| scholarly article | Q13442814 |
| P2093 | author name string | Li Ding | |
| Martin J Gallagher | |||
| Chengwen Zhou | |||
| Fazal Arain | |||
| Sahar Zaidi | |||
| P2860 | cites work | Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy | Q28216597 |
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| The GABAA receptor alpha1 subunit epilepsy mutation A322D inhibits transmembrane helix formation and causes proteasomal degradation | Q35928809 | ||
| Altered microstructural connectivity in juvenile myoclonic epilepsy: the missing link | Q35948522 | ||
| Effect of the alpha subunit subtype on the macroscopic kinetic properties of recombinant GABA(A) receptors | Q36156565 | ||
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| Altered cortical GABAA receptor composition, physiology, and endocytosis in a mouse model of a human genetic absence epilepsy syndrome | Q37175224 | ||
| Two molecular pathways (NMD and ERAD) contribute to a genetic epilepsy associated with the GABA(A) receptor GABRA1 PTC mutation, 975delC, S326fs328X | Q37204045 | ||
| GABRA1 and STXBP1: novel genetic causes of Dravet syndrome | Q37725930 | ||
| Epidemiology of juvenile myoclonic epilepsy | Q38113659 | ||
| What is special about the adolescent (JME) brain? | Q38113664 | ||
| The quest for juvenile myoclonic epilepsy genes | Q38113665 | ||
| Clinical aspects of juvenile myoclonic epilepsy | Q38113673 | ||
| Mechanisms involved in the reduction of GABAA receptor alpha1-subunit expression caused by the epilepsy mutation A322D in the trafficking-competent receptor | Q39974702 | ||
| GABA(A) receptors: immunocytochemical distribution of 13 subunits in the adult rat brain. | Q42497057 | ||
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| Cortical glutamatergic neurons mediate the motor sedative action of diazepam. | Q46927727 | ||
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| Laforin and malin deletions in mice produce similar neurologic impairments. | Q47997155 | ||
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| Changes in neocortical and hippocampal GABAA receptor subunit distribution during brain maturation and aging. | Q48494406 | ||
| Juvenile myoclonic epilepsy subsyndromes: family studies and long-term follow-up | Q48625878 | ||
| Dependence of the GABAA receptor gating kinetics on the alpha-subunit isoform: implications for structure-function relations and synaptic transmission. | Q52321710 | ||
| Spontaneous generalized spike-wave discharges in the electrocorticograms of albino rats | Q71327497 | ||
| Long-term prognosis of typical childhood absence epilepsy: remission or progression to juvenile myoclonic epilepsy | Q71656667 | ||
| A mutation in the GABA(A) receptor alpha(1)-subunit is associated with absence epilepsy | Q83828124 | ||
| Abnormal response to photic stimulation in juvenile myoclonic epilepsy: an EEG-fMRI study | Q87952352 | ||
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | juvenile myoclonic epilepsy | Q543517 |
| myoclonic epilepsy | Q11883686 | ||
| P304 | page(s) | 164-175 | |
| P577 | publication date | 2015-06-06 | |
| P1433 | published in | Neurobiology of Disease | Q15716606 |
| P1476 | title | The developmental evolution of the seizure phenotype and cortical inhibition in mouse models of juvenile myoclonic epilepsy | |
| P478 | volume | 82 |
| Q90603385 | Abnormal expression of GABAA receptor sub-units and hypomotility upon loss of gabra1 in zebrafish |
| Q48129765 | Defects at the crossroads of GABAergic signaling in generalized genetic epilepsies |
| Q41640904 | Dynamics of sensorimotor cortex activation during absence and myoclonic seizures in a mouse model of juvenile myoclonic epilepsy |
| Q40056976 | Heat induced temperature dysregulation and seizures in Dravet Syndrome/GEFS+ Gabrg2+/Q390X mice |
| Q47269323 | Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies |
| Q47371810 | Modulation of thalamocortical oscillations by TRIP8b, an auxiliary subunit for HCN channels. |
| Q99711198 | Neurophysiological and Genetic Findings in Patients With Juvenile Myoclonic Epilepsy |
| Q59807946 | Remodeling the endoplasmic reticulum proteostasis network restores proteostasis of pathogenic GABAA receptors |
| Q90704624 | Subtle Brain Developmental Abnormalities in the Pathogenesis of Juvenile Myoclonic Epilepsy |
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