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《分子药理学杂志》2007年第11期

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ligand-directed signaling: 50 ways to find a lover
parawixin1: a spider toxin opening new avenues for glutamate transporter pharmacology
regulation of glutathione synthesis via interaction between glutamate transport-associated protein 3-18 (gtrap3-18) and excitatory amino acid carrier-1 (eaac1) at p..
identification of two new synthetic histone deacetylase inhibitors that modulate globin gene expression in erythroid cells from healthy donors and patients with tha..
2-amino-n-{4-[5-(2-phenanthrenyl)-3-(trifluoromethyl)-1h-pyrazol-1-yl]-phenyl} acetamide (osu-03012), a celecoxib derivative, directly targets p21-activated kinase
purinergic 2x1 receptors mediate endothelial dependent vasodilation to atp
8-benzyl-4-oxo-8-azabicyclo[3.2.1]oct-2-ene-6,7-dicarboxylic acid (sd-1008), a novel janus kinase 2 inhibitor, increases chemotherapy sensitivity in human ovarian c..
capacitative calcium entry contributes to the differential transactivation of the epidermal growth factor receptor in response to thiazolidinediones
regulation of d1 dopamine receptor trafficking and signaling by caveolin-1
evaluation of action mechanisms of toxic chemicals using jfcr39, a panel of human cancer cell lines
dimerization region of soluble guanylate cyclase characterized by bimolecular fluorescence complementation in vivo
rational engineering of human cytochrome p450 2b6 for enhanced expression and stability: importance of a leu264phe substitution
assessment of the roles of serines 5.43(239) and 5.46(242) for binding and potency of agonist ligands at the human serotonin 5-ht2a receptor
g interferes with ca2+-dependent binding of synaptotagmin to the soluble n-ethylmaleimide-sensitive factor attachment protein receptor (snare) complex
mammalian skeletal muscle voltage-gated sodium channels are affected by scorpion depressant "insect-selective" toxins when preconditioned
enhancing glutamate transport: mechanism of action of parawixin1, a neuroprotective compound from parawixia bistriata spider venom
peroxisomal proliferator-activated receptor- protects renal tubular cells from doxorubicin-induced apoptosis
inhibition of trail gene expression by cyclopentenonic prostaglandin 15-deoxy-12,14-prostaglandin j2 in t lymphocytes
pharmacological characterization and molecular determinants of the activation of transient receptor potential v2 channel orthologs by 2-aminoethoxydiphenyl borate
ccaat/enhancer binding protein homologous protein-dependent death receptor 5 induction and ubiquitin/proteasome-mediated cellular flice-inhibitory protein down-regu..
polymorphic variants of cyp2c9: mechanisms involved in reduced catalytic activity
involvement of the 90-kda heat shock protein (hsp-90) in cb2 cannabinoid receptor-mediated cell migration: a new role of hsp-90 in migration signaling of a g protei..
role of protein kinase c and its adaptor protein p62 in voltage-gated potassium channel modulation in pulmonary arteries
association of nucleophosmin negatively regulates cxcr4-mediated g protein activation and chemotaxis
the neurosteroids dehydroepiandrosterone sulfate and pregnenolone sulfate inhibit the unc-49 gaba receptor through a common set of residues
inhibition of the na+/dicarboxylate cotransporter by anthranilic acid derivatives
geranylgeranylacetone, an inducer of the 70-kda heat shock protein (hsp70), elicits unfolded protein response and coordinates cellular fate independently of hsp70
disruption of clock gene expression alters responses of the aryl hydrocarbon receptor signaling pathway in the mouse mammary gland
ligand-directed signaling at the 3-adrenoceptor produced by 3-(2-ethylphenoxy)-1-[(1,s)-1,2,3,4-tetrahydronapth-1-ylamino]-2s-2-propanol oxalate (sr59230a) relative..
evidence for an aryl hydrocarbon receptor-mediated cytochrome p450 autoregulatory pathway
activation of nuclear factor (erythroid-2 like) factor 2 by toxic bile acids provokes adaptive defense responses to enhance cell survival at the emergence of oxidat..
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