Postnatal loss of P/Q-type channels confined to rhombic-lip-derived neurons alters synaptic transmission at the parallel fiber to purkinje cell synapse and replicates genomic Cacna1a mutation phenotype of ataxia and seizures in mice.

Postnatal loss of P/Q-type channels confined to rhombic-lip-derived neurons alters synaptic transmission at the parallel fiber to purkinje cell synapse and replicates genomic Cacna1a mutation phenotype of ataxia and seizures in mice.

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http://www.wikidata.org/entity/Q40299916
Toll-Like Receptor 4 Deficiency Impairs Motor Coordination.Abnormal synaptic Ca(2+) homeostasis and morphology in cortical neurons of familial hemiplegic migraine type 1 mutant miceGlucose Transporter Type I Deficiency (G1D) at 25 (1990-2015): Presumptions, Facts, and the Lives of Persons With This Rare DiseaseThe first knockin mouse model of episodic ataxia type 2Isolated P/Q Calcium Channel Deletion in Layer VI Corticothalamic Neurons Generates Absence Epilepsy.Altered short-term synaptic plasticity and reduced muscle strength in mice with impaired regulation of presynaptic CaV2.1 Ca2+ channelsPathway-driven discovery of epilepsy genes.Seizing Control: From Current Treatments to Optogenetic Interventions in EpilepsyCurrent Opinions and Areas of Consensus on the Role of the Cerebellum in Dystonia.Pharmacological correction of gating defects in the voltage-gated Ca(v)2.1 Ca²⁺ channel due to a familial hemiplegic migraine mutation.Does modulation of the endocannabinoid system have potential therapeutic utility in cerebellar ataxia?CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.Loss of the calcium channel β4 subunit impairs parallel fibre volley and Purkinje cell firing in cerebellum of adult ataxic mice.Conditional Loss of Hoxa5 Function Early after Birth Impacts on Expression of Genes with Synaptic Function.Combining Optogenetics with Artificial microRNAs to Characterize the Effects of Gene Knockdown on Presynaptic Function within Intact Neuronal Circuits.P/Q Type Calcium Channel Cav2.1 Defines a Unique Subset of Glomeruli in the Mouse Olfactory Bulb
P2860

Postnatal loss of P/Q-type channels confined to rhombic-lip-derived neurons alters synaptic transmission at the parallel fiber to purkinje cell synapse and replicates genomic Cacna1a mutation phenotype of ataxia and seizures in mice.

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http://www.wikidata.org/entity/Q40299916
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2013 nî lūn-bûn
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2013年の論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年论文
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2013年论文
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2013年论文
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name
Postnatal loss of P/Q-type cha ...... f ataxia and seizures in mice.
@en
type
label
Postnatal loss of P/Q-type cha ...... f ataxia and seizures in mice.
@en
prefLabel
Postnatal loss of P/Q-type cha ...... f ataxia and seizures in mice.
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698
P921
P932
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P1433
P1476
Postnatal loss of P/Q-type cha ...... of ataxia and seizures in mice
@en
P2093
P2860
P304
P31
P356
10.1523/JNEUROSCI.5442-12.2013
P407
P433
P478
P50
P577
P698
P921
P932