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《分子药理学杂志》2006年第08期

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osu-03012 in the treatment of glioblastoma
chromatin remodeling: a novel mechanism of psychotropic drug action
pharmacology meets vesicular trafficking at a central nervous system synapse: pregabalin effects on synaptic vesicle cycling in hippocampal neurons
a tail of two signals: the c terminus of the a2a-adenosine receptor recruits alternative signaling pathways
cimetidine induces interleukin-18 production through h2-agonist activity in monocytes
rescue of p53 blockage by the a2a adenosine receptor via a novel interacting protein, translin-associated protein x
pregabalin reduces the release of synaptic vesicles from cultured hippocampal neurons
cyp2c76, a novel cytochrome p450 in cynomolgus monkey, is a major cyp2c in liver, metabolizing tolbutamide and testosterone
fluoxetine and cocaine induce the epigenetic factors mecp2 and mbd1 in adult rat brain
isoliquiritigenin selectively inhibits h2 histamine receptor signaling
5'-o-tritylated nucleoside derivatives: inhibition of thymidine phosphorylase and angiogenesis
lithium inhibits ceramide- and etoposide-induced protein phosphatase 2a methylation, bcl-2 dephosphorylation, caspase-2 activation, and apoptosis
transforming growth factor- receptor type 1 (tgfri) kinase activity but not p38 activation is required for tgfri-induced myofibroblast differentiation and profibrot..
mammalian tolloid alters subcellular localization, internalization, and signaling of 1a-adrenergic receptors
regulation of dopamine transporter trafficking by intracellular amphetamine
aryl hydrocarbon receptor activation produces heart-specific transcriptional and toxic responses in developing zebrafish
discovery of a novel shp2 protein tyrosine phosphatase inhibitor
mapping residues in the ligand-binding domain of the 5-ht3 receptor onto d-tubocurarine structure
tamoxifen and raloxifene differ in their functional interactions with aspartate 351 of estrogen receptor
osu-03012 promotes caspase-independent but perk-, cathepsin b-, bid-, and aif-dependent killing of transformed cells
oligomerization of recombinant and endogenously expressed human histamine h4 receptors
a novel class of positive allosteric modulators of metabotropic glutamate receptor subtype 1 interact with a site distinct from that of negative allosteric modulators
hepatocyte nuclear factor (hnf) 1 and hnf4 mediate hepatic multidrug resistance protein 2 up-regulation during hepatitis c virus gene expression
polysaccharide purified from ganoderma lucidum induces gene expression changes in human dendritic cells and promotes t helper 1 immune response in balb/c mice
the three-substituted indolinone cyclin-dependent kinase 2 inhibitor 3-[1-(3h-imidazol-4-yl)-meth-(z)-ylidene]-5-methoxy-1,3-dihydro-indol-2-one (su9516) kills huma..
differences in kinetics of xanomeline binding and selectivity of activation of g proteins at m1 and m2 muscarinic acetylcholine receptors
allosteric interactions required for high-affinity binding of dihydropyridine antagonists to cav1.1 channels are modulated by calcium in the pore
agonist-selective mechanisms of µ-opioid receptor desensitization in human embryonic kidney 293 cells
simultaneous activation of the opioid receptor (or)/sensory neuron-specific receptor-4 (snsr-4) hetero-oligomer by the mixed bivalent agonist bovine adrenal medull..
validation of the anti-inflammatory properties of small-molecule ib kinase (ikk)-2 inhibitors by comparison with adenoviral-mediated delivery of dominant-negative i..
mechanisms of cardiolipin oxidation by cytochrome c: relevance to pro- and antiapoptotic functions of etoposide
state-dependent verapamil block of the cloned human cav3.1 t-type ca2+ channel
cross-talk between gs- and gq-coupled pathways in regulation of interleukin-4 by a2b adenosine receptors in human mast cells
interaction studies of multiple binding sites on m4 muscarinic acetylcholine receptors
divergent activities of human glutathione transferases in the bioactivation of azathioprine
42 nicotinic receptors with high and low acetylcholine sensitivity: pharmacology, stoichiometry, and sensitivity to long-term exposure to nicotine
capacitative and 1-oleyl-2-acetyl-sn-glycerol-activated ca2+ entry distinguished using adenylyl cyclase type 8
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