Stephen R. Ikeda, MD, PhD

Affiliations: 
National Institutes of Health, Bethesda, MD 
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"Stephen Ikeda"
Mean distance: 16.85 (cluster 11)
 
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Publications

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Jun SB, Ikeda SR, Sung JE, et al. (2020) Ethanol induces persistent potentiation of 5-HT receptor-stimulated GABA release at synapses on rat hippocampal CA1 neurons. Neuropharmacology. 108415
Colina C, Puhl HL, Ikeda SR. (2018) Selective tracking of FFAR3-expressing neurons supports receptor coupling to N-type calcium channels in mouse sympathetic neurons. Scientific Reports. 8: 17379
Lu VB, Ikeda SR. (2016) Strategies for Investigating G-Protein Modulation of Voltage-Gated Ca2+ Channels. Cold Spring Harbor Protocols. 2016: pdb.top087072
Lu VB, Ikeda SR. (2016) G-Protein Modulation of Voltage-Gated Ca2+ Channels from Isolated Adult Rat Superior Cervical Ganglion Neurons. Cold Spring Harbor Protocols. 2016: pdb.prot091223
Liput DJ, Lu VB, Davis MI, et al. (2016) Rem2, a member of the RGK family of small GTPases, is enriched in nuclei of the basal ganglia. Scientific Reports. 6: 25137
Puhl HL, Won YJ, Lu VB, et al. (2015) Human GPR42 is a transcribed multisite variant that exhibits copy number polymorphism and is functional when heterologously expressed. Scientific Reports. 5: 12880
Lu VB, Ikeda SR, Puhl HL. (2015) A 3.7 kb fragment of the mouse Scn10a gene promoter directs neural crest but not placodal lineage EGFP expression in a transgenic animal. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 8021-34
Puhl HL, Lu VB, Won YJ, et al. (2014) Ancient origins of RGK protein function: modulation of voltage-gated calcium channels preceded the protostome and deuterostome split. Plos One. 9: e100694
Won YJ, Lu VB, Puhl HL, et al. (2013) β-Hydroxybutyrate modulates N-type calcium channels in rat sympathetic neurons by acting as an agonist for the G-protein-coupled receptor FFA3. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 19314-25
Lu VB, Puhl HL, Ikeda SR. (2013) N-Arachidonyl glycine does not activate G protein-coupled receptor 18 signaling via canonical pathways. Molecular Pharmacology. 83: 267-82
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