Emerging evidence for astrocyte dysfunction in schizophrenia

EC de Oliveira Figueiredo, C Calì, F Petrelli, P Bezzi - Glia, 2022 - Wiley Online Library
Schizophrenia is a complex, chronic mental health disorder whose heterogeneous genetic
and neurobiological background influences early brain development, and whose precise …

Update on the 22q11. 2 deletion syndrome and its relevance to schizophrenia

L Van, E Boot, AS Bassett - Current opinion in psychiatry, 2017 - journals.lww.com
Progress in characterizing and predicting psychotic illness in 22q11. 2DS supports this
identifiable subpopulation as a molecular model with important implications for …

Shank3 mutation in a mouse model of autism leads to changes in the S-nitroso-proteome and affects key proteins involved in vesicle release and synaptic function

H Amal, B Barak, V Bhat, G Gong, BA Joughin… - Molecular …, 2020 - nature.com
Mutation in the SHANK3 human gene leads to different neuropsychiatric diseases including
Autism Spectrum Disorder (ASD), intellectual disabilities and Phelan-McDermid syndrome …

Rescue of neuropsychiatric phenotypes in a mouse model of 16p11. 2 duplication syndrome by genetic correction of an epilepsy network hub

MP Forrest, M Dos Santos, NH Piguel, YZ Wang… - Nature …, 2023 - nature.com
Neuropsychiatric disorders (NPDs) are frequently co-morbid with epilepsy, but the biological
basis of shared risk remains poorly understood. The 16p11. 2 duplication is a copy number …

Intellectual disability: dendritic anomalies and emerging genetic perspectives

TT Quach, HJ Stratton, R Khanna, PE Kolattukudy… - Acta …, 2021 - Springer
Intellectual disability (ID) corresponds to several neurodevelopmental disorders of
heterogeneous origin in which cognitive deficits are commonly associated with …

Systems analysis of the 22q11. 2 microdeletion syndrome converges on a mitochondrial interactome necessary for synapse function and behavior

A Gokhale, C Hartwig, AAH Freeman… - Journal of …, 2019 - Soc Neuroscience
Neurodevelopmental disorders offer insight into synaptic mechanisms. To unbiasedly
uncover these mechanisms, we studied the 22q11. 2 syndrome, a recurrent copy number …

MZB1 targeted by miR‐185‐5p inhibits the migration of human periodontal ligament cells through NF‐κB signaling and promotes alveolar bone loss

D Li, Y Zhu, L Zhang, L Shi, L Deng… - Journal of …, 2022 - Wiley Online Library
Objective To explore the role of Marginal Zone B and B‐1 Cell‐Specific Protein (MZB1), a
novel molecule associated with periodontitis, in migration of human periodontal ligament …

A mouse model of 22q11. 2 deletions: molecular and behavioral signatures of Parkinson's disease and schizophrenia

A Sumitomo, K Horike, K Hirai, N Butcher, E Boot… - Science …, 2018 - science.org
Individuals with chromosome 22q11. 2 deletions are at increased risk of developing
psychiatric conditions, most notably, schizophrenia (SZ). Recently, clinical studies have also …

22q11. 2 deletion syndrome–associated Parkinson's disease

E Boot, AS Bassett, C Marras - Movement disorders clinical …, 2019 - Wiley Online Library
Abstract Background 22q11. 2 deletion syndrome (22q11. 2DS) is a multisystem condition
associated with an increased risk of early‐onset Parkinson's disease (PD). Methods We …

Untargeted metabolomic, and proteomic analysis identifies metabolic biomarkers and pathway alterations in individuals with 22q11. 2 deletion syndrome

M Zafarullah, K Angkustsiri, A Quach, S Yeo… - Metabolomics, 2024 - Springer
Abstract Introduction The chromosome 22q11. 2 deletion syndrome (22q11. 2DS) is
characterized by a well-defined microdeletion and is associated with a wide range of brain …