Evaluating the effect of R-Baclofen and LP-211 on autistic behavior of the BTBR and Fmr1-KO mouse models

S Sharghi, S Flunkert, M Daurer, R Rabl… - Frontiers in …, 2023 - frontiersin.org
Introduction Autism spectrum disorder (ASD) is a persistent neurodevelopmental condition
characterized by two core behavioral symptoms: impaired social communication and …

[HTML][HTML] Genetic and environmental contributions to autism spectrum disorder through mechanistic target of rapamycin

A Sato, K Ikeda - Biological Psychiatry Global Open Science, 2022 - Elsevier
Autism spectrum disorder (ASD) is a neurodevelopmental disorder that affects an
individual's reciprocal social interaction and communication ability. Numerous genetic and …

Prefrontal cortex dysfunction in fragile X mice depends on the continued absence of fragile X mental retardation protein in the adult brain

JJ Siegel, RA Chitwood, JM Ding, C Payne… - Journal of …, 2017 - Soc Neuroscience
Fragile X Syndrome (FX) is generally considered a developmental disorder, arising from a
mutation that disrupts the transcription of Fragile X Mental Retardation Protein (FMRP) …

Dysregulated prefrontal cortex inhibition in prepubescent and adolescent fragile X mouse model

I Kramvis, R Van Westen, HCA Lammertse… - Frontiers in Molecular …, 2020 - frontiersin.org
Changes in excitation and inhibition are associated with the pathobiology of
neurodevelopmental disorders of intellectual disability and autism and are widely described …

Dissociating motor impairment from five-choice serial reaction time task performance in a mouse model of Angelman syndrome

PN Negrón-Moreno, DT Diep, CD Guoynes… - Frontiers in Behavioral …, 2022 - frontiersin.org
Angelman syndrome (AS) is a single-gene neurodevelopmental disorder associated with
cognitive and motor impairment, seizures, lack of speech, and disrupted sleep. AS is caused …

Extinction of an instrumental response: a cognitive behavioral assay in Fmr1 knockout mice

MS Sidorov, DD Krueger, M Taylor… - Genes, Brain and …, 2014 - Wiley Online Library
Fragile X (FX) is the most common genetic cause of intellectual disability and autism.
Previous studies have shown that partial inhibition of metabotropic glutamate receptor …

BK channel dysfunction disrupts attention-controlled behaviors and altered perseverative responses in murine instrumental learning

M Arake, H Ohta, T Nozawa, Y Satoh, M Fujita… - Behavioural Brain …, 2024 - Elsevier
This study examined the effect of knockout of KCNMA1 gene, coding for the BK channel, on
cognitive and attentional functions in mice, with an aim to better understand its implications …

Normal performance of Fmr1 mice on a touchscreen delayed nonmatching to position working memory task

PT Leach, J Hayes, M Pride, JL Silverman, JN Crawley - eneuro, 2016 - eneuro.org
Fragile X syndrome is a neurodevelopmental disorder characterized by mild-to-severe
cognitive deficits. The complete absence of Fmr1 and its protein product in the mouse model …

[HTML][HTML] Genetic factors underlying attention and impulsivity: mouse models of attention-deficit/hyperactivity disorder

S Itohara, Y Kobayashi, T Nakashiba - Current opinion in behavioral …, 2015 - Elsevier
Highlights•ADHD mouse models have diversified due to the progress in human
genetics.•Causal genes act on monoaminergic signaling, synaptic plasticity, and …

Differential Adulthood Onset mGlu5 Signaling Saves Prefrontal Function in the Fragile X Mouse

HGS Martin, O Lassalle, OJ Manzoni - Cerebral Cortex, 2017 - academic.oup.com
The final maturation of the prefrontal cortex (PFC) continues into early adulthood and is
delayed compared with other forebrain structures. However, how these late onset changes …