[HTML][HTML] The making of the Drosophila mushroom body

S Lin - Frontiers in Physiology, 2023 - frontiersin.org
The mushroom body (MB) is a computational center in the Drosophila brain. The intricate
neural circuits of the mushroom body enable it to store associative memories and process …

Molecular and cellular events linking variants in the histone demethylase KDM5C to the intellectual disability disorder Claes‐Jensen syndrome

HAM Hatch, J Secombe - The FEBS journal, 2022 - Wiley Online Library
The widespread availability of genetic testing for those with neurodevelopmental disorders
has highlighted the importance of many genes necessary for the proper development and …

[HTML][HTML] A circular RNA Edis-Relish-castor axis regulates neuronal development in Drosophila

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 …

[HTML][HTML] Proximity labeling reveals a new in vivo network of interactors for the histone demethylase KDM5

M Yheskel, S Sidoli, J Secombe - Epigenetics & Chromatin, 2023 - Springer
Background KDM5 family proteins are multi-domain regulators of transcription that when
dysregulated contribute to cancer and intellectual disability. KDM5 proteins can regulate …

[HTML][HTML] Genomic insights and advanced machine learning: characterizing autism spectrum disorder biomarkers and genetic interactions

LD Nahas, A Datta, AM Alsamman, MH Adly… - Metabolic Brain …, 2024 - Springer
Abstract Autism Spectrum Disorder (ASD) is a complex neurodevelopmental condition
characterized by altered brain connectivity and function. In this study, we employed …

[HTML][HTML] Notch signaling and Bsh homeodomain activity are integrated to diversify Drosophila lamina neuron types

C Xu, TB Ramos, OJ Marshall, CQ Doe - Elife, 2024 - elifesciences.org
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 …

Exploring links between 2‐oxoglutarate‐dependent oxygenases and Alzheimer's disease

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 …

KDM5-mediated transcriptional activation of ribosomal protein genes alters translation efficiency to regulate mitochondrial metabolism in neurons

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 …

[HTML][HTML] WNT signalling control by KDM5C during development affects cognition

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 …

Soma‐to‐germline transformation in chromatin‐linked neurodevelopmental disorders?

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 …