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Yong Lin

Researcher at Hunan Agricultural University

Publications -  9
Citations -  144

Yong Lin is an academic researcher from Hunan Agricultural University. The author has contributed to research in topics: Membrane protein & Integral membrane protein. The author has an hindex of 7, co-authored 9 publications receiving 97 citations.

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Anti-melanogenic effects of epigallocatechin-3-gallate (EGCG), epicatechin-3-gallate (ECG) and gallocatechin-3-gallate (GCG) via down-regulation of cAMP/CREB /MITF signaling pathway in B16F10 melanoma cells.

TL;DR: The results revealed catechins could be used as anti-melanogenic agents to protect cells from abnormal melanogenesis and regulated the melanogenesis of B16F10 cells through the cAMP/CREB/MITF pathway.
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Comparative proteomic analysis using 2DE-LC-MS/MS reveals the mechanism of Fuzhuan brick tea extract against hepatic fat accumulation in rats with nonalcoholic fatty liver disease

TL;DR: The reduced lipogenesis and enhanced β‐oxidation, tricarboxylic acid cycle and respiratory chain in HFD + HFTE‐fed rats, which mainly contributed to ameliorate hepatic fat accumulation and associated NAFLD.
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Improvement of a sample preparation method assisted by sodium deoxycholate for mass‐spectrometry‐based shotgun membrane proteomics

TL;DR: The enhanced sodium deoxycholate method exhibited superior sensitivity, coverage, and reliability for the identification of membrane proteins particularly those with high hydrophobicity and/or multiple transmembrane domains.
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Proteomic analysis of the inhibitory effect of epigallocatechin gallate on lipid accumulation in human HepG2 cells

TL;DR: The proteomic analysis hypothesized that EGCG reduced cellular lipid accumulation in FFA-induced HepG2 cells through the activation of AMP-activated protein kinase (AMPK) resulting from the generation of reactive oxygen species (ROS).
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Enhanced SDC-assisted digestion coupled with lipid chromatography-tandem mass spectrometry for shotgun analysis of membrane proteome.

TL;DR: An enhanced SDC-assisted digestion method was developed that incorporates the almost strongest ability of SDC with a high concentration to lyse membrane and extract/solubilize hydrophobic membrane proteins, and then dilution to 1% for more efficient digestion, demonstrating that the ESDC method provides a substantial improvement in the recovery and identification of membrane proteins.