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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 5, 2018
Chemogenetic Isolation Reveals Synaptic Contribution of δ GABAA Receptors in Mouse Dentate Granule NeuronsMin-Yu Sun, Hong-Jin Shu, Ann Benz, et al.
Molecular Pharmacology|May 7, 2021
Intrasubunit and Intersubunit Steroid Binding Sites Independently and Additively Mediate α1β2γ2L GABAA Receptor Potentiation by the Endogenous Neurosteroid AllopregnanoloneAllison L Germann, Spencer R Pierce, Hiroki Tateiwa, et al.
British Journal of Pharmacology|July 27, 2016
Activation and modulation of recombinant glycine and GABAA receptors by 4-halogenated analogues of propofolAllison L Germann, Daniel J Shin, Brad D Manion, et al.
ACS Chemical Neuroscience|June 16, 2025
Properties of Acute Activation and Inhibition of the β3 Homomeric GABAA Receptor Mediated by Protonation of Conserved Histidine ResiduesSpencer R Pierce, Allison L Germann, Yu Zhou, et al.
The Journal of Steroid Biochemistry and Molecular Biology|June 1, 2019
The molecular determinants of neurosteroid binding in the GABA(A) receptorYusuke Sugasawa, John R Bracamontes, Kathiresan Krishnan, et al.
Biomolecules|February 25, 2023
The Mechanism of Enantioselective Neurosteroid Actions on GABAA ReceptorsHiroki Tateiwa, Satyanarayana M Chintala, Ziwei Chen, et al.
Science Advances|November 1, 2023
UNC-49 is a redox-sensitive GABAA receptor that regulates the mitochondrial unfolded protein response cell nonautonomouslyFranziska Pohl, Allison L Germann, Jack Mao, et al.
Scientific Reports|July 10, 2018
Enhanced GABAergic actions resulting from the coapplication of the steroid 3α-hydroxy-5α-pregnane-11,20-dione (alfaxalone) with propofol or diazepamLily Q Cao, Michael C Montana, Allison L Germann, et al.
Molecular Pharmacology|June 14, 2023
Chemical, Pharmacological, and Structural Characterization of Novel Acrylamide-Derived Modulators of the GABAA ReceptorHugo R Arias, Spencer R Pierce, Allison L Germann, et al.
Journal of Medicinal Chemistry|December 17, 2013
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 allopregnanoloneMingxing Qian, Kathiresan Krishnan, Eva Kudova, et al.
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