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UnknownIdentification of diverse astrocyte populations and their malignant analogs.
Not available
S-EPMC5824716 | biostudies-literature
UnknownSensorineural deafness and seizures in mice lacking vesicular glutamate transporter 3.
Not available
S-EPMC2293283 | biostudies-literature
UnknownTherapeutic inhibition of mTORC2 rescues the behavioral and neurophysiological abnormalities associated with Pten-deficiency.
Not available
S-EPMC7082835 | biostudies-literature
UnknownBrain microvasculature defects and Glut1 deficiency syndrome averted by early repletion of the glucose transporter-1 protein.
Not available
S-EPMC5263887 | biostudies-literature
UnknownPlural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy.
Not available
S-EPMC10802467 | biostudies-literature
UnknownPlural molecular and cellular mechanisms of pore domain <i>KCNQ2</i> encephalopathy.
Not available
S-EPMC11703504 | biostudies-literature
UnknownExome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
Not available
S-EPMC9980234 | biostudies-literature
UnknownSub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals.
Not available
S-EPMC8206159 | biostudies-literature
UnknownExome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
Not available
S-EPMC11646479 | biostudies-literature
UnknownGenome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals.
Not available
S-EPMC10359300 | biostudies-literature
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