the coordination of prostaglandin e2 production by sphingosine-1-phosphate and ceramide-1-phosphate
molecular pharmacology of the interaction of anthracyclines with iron
arsenite-induced aryl hydrocarbon receptor nuclear translocation results in additive induction of phase i genes and synergistic induction of phase ii genes
single mutations at asn295 and leu305 in the cytoplasmic half of transmembrane -helix domain 7 of the at1 receptor induce promiscuous agonist specificity for angiot..
agonist-induced interactions between angiotensin at1 and epidermal growth factor receptors
spatial orientation of the antagonist granisetron in the ligand-binding site of the 5-ht3 receptor
chemotherapy compounds in cervical cancer cells primed by reconstitution of p53 function after short interfering rna-mediated degradation of human papillomavirus 18..
discovery of novel flavin-containing monooxygenase 3 (fmo3) single nucleotide polymorphisms and functional analysis of upstream haplotype variants
identification of indole derivatives exclusively interfering with a g protein-independent signaling pathway of the prostaglandin d2 receptor crth2
a pregnane x receptor agonist with unique species-dependent stereoselectivity and its implications in drug development
down-regulation of na+/ca2+ exchanger by fluvastatin in rat cardiomyoblast h9c2 cells: involvement of rhob in na+/ca2+ exchanger mrna stability
camp and extracellular signal-regulated kinase signaling in response to d-amphetamine and methylphenidate in the prefrontal cortex in vivo: role of 1-adrenoceptors
how the monoamine transporter garden grows
expression profiling of abc transporters in a drug-resistant breast cancer cell line using amparray
integrin engagement increases histone h3 acetylation and reduces histone h1 association with dna in murine lung endothelial cells
orphanin fq/nociceptin potentiates [d-ala2,n-me-phe4,gly5-ol]-enkephalinecinduced eopioid receptor phosphorylation
single nucleotide polymorphisms in the human norepinephrine transporter gene affect expression, trafficking, antidepressant interaction, and protein kinase c regula..
long-term morphine treatment enhances proteasome-dependent degradation of g in human neuroblastoma sh-sy5y cells: correlation with onset of adenylate cyclase sensit..
characterization of a human carcinoma cell line selected for resistance to the farnesyl transferase inhibitor 4-(2-(4-(8-chloro-3,10-dibromo-6,11-dihydro-5h-benzo-(..
mutations linked to autosomal dominant nocturnal frontal lobe epilepsy affect allosteric ca2+ activation of the 42 nicotinic acetylcholine receptor
kahalalide f induces necrosis-like cell death that involves depletion of erbb3 and inhibition of akt signaling
coactivation of the human vitamin d receptor by the peroxisome proliferator-activated receptor coactivator-1
conservation of functional and pharmacological properties in the distantly related temperature sensors trpv1 and trpm8
double feature at the signalplex
n-methyl-d-aspartate attenuates cxcr2-mediated neuroprotection through enhancing the receptor phosphorylation and blocking the receptor recycling
diketo hexenoic acid derivatives are novel selective non-nucleoside inhibitors of mammalian terminal deoxynucleotidyl transferases, with potent cytotoxic effect aga..
the methyl transferase prmt1 functions as co-activator of farnesoid x receptor (fxr)/9-cis retinoid x receptor and regulates transcription of fxr responsive genes
a major species of mouse e?opioid receptor mrna and its promoter-dependent functional polyadenylation signal
novel mechanism of inhibition of nuclear factor-b dna-binding activity by diterpenoids isolated from isodon rubescens
molecular basis of inward rectification: structural features of the blocker defined by extended polyamine analogs
a single residue in the s6 transmembrane domain governs the differential flecainide sensitivity of voltage-gated potassium channels
cyclooxygenase-2 inhibitors decrease vascular endothelial growth factor expression in colon cancer cells by enhanced degradation of sp1 and sp4 proteins