Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Stefanie Prilla"'
Autor:
Stella Blackburn, Henry Fitt, Ingemar Persson, Kevin Blake, Sophie Accadebled, Monica Biscaro, Marie Guimier, Stefanie Prilla, Peter Arlett
Publikováno v:
Pharmacoepidemiology and Drug Safety. 20:1021-1029
Purpose A review of post-authorisation studies requested in 2007 by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) was undertaken to determine compliance and the need for research capacity in the Euro
Publikováno v:
Molecular Pharmacology. 70:181-193
In general, the M2 subtype of muscarinic acetylcholine receptors has the highest sensitivity for allosteric modulators and the M5 subtype the lowest. The M2/M5 selectivity of some structurally diverse allosteric agents is known to be completely expla
Publikováno v:
Molecular Pharmacology. 68:769-778
The structurally divergent agents gallamine and hexamethylene-bis-[dimethyl-(3-phthalimidopropyl)ammonium]dibromide (W84) are known to interact competitively at a common allosteric site on muscarinic receptors. Previous studies reported that the M2 s
Autor:
Kevin V, Blake, Stefanie, Prilla, Sophie, Accadebled, Marie, Guimier, Monica, Biscaro, Ingemar, Persson, Peter, Arlett, Stella, Blackburn, Henry, Fitt
Publikováno v:
Pharmacoepidemiology and drug safety. 20(10)
A review of post-authorisation studies requested in 2007 by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) was undertaken to determine compliance and the need for research capacity in the European Uni
Autor:
Johannes Antony, Clelia Dallanoce, Klaus Mohr, Anna Kebig, Stefanie Prilla, Mathias Muth, Teresa Disingrini, Kerstin Kellershohn, Evi Kostenis, Eberhard Heller, Simona Bertoni, Hans-Dieter Höltje, Jasmin Schrobang, Ulrike Holzgrabe, Marco De Amici, Christian Tränkle, Marion Mohr-Andrä, Arthur Christopoulos, Elisabetta Barocelli
Publikováno v:
Monash University
Selective modulation of cell function by G protein-coupled receptor (GPCR) activation is highly desirable for basic research and therapy but difficult to achieve. We present a novel strategy toward this goal using muscarinic acetylcholine receptors a
Autor:
Klaus Mohr, Jasmin Schrobang, Christian Tränkle, Stefanie Prilla, Anna Kebig, Caroline Schmalenbach, Hans Dieter Höltje, Matthias Sennwitz, Dorothea Jäger, Eberhard Heller, Ulrike Holzgrabe
Publikováno v:
The Journal of biological chemistry. 282(48)
G protein-coupled receptors represent the largest superfamily of cell membrane-spanning receptors. We used allosteric small molecules as a novel approach to better understand conformational changes underlying the inactive-to-active switch in native r
Publikováno v:
Molecular pharmacology. 68(3)
The structurally divergent agents gallamine and hexamethylene-bis-[dimethyl-(3-phthalimidopropyl)ammonium]dibromide (W84) are known to interact competitively at a common allosteric site on muscarinic receptors. Previous studies reported that the M2 s