Gustav Akk, PhD

Affiliations: 
Washington University, Saint Louis, St. Louis, MO 
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"Gustav Akk"
Mean distance: 15.69 (cluster 11)
 
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Publications

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Germann AL, Shin DJ, Manion BD, et al. (2016) Activation and modulation of recombinant glycine and GABAA receptors by 4-halogenated analogues of propofol. British Journal of Pharmacology
Chakrabarti S, Qian M, Krishnan K, et al. (2016) Comparison of Steroid Modulation of Spontaneous Inhibitory Postsynaptic Currents in Cultured Hippocampal Neurons and Steady-State Single-Channel Currents from Heterologously Expressed α1β2γ2L GABAA Receptors. Molecular Pharmacology
Akk G. (2015) Meet Our Editorial Board Member. Current Neuropharmacology. 13: 1-0
Eaton MM, Cao LQ, Chen Z, et al. (2015) Mutational Analysis of the Putative High-Affinity Propofol Binding Site in Human β3 Homomeric GABAA Receptors. Molecular Pharmacology. 88: 736-45
Li P, Akk G. (2015) Synaptic-type α1β2γ2L GABAA receptors produce large persistent currents in the presence of ambient GABA and anesthetic drugs. Molecular Pharmacology. 87: 776-81
Eaton MM, Bracamontes J, Shu HJ, et al. (2014) γ-aminobutyric acid type A α4, β2, and δ subunits assemble to produce more than one functionally distinct receptor type. Molecular Pharmacology. 86: 647-56
Li P, Bracamontes JR, Manion BD, et al. (2014) The neurosteroid 5β-pregnan-3α-ol-20-one enhances actions of etomidate as a positive allosteric modulator of α1β2γ2L GABAA receptors. British Journal of Pharmacology. 171: 5446-57
Chen ZW, Wang C, Krishnan K, et al. (2014) 11-trifluoromethyl-phenyldiazirinyl neurosteroid analogues: potent general anesthetics and photolabeling reagents for GABAA receptors. Psychopharmacology. 231: 3479-91
Bracamontes JR, Li P, Akk G, et al. (2014) Mutations in the main cytoplasmic loop of the GABA(A) receptor α4 and δ subunits have opposite effects on surface expression. Molecular Pharmacology. 86: 20-7
Qian M, Krishnan K, Kudova E, et al. (2014) Neurosteroid analogues. 18. Structure-activity studies of ent-steroid potentiators of γ-aminobutyric acid type A receptors and comparison of their activities with those of alphaxalone and allopregnanolone. Journal of Medicinal Chemistry. 57: 171-90
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