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Jiang Wu

Researcher at University of Texas Southwestern Medical Center

Publications -  44
Citations -  4314

Jiang Wu is an academic researcher from University of Texas Southwestern Medical Center. The author has contributed to research in topics: Chromatin remodeling & Sonic hedgehog. The author has an hindex of 23, co-authored 43 publications receiving 3860 citations. Previous affiliations of Jiang Wu include Howard Hughes Medical Institute & Stanford University.

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An Essential Switch in Subunit Composition of a Chromatin Remodeling Complex during Neural Development

TL;DR: It is suggested that SWI/SNF-like complexes in vertebrates achieve biological specificity by combinatorial assembly of their subunits by preventing the subunit switch impairs neuronal differentiation.
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An embryonic stem cell chromatin remodeling complex, esBAF, is essential for embryonic stem cell self-renewal and pluripotency.

TL;DR: It is shown that BAF complexes are required for the self-renewal and pluripotency of mouse ES cells but not for the proliferation of fibroblasts or other cells, suggesting that esBAF complexes are specialized to interact with ES cell-specific regulators, providing a potential explanation for the requirement of BAF complex in pluripOTency.
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Regulation of Dendritic Development by Neuron-Specific Chromatin Remodeling Complexes

TL;DR: These studies suggest that the genes encoding the individual subunits of BAF complexes function like letters in a ten-letter word to produce biologically specific meanings (in this case dendritic outgrowth) by combinatorial assembly of their products.
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Understanding the words of chromatin regulation.

TL;DR: Combinatorial assembly of chromatin regulatory complexes may be critical for maximizing the information content provided by arrays of histone modifications.
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Olig2 Targets Chromatin Remodelers to Enhancers to Initiate Oligodendrocyte Differentiation

TL;DR: Regulation of the functional specificity and activity of a Smarca4/Brg1-dependent chromatin-remodeling complex by Olig2, coupled with transcriptionally linked chromatin modifications, is critical to precisely initiate and establish the transcriptional program that promotes oligodendrocyte differentiation and subsequent myelination of the CNS.