinical development. We evaluated the antiatherogenic potential of
Externí odkaz:
https://doaj.org/article/53e1f0f319af41358683cedf9dce15c4
Autor:
H.L. Schaefer, Susan Kühnast, Anusch Peyman, Hans M.G. Princen, Uwe Schwahn, A.M. van den Hoek, Joop Jukema, E.J. Pieterman, William J. Sasiela, Viktoria Gusarova, J.W.A. van der Hoorn
Publikováno v:
Atherosclerosis, 235(2), E19-E19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5662a893a215cea6a3e4bab4cd8a3ae
http://hdl.handle.net/1887/103247
http://hdl.handle.net/1887/103247
Autor:
Anusch Peyman, Elsbet J. Pieterman, Hans-Ludwig Schäfer, Anita M. van den Hoek, Uwe Schwahn, Susan Kühnast, José W.A. van der Hoorn, Viktoria Gusarova, William J. Sasiela, J. Wouter Jukema, Hans M.G. Princen
Publikováno v:
Journal of Lipid Research, 10, 55, 2103-2112
Journal of Lipid Research, 55(10), 2103-2112
Journal of Lipid Research, Vol 55, Iss 10, Pp 2103-2112 (2014)
Journal of Lipid Research
Journal of Lipid Research, 55(10), 2103-2112
Journal of Lipid Research, Vol 55, Iss 10, Pp 2103-2112 (2014)
Journal of Lipid Research
Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibition is a potential novel strategy for treatment of CVD. Alirocumab is a fully human PCSK9 monoclonal antibody in phase 3 clinical development. We evaluated the antiatherogenic potential of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f7b3416033f6aa49c622e6e0617ffe8
http://resolver.tudelft.nl/uuid:17ce4754-8fa8-4e08-b529-0e07e5ec7fb3
http://resolver.tudelft.nl/uuid:17ce4754-8fa8-4e08-b529-0e07e5ec7fb3
Autor:
Thomas R. Gadek, Denis Carniato, Martine Gaillard, Marielle Auberval, Jochen Knolle, Roland Baron, Jean-Marie Ruxer, Karl-Heinz Scheunemann, Jean-Francois Gourvest, Gerhard Breipohl, Hans Ulrich Stilz, Volkmar Wehner, Sarah C. Bodary, Bernard Doucet, David William Will, Anusch Peyman
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 11:2011-2015
A series of novel, highly potent αvβ3 antagonists based on a thiophene scaffold and containing an acylguanidine as an Arg-mimetic is described. A number of structural features, such as cyclic versus open guanidine and a variety of lipophilic side c
Autor:
Michael T. Lipari, Timothy J. A. Chico, Hans Ulrich Stilz, Julian Gunn, Michael A. Horton, David C. Crossman, Jochen Knolle, Stuart Bunting, L Shepherd, Clifford Quan, Thomas R. Gadek, Anusch Peyman, Sheila E. Francis, Sherron Bullens, Janet Chamberlain, N Arnold
Publikováno v:
Circulation. 103:1135-1141
Background —Thrombosis and neointima formation limit the efficacy of coronary angioplasty (PTCA). Clinical trials have implicated the adhesion molecules integrin α IIb β 3 and integrin α v β 3 in these processes. The roles of these molecules in
Publikováno v:
Angewandte Chemie. 112:2996-2999
Autor:
Jochen Knolle, Denis Carniato, Hans Ulrich Stilz, Jean-Marie Ruxer, Karl-Heinz Scheunemann, Anusch Peyman, Gerhard Breipohl, Thomas R. Gadek, Volkmar Wehner, Jean-Francois Gourvest, Sarah C. Bodary
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 10:179-182
The synthesis of a series of RGD mimetic α V β 3 antagonists containing a hydantoin scaffold is shown. The results demonstrate some of the structural requirements for the design of selective α V β 3 antagonists (vs α IIb β 3 ) in terms of the A
Publikováno v:
Angewandte Chemie International Edition. 37:2796-2823
The astonishing discovery that peptide nucleic acids (PNAs, B=nucleobase), in spite of their drastic structural difference to natural DNA, are better nucleic acid mimetics than many other oligonucleotides has resulted in an explosion of research into
Publikováno v:
Angewandte Chemie. 110:2954-2983
Auserst uberraschend war die Erkenntnis, das Peptidnucleinsauren (PNAs, B=Nucleobase) trotz ihrer drastisch vom naturlichen DNA-Ruckgrat abweichenden Struktur besser als die meisten Oligonucleotidderivate als Nucleinsauremimetica genutzt werden konne
Autor:
Gerhard Breipohl, Eugen Uhlmann, Anusch Peyman, Caroline Weiser, David William Will, Sascha Augustin, Konrad Wagner
Publikováno v:
Angewandte Chemie. 109:2919-2922