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Burton B. Yang

Researcher at University of Toronto

Publications -  178
Citations -  15589

Burton B. Yang is an academic researcher from University of Toronto. The author has contributed to research in topics: microRNA & Versican. The author has an hindex of 63, co-authored 163 publications receiving 12908 citations. Previous affiliations of Burton B. Yang include Sunnybrook Health Sciences Centre & Chinese Academy of Sciences.

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Foxo3 circular RNA retards cell cycle progression via forming ternary complexes with p21 and CDK2

TL;DR: This work demonstrates that the circular RNA circ-Foxo3 was highly expressed in non-cancer cells and were associated with cell cycle progression, and formed a ternary complex that arrested the function of CDK2 and blockedcell cycle progression.
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MiRNA-Directed Regulation of VEGF and Other Angiogenic Factors under Hypoxia

TL;DR: This work used CNE cells from a human nasopharyngeal carcinoma cell line as a cellular system to investigate miRNA-directed regulation of VEGF and other angiogenic factors under hypoxia, and to explore the principles of gene regulation by miRNAs.
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Structure and function of aggrecan

TL;DR: ABSTRACTAggrecan is the major proteoglycan in the articular cartilage because it provides a hydrated gel structure (via its interaction with hyaluronan and link protein) that endows the cartilage with load-bearing properties and is crucial in chondroskeletal morphogenesis during development.
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Foxo3 circular RNA promotes cardiac senescence by modulating multiple factors associated with stress and senescence responses

TL;DR: It is concluded that ID-1, E2F1, FAK, and HIF1&agr; interact with circ-Foxo3 and are retained in the cytoplasm and could no longer exert their anti-senescent and anti-stress roles, resulting in increased cellular senescence.
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MicroRNA-378 promotes cell survival, tumor growth, and angiogenesis by targeting SuFu and Fus-1 expression

TL;DR: It is suggested that miR-378 transfection enhanced cell survival, tumor growth, and angiogenesis through repression of the expression of two tumor suppressors, Sufu and Fus-1.