Zobrazeno 1 - 10
of 602
pro vyhledávání: '"A. Schwink"'
Publikováno v:
In Applied Radiation and Isotopes January 2017 119:1-5
Autor:
Joseph Gagliardo, J. P. Grossman, Andrew Parker, Anthony Forte, Jeremy Hunt, Peter J. Adams, Brian Towles, Adam McLaughlin, Michael Theobald, Jochen Spengler, Jon L. Peticolas, Keun Sup Shim, Mark A. Moraes, Madeleine J. Weingarten, Naseer Siddique, Gennette Gill, Lawrence J. Nociolo, Michael Wazlowski, Jhanvi Bhatt, Bryan L. Jackson, Brannon Batson, Timothy Correia, Jeffrey S. Kuskin, T. Carl Schwink, Stanley C. Wang, Terry Quan, Roy J. Mader, Alistair Bell, William Vick, Lief O'Donnell, Maria Gorlatova, Peter Feldmann, Bruce Edwards, Mollie M. Kirk, Mohamed H. Nasr, J. Adam Butts, Richard McGowen, John M. Williams, Brian Greskamp, David E. Shaw, Christopher H. Fenton
Publikováno v:
HCS
• Understand biomolecular systems through their motions •Numerical integration of Newton's laws of motion — Model atoms as point masses — Compute forces on every atom based on current positions — Update atom velocities and positions in disc
Autor:
Schwink, Mirjam1
Publikováno v:
Zeitschrift für das Gesamte Kreditwesen. 7/1/2022, Vol. 75 Issue 13, p14-17. 4p.
Publikováno v:
Journal of the Mechanical Behavior of Materials, Vol 11, Iss 1-3, Pp 157-164 (2000)
Externí odkaz:
https://doaj.org/article/dabf08a1776b4fc0bfc0d774fcb0e70a
Publikováno v:
Applied Radiation and Isotopes. 119:1-5
A radiochemical analysis of the valence state of uranium isotopes in minerals involves isolation of the U(IV) and U(VI) valence forms and determination of the radioactivity of the 234U and 238U isotopes in each fraction. If the nuclear decay of the u
Publikováno v:
In Tetrahedron 2003 59(18):3201-3217
Publikováno v:
Journal of Medicinal Chemistry. 59:3579-3592
In this Perspective, recent advances and challenges in the development of GPR119 agonists as new oral antidiabetic drugs will be discussed. Such agonists are expected to exhibit a low risk to induce hypoglycemia as well as to have a beneficial impact
Autor:
Raisa Nagorny, Pascal George, Zhongli Gao, Philippe Pichat, Hendrix James A, Siegfried Stengelin, Czechtizky Werngard, Lothar Schwink, Dominique Françon, Guy Griebel, Hurst William J
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 23:6141-6145
Previous studies have shown that compound 1 displayed high affinity towards histamine H3 receptor (H3R), (human (h-H3R), K(i)=8.6 nM, rhesus monkey (rh-H3R), K(i)=1.2 nM, and rat (r-H3R), K(i)=16.5 nM), but exhibited high affinity for hERG channel. H
Publikováno v:
The Journal of Infectious Diseases, 1951 Jul 01. 89(1), 95-102.
Externí odkaz:
https://www.jstor.org/stable/30093975