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Wei Wu

Researcher at University of California, Los Angeles

Publications -  10
Citations -  1096

Wei Wu is an academic researcher from University of California, Los Angeles. The author has contributed to research in topics: Chromatin remodeling & Alternative splicing. The author has an hindex of 7, co-authored 8 publications receiving 987 citations. Previous affiliations of Wei Wu include Stanford University.

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From neural development to cognition: unexpected roles for chromatin

TL;DR: Interestingly, mutations in EZH2 and certain BAF complex components have roles in both neurodevelopmental disorders and cancer, and overlapping point mutations are suggesting functionally important residues and domains.
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A vast repertoire of Dscam binding specificities arises from modular interactions of variable Ig domains.

TL;DR: This work develops a high-throughput ELISA-based binding assay and provides evidence that 95% (>18,000) of Dscam isoforms exhibit striking isoform-specific homophilic binding, thereby allowing neuronal processes to distinguish between self and nonself.
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Dscam2 mediates axonal tiling in the Drosophila visual system

TL;DR: It is shown that the immunoglobulin superfamily member Dscam2 restricts the connections formed by L1 lamina neurons to columns in the Drosophila visual system, and it is proposed that D scam2 is a tiling receptor for L1 neurons, which mediate repulsion between neurites of L1 cells in neighbouring columns.
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A Double S Shape Provides the Structural Basis for the Extraordinary Binding Specificity of Dscam Isoforms

TL;DR: Structural, genetic, and biochemical studies demonstrate that, in addition to variable domain "matching," intramolecular interactions between constant domains promote homophilic binding.
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Kinetic Analysis of npBAF to nBAF Switching Reveals Exchange of SS18 with CREST and Integration with Neural Developmental Pathways

TL;DR: The kinetics of neuron-specific BAF complex assembly in the formation of induced neurons from mouse embryonic stem cells, human fibroblasts, and normal mouse neural differentiation are defined and it is found that switching of chromatin remodeling mechanisms is highly correlated with a broad switch in the use of neurogenic transcription factors.