Forestwalk: A machine learning workflow brings new insights into posture and balance in rodent beam walking

F Tozzi, YP Zhang, D Roqueiro, R Narayanan… - bioRxiv, 2024 - biorxiv.org
The beam walk is widely used to study coordination and balance in rodents. While the task
has ethological validity, the main endpoints of foot slip counts and time to cross are prone to …

Characteristic development of the GABA-removal system in the mouse spinal cord

J Kim, Y Kosaka, C Shimizu-Okabe, A Niizaki… - Neuroscience, 2014 - Elsevier
GABA is a predominant inhibitory neurotransmitter in the CNS. Released GABA is removed
from the synaptic cleft by two GABA transporters (GATs), GAT-1 and GAT-3, and their …

Conditioned Aversion and Neuroplasticity Induced by a Superagonist of Extrasynaptic GABAA Receptors: Correlation With Activation of the Oval BNST Neurons and …

E De Miguel, O Vekovischeva, LV Elsilä… - Frontiers in Molecular …, 2019 - frontiersin.org
THIP (gaboxadol), a superagonist of the δ subunit-containing extrasynaptic GABAA
receptors, produces persistent neuroplasticity in dopamine (DA) neurons of the ventral …

Recovery of Angelman syndrome rat deficits with UBE3A protein supplementation

A Dodge, NK Morrill, EJ Weeber, KR Nash - Molecular and Cellular …, 2022 - Elsevier
We recently generated a novel Angelman syndrome (AS) rat model with a complete Ube3a
gene deletion, that recapitulates the loss of UBE3A protein and shows cognitive and EEG …

A longevity-specific bank of induced pluripotent stem cells from centenarians and their offspring

TW Dowrey, SF Cranston, N Skvir, Y Lok, B Gould… - bioRxiv, 2024 - biorxiv.org
Centenarians provide a unique lens through which to study longevity, healthy aging, and
resiliency. Moreover, models of human aging and resilience to disease that allow for the …

Translational research for the development of treatment of patients with neurogenetic diseases: An important step for Angelman syndrome

B Dan - European Journal of Paediatric Neurology, 2023 - ejpn-journal.com
Insights into mechanisms of neurogenetic diseases can inspire precision medicine
approaches, potentially paving the way for more targeted and effective treatments in the …

Deficits in higher visual area representations in a mouse model of Angelman syndrome

LB Townsend, KA Jones, CR Dorsett… - Journal of …, 2020 - Springer
Background Sensory processing deficits are common in individuals with
neurodevelopmental disorders. One hypothesis is that deficits may be more detectable in …

The hippocampal response to acute corticosterone elevation is altered in a mouse model for Angelman syndrome

EMG Viho, AM Punt, B Distel, R Houtman… - International journal of …, 2022 - mdpi.com
Angelman Syndrome (AS) is a severe neurodevelopmental disorder, caused by the
neuronal absence of the ubiquitin protein ligase E3A (UBE3A). UBE3A promotes ubiquitin …

Methods of treating developmental disorders with gaboxadol

M During - US Patent 11,096,929, 2021 - Google Patents
Methods of treating developmental disorders such as Angelman syndrome, Fragile X
syndrome, Fragile X-associated tremor/ataxia syndrome (FXTAS), Autistic Spectrum …

[HTML][HTML] Short-latency somatosensory-evoked potentials demonstrate cortical dysfunction in patients with Angelman syndrome

K Egawa, S Saitoh, N Asahina, H Shiraishi - Eneurologicalsci, 2021 - Elsevier
Background Angelman syndrome (AS) is neurodevelopmental disorder, causal gene of
which is maternally expressed UBE3A. A majority of patients results from the large deletion …