about
A novel biological activity of praziquantel requiring voltage-operated Ca2+ channel beta subunits: subversion of flatworm regenerative polarity'Death and axes': unexpected Ca²⁺ entry phenologs predict new anti-schistosomal agentsErgot Alkaloids (Re)generate New Leads as Antiparasitics.A Miniaturized Screen of a Schistosoma mansoni Serotonergic G Protein-Coupled Receptor Identifies Novel Classes of Parasite-Selective InhibitorsOpposing roles of voltage-gated Ca2+ channels in neuronal control of regenerative patterning.Characterization of a flatworm inositol (1,4,5) trisphosphate receptor (IP₃R) reveals a role in reproductive physiologyKinetic profiling an abundantly expressed planarian serotonergic GPCR identifies bromocriptine as a perdurant antagonist.Pharmacological profiling an abundantly expressed schistosome serotonergic GPCR identifies nuciferine as a potent antagonistCa²⁺ channels and praziquantel: a view from the free worldDataset for a Dugesia japonica de novo transcriptome assembly, utilized for defining the voltage-gated like ion channel superfamily.The anthelmintic praziquantel is a human serotoninergic G-protein-coupled receptor ligand.Unique pharmacological properties of serotonergic G-protein coupled receptors from cestodes.Coalescing beneficial host and deleterious antiparasitic actions as an antischistosomal strategyNon-sedating benzodiazepines cause paralysis and tissue damage in the parasitic blood fluke Schistosoma mansoni
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description
Forscher
@de
chercheur
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investigador
@es
researcher
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wetenschapper
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հետազոտող
@hy
研究者
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name
John D Chan
@ast
John D Chan
@en
John D Chan
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John D Chan
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type
label
John D Chan
@ast
John D Chan
@en
John D Chan
@es
John D Chan
@nl
prefLabel
John D Chan
@ast
John D Chan
@en
John D Chan
@es
John D Chan
@nl
P108
P106
P1153
34867854500
P31
P496
0000-0003-4986-972X