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Mingyang Lu

Researcher at Rice University

Publications -  71
Citations -  5310

Mingyang Lu is an academic researcher from Rice University. The author has contributed to research in topics: Gene regulatory network & Population. The author has an hindex of 30, co-authored 63 publications receiving 4513 citations. Previous affiliations of Mingyang Lu include Northeastern University & Baylor College of Medicine.

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The genome of the social amoeba Dictyostelium discoideum

Ludwig Eichinger, +98 more
- 05 May 2005 - 
TL;DR: A proteome-based phylogeny shows that the amoebozoa diverged from the animal–fungal lineage after the plant–animal split, but Dictyostelium seems to have retained more of the diversity of the ancestral genome than have plants, animals or fungi.
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Implications of the Hybrid Epithelial/Mesenchymal Phenotype in Metastasis

TL;DR: The operating principles of the core regulatory network for EMT/MET that acts as a “three-way” switch giving rise to three distinct phenotypes – E, M and hybrid E/M are reviewed and a theoretical framework that can elucidate the role of many other players in regulating epithelial plasticity is presented.
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MicroRNA-based regulation of epithelial-hybrid-mesenchymal fate determination.

TL;DR: A unique model of the microRNA (miR)-based coupled chimeric modules underlying this core circuit is devised, showing that the miR-200/ZEB module functions as a ternary switch, allowing not only for the epithelial and mesenchymal phenotypes but also for a hybrid phenotype with mixed characteristics of collective cell migration, as seen in branching morphogenesis and wound closure.
Posted Content

Implications of the hybrid epithelial/mesenchymal phenotype in metastasis

TL;DR: In this article, the operating principles of the core regulatory network for EMT/MET are reviewed, which acts as a three-way switch giving rise to three distinct phenotypes - epithelial, mesenchymal and hybrid epithelial/mesenchymals.
Journal ArticleDOI

Elucidating cancer metabolic plasticity by coupling gene regulation with metabolic pathways.

TL;DR: The experimental results confirm that TNBC cells can maintain a hybrid metabolic phenotype and targeting both glycolysis and OXPHOS is necessary to eliminate their metabolic plasticity, and the theoretical framework to decode the coupling of gene regulation and metabolic pathways is established.