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Wen Liu

Researcher at University of California, San Diego

Publications -  21
Citations -  3517

Wen Liu is an academic researcher from University of California, San Diego. The author has contributed to research in topics: Retinoid X receptor & Regulation of gene expression. The author has an hindex of 15, co-authored 21 publications receiving 3216 citations. Previous affiliations of Wen Liu include Howard Hughes Medical Institute & Sanford-Burnham Institute for Medical Research.

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Reprogramming transcription by distinct classes of enhancers functionally defined by eRNA

TL;DR: Evidence is presented that cell-lineage-specific factors, such as FoxA1, can simultaneously facilitate and restrict key regulated transcription factors, exemplified by the androgen receptor (AR), to act on structurally and functionally distinct classes of enhancer.
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Conversion of Bcl-2 from protector to killer by interaction with nuclear orphan receptor Nur77/TR3

TL;DR: It is shown that Bcl-2 interacts with orphan nuclear receptor Nur77 (also known as TR3), which is required for cancer cell apoptosis induced by many antineoplastic agents, and can manifest opposing phenotypes, induced by interactions with proteins such as Nur77, suggesting novel strategies for regulating apoptosis in cancer and other diseases.
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ncRNA- and Pc2 Methylation-Dependent Gene Relocation between Nuclear Structures Mediates Gene Activation Programs

TL;DR: Observations delineate a molecular pathway linking the actions of subnuclear structure-specific ncRNAs and nonhistone protein methylation to relocation of transcription units in the three-dimensional space of the nucleus, thus achieving coordinated gene expression programs.
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The Akt-SRPK-SR Axis Constitutes a Major Pathway in Transducing EGF Signaling to Regulate Alternative Splicing in the Nucleus

TL;DR: In this article, a massive reprogramming of alternative splicing in response to EGF signaling is reported, which reveals a major signal transduction pathway for regulated splicing and place SRPKs in a central position in the pathway, consistent with their reputed roles in a large number of human cancers.