[PDF][PDF] Distinct pathogenic genes causing intellectual disability and autism exhibit a common neuronal network hyperactivity phenotype

…, M Selten, B Mossink, JM Keller, K Linda, R Moerschen… - Cell reports, 2020 - cell.com
Pathogenic mutations in either one of the epigenetic modifiers EHMT1, MBD5, MLL3, or
SMARCB1 have been identified to be causative for Kleefstra syndrome spectrum (KSS), a …

Distinct pathogenic genes causing intellectual disability and autism exhibit overlapping effects on neuronal network development

…, M Selten, B Mossink, JM Keller, K Linda, R Moerschen… - bioRxiv, 2018 - biorxiv.org
… Keller, Katrin Linda, Rebecca Moerschen, Jieqiong Qu, Pierre Koerner, Sophie Jansen,
Elske Bijvank, Astrid Oudakker, Tjitske Kleefstra, View ORCID ProfileHans van Bokhoven, …

Characterization of Kleefstra syndrome neuronal networks on multi-electrode arrays and a drug screen on human induced pluripotent stem cells

R Moerschen - 2017 - theses.ubn.ru.nl
Kleefstra syndrome (KS) has been associated with haploinsufficiency of the epigenetic gene
Euchromatin histone methyltransferase 1 (EHMT1). Additional genes were found to cause …

Epigenetic Regulation of Gene Expression in Temporal Lobe Epilepsy

RM Hauser - 2022 - search.proquest.com
Temporal lobe epilepsy (TLE) is the most common form of focal epilepsy and is characterized
by seizures originating from the temporal lobe of the brain. A frequent seizure focus in TLE …

Dealing with the appellate caseload crisis: The report of the federal courts study committee revisited

RJ Miner - NYL Sch. L. Rev., 2012 - HeinOnline
The Federal Courts Study Committee (the" Committee"), created by an act of Congress in
1988, was charged with inquiring into the issues and problems confronting the federal courts of …