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Frontiers in Pharmacology
|
June 19, 2023
Corrigendum: Diclofenac and other non-steroidal anti-inflammatory drugs (NSAIDs) are competitive antagonists of the human P2X3 receptor
Laura Grohs, Linhan Cheng, Saskia Cönen, et al.
Frontiers in Pharmacology
|
April 3, 2023
Diclofenac and other non-steroidal anti-inflammatory drugs (NSAIDs) are competitive antagonists of the human P2X3 receptor
Laura Grohs, Linhan Cheng, Saskia Cönen, et al.
Journal of Medicinal Chemistry
|
October 28, 2005
Synthesis and structure-activity relationships of suramin-derived P2Y11 receptor antagonists with nanomolar potency
Heiko Ullmann, Sabine Meis, Darunee Hongwiset, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
October 10, 2009
NF546 [4,4'-(carbonylbis(imino-3,1-phenylene-carbonylimino-3,1-(4-methyl-phenylene)-carbonylimino))-bis(1,3-xylene-alpha,alpha'-diphosphonic acid) tetrasodium salt] is a non-nucleotide P2Y11 agonist and stimulates release of interleukin-8 from human monocyte-derived dendritic cells
Sabine Meis, Alexandra Hamacher, Darunee Hongwiset, et al.
The Journal of Biological Chemistry
|
November 25, 2010
Amino acid residues constituting the agonist binding site of the human P2X3 receptor
Mandy Bodnar, Haihong Wang, Thomas Riedel, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology
|
April 14, 2021
Effects of Perfusion Pressures on Podocyte Loss in the Isolated Perfused Mouse Kidney
Thiago Strieder, Victor G Puelles, Michael Vogt, et al.
The Journal of Biological Chemistry
|
March 2, 2012
ATP binding site mutagenesis reveals different subunit stoichiometry of functional P2X2/3 and P2X2/6 receptors
Ralf Hausmann, Mandy Bodnar, Ronja Woltersdorf, et al.
British Journal of Pharmacology
|
July 15, 2020
Uncoupling sodium channel dimers restores the phenotype of a pain-linked Na<sub>v</sub> 1.7 channel mutation
Annika H Rühlmann, Jannis Körner, Ralf Hausmann, et al.
Purinergic Signalling
|
May 29, 2021
BAC transgenic mice to study the expression of P2X2 and P2Y<sub>1</sub> receptors
Marcus Grohmann, Michaela Schumacher, Janka Günther, et al.
Nature Communications
|
August 19, 2018
Author Correction: The ASIC3/P2X3 cognate receptor is a pain-relevant and ligand-gated cationic channel
Gabriele Stephan, Lumei Huang, Yong Tang, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 45) with videos related to
Sort By:
Page
of 5
Frontiers in Pharmacology
|
June 19, 2023
Corrigendum: Diclofenac and other non-steroidal anti-inflammatory drugs (NSAIDs) are competitive antagonists of the human P2X3 receptor
Laura Grohs, Linhan Cheng, Saskia Cönen, et al.
Frontiers in Pharmacology
|
April 3, 2023
Diclofenac and other non-steroidal anti-inflammatory drugs (NSAIDs) are competitive antagonists of the human P2X3 receptor
Laura Grohs, Linhan Cheng, Saskia Cönen, et al.
Journal of Medicinal Chemistry
|
October 28, 2005
Synthesis and structure-activity relationships of suramin-derived P2Y11 receptor antagonists with nanomolar potency
Heiko Ullmann, Sabine Meis, Darunee Hongwiset, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
October 10, 2009
NF546 [4,4'-(carbonylbis(imino-3,1-phenylene-carbonylimino-3,1-(4-methyl-phenylene)-carbonylimino))-bis(1,3-xylene-alpha,alpha'-diphosphonic acid) tetrasodium salt] is a non-nucleotide P2Y11 agonist and stimulates release of interleukin-8 from human monocyte-derived dendritic cells
Sabine Meis, Alexandra Hamacher, Darunee Hongwiset, et al.
The Journal of Biological Chemistry
|
November 25, 2010
Amino acid residues constituting the agonist binding site of the human P2X3 receptor
Mandy Bodnar, Haihong Wang, Thomas Riedel, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology
|
April 14, 2021
Effects of Perfusion Pressures on Podocyte Loss in the Isolated Perfused Mouse Kidney
Thiago Strieder, Victor G Puelles, Michael Vogt, et al.
The Journal of Biological Chemistry
|
March 2, 2012
ATP binding site mutagenesis reveals different subunit stoichiometry of functional P2X2/3 and P2X2/6 receptors
Ralf Hausmann, Mandy Bodnar, Ronja Woltersdorf, et al.
British Journal of Pharmacology
|
July 15, 2020
Uncoupling sodium channel dimers restores the phenotype of a pain-linked Na<sub>v</sub> 1.7 channel mutation
Annika H Rühlmann, Jannis Körner, Ralf Hausmann, et al.
Purinergic Signalling
|
May 29, 2021
BAC transgenic mice to study the expression of P2X2 and P2Y<sub>1</sub> receptors
Marcus Grohmann, Michaela Schumacher, Janka Günther, et al.
Nature Communications
|
August 19, 2018
Author Correction: The ASIC3/P2X3 cognate receptor is a pain-relevant and ligand-gated cationic channel
Gabriele Stephan, Lumei Huang, Yong Tang, et al.
Page
of 5