NMDA receptors mediate calcium accumulation in myelin during chemical ischaemia

Ileana Micu, Quan Jiang, Elaine Coderre, +10

Nature

NeurophysiologyPhysiologyNmda ReceptorsNeuroprotectionNeuroscience +7

Specific T-type calcium channel isoforms are associated with distinct burst phenotypes in deep cerebellar nuclear neurons

Michael L. Molineux, John E. McRory, Bruce E. McKay, +6

Proceedings of the National Academy of Sciences

Different IsoformsDistinct Burst PhenotypesNeurotransmissionSynaptic SignalingCellular Physiology +15

Regulation of neuronal activity by Cav3-Kv4 channel signaling complexes

Dustin Anderson, W. Hamish Mehaffey, Mircea Iftinca, +5

Nature Neuroscience

Molecular NeuroscienceMolecular PhysiologyHyperpolarization (Biology)NeurophysiologyNeuroscience +6

Intermediate conductance calcium-activated potassium channels modulate summation of parallel fiber input in cerebellar Purkinje cells

Jordan D. T. Engbers, Dustin Anderson, Hadhimulya Asmara, +7

Proceedings of the National Academy of Sciences

Glutamate receptors on myelinated spinal cord axons: I. GluR6 kainate receptors

Mohamed Ouardouz, Elaine Coderre, Ajoy Basak, +7

Annals of Neurology

Low Voltage Activation of KCa1.1 Current by Cav3-KCa1.1 Complexes

Renata Rehak, Theodore M. Bartoletti, Jordan D. T. Engbers, +3

PLoS ONE

A novel metabolism-based phenotypic drug discovery platform in zebrafish uncovers HDACs 1 and 3 as a potential combined anti-seizure drug target

Kingsley Ibhazehiebo, Cezar Gavrilovici, Cristiane L de la Hoz, +9

Brain

Hdacs 1Zebrafish UncoversCellular PharmacologyZebrafish GeneticsExperimental Pharmacology +18

RIM1/2-Mediated Facilitation of Cav1.4 Channel Opening Is Required for Ca²⁺-Stimulated Release in Mouse Rod Photoreceptors

Chad P. Grabner, María A. Gandini, Renata Rehak, +3

Journal of Neuroscience

Synaptic TransmissionMolecular BiologyNeurotransmissionOptogeneticsSynaptic Signaling +22

Regulation of the K_V4.2 complex by Ca_V3.1 calcium channels

Dustin Anderson, Renata Rehak, Shahid Hameed, +3

Channels

Functional analysis of congenital stationary night blindness type-2 CACNA1F mutations F742C, G1007R, and R1049W

Jean B. Peloquin, Renata Rehak, Clinton J. Doering, +1

Neuroscience

Developmental BiologyMendelian DisorderOphthalmologyGenetic DisorderGenetics +4