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《分子药理学杂志》2007年第05期

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vitamin e analogs, a novel group of "mitocans," as anticancer agents: the importance of being redox-silent
missing links: mechanisms of protean agonism
the thrill can kill: murder by methylation
all aglow about presynaptic receptor regulation of neurotransmitter transporters
activation of trpa1 channels by the fatty acid amide hydrolase inhibitor 3'-carbamoylbiphenyl-3-yl cyclohexylcarbamate (urb597)
extracellular signal-regulated kinase is an endogenous signal retaining the nuclear constitutive active/androstane receptor (car) in the cytoplasm of mouse primary ..
d2 receptors regulate dopamine transporter function via an extracellular signal-regulated kinases 1 and 2-dependent and phosphoinositide 3 kinase-independent mechan..
reversal of stathmin-mediated resistance to paclitaxel and vinblastine in human breast carcinoma cells
solute-inhibitor interactions in the plasmodial surface anion channel reveal complexities in the transport process
a widely used retinoic acid receptor antagonist induces peroxisome proliferator-activated receptor- activity
synergistic neuroprotection by bis(7)-tacrine via concurrent blockade of n-methyl-d-aspartate receptors and neuronal nitric-oxide synthase
domains necessary for g12 binding and stimulation of protein phosphatase-2a (pp2a): is g12 a novel regulatory subunit of pp2a?
insulin increases the potency of glycine at ionotropic glycine receptors
analogs of methyllycaconitine as novel noncompetitive inhibitors of nicotinic receptors: pharmacological characterization, computational modeling, and pharmacophore..
vitamin d3 derivatives with adamantane or lactone ring side chains are cell type-selective vitamin d receptor modulators
agonist-driven conformational changes in the inner -sheet of 7 nicotinic receptors
maternal cocaine administration causes an epigenetic modification of protein kinase c gene expression in fetal rat heart
real-time analysis of agonist-induced activation of protease-activated receptor 1/gi1 protein complex measured by bioluminescence resonance energy transfer in livin..
conformationally sensitive reactivity to permeant sulfhydryl reagents of cysteine residues engineered into helical hairpin 1 of the glutamate transporter glt-1
protean agonism at the dopamine d2 receptor: (s)-3-(3-hydroxyphenyl)-n-propylpiperidine is an agonist for activation of go1 but an antagonist/inverse agonist for gi..
identification of a second blocker binding site at the cytoplasmic mouth of the cystic fibrosis transmembrane conductance regulator chloride channel pore
molecular signalling mediating the protective effect of a1 adenosine and mglu3 metabotropic glutamate receptor activation against apoptosis by oxygen/glucose depriv..
a critical role of luteolin-induced reactive oxygen species in blockage of tumor necrosis factor-activated nuclear factor-b pathway and sensitization of apoptosis i..
interaction of novel positive allosteric modulators of metabotropic glutamate receptor 5 with the negative allosteric antagonist site is required for potentiation o..
par1, but not par4, activates human platelets through a gi/o/phosphoinositide-3 kinase signaling axis
activation of single nicotinic receptor channels from caenorhabditis elegans muscle
quantitative evaluation of human opioid receptor desensitization using the operational model of drug action
post-transcriptional regulation of human inducible nitric-oxide synthase expression by the jun n-terminal kinase
antiproliferative mechanisms of a transcription factor decoy targeting signal transducer and activator of transcription (stat) 3: the role of stat1
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