Boehm, S.
Stefan Boehm
Böhm, Stefan 1963-
VIAF ID: 70136009 (Personal)
Permalink: http://viaf.org/viaf/70136009
Preferred Forms
- 100 1 _ ‡a Boehm, S.
- 100 1 _ ‡a Boehm, S.
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- 100 1 _ ‡a Böhm, Stefan ‡d 1963-
- 100 0 _ ‡a Stefan Boehm
4xx's: Alternate Name Forms (3)
5xx's: Related Names (3)
- 510 2 _ ‡a Medizinische Universität Wien ‡b Zentrum für Physiologie und Pharmakologie ‡4 affi ‡4 https://d-nb.info/standards/elementset/gnd#affiliation ‡e Affiliation
- 551 _ _ ‡a Wien ‡4 ortg ‡4 https://d-nb.info/standards/elementset/gnd#placeOfBirth
- 551 _ _ ‡a Wien ‡4 ortw ‡4 https://d-nb.info/standards/elementset/gnd#placeOfActivity
Works
Title | Sources |
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Age-dependent sensitivity to glucocorticoids in the developing mouse basolateral nucleus of the amygdala. | |
Amphetamine actions at the serotonin transporter rely on the availability of phosphatidylinositol-4,5-bisphosphate | |
Anti-addiction drug ibogaine inhibits hERG channels: a cardiac arrhythmia risk | |
Anti-addiction Drug Ibogaine Prolongs the Action Potential in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes | |
The anticonvulsant retigabine is a subtype selective modulator of GABAA receptors. | |
The brain-specific double-stranded RNA-binding protein Staufen2 is required for dendritic spine morphogenesis | |
Calcium-activated chloride channels: Potential targets for antinociceptive therapy | |
Concomitant facilitation of GABAA receptors and KV7 channels by the non-opioid analgesic flupirtine. | |
Constitutive activity of the A2A adenosine receptor and compartmentalised cyclic AMP signalling fine-tune noradrenaline release | |
Control of sensory neuron excitability by serotonin involves 5HT2C receptors and Ca(2+)-activated chloride channels. | |
CSTX-1, a toxin from the venom of the hunting spider Cupiennius salei, is a selective blocker of L-type calcium channels in mammalian neurons. | |
Differential fading of inhibitory and excitatory B2 bradykinin receptor responses in rat sympathetic neurons: a role for protein kinase C. | |
Distribution of M-channel subunits KCNQ2 and KCNQ3 in rat hippocampus | |
Dynamic interplay of excitatory and inhibitory coupling modes of neuronal L-type calcium channels. | |
Electrophysiological Investigation of the Subcellular Fine Tuning of Sympathetic Neurons by Hydrogen Sulfide. | |
Electrophysiological profiles of induced neurons converted directly from adult human fibroblasts indicate incomplete neuronal conversion | |
Evidence for structural and functional diversity among SDS-resistant SNARE complexes in neuroendocrine cells | |
G proteins as drug targets | |
The human D2 dopamine receptor synergizes with the A2A adenosine receptor to stimulate adenylyl cyclase in PC12 cells. | |
Mapping of calmodulin and Gbetagamma binding domains within the C-terminal region of the metabotropic glutamate receptor 7A. | |
The mechanistic basis for noncompetitive ibogaine inhibition of serotonin and dopamine transporters | |
A membrane network of receptors and enzymes for adenine nucleotides and nucleosides. | |
Modulation of calcium currents via ?2-adrenoceptors in embryonic chick sympathetic neurons | |
Modulation of the heart's electrical properties by the anticonvulsant drug retigabine. | |
Molecular mechanisms underlying the modulation of exocytotic noradrenaline release via presynaptic receptors | |
Nucleotides control the excitability of sensory neurons via two P2Y receptors and a bifurcated signaling cascade. | |
Opposite effects of presynaptic 5-HT3 receptor activation on spontaneous and action potential-evoked GABA release at hippocampal synapses. | |
The paracetamol metabolite N-acetylp-benzoquinone imine reduces excitability in first- and second-order neurons of the pain pathway through actions on KV7 channels | |
The Paroxysmal Depolarization Shift: Reconsidering Its Role in Epilepsy, Epileptogenesis and Beyond | |
Pharmacological characterization of P2 purinoceptor types in rat locus coeruleus neurons. | |
Pharmacology of neurotransmitter release, c2008: | |
Pharmakologie und Toxikologie Von den molekularen Grundlagen zur Pharmakotherapie | |
Presynaptic alpha2-adrenoceptors control excitatory, but not inhibitory, transmission at rat hippocampal synapses. | |
Raised activity of L-type calcium channels renders neurons prone to form paroxysmal depolarization shifts. | |
Receptors controlling transmitter release from sympathetic neurons in vitro. | |
Regulation of neuronal ion channels via P2Y receptors | |
Selective inhibition of M-type potassium channels in rat sympathetic neurons by uridine nucleotide preferring receptors | |
Serotonin-transporter mediated efflux: a pharmacological analysis of amphetamines and non-amphetamines | |
Signaling via nucleotide receptors in the sympathetic nervous system | |
Somatic and prejunctional nicotinic receptors in cultured rat sympathetic neurones show different agonist profiles | |
Synthesis and Calcium Antagonistic Activity of 8-[N-[2-(3,4-Dimethoxyphenyl)ethyl]-β-alanyl]-5,6,7,8-tetrahydrothieno[3,2-b][1,4]thiazepine Fumarate | |
Time-dependent reversal of synaptic plasticity induced by physiological concentrations of oligomeric Aβ42: an early index of Alzheimer's disease. | |
L-type Ca2+ channel-mediated Ca2+ influx adjusts neuronal mitochondrial function to physiological and pathophysiological conditions | |
The ubiquitin-specific protease Usp4 regulates the cell surface level of the A2A receptor | |
Unifying concept of serotonin transporter-associated currents | |
An unsuspected role for organic cation transporter 3 in the actions of amphetamine | |
Updating in vivo and in vitro phosphorylation and methylation sites of voltage-gated Kv7.2 potassium channels | |
α2-adrenoreceptor-mediated inhibition of acetylcholine-induced noradrenaline release from rat sympathetic neurons: An action at voltage-gated Ca2+ channels | |
δ Subunit-containing GABAA receptors are preferred targets for the centrally acting analgesic flupirtine. |