Related references
Note: Only part of the references are listed.Heterodimerization within the TREK channel subfamily produces a diverse family of highly regulated potassium channels
Joshua Levitz et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2016)
Mixing and matching TREK/TRAAK subunits generate heterodimeric K2P channels with unique properties
Sandy Blin et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2016)
Differential sensitivity of TREK-1, TREK-2 and TRAAK background potassium channels to the polycationic dye ruthenium red
G. Braun et al.
BRITISH JOURNAL OF PHARMACOLOGY (2015)
K+ efflux through two-pore domain K+ channels is required for mouse embryonic development
Chang-Gi Hur et al.
REPRODUCTION (2012)
The primacy of mania: A reconsideration of mood disorders
Athanasios Koukopoulos et al.
EUROPEAN PSYCHIATRY (2009)
Alternative translation initiation in rat brain yields K2P2.1 potassium channels permeable to sodium
Dierk Thomas et al.
NEURON (2008)
Antipsychotics inhibit TREK but not TRAAK channels
Susanne Thummler et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2007)
Animal models of mood disorders: recent developments
John F. Cryan et al.
CURRENT OPINION IN PSYCHIATRY (2007)
Phenytoin and carbamazepine delay the initial depression of the population spike upon exposure to in vitro ischemia and promote its post-ischemic functional recovery in rat hippocampal slices
Mitsuo Tanabe et al.
EUROPEAN JOURNAL OF PHARMACOLOGY (2006)
Mechanism of inhibition of TREK-2 (K2P10.1) by the Gq-coupled M3 muscarinic receptor
Dawon Kang et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2006)
Deletion of the background potassium channel TREK-1 results in a depression-resistant phenotype
Catherine Heurteaux et al.
NATURE NEUROSCIENCE (2006)
Thermosensitivity of the two-pore domain K+ channels TREK-2 and TRAAK
D Kang et al.
JOURNAL OF PHYSIOLOGY-LONDON (2005)
Inhibition of the human two-pore domain potassium channel, TREK-1, by fluoxetine and its metabolite norfluoxetine
LE Kennard et al.
BRITISH JOURNAL OF PHARMACOLOGY (2005)
Physiology and pharmacology of two-pore domain potassium channels
D Kim
CURRENT PHARMACEUTICAL DESIGN (2005)
Mechanisms underlying excitatory effects of group I metabotropic glutamate receptors via inhibition of 2P domain K+ channels
J Chemin et al.
EMBO JOURNAL (2003)
Attenuation of N-methyl-D-aspartate-mediated cytoplasmic vacuolization in primary rat hippocampal neurons by mood stabilizers
CD Bown et al.
NEUROSCIENCE (2003)
Fatty acid-sensitive two-pore domain K+ channels
D Kim
TRENDS IN PHARMACOLOGICAL SCIENCES (2003)
Glycogen synthase kinase-3β, mood stabilizers, and neuroprotection
XH Li et al.
BIPOLAR DISORDERS (2002)
A placebo-controlled study of lamotrigine and gabapentin monotherapy in refractory mood disorders
MA Frye et al.
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY (2000)
A novel evidence of different mechanisms of lithium and valproate neuroprotective action on human SY5Y neuroblastoma cells: caspase-3 dependency
RN Li et al.
NEUROSCIENCE LETTERS (2000)
Brain pharmacokinetics and tissue distribution in vivo of fluvoxamine and fluoxetine by fluorine magnetic resonance spectroscopy
NR Bolo et al.
NEUROPSYCHOPHARMACOLOGY (2000)
TREK-1 is a heat-activated background K+ channel
F Maingret et al.
EMBO JOURNAL (2000)
Share Paper
