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Journal of Cellular Physiology
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November 18, 2006
Cell cycle-dependent activity of the volume- and Ca2+-activated anion currents in Ehrlich lettre ascites cells
Thomas Kjaer Klausen, Andreas Bergdahl, Charlotte Hougaard, et al.
Glia
|
July 30, 2016
Quantification of the functional expression of the Ca<sup>2+</sup> -activated K<sup>+</sup> channel K<sub>Ca</sub> 3.1 on microglia from adult human neocortical tissue
Linda V Blomster, Dorte Strøbaek, Charlotte Hougaard, et al.
The Journal of Physiology
|
June 18, 2002
Rho family GTP binding proteins are involved in the regulatory volume decrease process in NIH3T3 mouse fibroblasts
Stine F Pedersen, Kristine H Beisner, Charlotte Hougaard, et al.
Molecular Pharmacology
|
November 3, 2011
Evidence for a common pharmacological interaction site on K(Ca)2 channels providing both selective activation and selective inhibition of the human K(Ca)2.1 subtype
Charlotte Hougaard, Sofia Hammami, Birgitte L Eriksen, et al.
The Journal of Biological Chemistry
|
October 22, 2005
Specific enhancement of SK channel activity selectively potentiates the afterhyperpolarizing current I(AHP) and modulates the firing properties of hippocampal pyramidal neurons
Paola Pedarzani, Jaime E McCutcheon, Gregor Rogge, et al.
Journal of Medicinal Chemistry
|
November 13, 2008
Synthesis and structure-activity relationship studies of 2-(N-substituted)-aminobenzimidazoles as potent negative gating modulators ofsmall conductance Ca2+-activated K+ channels
Ulrik S Sørensen, Dorte Strøbaek, Palle Christophersen, et al.
Molecular Pharmacology
|
March 3, 2011
Negative gating modulation by (R)-N-(benzimidazol-2-yl)-1,2,3,4-tetrahydro-1-naphthylamine (NS8593) depends on residues in the inner pore vestibule: pharmacological evidence of deep-pore gating of K(Ca)2 channels
David Paul Jenkins, Dorte Strøbæk, Charlotte Hougaard, et al.
Neuropharmacology
|
March 1, 2017
K<sub>v</sub>3.1/K<sub>v</sub>3.2 channel positive modulators enable faster activating kinetics and increase firing frequency in fast-spiking GABAergic interneurons
Kim Boddum, Charlotte Hougaard, Julie Xiao-Ying Lin, et al.
Molecular Pharmacology
|
August 24, 2006
Inhibitory gating modulation of small conductance Ca2+-activated K+ channels by the synthetic compound (R)-N-(benzimidazol-2-yl)-1,2,3,4-tetrahydro-1-naphtylamine (NS8593) reduces afterhyperpolarizing current in hippocampal CA1 neurons
Dorte Strøbaek, Charlotte Hougaard, Tina H Johansen, et al.
Molecular Pharmacology
|
June 12, 2009
Selective activation of the SK1 subtype of human small-conductance Ca2+-activated K+ channels by 4-(2-methoxyphenylcarbamoyloxymethyl)-piperidine-1-carboxylic acid tert-butyl ester (GW542573X) is dependent on serine 293 in the S5 segment
Charlotte Hougaard, Marianne L Jensen, Tim J Dale, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 27) with videos related to
Sort By:
Page
of 3
Journal of Cellular Physiology
|
November 18, 2006
Cell cycle-dependent activity of the volume- and Ca2+-activated anion currents in Ehrlich lettre ascites cells
Thomas Kjaer Klausen, Andreas Bergdahl, Charlotte Hougaard, et al.
Glia
|
July 30, 2016
Quantification of the functional expression of the Ca<sup>2+</sup> -activated K<sup>+</sup> channel K<sub>Ca</sub> 3.1 on microglia from adult human neocortical tissue
Linda V Blomster, Dorte Strøbaek, Charlotte Hougaard, et al.
The Journal of Physiology
|
June 18, 2002
Rho family GTP binding proteins are involved in the regulatory volume decrease process in NIH3T3 mouse fibroblasts
Stine F Pedersen, Kristine H Beisner, Charlotte Hougaard, et al.
Molecular Pharmacology
|
November 3, 2011
Evidence for a common pharmacological interaction site on K(Ca)2 channels providing both selective activation and selective inhibition of the human K(Ca)2.1 subtype
Charlotte Hougaard, Sofia Hammami, Birgitte L Eriksen, et al.
The Journal of Biological Chemistry
|
October 22, 2005
Specific enhancement of SK channel activity selectively potentiates the afterhyperpolarizing current I(AHP) and modulates the firing properties of hippocampal pyramidal neurons
Paola Pedarzani, Jaime E McCutcheon, Gregor Rogge, et al.
Journal of Medicinal Chemistry
|
November 13, 2008
Synthesis and structure-activity relationship studies of 2-(N-substituted)-aminobenzimidazoles as potent negative gating modulators ofsmall conductance Ca2+-activated K+ channels
Ulrik S Sørensen, Dorte Strøbaek, Palle Christophersen, et al.
Molecular Pharmacology
|
March 3, 2011
Negative gating modulation by (R)-N-(benzimidazol-2-yl)-1,2,3,4-tetrahydro-1-naphthylamine (NS8593) depends on residues in the inner pore vestibule: pharmacological evidence of deep-pore gating of K(Ca)2 channels
David Paul Jenkins, Dorte Strøbæk, Charlotte Hougaard, et al.
Neuropharmacology
|
March 1, 2017
K<sub>v</sub>3.1/K<sub>v</sub>3.2 channel positive modulators enable faster activating kinetics and increase firing frequency in fast-spiking GABAergic interneurons
Kim Boddum, Charlotte Hougaard, Julie Xiao-Ying Lin, et al.
Molecular Pharmacology
|
August 24, 2006
Inhibitory gating modulation of small conductance Ca2+-activated K+ channels by the synthetic compound (R)-N-(benzimidazol-2-yl)-1,2,3,4-tetrahydro-1-naphtylamine (NS8593) reduces afterhyperpolarizing current in hippocampal CA1 neurons
Dorte Strøbaek, Charlotte Hougaard, Tina H Johansen, et al.
Molecular Pharmacology
|
June 12, 2009
Selective activation of the SK1 subtype of human small-conductance Ca2+-activated K+ channels by 4-(2-methoxyphenylcarbamoyloxymethyl)-piperidine-1-carboxylic acid tert-butyl ester (GW542573X) is dependent on serine 293 in the S5 segment
Charlotte Hougaard, Marianne L Jensen, Tim J Dale, et al.
Page
of 3