Zobrazeno 1 - 10
of 14
pro vyhledávání: '"D W, Ford"'
Autor:
Alicja J Copik, Aleksander Baldys, Khanh Nguyen, Sunil Sahdeo, Hoangdung Ho, Alan Kosaka, Paul J Dietrich, Bill Fitch, John R Raymond, Anthony P D W Ford, Donald Button, Marcos E Milla
Publikováno v:
PLoS ONE, Vol 10, Iss 1, p e0115701 (2015)
The α1A-AR is thought to couple predominantly to the Gαq/PLC pathway and lead to phosphoinositide hydrolysis and calcium mobilization, although certain agonists acting at this receptor have been reported to trigger activation of arachidonic acid fo
Externí odkaz:
https://doaj.org/article/f47f66804c3a42b0a43ac356b5af6f80
Autor:
Anthony P D W, Ford, Debra A, Cockayne
Publikováno v:
Handbook of experimental pharmacology. (202)
The pharmacological concept of specifically targeting purinoceptors (receptors for ATP and related nucleotides) has emerged over the last two decades in the quest for novel, differentiated therapeutics. Investigations from many laboratories have esta
Autor:
Joel R, Gever, Rothschild, Soto, Robert A, Henningsen, Renee S, Martin, David H, Hackos, Sandip, Panicker, Werner, Rubas, Ian B, Oglesby, Michael P, Dillon, Marcos E, Milla, Geoffrey, Burnstock, Anthony P D W, Ford
Publikováno v:
British journal of pharmacology. 160(6)
Purinoceptors containing the P2X3 subunit (P2X3 homotrimeric and P2X2/3 heterotrimeric) are members of the P2X family of ion channels gated by ATP and may participate in primary afferent sensitization in a variety of pain-related diseases. The curren
Autor:
Keith R, Bley, Anindya, Bhattacharya, Don V, Daniels, Joel, Gever, Alam, Jahangir, Counde, O'Yang, Steven, Smith, Dinesh, Srinivasan, Anthony P D W, Ford, Mary-Frances, Jett
Publikováno v:
British journal of pharmacology. 147(3)
Prostacyclin (PGI2) possesses various physiological functions, including modulation of nociception, inflammation and cardiovascular activity. Elucidation of these functions has been hampered by the absence of selective IP receptor antagonists. Two st
Autor:
Debra A, Cockayne, Philip M, Dunn, Yu, Zhong, Weifang, Rong, Sara G, Hamilton, Gillian E, Knight, Huai-Zhen, Ruan, Bei, Ma, Ping, Yip, Philip, Nunn, Stephen B, McMahon, Geoffrey, Burnstock, Anthony P D W, Ford
Publikováno v:
The Journal of physiology. 567(Pt 2)
Extracellular ATP plays a role in nociceptive signalling and sensory regulation of visceral function through ionotropic receptors variably composed of P2X2 and P2X3 subunits. P2X2 and P2X3 subunits can form homomultimeric P2X2, homomultimeric P2X3, o
Autor:
Bikramjit, Chopra, Stacey R, Barrick, Susan, Meyers, Jonathan M, Beckel, Mark L, Zeidel, Anthony P D W, Ford, William C, de Groat, Lori A, Birder
Publikováno v:
The Journal of physiology. 562(Pt 3)
The bladder urothelium exhibits dynamic sensory properties that adapt to changes in the local environment. These studies investigated the localization and function of bradykinin receptor subtypes B1 and B2 in the normal and inflamed (cyclophosphamide
Publikováno v:
Neurophysiological Techniques, I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bf78a3867857c3bebb83c2370fcbde0
https://doi.org/10.1385/0-89603-160-8:321
https://doi.org/10.1385/0-89603-160-8:321
Autor:
Barry A, O'Reilly, Alan H, Kosaka, Gillian F, Knight, Thomas K, Chang, Anthony P D W, Ford, Janice M, Rymer, Rick, Popert, Geoffrey, Burnstock, Stephen B, McMahon
Publikováno v:
The Journal of urology. 167(1)
It is clear from previous studies that adenosine triphosphate is released as a contractile co-transmitter with acetylcholine from parasympathetic nerves supplying the mammalian bladder but the physiological significance of ligand gated purinergic P2X
Publikováno v:
Journal of the American College of Surgeons. 181(6)
The American College of Surgeons' Committee on Trauma (ACSCOT) has developed field triage guidelines intended to identify seriously injured patients. Unlike the 1990 version, the 1993 revision calls for on-line medical control assistance with the tri
Autor:
E. H. F. Wong, A. P. D. W. Ford, Richard M. Eglen, Roger L. Whiting, G.C. Harris, J. R. Pfister
Publikováno v:
Naunyn-Schmiedeberg's archives of pharmacology. 345(4)
1. The muscarinic pharmacology of a novel oxadiazole muscarinic agonist, (+/-) L-660,863, [+/-3-(3-amino-1,2,4-oxadiazole-5-yl)-quinuclidine] has been studied using pharmacological, radioligand binding and biochemical techniques, in vitro. 2. In isol