about
Tools for GPCR drug discovery.Dopamine D(2) receptor function is compromised in the brain of the methionine sulfoxide reductase A knockout mouseBinding of NIR-conPK and NIR-6T to astrocytomas and microglial cells: evidence for a protein related to TSPO.Agonists and antagonists bind to an A-A interface in the heteromeric 5-HT3AB receptor.Ligand-receptor interaction rates in the presence of convective mass transport.Diclofenac distinguishes among homomeric and heteromeric potassium channels composed of KCNQ4 and KCNQ5 subunitsNesfatin-1 induces the phosphorylation levels of cAMP response element-binding protein for intracellular signaling in a neural cell lineIdentification of the alpha1L-adrenoceptor in rat cerebral cortex and possible relationship between alpha1L- and alpha1A-adrenoceptorsAlpha-1 adrenoceptors: evaluation of receptor subtype-binding kinetics in intact arterial tissues and comparison with membrane bindingCross-platform comparison of nucleic acid hybridization: toward quantitative reference standards.Novel fluorescent antagonist as a molecular probe in A(3) adenosine receptor binding assays using flow cytometry.Analytical expressions for the homotropic binding of ligand to protein dimers and trimersLighting up G protein-coupled purinergic receptors with engineered fluorescent ligands.Loop B is a major structural component of the 5-HT3 receptor.Radioligand saturation binding for quantitative analysis of ligand-receptor interactions.Optimum conditions of radioligand receptor binding assay of ligands of benzodiazepine receptors.Low affinity GPCRs for metabolic intermediates: challenges for pharmacologists.Re-evaluation of nicotinic acetylcholine receptors in rat brain by a tissue-segment binding assay.Considerations in the Development of Reversibly Binding PET Radioligands for Brain Imaging.Maternal separation diminishes α-adrenergic receptor density and function in renal vasculature from male Wistar-Kyoto rats.Tactics for preclinical validation of receptor-binding radiotracers.Decorin is a novel VEGFR-2-binding antagonist for the human extravillous trophoblast[(3)H]Adenine is a suitable radioligand for the labeling of G protein-coupled adenine receptors but shows high affinity to bacterial contaminations in buffer solutions.A general protocol for the crystallization of membrane proteins for X-ray structural investigation.Development of DOTA-Rituximab to be Labeled with 90Y for Radioimmunotherapy of B-cell Non-Hodgkin Lymphoma.Cell-Binding Assays for Determining the Affinity of Protein-Protein Interactions: Technologies and Considerations.Overview of the detection methods for equilibrium dissociation constant KD of drug-receptor interaction.
P2860
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P2860
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年学术文章
@wuu
1993年学术文章
@zh-cn
1993年学术文章
@zh-hans
1993年学术文章
@zh-my
1993年学术文章
@zh-sg
1993年學術文章
@yue
1993年學術文章
@zh
1993年學術文章
@zh-hant
name
Radioligand binding methods: practical guide and tips.
@en
type
label
Radioligand binding methods: practical guide and tips.
@en
prefLabel
Radioligand binding methods: practical guide and tips.
@en
P1476
Radioligand binding methods: practical guide and tips.
@en
P2093
P304
P356
10.1152/AJPLUNG.1993.265.5.L421
P407
P433
P577
1993-11-01T00:00:00Z