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Editorial A new era for GPCR research: structures, biology and drug discovery [P 289-290] Review Structure
and activation of rhodopsin [P 291-299] Structure
and mechanism for recognition of peptide hormones by Class B G-protein-coupled
receptors [P 300-311] Structure
and ligand recognition of class C GPCRs [P 312-323] Ice
breaking in GPCR structural biology [P 324-334] β-Adrenergic
receptor subtype signaling in heart: From bench to bedside [P 335-341] Role
of G protein-coupled receptors in inflammation [P 342-350] GPCRs
and cancer [P 351-362] Orphan
G protein-coupled receptors (GPCRs): biological functions and potential drug
targets [P 363-371] Tools
for GPCR drug discovery [P 372-384]
Neuropharmacology Rapamycin
prevents the mutant huntingtin-suppressed GLT-1 expression in cultured
astrocytes [P 385-392]
High-sodium
intake aggravates myocardial injuries induced by aldosterone via oxidative
stress in Sprague-Dawley rats [P 393-400]
Heterogeneity
of chemosensitivity in esophageal cancer using ATP-tumor chemosensitivity
assay [P 401-406] Novel
microtubule-targeted agent 6-chloro-4-(methoxyphenyl) coumarin induces G2-M
arrest and apoptosis in HeLa cells [P 407-417]
Thiazolidione
derivatives targeting the histidine kinase YycG are effective against both
planktonic and biofilm-associated Staphylococcus epidermidis [P 418-425]
Differential
sensitivity of RIP3-proficient and deficient murine fibroblasts to camptothecin
anticancer drugs [P 426-428] |
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