Hochschulschrift
Local-anesthetic like inhibition of the cardiac sodium channel Nav1.5 α-subunit by 5-HT3 receptor antagonists
- Alternative title
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alpha-subunit
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Dimensions
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30 cm
- Extent
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27 Blätter
- Language
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Englisch
- Notes
-
Diagramme
Im Titel ist "3" tiefgestellt
Enthält 1 Sonderabdruck aus: European Journal of Pharmacology ; 789.2016. Seite 119-126
Medizinische Hochschule Hannover, Dissertation, 2019
- Event
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Veröffentlichung
- (where)
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Hannover
- (when)
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2018
- Table of contents
- Rights
-
Bei diesem Objekt liegt nur das Inhaltsverzeichnis digital vor. Der Zugriff darauf ist unbeschränkt möglich.
- Last update
-
11.03.2025, 11:45 AM CET
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Object type
- Hochschulschrift
Associated
Time of origin
- 2018
Other Objects (12)
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Sodium channel slow inactivation interferes with open channel block
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Bisphenol A Binds to the Local Anesthetic Receptor Site to Block the Human Cardiac Sodium Channel
An Inhibitory Peptide Derived from the α-subunit of the Epithelial Sodium Channel (ENaC) Shows a Helical Conformation
Novel functions of the calcium channel β3 subunit
Pharmacological modification of sodium channel Nav1.9 activity
Coupling the cardiac voltage-gated sodium channel to channelrhodopsin-2 generates novel optical switches for action potential studies
Functional analysis of the potassium channel beta subunit KCNE3
Molecular modeling of human voltage-gated sodium channel complexes
The contribution of the sodium channel subunit NaV1.6 to neuronal excitability
Effects of the δ-subunit [delta-subunit] and of proteolytic channel cleavage on the function of the epithelial sodium channel (ENaC)
Modifications of sodium channel voltage dependence induce arrhythmia-favouring dynamics of cardiac action potentials
Sodium channel slow inactivation interferes with open channel block
Veratridine Can Bind to a Site at the Mouth of the Channel Pore at Human Cardiac Sodium Channel NaV1.5
Bisphenol A Binds to the Local Anesthetic Receptor Site to Block the Human Cardiac Sodium Channel
An Inhibitory Peptide Derived from the α-subunit of the Epithelial Sodium Channel (ENaC) Shows a Helical Conformation
Novel functions of the calcium channel β3 subunit
Pharmacological modification of sodium channel Nav1.9 activity
Coupling the cardiac voltage-gated sodium channel to channelrhodopsin-2 generates novel optical switches for action potential studies
Functional analysis of the potassium channel beta subunit KCNE3
Molecular modeling of human voltage-gated sodium channel complexes
The contribution of the sodium channel subunit NaV1.6 to neuronal excitability
Effects of the δ-subunit [delta-subunit] and of proteolytic channel cleavage on the function of the epithelial sodium channel (ENaC)
Modifications of sodium channel voltage dependence induce arrhythmia-favouring dynamics of cardiac action potentials
Sodium channel slow inactivation interferes with open channel block
Veratridine Can Bind to a Site at the Mouth of the Channel Pore at Human Cardiac Sodium Channel NaV1.5
Bisphenol A Binds to the Local Anesthetic Receptor Site to Block the Human Cardiac Sodium Channel
An Inhibitory Peptide Derived from the α-subunit of the Epithelial Sodium Channel (ENaC) Shows a Helical Conformation
Novel functions of the calcium channel β3 subunit
Pharmacological modification of sodium channel Nav1.9 activity
Coupling the cardiac voltage-gated sodium channel to channelrhodopsin-2 generates novel optical switches for action potential studies
Functional analysis of the potassium channel beta subunit KCNE3