Deletion of TASK1 and TASK3 channels disrupts intrinsic excitability but does not abolish glucose or pH responses of orexin/hypocretin neurons

European Journal of Neuroscience

Volumn 30, Issue 1, 2009, Pages 57-64

  Gonzalez J A ^a   Jensen, Lise T ^b   Doyle, Susan E ^c   Miranda Anaya, Manuel ^d   Menaker, Michael ^c   Fugger, Lars ^e   Bayliss, Douglas A ^f   Burdakov, Denis ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b AARHUS UNIVERSITY HOSPITAL   (Denmark)

^c UNIVERSITY OF VIRGINIA   (United States)

^d UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

^e UNIVERSITY OF OXFORD   (United Kingdom)

^f UNIVERSITY OF VIRGINIA   (United States)

Author keywords

Appetite; Firing; Glucose; Hypothalamus; K channels; Mice; Sleep

Indexed keywords

GLUCOSE; GREEN FLUORESCENT PROTEIN; OREXIN; POTASSIUM CHANNEL; POTASSIUM CHANNEL TASK1; POTASSIUM CHANNEL TASK3; UNCLASSIFIED DRUG;

ACTION POTENTIAL; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN SLICE; CONTROLLED STUDY; KNOCKOUT MOUSE; LOCOMOTION; MOUSE; NONHUMAN; PATCH CLAMP; PH; PRIORITY JOURNAL; SYNAPTIC TRANSMISSION;

ACTION POTENTIALS; ANIMALS; BRAIN; FEEDING BEHAVIOR; GLUCOSE; GREEN FLUORESCENT PROTEINS; HYDROGEN-ION CONCENTRATION; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MEMBRANE POTENTIALS; MICE; MICE, KNOCKOUT; MICE, TRANSGENIC; MOTOR ACTIVITY; NERVE TISSUE PROTEINS; NEURONS; NEUROPEPTIDES; PATCH-CLAMP TECHNIQUES; POTASSIUM CHANNELS; POTASSIUM CHANNELS, TANDEM PORE DOMAIN;

EID: 67649865276     PISSN: 0953816X     EISSN: 14609568     Source Type: Journal    
DOI: 10.1111/j.1460-9568.2009.06789.x     Document Type: Article

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