UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 1.243

Sortiert nach

Thallium-sensitive fluorescent assay reveals loperamide as a new inhibitor of the potassium channel Kv10.1

Pharmacological reports, 2021-12, Vol.73 (6), p.1744-1753

2021

Link zum Volltext

Verfügbarkeit prüfen

Atypical antipsychotic olanzapine inhibits voltage-dependent K+ channels in coronary arterial smooth muscle cells

Pharmacological reports, 2021-12, Vol.73 (6), p.1724-1733

2021

Link zum Volltext

Verfügbarkeit prüfen

Complexes of Peptide Blockers with Kv1.6 Pore Domain: Molecular Modeling and Studies with KcsA-Kv1.6 Channel

Journal of neuroimmune pharmacology, 2017-06, Vol.12 (2), p.260-276

2017

Link zum Volltext

Verfügbarkeit prüfen

Escitalopram block of hERG potassium channels

Naunyn-Schmiedeberg's archives of pharmacology, 2014, Vol.387 (1), p.23-32

2014

Link zum Volltext

Verfügbarkeit prüfen

Phytochemicals genistein and capsaicin modulate Kv2.1 channel gating

Pharmacological reports, 2017-12, Vol.69 (6), p.1145-1153

2017

Link zum Volltext

Verfügbarkeit prüfen

In vitro evidence that endothelium-dependent vasodilatation induced by clozapine is mediated by an ATP-sensitive potassium channel

Pharmacological reports, 2019-06, Vol.71 (3), p.522-527

2019

Link zum Volltext

Verfügbarkeit prüfen

Fampridine is a Substrate and Inhibitor of Human OCT2, but not of Human MATE1, or MATE2K

Pharmaceutical research, 2018-08, Vol.35 (8), p.159-8, Article 159

2018

Link zum Volltext

Verfügbarkeit prüfen

Novel electrophysiological properties of dronedarone: inhibition of human cardiac two-pore-domain potassium (K2P) channels

Naunyn-Schmiedeberg's archives of pharmacology, 2012-10, Vol.385 (10), p.1003-1016

2012

Link zum Volltext

Verfügbarkeit prüfen

Antiarrhythmic activity of a new spiro-cyclic benzopyran activator of the cardiac mitochondrial ATP dependent potassium channels

Archives of Pharmacal Research, 2016, 39(9), , pp.1212-1222

2016

Link zum Volltext

Verfügbarkeit prüfen

The class III anti-arrhythmic agent, amiodarone, inhibits voltage-dependent K+ channels in rabbit coronary arterial smooth muscle cells

Naunyn-Schmiedeberg's archives of pharmacology, 2016-07, Vol.389 (7), p.713-721

2016

Link zum Volltext

Verfügbarkeit prüfen

Inhibition of cardiac Kv1.5 and Kv4.3 potassium channels by the class Ia anti-arrhythmic ajmaline: mode of action

Naunyn-Schmiedeberg's archives of pharmacology, 2013-11, Vol.386 (11), p.991-999

2013

Link zum Volltext

Verfügbarkeit prüfen

Activation of KCNQ channels located on the skeletal muscle membrane by retigabine and its influence on the maximal muscle force in rat muscle strips

Naunyn-Schmiedeberg's archives of pharmacology, 2016-04, Vol.389 (4), p.439-446

2016

Link zum Volltext

Verfügbarkeit prüfen

Lack of effect of Z-butylidenephthalide on presynaptic N-type Ca2+ channels in isolated guinea-pig ileum

Naunyn-Schmiedeberg's archives of pharmacology, 2016-02, Vol.389 (2), p.159-166

2016

Link zum Volltext

Verfügbarkeit prüfen

Identification of undecylenic acid as EAG channel inhibitor using surface plasmon resonance-based screen of KCNH channels

BMC pharmacology & toxicology, 2019-07, Vol.20 (1), p.42-42, Article 42

2019

Link zum Volltext

Verfügbarkeit prüfen

Cortisone and hydrocortisone inhibit human Kv1.3 activity in a non-genomic manner

Naunyn-Schmiedeberg's archives of pharmacology, 2015-06, Vol.388 (6), p.653-661

2015

Link zum Volltext

Verfügbarkeit prüfen

Effect of mosapride on Kv4.3 potassium channels expressed in CHO cells

Naunyn-Schmiedeberg's archives of pharmacology, 2013-10, Vol.386 (10), p.905-916

2013

Link zum Volltext

Verfügbarkeit prüfen

Pergolide block of the cloned Kv1.5 potassium channels

Naunyn-Schmiedeberg's archives of pharmacology, 2013-02, Vol.386 (2), p.125-133

2013

Link zum Volltext

Verfügbarkeit prüfen

Inhibition of Kv4.3 potassium channels by trazodone

Naunyn-Schmiedeberg's archives of pharmacology, 2013-08, Vol.386 (8), p.711-719

2013

Link zum Volltext

Verfügbarkeit prüfen

Inhibition of human Kv3.1 current expressed in Xenopus oocytes by the toxic venom fraction of Androctonus australis hector

Archives of Pharmacal Research, 2014, 37(11), , pp.1445-1453

2014

Link zum Volltext

Verfügbarkeit prüfen

K+ Channels Expression in Hypertension After Arterial Injury, and Effect of Selective Kv1.3 Blockade with PAP-1 on Intimal Hyperplasia Formation

Cardiovascular drugs and therapy, 2014-12, Vol.28 (6), p.501-511

2014

Link zum Volltext

Verfügbarkeit prüfen

Similarity-based SIBAR descriptors for classification of chemically diverse hERG blockers

Molecular diversity, 2009-08, Vol.13 (3), p.321-336

2009

Link zum Volltext

Verfügbarkeit prüfen

Electrophysiological analysis of mammalian cells expressing hERG using automated 384-well-patch-clamp

BMC pharmacology & toxicology, 2015-12, Vol.16 (38), p.39, Article 39

2015

Link zum Volltext

Verfügbarkeit prüfen

Inhibitory effects of imperatorin on voltage-gated K+ channels and ATP-sensitive K+ channels

Pharmacological reports, 2015-02, Vol.67 (1), p.134-139

2015

Link zum Volltext

Verfügbarkeit prüfen

Does hypercholesterolemia affect the relaxation of the detrusor smooth muscle in rats? In vitro and in vivo studies

Naunyn-Schmiedeberg's archives of pharmacology, 2015-07, Vol.388 (7), p.761-771

2015

Link zum Volltext

Verfügbarkeit prüfen

Voltage-dependent open-channel block of G protein-gated inward-rectifying K+ (GIRK) current in rat atrial myocytes by tamoxifen

Naunyn-Schmiedeberg's archives of pharmacology, 2012-12, Vol.385 (12), p.1149-1160

2012

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 1.243

Suche als RSS-Feed

Aktive Filter

KollektionNexis Uni

KollektionSpringerLink

ThemaLife Sciences & Biomedicine

ThemaPharmacology & Pharmacy

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(1.231)
Mit Volltextzugriff
(1.231)

Publikationsform

Artikel
(1.243)

Sprache

Englisch
(1.243)
Japanisch
(156)
Norwegisch
(2)
Koreanisch
(1)

Erscheinungsjahr

n.n

Thema

13 weitere anzeigen...

Weniger anzeigen...

Kollektion

2022 ECC(Springer)
(1.243)
MEDLINE
(1.001)
SpringerLINK Contemporary (Konsortium Baden-Württemberg)
(911)
Ingenta
(598)
Journals@Ovid Ovid Full Text
(531)
EZB Free E-Journals
(143)
Single Journals
(135)
IngentaConnect Journals
(60)
Brill Online Journals
(28)
EBSCOhost Psychology and Behavioral Sciences Collection
(21)
SAGE Journals
(7)

6 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Naunyn-Schmiedeberg's Archives Of Pharmacology
(302)
Cardiovascular Drugs And Therapy
(181)
Drugs
(101)
European Journal Of Clinical Pharmacology
(78)
Cns Drugs
(54)
Neurotherapeutics
(54)
Psychopharmacology
(41)
Advances In Therapy
(40)
Medicinal Chemistry Research
(35)
Pharmacological Reports
(32)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

Thallium-sensitive fluorescent assay reveals loperamide as a new inhibitor of the potassium channel Kv10.1

Atypical antipsychotic olanzapine inhibits voltage-dependent K+ channels in coronary arterial smooth muscle cells

Complexes of Peptide Blockers with Kv1.6 Pore Domain: Molecular Modeling and Studies with KcsA-Kv1.6 Channel

Escitalopram block of hERG potassium channels

Phytochemicals genistein and capsaicin modulate Kv2.1 channel gating

In vitro evidence that endothelium-dependent vasodilatation induced by clozapine is mediated by an ATP-sensitive potassium channel

Fampridine is a Substrate and Inhibitor of Human OCT2, but not of Human MATE1, or MATE2K

Novel electrophysiological properties of dronedarone: inhibition of human cardiac two-pore-domain potassium (K2P) channels

Antiarrhythmic activity of a new spiro-cyclic benzopyran activator of the cardiac mitochondrial ATP dependent potassium channels

The class III anti-arrhythmic agent, amiodarone, inhibits voltage-dependent K+ channels in rabbit coronary arterial smooth muscle cells

Inhibition of cardiac Kv1.5 and Kv4.3 potassium channels by the class Ia anti-arrhythmic ajmaline: mode of action

Activation of KCNQ channels located on the skeletal muscle membrane by retigabine and its influence on the maximal muscle force in rat muscle strips

Lack of effect of Z-butylidenephthalide on presynaptic N-type Ca2+ channels in isolated guinea-pig ileum

Identification of undecylenic acid as EAG channel inhibitor using surface plasmon resonance-based screen of KCNH channels

Cortisone and hydrocortisone inhibit human Kv1.3 activity in a non-genomic manner

Effect of mosapride on Kv4.3 potassium channels expressed in CHO cells

Pergolide block of the cloned Kv1.5 potassium channels

Inhibition of Kv4.3 potassium channels by trazodone

Inhibition of human Kv3.1 current expressed in Xenopus oocytes by the toxic venom fraction of Androctonus australis hector

K+ Channels Expression in Hypertension After Arterial Injury, and Effect of Selective Kv1.3 Blockade with PAP-1 on Intimal Hyperplasia Formation

Similarity-based SIBAR descriptors for classification of chemically diverse hERG blockers

Electrophysiological analysis of mammalian cells expressing hERG using automated 384-well-patch-clamp

Inhibitory effects of imperatorin on voltage-gated K+ channels and ATP-sensitive K+ channels

Does hypercholesterolemia affect the relaxation of the detrusor smooth muscle in rats? In vitro and in vivo studies

Voltage-dependent open-channel block of G protein-gated inward-rectifying K+ (GIRK) current in rat atrial myocytes by tamoxifen

Aktive Filter

Suchergebnisse filtern