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XPHuang
@ahuangxp
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@xphuang.bsky.social Biased for GPCRs, NIMH Psychoactive Drug Screening Program (PDSP), Roth Lab, UNC Pharmacology
North Carolina, USA
Joined December 2015
@zenbrainest @DR_WANG_SIBCB Congratulations on the great work @DR_WANG_SIBCB @chengjj_iHuman, and Eric Xu
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Discovery of Guanfacine as a Novel TAAR1 Agonist: A Combination Strategy through Molecular Modeling Studies and Biological Assays #mdpipharmaceuticals via @MDPIOpenAccess
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RT @bopengmicroglia: This is our latest study, about microglia and general anesthesia. The most important part is in the Discussion. https:…
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@zenbrainest "Interestingly, the chemokine ligands CXCL11 and CXCL12 are not able to displace the binding of [3H]VUF15485 to ACKR3." The small ligand is a PAM agonist.
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RT @WackerLab: Tetracyclic antidepressants potently activate serotonin receptors 5-HT1e and 5-HT1F, explaining some of their clinically obs…
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@GpcReid @GPCRHenry @Nedjma36193203 Here is a set of old Gs DREADD GloSensor cAMP data in transiently transfected HEK293 T cells.
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RT @GPCRHenry: An incredible study and resource with many important findings: including reclassification of group I mGluRs and some DREADDs…
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@weinberz @LoydaMorales1 At room temperature, proton potency is about pH 7.5 in Gs GloSensor cAMP assays in HEK293 cells. GPR65 is 'constitutively' activated under neutral condition, assuming medium pH is about 7.4.
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