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《分子药理学杂志》2006年第07期

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class b gpcrs: a hidden agonist within?
interleukin-2 suppression by 2-arachidonyl glycerol is mediated through peroxisome proliferator-activated receptor independently of cannabinoid receptors 1 and 2
resveratrol suppresses tumor necrosis factor--induced fractalkine expression in endothelial cells
structure-function analysis of vitamin d 24-hydroxylase (cyp24a1) by site-directed mutagenesis: amino acid residues responsible for species-based difference of cyp2..
novel 1-adrenergic receptor signaling pathways: secreted factors and interactions with the extracellular matrix
comparative study of ortho- and meta-nitrated inhibitors of catechol-o-methyltransferase: interactions with the active site and regioselectivity of o-methylation
estrogens cross-talk to 1b-adrenergic receptors
role of the outer -sheet in divalent cation modulation of 7 nicotinic receptors
sustained aryl hydrocarbon receptor activity attenuates liver regeneration
zip8, member of the solute-carrier-39 (slc39) metal-transporter family: characterization of transporter properties
allosteric interactions with muscarinic acetylcholine receptors: complex role of the conserved tryptophan m2422trp in a critical cluster of amino acids for baseline..
analysis of g protein dimer formation in live cells using multicolor bimolecular fluorescence complementation demonstrates preferences of 1 for particular subunits
possible endogenous agonist mechanism for the activation of secretin family g protein-coupled receptors
relaxin family peptide receptors rxfp1 and rxfp2 modulate camp signaling by distinct mechanisms
untranslated region-dependent exclusive expression of high-sensitivity subforms of 42 and 32 nicotinic acetylcholine receptors
high accumulation of platinum-dna adducts in strial marginal cells of the cochlea is an early event in cisplatin but not carboplatin ototoxicity
serum amyloid a induces contrary immune responses via formyl peptide receptor-like 1 in human monocytes
soluble mimics of the cytoplasmic face of the human v1-vascular vasopressin receptor bind arrestin2 and calmodulin
structural determinants of 4-chloro-m-cresol required for activation of ryanodine receptor type 1
the promoter region of the mdr1 gene is largely invariant, but different single nucleotide polymorphism haplotypes affect mdr1 promoter activity differently in diff..
chemical inducers of rodent glutathione s-transferases down-regulate human gsta1 transcription through a mechanism involving variant hepatic nuclear factor 1-c
functional validation of the genetic polymorphisms of human atp-binding cassette (abc) transporter abcg2: identification of alleles that are defective in porphyrin ..
specific rescue of cystic fibrosis transmembrane conductance regulator processing mutants using pharmacological chaperones
the phenotypic differentiation of locus ceruleus noradrenergic neurons mediated by brain-derived neurotrophic factor is enhanced by corticotropin releasing factor t..
the role of human nucleoside transporters in cellular uptake of 4'-thio--d-arabinofuranosylcytosine and -d-arabinosylcytosine
direct modulation of phospholipase d activity by g
retinoic acids increase p2x2 receptor expression through the 5'-flanking region of p2rx2 gene in rat phaeochromocytoma pc-12 cells
ketoconazole and miconazole are antagonists of the human glucocorticoid receptor: consequences on the expression and function of the constitutive androstane recepto..
subtype specificity of scorpion -toxin tz1 interaction with voltage-gated sodium channels is determined by the pore loop of domain 3
modification and uptake of a cisplatin carbonato complex by jurkat cells
transfection of drug-specific t-cell receptors into hybridoma cells: tools to monitor drug interaction with t-cell receptors and evaluate cross-reactivity to relate..
inhibition of human tyrosyl-dna phosphodiesterase by aminoglycoside antibiotics and ribosome inhibitors
experimental and modeling studies of desensitization of p2x3 receptors
reducing and oxidizing agents sensitize heat-activated vanilloid receptor (trpv1) current
neuroprotective effects of 17-estradiol and nonfeminizing estrogens against h2o2 toxicity in human neuroblastoma sk-n-sh cells
potent modulation of the voltage-gated sodium channel nav1.7 by od1, a toxin from the scorpion odonthobuthus doriae
sphingosine and its analog, the immunosuppressant 2-amino-2-(2-[4-octylphenyl]ethyl)-1,3-propanediol, interact with the cb1 cannabinoid receptor
peroxisome proliferator-activated receptor- and retinoic acid x receptor represses the tgf1 gene via pten-mediated p70 ribosomal s6 kinase-1 inhibition: role for z..
a boronic-chalcone derivative exhibits potent anticancer activity through inhibition of the proteasome
correction to "no nitric oxide for ho-1 from sodium nitroprusside"
potentiation of acetylcholine receptors by divalent cations
a cannabinoid quinone inhibits angiogenesis by targeting vascular endothelial cells
identification of tubulin as the molecular target of proapoptotic pyrrolo-1,5-benzoxazepines
receptor regulation of gene expression of axon guidance molecules: implications for adaptation
agonist-induced cell surface trafficking of an intracellularly sequestered d1 dopamine receptor homo-oligomer
the aryl hydrocarbon receptor signaling pathway is modified through interactions with a kelch protein
phosducin and phosducin-like protein attenuate g-protein-coupled receptor-mediated inhibition of voltage-gated calcium channels in rat sympathetic neurons
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