about
The binding orientation of epibatidine at α7 nACh receptorsThe binding orientations of structurally-related ligands can differ; A cautionary noteThe antimalarial drugs quinine, chloroquine and mefloquine are antagonists at 5-HT3 receptors.Loop B is a major structural component of the 5-HT3 receptor.The SLC1 high-affinity glutamate and neutral amino acid transporter family.A review of fluorescent ligands for studying 5-HT3 receptors.Tracking individual membrane proteins and their biochemistry: The power of direct observation.The origin of the low-spin character of the resting state of cytochrome P450cam investigated by means of active site analogues.Design, synthesis and pharmacological characterization of analogs of 2-aminoethyl diphenylborinate (2-APB), a known store-operated calcium channel blocker, for inhibition of TRPV6-mediated calcium transport.Synthesis and Pharmacological Evaluation of [11C]Granisetron and [18F]Fluoropalonosetron as PET Probes for 5-HT3 Receptor Imaging.Discovery of Novel Adenosine Receptor Agonists That Exhibit Subtype Selectivity.The antimalarial drug proguanil is an antagonist at 5-HT3 receptors.Characterizing new fluorescent tools for studying 5-HT₃ receptor pharmacology.Identification of potent and selective small molecule inhibitors of the cation channel TRPM4.Lighting up neuroscienceMapping the Orthosteric Binding Site of the Human 5-HT3 Receptor Using Photo-cross-linking AntagonistsA challenge finding P2X1 and P2X4 ligands
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Martin Lochner
@ast
Martin Lochner
@en
Martin Lochner
@es
Martin Lochner
@nl
Martin Lochner
@sl
type
label
Martin Lochner
@ast
Martin Lochner
@en
Martin Lochner
@es
Martin Lochner
@nl
Martin Lochner
@sl
prefLabel
Martin Lochner
@ast
Martin Lochner
@en
Martin Lochner
@es
Martin Lochner
@nl
Martin Lochner
@sl
P106
P21
P31
P496
0000-0003-4930-1886
P569
2000-01-01T00:00:00Z