Consciousness among delta waves: a paradox?

J Frohlich, D Toker, MM Monti - Brain, 2021 - academic.oup.com
A common observation in EEG research is that consciousness vanishes with the
appearance of delta (1–4 Hz) waves, particularly when those waves are high amplitude …

Consciousness and complexity: a consilience of evidence

S Sarasso, AG Casali, S Casarotto… - Neuroscience of …, 2021 - academic.oup.com
Over the last years, a surge of empirical studies converged on complexity-related measures
as reliable markers of consciousness across many different conditions, such as sleep …

A comprehensive atlas of E3 ubiquitin ligase mutations in neurological disorders

AJ George, YC Hoffiz, AJ Charles, Y Zhu… - Frontiers in …, 2018 - frontiersin.org
Protein ubiquitination is a posttranslational modification that plays an integral part in
mediating diverse cellular functions. The process of protein ubiquitination requires an …

Potassium channel dysfunction in human neuronal models of Angelman syndrome

AX Sun, Q Yuan, M Fukuda, W Yu, H Yan, GGY Lim… - Science, 2019 - science.org
Disruptions in the ubiquitin protein ligase E3A (UBE3A) gene cause Angelman syndrome
(AS). Whereas AS model mice have associated synaptic dysfunction and altered plasticity …

[HTML][HTML] Level of consciousness is dissociable from electroencephalographic measures of cortical connectivity, slow oscillations, and complexity

D Pal, D Li, JG Dean, MA Brito, T Liu… - Journal of …, 2020 - Soc Neuroscience
Leading neuroscientific theories posit a central role for the functional integration of cortical
areas in conscious states. Considerable evidence supporting this hypothesis is based on …

Reduced prefrontal synaptic connectivity and disturbed oscillatory population dynamics in the CNTNAP2 model of autism

MT Lazaro, J Taxidis, T Shuman, I Bachmutsky, T Ikrar… - Cell reports, 2019 - cell.com
Loss-of-function mutations in CNTNAP2 cause a syndromic form of autism spectrum
disorder in humans and produce social deficits, repetitive behaviors, and seizures in mice …

[HTML][HTML] Multielectrode array analysis of EEG biomarkers in a mouse model of Fragile X Syndrome

CR Jonak, JW Lovelace, IM Ethell, KA Razak… - Neurobiology of …, 2020 - Elsevier
Abstract Fragile X Syndrome (FXS) is a leading known genetic cause of intellectual disability
with symptoms that include increased anxiety and social and sensory processing deficits …

[HTML][HTML] Angelman syndrome: from mouse models to therapy

DC Rotaru, EJ Mientjes, Y Elgersma - Neuroscience, 2020 - Elsevier
The UBE3A gene is part of the chromosome 15q11-q13 region that is frequently deleted or
duplicated, leading to several neurodevelopmental disorders (NDD). Angelman syndrome …

[HTML][HTML] Electrophysiological phenotype in Angelman syndrome differs between genotypes

J Frohlich, MT Miller, LM Bird, P Garces, H Purtell… - Biological …, 2019 - Elsevier
Background Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by
either disruptions of the gene UBE3A or deletion of chromosome 15 at 15q11-q13, which …

Functional rescue in an Angelman syndrome model following treatment with lentivector transduced hematopoietic stem cells

A Adhikari, NA Copping, J Beegle… - Human molecular …, 2021 - academic.oup.com
Angelman syndrome (AS) is a rare neurodevelopmental disorder characterized by impaired
communication skills, ataxia, motor and balance deficits, intellectual disabilities, and …