K. Wenzel-Seifert

发表

The olfactory G protein Gαolf possesses a lower GDP‐affinity and deactivates more rapidly than Gsαshort: consequences for receptor‐coupling and adenylyl cyclase activation

Hui-yu Liu, K. Wenzel-Seifert, R. Seifert, 2001 .

The olfactory G protein G(alphaolf) possesses a lower GDP-affinity and deactivates more rapidly than G(salphashort): consequences for receptor-coupling and adenylyl cyclase activation.

K. Wenzel-Seifert, R. Seifert, H. Y. Liu, 2001, Journal of neurochemistry.

Partial inhibition of human neutrophil activation by FK-506 at supratherapeutic concentrations

K. Wenzel-Seifert, R. Seifert, K. Wenzel‐Seifert, 1993, Naunyn-Schmiedeberg's Archives of Pharmacology.

Oleic acid inhibition of Na+/D-glucose transport in isolated renal brush-border membranes: role of lipid physical parameters and trans Na(+)-inhibition.

K. Wenzel-Seifert, S. Wagner, L. Volbracht, 1994, Biochimica et biophysica acta.

GPCR-Galpha fusion proteins: molecular analysis of receptor-G-protein coupling.

B. Kobilka, K. Wenzel-Seifert, R. Seifert, 1999, Trends in pharmacological sciences.

Cyclosporin H Is a Potent and Selective Formyl Peptide Receptor Antagonist Comparison with Nt-Butoxycarbonyl-~-phenylalanyl-L-leucyl-L-phenylalanyl-1-leucyl-L-phenylalanine and Cyclosporins

K. Wenzel-Seifert, R. Seifert, K. Wenzel‐Seifert, 2001 .

Rating The Delirogenic Potential of Drugs for Prediction of Side Effects in Elderly Psychiatric Inpatients

A. Fellgiebel, K. Wenzel-Seifert, C. Hiemke, 2015 .

Differential inhibition of human neutrophil activation by cyclosporins A, D, and H. Cyclosporin H is a potent and effective inhibitor of formyl peptide-induced superoxide formation.

K. Wenzel-Seifert, R. Seifert, L. Grünbaum, 1991, Journal of immunology.

Cyclosporin H is a potent and selective formyl peptide receptor antagonist. Comparison with N-t-butoxycarbonyl-L-phenylalanyl-L-leucyl-L-phenylalanyl-L- leucyl-L-phenylalanine and cyclosporins A, B, C, D, and E.

K. Wenzel-Seifert, R. Seifert, K. Wenzel‐Seifert, 1993, Journal of immunology.

Defective Gi Protein Coupling in Two Formyl Peptide Receptor Mutants Associated with Localized Juvenile Periodontitis*

K. Wenzel-Seifert, R. Seifert, K. Wenzel‐Seifert, 2001, The Journal of Biological Chemistry.

High Constitutive Activity of the Human Formyl Peptide Receptor*

K. Wenzel-Seifert, R. Seifert, C. Hurt, 1998, The Journal of Biological Chemistry.

N-protein kinase C isoenzymes may be involved in the regulation of various neutrophil functions.

K. Wenzel-Seifert, R. Seifert, C. Schächtele, 1994, Biochemical and biophysical research communications.

Unmasking different constitutive activity of four chemoattractant receptors using Na+ as universal stabilizer of the inactive (R) state.

K. Wenzel-Seifert, R. Seifert, K. Wenzel‐Seifert, 2001, Receptors & channels.

In U-937 promonocytes, misteltoe lectin I increases basal [Ca2+]i, enhances histamine H1- and complement C5a-receptor-mediated rises in [Ca2+]i, and induces cell death

K. Wenzel-Seifert, R. Seifert, H. Lentzen, 1997, Naunyn-Schmiedeberg's Archives of Pharmacology.

Different Effects of Gsα Splice Variants on β2-Adrenoreceptor-mediated Signaling

B. Kobilka, K. Wenzel-Seifert, R. Seifert, 1998, The Journal of Biological Chemistry.

Functional differences between human formyl peptide receptor isoforms 26, 98, and G6

K. Wenzel-Seifert, R. Seifert, K. Wenzel‐Seifert, 2003, Naunyn-Schmiedeberg's Archives of Pharmacology.

Multiple Differences in Agonist and Antagonist Pharmacology between Human and Guinea Pig Histamine H1-Receptor

T. Bürckstümmer, K. Wenzel-Seifert, R. Seifert, 2003, Journal of Pharmacology and Experimental Therapeutics.

Complex regulation of human neutrophil activation by actin filaments: dihydrocytochalasin B and botulinum C2 toxin uncover the existence of multiple cation entry pathways

K. Wenzel-Seifert, R. Seifert, K. Aktories, 1997, Journal of leukocyte biology.

Concanavalin A and mistletoe lectin I differentially activate cation entry and exocytosis in human neutrophils: lectins may activate multiple subtypes of cation channels

K. Wenzel-Seifert, R. Seifert, D. Krautwurst, 1996, Journal of leukocyte biology.

Thapsigargin activates univalent- and bivalent-cation entry in human neutrophils by a SK&F I3 96365- and Gd3+-sensitive pathway and is a partial secretagogue: involvement of pertussis-toxin-sensitive G-proteins and protein phosphatases 1/2A and 2B in the signal-transduction pathway.

K. Wenzel-Seifert, R. Seifert, D. Krautwurst, 1996, The Biochemical journal.

Differential inhibition and potentiation by cell-permeant analogues of cyclic AMP and cyclic GMP and NO-containing compounds of exocytosis in human neutrophils

K. Wenzel-Seifert, R. Seifert, J. Ervens, 1991, Naunyn-Schmiedeberg's Archives of Pharmacology.

Examining the efficiency of receptor/G‐protein coupling with a cleavable β2‐adrenoceptor–Gsα fusion protein

B. Kobilka, K. Wenzel-Seifert, R. Seifert, 1999 .

Different effects of Gsalpha splice variants on beta2-adrenoreceptor-mediated signaling. The beta2-adrenoreceptor coupled to the long splice variant of Gsalpha has properties of a constitutively active receptor.

B. Kobilka, K. Wenzel-Seifert, R. Seifert, 1998, The Journal of biological chemistry.

Distinct interaction of human and guinea pig histamine H2-receptor with guanidine-type agonists.

T. Bürckstümmer, K. Wenzel-Seifert, R. Seifert, 2001, Molecular pharmacology.

Evidence that inhibition of phorbol ester-induced superoxide anion formation by cyclosporin A in phagocytes is not mediated by direct inhibition of protein kinase C.

K. Wenzel-Seifert, R. Seifert, C. Schächtele, 1994, Biochemical pharmacology.

Critical role of N-terminal N-glycosylation for proper folding of the human formyl peptide receptor.

K. Wenzel-Seifert, R. Seifert, K. Wenzel‐Seifert, 2003, Biochemical and biophysical research communications.