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Li Ye

Researcher at Stanford University

Publications -  39
Citations -  11528

Li Ye is an academic researcher from Stanford University. The author has contributed to research in topics: Adipose tissue & Thermogenesis. The author has an hindex of 22, co-authored 38 publications receiving 9685 citations. Previous affiliations of Li Ye include Howard Hughes Medical Institute & Harvard University.

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Beige Adipocytes Are a Distinct Type of Thermogenic Fat Cell in Mouse and Human

TL;DR: Beige cells have a gene expression pattern distinct from either white or brown fat and are preferentially sensitive to the polypeptide hormone irisin, providing evidence that previously identified brown fat deposits in adult humans are composed of beige adipocytes.
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Advanced CLARITY for rapid and high-resolution imaging of intact tissues

TL;DR: Protocols spanning multiple dimensions of the CLARITY workflow are described, ranging from simple, reliable and efficient lipid removal without electrophoretic instrumentation to optimized objectives and integration with light-sheet optics (CLARITY-optimized light- sheet microscopy (COLM)) for accelerating data collection from clarified samples by several orders of magnitude while maintaining or increasing quality and resolution.
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Ablation of PRDM16 and Beige Adipose Causes Metabolic Dysfunction and a Subcutaneous to Visceral Fat Switch

TL;DR: It is shown that adipocyte-specific deletion of the coregulatory protein PRDM16 caused minimal effects on classical brown fat but markedly inhibited beige adipocyte function in subcutaneous fat following cold exposure or β3-agonist treatment, indicating that PRDM 16 and beige fat cells are required for the "browning" of white fat and the healthful effects of sub cutaneous adipose tissue.
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Transcriptional control of preadipocyte determination by Zfp423

TL;DR: Using a new method for the quantitative analysis of transcriptional components, the zinc-finger protein Zfp423 is identified as a factor enriched in preadipose versus non-preadipose fibroblasts and regulates Pparg expression through amplification of the BMP signalling pathway.