Autism spectrum disorder: focus on glutamatergic neurotransmission

M Montanari, G Martella, P Bonsi… - International Journal of …, 2022 - mdpi.com
Disturbances in the glutamatergic system have been increasingly documented in several
neuropsychiatric disorders, including autism spectrum disorder (ASD). Glutamate-centered …

Dissecting the relationship between neuropsychiatric and neurodegenerative disorders

R Gupta, D Advani, D Yadav, RK Ambasta… - Molecular …, 2023 - Springer
Neurodegenerative diseases (NDDs) and neuropsychiatric disorders (NPDs) are two
common causes of death in elderly people, which includes progressive neuronal cell death …

Invited review: epigenetics in neurodevelopment

RD Salinas, DR Connolly… - … and applied neurobiology, 2020 - Wiley Online Library
Neural development requires the orchestration of dynamic changes in gene expression to
regulate cell fate decisions. This regulation is heavily influenced by epigenetics, heritable …

[HTML][HTML] m6A methyltransferase METTL3 reduces hippocampal neuron apoptosis in a mouse model of autism through the MALAT1/SFRP2/wnt/β-catenin Axis

Y Ming, Z Deng, X Tian, Y Jia, M Ning… - Psychiatry …, 2022 - ncbi.nlm.nih.gov
Objective Hippocampal neuron apoptosis contributes to autism, while METTL3 has been
documented to possess great potentials in neuron apoptosis. Our study probed into the role …

Impacts of cannabinoid epigenetics on human development: reflections on Murphy et. al.'cannabinoid exposure and altered DNA methylation in rat and human sperm' …

AS Reece, GK Hulse - Epigenetics, 2019 - Taylor & Francis
Recent data from the Kollins lab ('Cannabinoid exposure and altered DNA methylation in rat
and human sperm'Epigenetics 2018; 13: 1208–1221) indicated epigenetic effects of …

Hearing loss and brain disorders: A review of multiple pathologies

OG Oluwole, K James, A Yalcouye, A Wonkam - Open Medicine, 2021 - degruyter.com
Several causative factors are associated with hearing loss (HL) and brain disorders.
However, there are many unidentified disease modifiers in these conditions. Our study …

[HTML][HTML] Interaction-integrated linear mixed model reveals 3D-genetic basis underlying Autism

Q Li, D Perera, C Cao, J He, J Bian, X Chen, F Azeem… - Genomics, 2023 - Elsevier
Genetic interactions play critical roles in genotype-phenotype associations. We developed a
novel interaction-integrated linear mixed model (ILMM) that integrates a priori knowledge …

Evaluating the regulatory function of non‐coding autism‐associated single nucleotide polymorphisms on gene expression in human brain tissue

K Pugsley, A Namipashaki, MA Bellgrove… - Autism …, 2024 - Wiley Online Library
Common variants account for most of the estimated heritability associated with autism
spectrum disorder (autism). Although several replicable single nucleotide polymorphisms …

The key role of purine metabolism in the folate-dependent phenotype of autism spectrum disorders: an in silico analysis

J Geryk, D Krsička, M Vlčková, M Havlovicová… - Metabolites, 2020 - mdpi.com
Folate deficiency in the critical developmental period has been repeatedly associated with
an increased risk of Autism spectrum disorders (ASD), but the key pathophysiological …

DNMT1 downregulation as well as its overexpression distinctly affect mostly overlapping genes implicated in schizophrenia, autism spectrum, epilepsy, and bipolar …

M Singh, S Saxena, KN Mohan - Frontiers in Molecular Neuroscience, 2023 - frontiersin.org
Data on schizophrenia (SZ), epilepsy (EPD) and bipolar disorders (BPD) suggested an
association of DNMT1 overexpression whereas certain variants of the gene were predicted …