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UnknownImpaired gephyrin G-domain trimerization and phase separation in a patient with developmental epileptic encephalopathy
Not available
S-SCDT-10_1038-S44321-026-00474-W | biostudies-other
ProteomicsIdentifying altered mouse gephyrin interactome after sleep deprivation
GABAergic transmission controls cortical sleep, however the molecular determinants of GABAergic control of this phenomenon are unknown. We used immunoprecipitation of the inhibitory postsynaptic protein gephyrin to identify gephyrin interactors at ZT6 (sleep) and ZT6 with sleep deprivation (ZT6SD).
ORGANISM(S): Mus musculus (Mouse) 
2024-07-25 | PXD048929 | Pride
Mouse Gephyrin interactome Sleep deprivation 
GenomicsEGAS00001000386-sc-20130520 - samples
We are sequencing the exomes of patients with paroxysmal neurological disorders mainly focusing on migraine and epilepsy. Cases are collected from performance sites of members of the International Headache Genetics consortium and EuroEPINOMICS. Most cases have a strong family history. The study samp...
EGAD00001000412 | EGA
GenomicsEGAS00001000048-sc-20110602 - samples
Paroxysmal neurological disorders
EGAD00001000021 | EGA
GenomicsEGAS00001000190-sc-20130520 - samples
We are sequencing the exomes of patients with paroxysmal neurological disorders mainly focusing on migraine and epilepsy. Cases are collected from performance sites of members of the International Headache Genetics consortium and EuroEPINOMICS. Most cases have a strong family history. The study samp...
EGAD00001000407 | EGA
GenomicsEGAS00001000048-sc-20120215 - samples
Paroxysmal neurological disorders
EGAD00001000108 | EGA
GenomicsParoxysmal neurological disorders
We are sequencing the exomes of patients with paroxysmal neurological disorders mainly focusing on migraine and epilepsy. Cases are collected from performance sites of members of the International Headache Genetics consortium and EuroEPINOMICS. Most cases have a strong family history. The study samp...
EGAS00001000048 | EGA
GenomicsParoxysmal Neurological Disorders 2
We are sequencing the exomes of patients with paroxysmal neurological disorders mainly focusing on migraine and epilepsy. Cases are collected from performance sites of members of the International Headache Genetics consortium and EuroEPINOMICS. Most cases have a strong family history. The study samp...
EGAS00001000190 | EGA
GenomicsParoxysmal neurological Disorders
We are sequencing the exomes of patients with paroxysmal neurological disorders mainly focusing on migraine and epilepsy. Cases are collected from performance sites of members of the International Headache Genetics consortium and EuroEPINOMICS. Most cases have a strong family history. The study samp...
EGAS00001000386 | EGA
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