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Heike Wulff

Showing results (41-50 of 222) with videos related to

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Journal of Molecular and Cellular Cardiology|May 3, 2014
A pharmacologic activator of endothelial KCa channels enhances coronary flow in the hearts of type 2 diabetic ratsRamesh C Mishra, Heike Wulff, William C Cole, et al.
Elife|November 9, 2020
New capsaicin analogs as molecular rulers to define the permissive conformation of the mouse TRPV1 ligand-binding pocketSimon Vu, Vikrant Singh, Heike Wulff, et al.
British Journal of Pharmacology|June 6, 2013
Activation of KCa3.1 by SKA-31 induces arteriolar dilatation and lowers blood pressure in normo- and hypertensive connexin40-deficient miceJosephine Radtke, Kjestine Schmidt, Heike Wulff, et al.
Journal of Cardiovascular Pharmacology|March 28, 2015
Inhibition of Myogenic Tone in Rat Cremaster and Cerebral Arteries by SKA-31, an Activator of Endothelial KCa2.3 and KCa3.1 ChannelsRamesh C Mishra, Heike Wulff, Michael A Hill, et al.
Journal of Autoimmunity|September 2, 2014
Kv1.3 in psoriatic disease: PAP-1, a small molecule inhibitor of Kv1.3 is effective in the SCID mouse psoriasis--xenograft modelSmriti Kundu-Raychaudhuri, Yi-Je Chen, Heike Wulff, et al.
Annals of Clinical and Translational Neurology|March 24, 2022
The seizure-inducing plastic explosive RDX inhibits the α1β2γ2 GABA<sub>A</sub> receptorBrandon Pressly, Ruth D Lee, Vikrant Singh, et al.
Fibrogenesis & Tissue Repair|April 2, 2015
Human lung myofibroblast TGFβ1-dependent Smad2/3 signalling is Ca(2+)-dependent and regulated by KCa3.1 K(+) channelsKaty M Roach, Carol Feghali-Bostwick, Heike Wulff, et al.
Molecular Pharmacology|October 28, 2020
Identification of the Functional Binding Site for the Convulsant Tetramethylenedisulfotetramine in the Pore of the <i>α</i> <sub>2</sub> <i>β</i> <sub>3</sub> <i>γ</i> <sub>2</sub> GABA<sub>A</sub> ReceptorBrandon Pressly, Ruth D Lee, Bogdan Barnych, et al.
Journal of Medicinal Chemistry|February 17, 2006
A new class of blockers of the voltage-gated potassium channel Kv1.3 via modification of the 4- or 7-position of khellinoneAndrew J Harvey, Jonathan B Baell, Nathan Toovey, et al.
Molecular Pharmacology|August 2, 2017
Structural Determinants for the Selectivity of the Positive KCa3.1 Gating Modulator 5-Methylnaphtho[2,1-<i>d</i>]oxazol-2-amine (SKA-121)Brandon M Brown, Heesung Shim, Miao Zhang, et al.
Pageof 23

Showing results (41-50 of 222) with videos related to

Sort By:
Pageof 23
Journal of Molecular and Cellular Cardiology|May 3, 2014
A pharmacologic activator of endothelial KCa channels enhances coronary flow in the hearts of type 2 diabetic ratsRamesh C Mishra, Heike Wulff, William C Cole, et al.
Elife|November 9, 2020
New capsaicin analogs as molecular rulers to define the permissive conformation of the mouse TRPV1 ligand-binding pocketSimon Vu, Vikrant Singh, Heike Wulff, et al.
British Journal of Pharmacology|June 6, 2013
Activation of KCa3.1 by SKA-31 induces arteriolar dilatation and lowers blood pressure in normo- and hypertensive connexin40-deficient miceJosephine Radtke, Kjestine Schmidt, Heike Wulff, et al.
Journal of Cardiovascular Pharmacology|March 28, 2015
Inhibition of Myogenic Tone in Rat Cremaster and Cerebral Arteries by SKA-31, an Activator of Endothelial KCa2.3 and KCa3.1 ChannelsRamesh C Mishra, Heike Wulff, Michael A Hill, et al.
Journal of Autoimmunity|September 2, 2014
Kv1.3 in psoriatic disease: PAP-1, a small molecule inhibitor of Kv1.3 is effective in the SCID mouse psoriasis--xenograft modelSmriti Kundu-Raychaudhuri, Yi-Je Chen, Heike Wulff, et al.
Annals of Clinical and Translational Neurology|March 24, 2022
The seizure-inducing plastic explosive RDX inhibits the α1β2γ2 GABA<sub>A</sub> receptorBrandon Pressly, Ruth D Lee, Vikrant Singh, et al.
Fibrogenesis & Tissue Repair|April 2, 2015
Human lung myofibroblast TGFβ1-dependent Smad2/3 signalling is Ca(2+)-dependent and regulated by KCa3.1 K(+) channelsKaty M Roach, Carol Feghali-Bostwick, Heike Wulff, et al.
Molecular Pharmacology|October 28, 2020
Identification of the Functional Binding Site for the Convulsant Tetramethylenedisulfotetramine in the Pore of the <i>α</i> <sub>2</sub> <i>β</i> <sub>3</sub> <i>γ</i> <sub>2</sub> GABA<sub>A</sub> ReceptorBrandon Pressly, Ruth D Lee, Bogdan Barnych, et al.
Journal of Medicinal Chemistry|February 17, 2006
A new class of blockers of the voltage-gated potassium channel Kv1.3 via modification of the 4- or 7-position of khellinoneAndrew J Harvey, Jonathan B Baell, Nathan Toovey, et al.
Molecular Pharmacology|August 2, 2017
Structural Determinants for the Selectivity of the Positive KCa3.1 Gating Modulator 5-Methylnaphtho[2,1-<i>d</i>]oxazol-2-amine (SKA-121)Brandon M Brown, Heesung Shim, Miao Zhang, et al.
Pageof 23