Over the lifetime of an organism, neurons must establish, remodel, and maintain precise connections in order to form neural circuits that are required for proper nervous system functioning. Disruptions in these processes can lead to neurodevelopmental disorders such as intellectual disability (ID) and autism spectrum disorder. Mutations in genes encoding subunits of the SWI/SNF chromatin remodeling complex have been implicated in ID, yet the role of this complex in neurons is poorly understood. In this project, I established cell-type specific methods to examine the effect of SWI/SNF subunit knockdowns on gene transcription and chromatin structure in the memory-forming neurons of the Drosophila mushroom body (MB) during periods of neuronal ...
The central nervous system is the most complex and highly organized tissue in animals; composed of t...
The central nervous system (CNS) consists of an enormous number of cells, and large cellular varianc...
Recent literature has highlighted that mutations causing neurodevelopmental syndromes are particular...
The SWI/SNF complex is an evolutionarily conserved ATP-dependent chromatin remodelling complex that ...
Technology has led to rapid progress in the identification of genes involved in neurodevelopmental d...
Mutations in the lysine demethylase 5 (KDM5) family of transcriptional regulators areassociated with...
Mutations in several genes encoding components of the SWI/SNF chromatin remodeling complex cause neu...
Long-term memory formation requires the coordinated regulation of gene expression. Until recently nu...
Intellectual disability (ID) is a neurodevelopmental disorder associated with many epigenetic regula...
Drosophila mushroom body (MB) {gamma} neurons undergo axon pruning during metamorphosis through a pr...
The causal link between the three-dimensional conformation of the genome and spatiotemporal control ...
Purpose: Pathogenic variants in the chromatin organizer CTCF were previously reported in seven indiv...
Background: The SWI/SNF chromatin remodeling factors have the ability to remodel nucleosomes and...
The most common cause of inherited mental deficiency and monogenetic cause of autism is Fragile X Sy...
Cell-type specific transcriptional programs are thought to be defined by cell-type specific transcri...
The central nervous system is the most complex and highly organized tissue in animals; composed of t...
The central nervous system (CNS) consists of an enormous number of cells, and large cellular varianc...
Recent literature has highlighted that mutations causing neurodevelopmental syndromes are particular...
The SWI/SNF complex is an evolutionarily conserved ATP-dependent chromatin remodelling complex that ...
Technology has led to rapid progress in the identification of genes involved in neurodevelopmental d...
Mutations in the lysine demethylase 5 (KDM5) family of transcriptional regulators areassociated with...
Mutations in several genes encoding components of the SWI/SNF chromatin remodeling complex cause neu...
Long-term memory formation requires the coordinated regulation of gene expression. Until recently nu...
Intellectual disability (ID) is a neurodevelopmental disorder associated with many epigenetic regula...
Drosophila mushroom body (MB) {gamma} neurons undergo axon pruning during metamorphosis through a pr...
The causal link between the three-dimensional conformation of the genome and spatiotemporal control ...
Purpose: Pathogenic variants in the chromatin organizer CTCF were previously reported in seven indiv...
Background: The SWI/SNF chromatin remodeling factors have the ability to remodel nucleosomes and...
The most common cause of inherited mental deficiency and monogenetic cause of autism is Fragile X Sy...
Cell-type specific transcriptional programs are thought to be defined by cell-type specific transcri...
The central nervous system is the most complex and highly organized tissue in animals; composed of t...
The central nervous system (CNS) consists of an enormous number of cells, and large cellular varianc...
Recent literature has highlighted that mutations causing neurodevelopmental syndromes are particular...