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Published in 2022 at "Epilepsy Research"
DOI: 10.1016/j.eplepsyres.2022.106891
Abstract: The prevalence of seizures in individuals with fragile X syndrome (FXS) is ~25%; however, there are no reports of spontaneous seizures in the Fmr1 knockout mouse model of FXS. Herein, we report that 48% of…
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Keywords:
adult fmr1;
knockout mice;
fmr1 knockout;
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Published in 2022 at "ACS chemical neuroscience"
DOI: 10.1021/acschemneuro.2c00574
Abstract: There are no approved medicines for fragile X syndrome (FXS), a monogenic, neurodevelopmental disorder. Electroencephalogram (EEG) studies show alterations in resting-state cortical EEG spectra, such as increased gamma-band power, in patients with FXS that are…
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Keywords:
fpt;
power;
fmr1 knockout;
knockout mice ... See more keywords
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Published in 2017 at "Scientific Reports"
DOI: 10.1038/s41598-017-18598-y
Abstract: While mutations in the fragile X mental retardation-1 (FMR1) gene are associated with varying reproductive outcomes in females, the effects of a complete lack of FMR1 expression are not known. Here, we studied the ovarian…
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Keywords:
pool;
mtor signaling;
mtor;
mice ... See more keywords
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Published in 2017 at "NeuroReport"
DOI: 10.1097/wnr.0000000000000905
Abstract: Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by a single genetic mutation in the FMR1 gene. Mutations in the FMR1 gene are the largest monogenic cause of autism spectrum disorder (ASD), and thus…
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Keywords:
fmr1;
expression;
tumor necrosis;
mice ... See more keywords
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Published in 2022 at "Developmental Neuroscience"
DOI: 10.1159/000524898
Abstract: Fragile X syndrome (FXS) is the leading monogenic cause of intellectual disability and a significant contributor to Autism Spectrum Disorder. Individuals with FXS are subject to developing numerous comorbidities, one of the most prevalent being…
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Keywords:
early life;
life seizures;
knockout mice;
fmr1 knockout ... See more keywords