Zobrazeno 1 - 10
of 71
pro vyhledávání: '"P. W. Schiller"'
Autor:
M. Weber, U. Klein, A. Weigert, W. Schiller, V. Bayley-Ezziddin, D. C. Wirtz, A. Welz, N. Werner, E. Grube, G. Nickenig, J.-M. Sinning, A. Ghanem
Publikováno v:
Journal of Interventional Cardiology, Vol 2021 (2021)
Background. Physiotherapy prior to open-heart surgery lowers the rate of pneumonia and length of the hospital stay. Pneumonia is a major contributor to short-term mortality following transcatheter aortic valve replacement (TAVR). Hence, we hypothesiz
Externí odkaz:
https://doaj.org/article/ffdd9ebc07cd40218cf47159605a6351
Autor:
Jordan D Lewicky, Alexandrine L Martel, Nya L Fraleigh, Amanda Boraman, Thi M-D Nguyen, Peter W Schiller, Tze Chieh Shiao, René Roy, Hoang-Thanh Le
Publikováno v:
PLoS ONE, Vol 13, Iss 9, p e0204472 (2018)
The therapeutic application of peptide-based drugs is significantly limited by the rapid proteolytic degradation that occurs when in blood. Encapsulation of these peptide structures within a delivery system, such as liposomes, can greatly improve bot
Externí odkaz:
https://doaj.org/article/84e1b41a2ce54f7cad73c25d5a19d4af
The Cardiovascular and Renal Effects of the Potent and Highly Selective μ Opioid Agonist [Dmt1]DALDA
Publikováno v:
Journal of Cardiovascular Pharmacology. 44:651-658
The cardiovascular and renal effects of a mu opioid agonist, [Dmt]DALDA, were studied in conscious Sprague-Dawley rats. During the first hour postinjection, [Dmt]DALDA (0.025-250 microg/rat, IV) evoked a dose-dependent diuresis. The dose of 2.5 micro
Publikováno v:
Acta Biochimica Polonica. 48:1159-1163
A new pathway leading to a mixture of four isomers of 4-aminopyroglutamic acid is described. Michael type addition of Z-deltaAla-OMe to enolates prepared from acylaminomalonates, followed by hydrolysis and decarboxylation give protected 4-aminopyrogl
Autor:
Atsushi Yagasaki, P. W. Schiller, Walter G. Klemperer, Roy P. Planalp, Bianxiao Zhong, Todd A. Eberspacher, Victor W. Day
Publikováno v:
Inorganic Chemistry. 32:1629-1637
Autor:
P. W. Schiller
Publikováno v:
ChemInform. 23
Autor:
Julie L. Lavoie, Paul Tan, P. W. Schiller, S. Kajla, T.M.D. Nguyen, Catherine Michel, Jolanta Gutkowska, C. Blais
Publikováno v:
Canadian Journal of Diabetes. 39:169
Autor:
N. N. Chung, Klaus Burger, Michael Thormann, P. W. Schiller, Hans-Jörg Hofmann, Norbert Sewald, M. Gussmann, Dirk Winkler
Publikováno v:
Peptide Science — Present and Future ISBN: 0792352718
Several peptides isolated from mammalian brain are endogenous agonists of the opiate receptors (μ, δ, and κ ). They are of current interest in medicinal chemistry and neurobiology because of their mediation of strong analgesic effects. New analogu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4c9427db0a6a0925582a4505e7e53fc
https://doi.org/10.1007/0-306-46864-6_156
https://doi.org/10.1007/0-306-46864-6_156
Publikováno v:
The journal of peptide research : official journal of the American Peptide Society. 65(6)
The dermorphin-derived tetrapeptide H-Dmt-d-Arg-Phe-Lys-NH(2) (Dmt = 2',6'-dimethyltyrosine) ([Dmt(1)]DALDA) is a highly potent and selective mu-opioid agonist capable of crossing the blood-brain barrier and producing a potent, centrally mediated ana
Publikováno v:
The journal of peptide research : official journal of the American Peptide Society. 65(1)
The cyclic enkephalin analog H-Tyr-c[D-Cys-Gly-Phe(pNO(2))-D-Cys]NH(2) is a highly potent opioid agonist with IC(50)s of 35 pm and 19 pm in the guinea-pig ileum (GPI) and mouse vas deferens (MVD) assays, respectively. The Phe(1)-analog of this peptid