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Katharina Wenzel-Seifert

Explore the profile of Katharina Wenzel-Seifert including associated specialties, affiliations and a list of published articles. Areas
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Articles 15
Citations 386
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Recent Articles
1.
Seifert J, Fay B, Strueven N, Schiekofer S, Wenzel-Seifert K, Haen E
Psychiatr Prax . 2021 Mar; 49(1):37-45. PMID: 33773503
Objective: The purpose of this study was to examine the extent to which "potentially inappropriate drugs" (PID) are associated with an increased risk for adverse drug reactions (ADR). Methods: Data...
2.
Stegmann B, Rexroth C, Wenzel-Seifert K, Haen E
Z Kinder Jugendpsychiatr Psychother . 2015 May; 43(2):101-14. PMID: 25951625
Objective: This contribution evaluates the prevalence, medication use as well as age and sex distribution in inpatients with hyperkinetic disorders at the KinderAGATE hospitals for 2009-2012. Method: The age, sex,...
3.
Wenzel-Seifert K, Haen E
Med Monatsschr Pharm . 2013 Sep; 36(9):346-7. PMID: 24069648
No abstract available.
4.
Stegmann B, Wenzel-Seifert K, Haen E
Z Kinder Jugendpsychiatr Psychother . 2013 Feb; 41(2):109-19. PMID: 23425613
Objective: The present analysis evaluates the prevalence and medication use in inpatients with depression during childhood and adolescence at the KinderAGATE hospitals in 2010. Also discussed are age and sex...
5.
Wenzel-Seifert K, Wittmann M, Haen E
Dtsch Arztebl Int . 2011 Nov; 108(41):687-93. PMID: 22114630
Introduction: Many psychotropic drugs can delay cardiac repolarization and thereby prolong the rate-corrected QT interval (QTc). A prolonged QTc often arouses concern in clinical practice, as it can be followed,...
6.
Wenzel-Seifert K, Seifert R
Recept Channels . 2003 Oct; 9(5):315-23. PMID: 14527875
The human beta1-adrenoceptor (beta1AR) exists in several isoforms and activates adenylyl cyclase (AC) via Gs-proteins. The Arg389-isoform of the beta1AR (beta1AR-R389) expressed in CHW cells is much more efficient than...
7.
Seifert R, Wenzel-Seifert K
Life Sci . 2003 Aug; 73(18):2263-80. PMID: 12941430
According to the two-state model of G-protein-coupled receptor (GPCR) activation, GPCRs isomerize from an inactive (R) state to an active (R*) state. In the R* state, GPCRs activate G-proteins. Agonist-independent...
8.
Wenzel-Seifert K, Seifert R
Naunyn Schmiedebergs Arch Pharmacol . 2003 Apr; 367(5):509-15. PMID: 12679864
The formyl peptide receptor (FPR) is expressed in neutrophils, couples to G(i)-proteins and activates phospholipase C, chemotaxis and cytotoxic cell functions. FPR isoforms 26, 98, and G6 differ from each...
9.
Seifert R, Wenzel-Seifert K, Burckstummer T, Pertz H, Schunack W, Dove S, et al.
J Pharmacol Exp Ther . 2003 Mar; 305(3):1104-15. PMID: 12626648
Species isoforms of histamine H2-, H3-, and H4-receptors differ in their pharmacological properties. The study aim was to dissect differences between the human H1R (hH1R) and guinea pig H1R (ghH1R)....
10.
Wenzel-Seifert K, Seifert R
Biochem Biophys Res Commun . 2003 Feb; 301(3):693-8. PMID: 12565836
The human formyl peptide receptor (FPR) is N-glycosylated and activates phagocytes via G(i)-proteins. The FPR expressed with G(i)alpha(2)beta(1)gamma(2) in Sf9 insect cells exhibits high constitutive activity as assessed by strong...