multiple independent functions of arrestins in the regulation of protease-activated receptor-2 signaling and trafficking
the cardiovascular actions of protease-activated receptors
multiple mechanisms are involved in ah receptor-mediated cell cycle arrest
interaction between cardiac calsequestrin and drugs with known cardiotoxicity
estrogen receptor activation of phosphoinositide-3 kinase, akt, and nitric oxide signaling in cerebral blood vessels: rapid and long-term effects
regulation of p2y1 receptor-mediated signaling by the ectonucleoside triphosphate diphosphohydrolase isozymes ntpdase1 and ntpdase2
structural basis for epibatidine selectivity at desensitized nicotinic receptors
palmitoylation and plasma membrane targeting of rgs7 are promoted by o
amphetamines take two to tango: an oligomer-based counter-transport model of neurotransmitter transport explores the amphetamine action
protein kinase c-independent effects of protein kinase d3 in glucose transport in l6 myotubes
dynamics of ca2+-dependent cl- channel modulation by niflumic acid in rabbit coronary arterial myocytes
down-regulation does not mediate natriuretic peptide-dependent desensitization of natriuretic peptide receptor (npr)-a or npr-b: guanylyl cyclase-linked natriuretic..
agonists at opioid receptors spin the wheels to keep the action going
the protein kinase c inhibitor go6976 [12-(2-cyanoethyl)-6,7,12,13-tetrahydro-13-methyl-5-oxo-5h-indolo(2,3-a)pyrrolo(3,4-c)-carbazole] potentiates agonist-induced ..
h3 autoreceptors modulate histamine synthesis through calcium/calmodulin- and camp-dependent protein kinase pathways
gene transfer of cocaine hydrolase suppresses cardiovascular responses to cocaine in rats
antitumor activity of methoxymorpholinyl doxorubicin: potentiation by cytochrome p450 3a metabolism
alternative promoters determine tissue-specific expression profiles of the human microsomal epoxide hydrolase gene (ephx1)
relaxin-3/insulin-like peptide 5 chimeric peptide, a selective ligand for g protein-coupled receptor (gpcr)135 and gpcr142 over leucine-rich repeat-containing g pro..
hepatic expression of the ugt1a9 gene is governed by hepatocyte nuclear factor 4
protein kinase c and epidermal growth factor stimulation of raf1 potentiates adenylyl cyclase type 6 activation in intact cells
coimmunoprecipitation of udp-glucuronosyltransferase isoforms and cytochrome p450 3a4
vascular endothelial cell cyclic nucleotide phosphodiesterases and regulated cell migration: implications in angiogenesis
the nuclear receptor peroxisome proliferator-activated receptor- mediates the anti-inflammatory actions of palmitoylethanolamide
role of human nucleoside transporters in the cellular uptake of two inhibitors of imp dehydrogenase, tiazofurin and benzamide riboside
receptor endocytosis counteracts the development of opioid tolerance
the composition of the -2 adrenergic receptor oligomer affects its membrane trafficking after ligand-induced endocytosis
alterations in activating protein 1 composition correlate with phenotypic differentiation changes induced by resveratrol in human melanoma
b1 bradykinin receptor homo-oligomers in receptor cell surface expression and signaling: effects of receptor fragments
retinoid-induced apoptosis in hl-60 cells is associated with nucleolin down-regulation and destabilization of bcl-2 mrna
2,3,7,8-tetrachlorodibenzo-p-dioxin enhances negative selection of t cells in the thymus but allows autoreactive t cells to escape deletion and migrate to the perip..
reciprocal regulation of agonist and inverse agonist signaling efficacy upon short-term treatment of the human -opioid receptor with an inverse agonist
subunit composition of nicotinic receptors in monkey striatum: effect of treatments with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine or l-dopa
histidine residues 912 and 913 in protein associated with myc are necessary for the inhibition of adenylyl cyclase activity
proteochemometric mapping of the interaction of organic compounds with melanocortin receptor subtypes
development of nonsteroidal anti-inflammatory drug analogs and steroid carboxylates selective for human aldo-keto reductase isoforms: potential antineoplastic agent..
ertiprotafib improves glycemic control and lowers lipids via multiple mechanisms