Topologically controlled circuits of human iPSC-derived neurons for electrophysiology recordings

S Girardin, B Clement, SJ Ihle, S Weaver, JB Petr… - Lab on a Chip, 2022 - pubs.rsc.org
Bottom-up neuroscience, which consists of building and studying controlled networks of
neurons in vitro, is a promising method to investigate information processing at the neuronal …

Impairments in sensory-motor gating and information processing in a mouse model of Ehmt1 haploinsufficiency

BA Davis, F David, C O'Regan… - Brain and …, 2020 - journals.sagepub.com
Regulators of chromatin dynamics and transcription are increasingly implicated in the
aetiology of neurodevelopmental disorders. Haploinsufficiency of EHMT1, encoding a …

[HTML][HTML] The Object Space Task reveals increased expression of cumulative memory in a mouse model of Kleefstra syndrome

EHS Schut, A Alonso, S Smits, M Khamassi… - … of Learning and …, 2020 - Elsevier
Kleefstra syndrome is a disorder caused by a mutation in the EHMT1 gene characterized in
humans by general developmental delay, mild to severe intellectual disability and autism …

Sex-dependent effects of Setd1a haploinsufficiency on development and adult behaviour

ML Bosworth, AR Isles, LS Wilkinson, T Humby - Plos one, 2024 - journals.plos.org
Loss of function (LoF) mutations affecting the histone methyl transferase SETD1A are
implicated in the aetiology of a range of neurodevelopmental disorders including …

Brunner Syndrome associated MAOA dysfunction in human induced dopaminergic neurons results in dysregulated NMDAR expression and increased network activity

Y Shi, JR Van Rhijn, M Bormann, B Mossink, M Frega… - bioRxiv, 2019 - biorxiv.org
Monoamine oxidase A (MAOA) is an enzyme that catalyzes the degradation of dopamine,
noradrenaline, and serotonin. Regulation of monoamine neurotransmitter abundance …

Dysregulation of NRSF/REST via EHMT1 is associated with psychiatric disorders

M Alsaqati, BA Davis, J Wood, M Jones, L Jones… - bioRxiv, 2021 - biorxiv.org
Genetic evidence indicates disrupted epigenetic regulation as a major risk factor for
psychiatric disorders, but the molecular mechanisms that drive this association are …

Ehmt1 forebrain haploinsufficiency leads to impaired memory, sensory gating and information processing

BA Davis, F David, C O'Regan, MA Adam, AJ Harwood… - bioRxiv, 2018 - biorxiv.org
Regulators of chromatin dynamics and transcription are increasingly implicated in the
aetiology of neurodevelopmental disorders (NDDs). Haploinsufficiency of EHMT1, encoding …