The widespread availability of genetic testing for those with neurodevelopmental disorders has highlighted the importance of many genes necessary for the proper development and …
W Liu, W Liang, XP Xiong, JL Li, R Zhou - PLoS genetics, 2022 - journals.plos.org
Circular RNAs (circRNAs) are a new group of noncoding/regulatory RNAs that are particularly abundant in the nervous system, however, their physiological functions are …
Background KDM5 family proteins are multi-domain regulators of transcription that when dysregulated contribute to cancer and intellectual disability. KDM5 proteins can regulate …
Abstract Autism Spectrum Disorder (ASD) is a complex neurodevelopmental condition characterized by altered brain connectivity and function. In this study, we employed …
Notch signaling is an evolutionarily conserved pathway for specifying binary neuronal fates, yet how it specifies different fates in different contexts remains elusive. In our accompanying …
H Liu, Y Xie, X Wang, MI Abboud, C Ma… - Alzheimer's & …, 2022 - Wiley Online Library
Hypoxia, that is, an inadequate oxygen supply, is linked to neurodegeneration and patients with cardiovascular disease are prone to Alzheimer's disease (AD). 2‐Oxoglutarate and …
M Yheskel, HAM Hatch, E Pedrosa… - Nucleic Acids …, 2024 - academic.oup.com
Genes encoding the KDM5 family of transcriptional regulators are disrupted in individuals with intellectual disability (ID). To understand the link between KDM5 and ID, we …
V Karwacki-Neisius, A Jang, E Cukuroglu, A Tai, A Jiao… - Nature, 2024 - nature.com
Although KDM5C is one of the most frequently mutated genes in X-linked intellectual disability, the exact mechanisms that lead to cognitive impairment remain unknown. Here we …
KM Bonefas, S Iwase - The FEBS journal, 2022 - Wiley Online Library
Mutations in numerous chromatin regulators cause neurodevelopmental disorders (NDDs) with unknown mechanisms. Understandably, most research has focused on how chromatin …