K. May

发表

Disposition and Antimuscarinic Effects of the Urinary Bladder Spasmolytics Propiverine: Influence of Dosage Forms and Circadian‐Time Rhythms

M. Lerch, W. Weitschies, R. Oertel, 2008, Journal of clinical pharmacology.

Oral absorption of propiverine solution and of the immediate and extended release dosage forms: influence of regioselective intestinal elimination

S. Oswald, R. Oertel, W. Siegmund, 2008, European Journal of Clinical Pharmacology.

Synergistic influence of Abcb1 and Abcc2 on disposition and sterol lowering effects of ezetimibe in rats.

D. Lütjohann, S. Oswald, W. Siegmund, 2010, Journal of pharmaceutical sciences.

Drug-Related Hospital Admissions with Digitalis Glycosides

M. Hippius, W. Siegmund, J. Szymański, 2006 .

Tolerability of β‐blockers metabolized via cytochrome P450 2D6 is sex‐dependent

J. Hasford, M. Hippius, W. Siegmund, 2006 .

Identification and Characterization of a Potent, Selective, and Orally Active Antagonist of the CC Chemokine Receptor-1*

D. Taub, S. Harvey, R. Horuk, 2000, The Journal of Biological Chemistry.

Species selectivity of a small molecule antagonist for the CCR1 chemokine receptor.

R. Horuk, P. Kretschmer, M. Morrissey, 2000, European journal of pharmacology.

Antibody-Dependent Transplacental Transfer of Malaria Blood-Stage Antigen Using a Human Ex Vivo Placental Perfusion Model

C. Fusch, C. King, K. Mandaliya, 2009, PloS one.

Influence of genetic polymorphisms on intestinal expression and rifampicin-type induction of ABCC2 and on bioavailability of talinolol

A. Caliebe, I. Cascorbi, W. Siegmund, 2008, Pharmacogenetics and genomics.

Expression and activity of vitamin D receptor in the human placenta and in choriocarcinoma BeWo and JEG-3 cell lines

Z. Dvořák, R. Vrzal, P. Pávek, 2009, Molecular and Cellular Endocrinology.

Synthesis of N-alkyl glycine amides as potent inhibitors of leukotriene A4 hydrolase.

H. Ye, D. Davey, J. Parkinson, 2008, Bioorganic & Medicinal Chemistry Letters.

CCR5 receptor antagonists: discovery and SAR of novel 4-hydroxypiperidine derivatives.

D. Davey, G. Phillips, J. Onuffer, 2007, Bioorganic & medicinal chemistry letters.

Role of the Multidrug Transporter Proteins ABCB1 and ABCC2 in the Diaplacental Transport of Talinolol in the Term Human Placenta

H. Kroemer, C. Fusch, M. Zygmunt, 2008, Drug Metabolism and Disposition.

A Non-peptide Functional Antagonist of the CCR1 Chemokine Receptor Is Effective in Rat Heart Transplant Rejection*

C. Weber, A. Krensky, H. Gröne, 2001, The Journal of Biological Chemistry.

CCR1-specific non-peptide antagonist: efficacy in a rabbit allograft rejection model.

R. Horuk, M. Morrissey, H. Perez, 2001, Immunology letters.

Identification and Characterization of Small Molecule Functional Antagonists of the CCR1 Chemokine Receptor*

D. Taub, Wei Zheng, R. Horuk, 1998, The Journal of Biological Chemistry.

Long term lymphocyte reconstitution after alemtuzumab treatment of multiple sclerosis

G. Giovannoni, A. Coles, A. Green, 2011, Journal of Neurology, Neurosurgery & Psychiatry.

Carbamazepine regulates intestinal P‐glycoprotein and multidrug resistance protein MRP2 and influences disposition of talinolol in humans

Michael Zschiesche, Markus Grube, Christiane Modess, 2004, Clinical pharmacology and therapeutics.

Commonly used nonionic surfactants interact differently with the human efflux transporters ABCB1 (p-glycoprotein) and ABCC2 (MRP2).

Werner Weitschies, Werner Siegmund, W. Weitschies, 2010, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Discovery of novel non-peptide CCR1 receptor antagonists.

R. Horuk, M. Morrissey, H. Perez, 1999, Journal of medicinal chemistry.

Crystal structures of potent thiol-based inhibitors bound to carboxypeptidase B.

M. Adler, M. Whitlow, I. Islam, 2005, Biochemistry.

Rapid Modulation of the Organic Anion Transporting Polypeptide 2B1 (OATP2B1, SLCO2B1) Function by Protein Kinase C-mediated Internalization*

M. Fraunholz, U. Völker, H. Kroemer, 2010, The Journal of Biological Chemistry.

3-Mercaptopropionic acids as efficacious inhibitors of activated thrombin activatable fibrinolysis inhibitor (TAFIa).

M. Adler, M. Whitlow, R. Vergona, 2007, Bioorganic & medicinal chemistry letters.

Keratinocyte growth factor impairs human thymic recovery from lymphopenia

D. Douek, J. Isaacs, J. W. Brown, 2019, JCI insight.

Alemtuzumab treatment of multiple sclerosis: long-term safety and efficacy

A. Compston, A. Coles, G. Hill-Cawthorne, 2014, Journal of Neurology, Neurosurgery & Psychiatry.

Tolerability of beta-blockers metabolized via cytochrome P450 2D6 is sex-dependent.

J. Hasford, M. Hippius, W. Siegmund, 2006, Clinical pharmacology and therapeutics.

High-throughput LC-MS-UV-ELSD analysis of drug discovery sScreening libraries

B. Lin, M. Wan, K. May, 2007 .

Expression and activity of vitamin D receptor in the human placenta and in choriocarcinoma BeWo and JEG-3 cell lines

Z. Dvořák, R. Vrzal, P. Pávek, 2009, Molecular and Cellular Endocrinology.

Long term lymphocyte reconstitution after alemtuzumab treatment of multiple sclerosis

G. Giovannoni, A. Coles, A. Green, 2011, Journal of Neurology, Neurosurgery & Psychiatry.