Abnormal expression of GABAA receptor subunits and hypomotility upon loss of gabra1 in zebrafish

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Gastrodin Suppresses Pentylenetetrazole-Induced Seizures Progression by Modulating Oxidative Stress in Zebrafish

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Expression of the eight GABAA receptor α subunits in the developing zebrafish central nervous system

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γ-Aminobutyric acid receptor alpha 1 subunit loss of function causes genetic generalized epilepsy by impairing inhibitory network neurodevelopment

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Gene expression analysis in untreated absence epilepsy demonstrates an inconsistent pattern

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Model Organisms Facilitate Rare Disease Diagnosis and Therapeutic Research

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Model Organisms Facilitate Rare Disease Diagnosis and Therapeutic Research

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De novoGABRA1mutations in Ohtahara and West syndromes

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Anxiety-related behavioral responses of pentylenetetrazole-treated zebrafish larvae to light-dark transitions

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Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care

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Altered intrathalamic GABAA neurotransmission in a mouse model of a human genetic absence epilepsy syndrome

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The developmental evolution of the seizure phenotype and cortical inhibition in mouse models of juvenile myoclonic epilepsy

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Validation of the Zebrafish Pentylenetetrazol Seizure Model: Locomotor versus Electrographic Responses to Antiepileptic Drugs

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Decreased viability and absence-like epilepsy in mice lacking or deficient in the GABAA receptor α1 subunit

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Structure, Function, and Modulation of GABAAReceptors

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Novel α1 and γ2 GABAA receptor subunit mutations in families with idiopathic generalized epilepsy

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The GABRA6 mutation, R46W, associated with childhood absence epilepsy, alters α6β2γ2 and α6β2δ GABAAreceptor channel gating and expression

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Unlocking Mendelian disease using exome sequencing

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Fast and accurate short read alignment with Burrows-Wheeler transform

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High-resolution in situ hybridization to whole-mount zebrafish embryos

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