[HTML][HTML] Striatal circuits as a common node for autism pathophysiology

MV Fuccillo - Frontiers in neuroscience, 2016 - frontiersin.org
Autism spectrum disorders (ASD) are characterized by two seemingly unrelated symptom
domains—deficits in social interactions and restrictive, repetitive patterns of behavioral …

Modeling fragile X syndrome in the Fmr1 knockout mouse

TM Kazdoba, PT Leach, JL Silverman… - Intractable & rare …, 2014 - jstage.jst.go.jp
Summary Fragile X Syndrome (FXS) is a commonly inherited form of intellectual disability
and one of the leading genetic causes for autism spectrum disorder. Clinical symptoms of …

Impaired cognitive discrimination and discoordination of coupled theta–gamma oscillations in Fmr1 knockout mice

B Radwan, D Dvorak, AA Fenton - Neurobiology of disease, 2016 - Elsevier
Fragile X syndrome (FXS) patients do not make the fragile X mental retardation protein
(FMRP). The absence of FMRP causes dysregulated translation, abnormal synaptic …

Repurposing available drugs for neurodevelopmental disorders: the fragile X experience

MR Tranfaglia, C Thibodeaux, DJ Mason, D Brown… - …, 2019 - Elsevier
Many available drugs have been repurposed as treatments for neurodevelopmental
disorders. In the specific case of fragile X syndrome, many clinical trials of available drugs …

Age-Dependent Long-Term Potentiation Deficits in the Prefrontal Cortex of the Fmr1 Knockout Mouse Model of Fragile X Syndrome

HGS Martin, O Lassalle, JT Brown… - Cerebral cortex, 2016 - academic.oup.com
The most common inherited monogenetic cause of intellectual disability is Fragile X
syndrome (FXS). The clinical symptoms of FXS evolve with age during adulthood; however …

[HTML][HTML] Molecular and behavioral consequences of Ube3a gene overdosage in mice

AM Punt, MC Judson, MS Sidorov, BN Williams… - JCI insight, 2022 - ncbi.nlm.nih.gov
Abstract Chromosome 15q11. 2–q13. 1 duplication syndrome (Dup15q syndrome) is a
severe neurodevelopmental disorder characterized by intellectual disability, impaired motor …

Deletion of the KH1 Domain of Fmr1 Leads to Transcriptional Alterations and Attentional Deficits in Rats

CEM Golden, MS Breen, L Koro, S Sonar… - Cerebral …, 2019 - academic.oup.com
Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by mutations in the
FMR1 gene. It is a leading monogenic cause of autism spectrum disorder and inherited …

Restoration of FMRP expression in adult V1 neurons rescues visual deficits in a mouse model of fragile X syndrome

C Yang, Y Tian, F Su, Y Wang, M Liu, H Wang… - Protein & …, 2022 - academic.oup.com
Many people affected by fragile X syndrome (FXS) and autism spectrum disorders have
sensory processing deficits, such as hypersensitivity to auditory, tactile, and visual stimuli …

[HTML][HTML] Role of the TRPC1 channel in hippocampal long-term depression and in spatial memory extinction

X Yerna, O Schakman, I Ratbi, A Kreis… - International journal of …, 2020 - mdpi.com
Group I metabotropic glutamate receptors (mGluR) are involved in various forms of synaptic
plasticity that are believed to underlie declarative memory. We previously showed that …

Enhanced operant extinction and prefrontal excitability in a mouse model of Angelman syndrome

MS Sidorov, MC Judson, H Kim, M Rougie… - Journal of …, 2018 - Soc Neuroscience
Angelman syndrome (AS), a neurodevelopmental disorder associated with intellectual
disability, is caused by loss of maternal allele expression of UBE3A in neurons. Mouse …