[HTML][HTML] Translational validity and methodological underreporting in animal research: A systematic review and meta-analysis of the Fragile X syndrome (Fmr1 KO)�…

R Kat, M Arroyo-Araujo, RBM de Vries…�- Neuroscience &�…, 2022 - Elsevier
Predictive models are essential for advancing knowledge of brain disorders. High variation
in study outcomes hampers progress. To address the validity of predictive models, we�…

[HTML][HTML] Abnormalities of synaptic mitochondria in autism spectrum disorder and related neurodevelopmental disorders

L Rojas-Charry, L Nardi, A Methner…�- Journal of Molecular�…, 2021 - Springer
Autism spectrum disorder (ASD) is a neurodevelopmental condition primarily characterized
by an impairment of social interaction combined with the occurrence of repetitive behaviors�…

[HTML][HTML] Keeping excitation–inhibition ratio in balance

S Kirischuk�- International journal of molecular sciences, 2022 - mdpi.com
Unrelated genetic mutations can lead to convergent manifestations of neurological disorders
with similar behavioral phenotypes. Experimental data frequently show a lack of dramatic�…

[HTML][HTML] Spatially coordinated heterochromatinization of long synaptic genes in fragile X syndrome

T Malachowski, KR Chandradoss, R Boya, L Zhou…�- Cell, 2023 - cell.com
Short tandem repeat (STR) instability causes transcriptional silencing in several repeat
expansion disorders. In fragile X syndrome (FXS), mutation-length expansion of a CGG STR�…

Anandamide and 2-arachidonoylglycerol differentially modulate autistic-like traits in a genetic model of autism based on FMR1 deletion in rats

S Schiavi, A Manduca, E Carbone, V Buzzelli…�- …, 2023 - nature.com
Autism spectrum disorder (ASD) has a multifactorial etiology. Major efforts are underway to
understand the neurobiological bases of ASD and to develop efficacious treatment�…

[HTML][HTML] mGluR5 negative modulators for fragile X: treatment resistance and persistence

DC Stoppel, PK McCamphill, RK Senter…�- Frontiers in�…, 2021 - frontiersin.org
Fragile X syndrome (FXS) is caused by silencing of the human FMR1 gene and is the
leading monogenic cause of intellectual disability and autism. Abundant preclinical data�…

[HTML][HTML] Directly reprogrammed fragile X syndrome dorsal forebrain precursor cells generate cortical neurons exhibiting impaired neuronal maturation

N Edwards, C Combrinck…�- Frontiers in Cellular�…, 2023 - frontiersin.org
Introduction The neurodevelopmental disorder fragile X syndrome (FXS) is the most
common monogenic cause of intellectual disability associated with autism spectrum�…

[HTML][HTML] Dendritic integration dysfunction in neurodevelopmental disorders

AD Nelson, KJ Bender�- Developmental neuroscience, 2021 - karger.com
Neurodevelopmental disorders (NDDs) that affect cognition, social interaction, and learning,
including autism spectrum disorder (ASD) and intellectual disability (ID), have a strong�…

Chemical analysis of the human brain by imaging mass spectrometry

A Ajith, Y Sthanikam, S Banerjee�- Analyst, 2021 - pubs.rsc.org
Analysis of the chemical makeup of the brain enables a deeper understanding of several
neurological processes. Molecular imaging that deciphers the spatial distribution of�…

[HTML][HTML] Deletion of the autism-associated protein SHANK3 abolishes structural synaptic plasticity after brain trauma

C Urrutia-Ruiz, D Rombach, S Cursano…�- International journal of�…, 2022 - mdpi.com
Autism spectrum disorders (ASDs) are characterized by repetitive behaviors and
impairments of sociability and communication. About 1% of ASD cases are caused by�…