Hee-Sup Shin

Molecular basis of R-type calcium channels in central amygdala neurons of the mouse.

Role of the beta(2) subunit of voltage-dependent calcium channels in the retinal outer plexiform layer.

Functional Roles of Ca(v)1.3 (alpha(1D)) calcium channel in sinoatrial nodes: insight gained using gene-targeted null mutant mice.

Acetylcholine-induced phosphatidylinositol 4,5-bisphosphate depletion does not cause short-term desensitization of G protein-gated inwardly rectifying K+ current in mouse atrial myocytes.

A perforated patch-clamp study of calcium currents and exocytosis in chromaffin cells of wild-type and alpha(1A) knockout mice.

In vivo differentiation of mouse embryonic stem cells into hepatocytes.

Impaired D2 dopamine receptor function in mice lacking type 5 adenylyl cyclase.

Role of synaptic metabotropic glutamate receptors in epileptiform discharges in hippocampal slices.

Cerebellar slice cultures from mice lacking the P/Q calcium channel: electroresponsiveness of Purkinje cells.

Molecular characterization of a two-domain form of the neuronal voltage-gated P/Q-type calcium channel alpha(1)2.1 subunit.

Peroxiredoxin II is essential for sustaining life span of erythrocytes in mice.

Altered properties of quantal neurotransmitter release at endplates of mice lacking P/Q-type Ca2+ channels.

Translation of clock rhythmicity into neural firing in suprachiasmatic nucleus requires mGluR-PLCbeta4 signaling.

Partial rescue of the Na+-Ca2+ exchanger (NCX1) knock-out mouse by transgenic expression of NCX1.

Enhanced learning and memory in mice lacking Na+/Ca2+ exchanger 2.

Repression of phospho-JNK and infarct volume in ischemic brain of JIP1-deficient mice.

Thalamic control of visceral nociception mediated by T-type Ca2+ channels.

P/Q-type Ca2+ channel alpha1A regulates synaptic competition on developing cerebellar Purkinje cells.

Altered GABAergic neurotransmission in mice lacking dopamine D2 receptors.

Biophysical and pharmacological characterization of spermatogenic T-type calcium current in mice lacking the CaV3.1 (alpha1G) calcium channel: CaV3.2 (alpha1H) is the main functional calcium channel in wild-type spermatogenic cells.

Role of the alpha1G T-type calcium channel in spontaneous absence seizures in mutant mice.

Null mutation of alpha1D Ca2+ channel gene results in deafness but no vestibular defect in mice.

Human neural stem cell transplantation reduces spontaneous recurrent seizures following pilocarpine-induced status epilepticus in adult rats.

Deletion of N-type calcium channels alters ethanol reward and reduces ethanol consumption in mice.

The axon guidance defect of the telencephalic commissures of the JSAP1-deficient brain was partially rescued by the transgenic expression of JIP1.

Lack of delta waves and sleep disturbances during non-rapid eye movement sleep in mice lacking alpha1G-subunit of T-type calcium channels.

Phospholipase Cbeta serves as a coincidence detector through its Ca2+ dependency for triggering retrograde endocannabinoid signal.

Phospholipase C-beta3 mediates the thrombin-induced Ca2+ response in glial cells.

Presynaptic N-type and P/Q-type Ca2+ channels mediating synaptic transmission at the calyx of Held of mice.

Functional roles of Cav1.3(alpha1D) calcium channels in atria: insights gained from gene-targeted null mutant mice.

Genetic dissection of theta rhythm heterogeneity in mice.

Multiple receptors coupled to phospholipase C gate long-term depression in visual cortex.

Editorial retraction.

Bradycardia and slowing of the atrioventricular conduction in mice lacking CaV3.1/alpha1G T-type calcium channels.

T-type Ca2+ channels and absence epilepsy.

Thyrotropin-releasing hormone increases GABA release in rat hippocampus.

Reduced nicotinic receptor function in sympathetic ganglia is responsible for the hypothermia in the acetylcholinesterase knockout mouse.

Molecular coupling of a Ca2+-activated K+ channel to L-type Ca2+ channels via alpha-actinin2.

Genetic studies on the role of T-type Ca2+ channels in sleep and absence epilepsy.

Receptor-specific inhibition of GABAB-activated K+ currents by muscarinic and metabotropic glutamate receptors in immature rat hippocampus.

T-type calcium channels and thalamocortical rhythms in sleep: a perspective from studies of T-type calcium channel knockout mice.

Proteomic analysis of gamma-butyrolactone-treated mouse thalamus reveals dysregulated proteins upon absence seizure.

Expression, localization and functions in acrosome reaction and sperm motility of Ca(V)3.1 and Ca(V)3.2 channels in sperm cells: an evaluation from Ca(V)3.1 and Ca(V)3.2 deficient mice.

Reducing agents sensitize C-type nociceptors by relieving high-affinity zinc inhibition of T-type calcium channels.

Adrenergic facilitation of GABAergic transmission in rat entorhinal cortex.

Na(+)/Ca(2+) exchanger 2 is neuroprotective by exporting Ca(2+) during a transient focal cerebral ischemia in the mouse.

Gamma-band deficiency and abnormal thalamocortical activity in P/Q-type channel mutant mice.

Proteomic analysis of stargazer mutant mouse neuronal proteins involved in absence seizure.

T-type Ca2+ channels as therapeutic targets in the nervous system.

Ablation of Ca2+ channel beta3 subunit leads to enhanced N-methyl-D-aspartate receptor-dependent long term potentiation and improved long term memory.

Attenuated neuropathic pain in Cav3.1 null mice.

Modulation of Ca(v)3.1 T-type Ca2+ channels by the ran binding protein RanBPM.

A blocker of N- and T-type voltage-gated calcium channels attenuates ethanol-induced intoxication, place preference, self-administration, and reinstatement.

Deletion of N-type Ca(2+) channel Ca(v)2.2 results in hyperaggressive behaviors in mice.

Tuning thalamic firing modes via simultaneous modulation of T- and L-type Ca2+ channels controls pain sensory gating in the thalamus.

The Ca(v)3.2 T-type Ca(2+) channel is required for pressure overload-induced cardiac hypertrophy in mice.

Piezo motor based microdrive for neural signal recording.

Comprehensive analysis of microRNA-mRNA co-expression in circadian rhythm.

Ca2+ entry via alpha1G and TRPV4 channels differentially regulates surface expression of P-selectin and barrier integrity in pulmonary capillary endothelium.

Inositol 1,4,5-trisphosphate 3-kinase a functions as a scaffold for synaptic Rac signaling.

Deletion of phospholipase C beta4 in thalamocortical relay nucleus leads to absence seizures.

A flexible microelectrode for mouse EEG.

Simultaneous recording of brain activity and functional connectivity in the mouse brain.

Phospholipase C beta 4 in the medial septum controls cholinergic theta oscillations and anxiety behaviors.

Selective T-type calcium channel block in thalamic neurons reveals channel redundancy and physiological impact of I(T)window.

Deletion of Cav2.1(alpha1(A)) subunit of Ca2+-channels impairs synaptic GABA and glutamate release in the mouse cerebellar cortex in cultured slices.

The forced walking test: a novel test for pinpointing the anesthetic-induced transition in consciousness in mouse.

Observational fear learning involves affective pain system and Cav1.2 Ca2+ channels in ACC.

Cholecystokinin facilitates glutamate release by increasing the number of readily releasable vesicles and releasing probability.

Alpha1G T-type calcium channel selectively regulates P-selectin surface expression in pulmonary capillary endothelium.

Ca(V)3.1 is a tremor rhythm pacemaker in the inferior olive.

Subthreshold membrane potential oscillations in inferior olive neurons are dynamically regulated by P/Q- and T-type calcium channels: a study in mutant mice.

High resolution electroencephalography in freely moving mice.

T-type channels control the opioidergic descending analgesia at the low threshold-spiking GABAergic neurons in the periaqueductal gray.

Ca(v)3.2 T-type Ca2+ channel-dependent activation of ERK in paraventricular thalamus modulates acid-induced chronic muscle pain.

Feedback controlled piezo-motor microdrive for accurate electrode positioning in chronic single unit recording in behaving mice.

Channel-mediated tonic GABA release from glia.

Expression and roles of Cav1.3 (α1D) L-type Ca²+ channel in atrioventricular node automaticity.

Requirements for synaptically evoked plateau potentials in relay cells of the dorsal lateral geniculate nucleus of the mouse.

Modulation of synaptic transmission from primary afferents to spinal substantia gelatinosa neurons by group III mGluRs in GAD65-EGFP transgenic mice.

Thalamic ryanodine receptors are involved in controlling the tonic firing of thalamocortical neurons and inflammatory pain signal processing.

Basal sympathetic activity generated in neonatal mouse brainstem-spinal cord preparation requires T-type calcium channel subunit 1H.

Pacemaker activity and ionic currents in mouse atrioventricular node cells.

Functional roles of Ca(v)1.3, Ca(v)3.1 and HCN channels in automaticity of mouse atrioventricular cells: insights into the atrioventricular pacemaker mechanism.

Thalamic T-type Ca²+ channels mediate frontal lobe dysfunctions caused by a hypoxia-like damage in the prefrontal cortex.

Cav2.3 channels are critical for oscillatory burst discharges in the reticular thalamus and absence epilepsy.

Postsynaptic P/Q-type Ca2+ channel in Purkinje cell mediates synaptic competition and elimination in developing cerebellum.

Distribution of voltage gated calcium channel β subunits in the mouse retina.

A mouse model for observational fear learning and the empathetic response.

Cyclic ADP ribose-dependent Ca2+ release by group I metabotropic glutamate receptors in acutely dissociated rat hippocampal neurons.

Requirement of phospholipase C and protein kinase C in cholecystokinin-mediated facilitation of NMDA channel function and anxiety-like behavior.

Bidirectional modulation of fear extinction by mediodorsal thalamic firing in mice.

Cortical mapping of the optically evoked responses in channelrhodopsin-2 mouse model.

Interactive responses of a thalamic neuron to formalin induced lasting pain in behaving mice.