Do the K+ channel openers relax smooth muscle by opening K+ channels?
U Quast - Trends in Pharmacological Sciences, 1993 - Elsevier
… In addition, recent evidence reviewed here by Ulrich Quast suggests that the K + channel
openers possess further mechanisms of vasorelaxation not linked to the opening of …
openers possess further mechanisms of vasorelaxation not linked to the opening of …
The Impact of ATP-Sensitive K+ Channel Subtype Selectivity of Insulin Secretagogues for the Coronary Vasculature and the Myocardium
U Quast, D Stephan, S Bieger, U Russ - Diabetes, 2004 - Am Diabetes Assoc
Insulin secretagogues (sulfonylureas and glinides) increase insulin secretion by closing the
ATP-sensitive K + channel (K ATP channel) in the pancreatic β-cell membrane. K ATP …
ATP-sensitive K + channel (K ATP channel) in the pancreatic β-cell membrane. K ATP …
[HTML][HTML] Whole body radiotherapy: A TBI-guideline
U Quast - Journal of medical physics, 2006 - journals.lww.com
Total Body Irradiation (TBI) is one main component in the interdisciplinary treatment of widely
disseminated malignancies predominantly of haematopoietic diseases. Combined with …
disseminated malignancies predominantly of haematopoietic diseases. Combined with …
Total body irradiation—review of treatment techniquesin Europe
U Quast - Radiotherapy and Oncology, 1987 - Elsevier
In treatment of acute leukaemia and other disseminated diseases, high dose total body
irradiation (TBI)combined with intensive chemotherapy and bone marrow transplantation (BMT) …
irradiation (TBI)combined with intensive chemotherapy and bone marrow transplantation (BMT) …
Glibenclamide binding to sulphonylurea receptor subtypes: dependence on adenine nucleotides
…, C Löffler‐Walz, U Quast - British journal of …, 2002 - Wiley Online Library
ATP‐sensitive K + channels are composed of pore‐forming subunits Kir6.2 and of sulphonylurea
receptors (SURs); the latter are the target of the hypoglycaemic sulphonylureas like …
receptors (SURs); the latter are the target of the hypoglycaemic sulphonylureas like …
Cellular pharmacology of potassium channel openers in vascular smooth muscle.
U Quast, JM Guillon, I Cavero - Cardiovascular research, 1994 - europepmc.org
Potassium channel opening is a physiological mechanism which excitable cells exploit to
maintain or restore their resting state. Thus drugs that open vascular potassium channels have …
maintain or restore their resting state. Thus drugs that open vascular potassium channels have …
Physical treatment planning of total‐body irradiation: patient translation and beam‐zone method
U Quast - Medical Physics, 1985 - Wiley Online Library
In the treatment of acute leukemias, high doses of chemotherapy and total‐body irradiation (TBI)
are used prior to bone marrow transplantation. However, the doses needed equal or …
are used prior to bone marrow transplantation. However, the doses needed equal or …
Functional acetylcholine receptor from Torpedo marmorata in planar membranes.
H Schindler, U Quast - … of the National Academy of Sciences, 1980 - National Acad Sciences
Planar bilayer membranes containing functional acetylcholine receptor were formed from
vesicles of Torpedo marmorata electric organ without extracting the acetylcholine receptor from …
vesicles of Torpedo marmorata electric organ without extracting the acetylcholine receptor from …
[HTML][HTML] A specific binding site for K+ channel openers in rat aorta.
KM Bray, U Quast - Journal of Biological Chemistry, 1992 - Elsevier
The K+ channel openers, including cromakalim, pinacidil, minoxidil sulfate, diazoxide, and
nicorandil, form a chemically heterogeneous group of compounds, which relax smooth …
nicorandil, form a chemically heterogeneous group of compounds, which relax smooth …
ATP-sensitive K+ channel modulator binding to sulfonylurea receptors SUR2A and SUR2B: opposite effects of MgADP
…, D Kloor, U Delabar, Y Horio, Y Kurachi, U Quast - Molecular …, 1999 - ASPET
K ATP channels are heteromeric complexes of inwardly rectifying K + channel subunits and
sulfonylurea receptors (SURs). SUR2A and SUR2B, which differ within the carboxyl terminal …
sulfonylurea receptors (SURs). SUR2A and SUR2B, which differ within the carboxyl terminal …