Author pages are created from data sourced from our academic publisher partnerships and public sources.
- Publications
- Influence
The peril of dating beetles
- Emmanuel F. A. Toussaint, M. Seidel, +5 authors M. Fikáček
- Biology
- 1 January 2017
Recently, McKenna et al., 2015 (MCK15 hereafter) investigated the higher level phylogenetic relationships of beetles (Insecta, Coleoptera) using the most comprehensive molecular dataset to date, and… Expand
Clinical Utility of the Anti‐CCP Assay: Experiences with 700 Patients
- U. Sauerland, H. Becker, +6 authors M. Gaubitz
- Medicine
- Annals of the New York Academy of Sciences
- 1 June 2005
Abstract: Our objective was to determine the frequency of antibodies to cyclic citrullinated peptides (CCPs) in a series of patients with a variety of rheumatic diseases. Seven hundred consecutive… Expand
Synopsis of the pelidnotine scarabs (Coleoptera, Scarabaeidae, Rutelinae, Rutelini) and annotated catalog of the species and subspecies
- M. R. Moore, M. Jameson, B. Garner, Cédric Audibert, A. Smith, M. Seidel
- Biology, Medicine
- ZooKeys
- 6 April 2017
Abstract The pelidnotine scarabs (Scarabaeidae: Rutelinae: Rutelini) are a speciose, paraphyletic assemblage of beetles that includes spectacular metallic species (“jewel scarabs”) as well as species… Expand
Multifunctional nanoparticles for dual imaging.
- Z. Ali, A. Z. Abbasi, +11 authors W. Parak
- Chemistry, Medicine
- Analytical chemistry
- 17 March 2011
For imaging with different modalities, labels, which provide contrast for all modalities, are required. Colloidal nanoparticles composed out of an inorganic core and a polymer shell offer progress in… Expand
Dithranol, glucose-6-phosphate dehydrogenase inhibition and active oxygen species.
- K. Müller, M. Seidel, Curtis Braun, K. Zieresi, W. Wiegrebe
- Chemistry, Medicine
- Arzneimittel-Forschung
- 1 November 1991
Inhibition of glucose-6-phosphate dehydrogenase (G6-PDH) by dithranol (anthralin, CAS 480-22-8) has been studied in the presence of catalase, superoxide dismutase (SOD) and various scavengers of… Expand
Endoluminal Gastroplasty (EndoCinch™) versus Endoscopic Polymer Implantation (Enteryx™) for Treatment of Gastroesophageal Reflux Disease: 6-Month Results of a Prospective, Randomized Trial
- D. Domagk, J. Menzel, +5 authors T. Kucharzik
- Medicine
- The American Journal of Gastroenterology
- 1 March 2006
OBJECTIVES:The aim of this study was to compare and determine the efficiency and safety of two newly introduced endoscopic antireflux procedures in the treatment of gastroesophageal reflux disease… Expand
Structure‐function relationship of new anthralin derivatives assayed for growth inhibition and cytotoxicity in human keratinocyte cultures
- B. Bonnekoh, H. Tanzer, +4 authors W. Wiegrebe
- Chemistry, Medicine
- Archiv der Pharmazie
- 1 November 1991
HaCaT keratinocyte cultures were exposed to twelve hydrophilic anthralin derivatives 1 to 12 with substituents at C‐1 and C‐8 of the anthrone skeleton, of one H at C‐10 and of both H's at C‐10 by… Expand
Hydrophilic Derivatives of Dithranol
- H. Tanzer, M. Seidel, W. Wiegrebe
- Chemistry
- 1988
The syntheses of dithranol derivatives with ω‐carboxyalkyl side chains at C‐2 (and C‐7) or ω‐methoxycarbonylacyl‐substituents at C‐10, respectively, are described.
Use of physiological substrates for zymograms of disaccharidases after separation in immobilized pH gradients.
- P. Sinha, M. Seidel, P. G. Righetti, I. Bause-Niedrig, E. Köttgen
- Chemistry, Medicine
- Journal of biochemical and biophysical methods
- 1 May 1989
A new technique is described for in situ visualization of the activity of intestinal disaccharidases after isoelectric focusing in immobilized pH gradients using their physiological substrates. The… Expand
Anthralin derivatives—inhibition of 5‐lipoxygenase—antipsoriatic efficacy
- H. Tanzer, Curtis Braun, M. Seidel, W. Wiegrebe
- Chemistry, Medicine
- Archiv der Pharmazie
- 1 November 1991
Inhibition of 5‐lipoxygenase by anthralin (1) and 41 derivatives is determined: the acids 38 and 39, the lactones 40–42 and 9‐anthrone (8) are the most potent inhibitors, the lactone 41 reaching the… Expand