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Resveratrol differentially regulates NAMPT and SIRT1 in Hepatocarcinoma cells and primary human hepatocytes.

机译：白藜芦醇差异调节肝癌细胞和原代人肝细胞中的NampT和sIRT1。

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Susanne Schuster; Melanie Penke; Theresa Gorski; Stefanie Petzold-Quinque; Georg Damm; Rolf Gebhardt; Wieland Kiess; Antje Garten;
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1. Resveratrol differentially regulates NAMPT and SIRT1 in hepatocarcinoma cells and primary human hepatocytes [J] . Susanne Schuster, Melanie Penke, Theresa Gorski, Cancer & Metabolism . 2014,第S1期

机译：白藜芦醇在肝癌细胞和原代人肝细胞中差异调节NAMPT和SIRT1
2. Shelterin differentially respond to oxidative stress induced by TiO 2 -NPs and regulate telomere length in human hepatocytes and?hepatocarcinoma cells in?vitro [J] . Han Wang, Juan Ni, Xihan Guo, Biochemical and Biophysical Research Communications . 2018,第2期

机译：避难液差异地应对由TiO 2-NPS诱导的氧化应激，并调节人肝细胞中的端粒长度，体外肝癌细胞
3. A novel herbal formulation "LiverCare" differentially regulates primary rat hepatocyte and hepatocarcinoma cell proliferation in vitro. [J] . Vidyashankar S, Varma SR, Azeemudin M, Journal of medicinal food . 2011,第9期

机译：新型草药制剂“ LiverCare”在体外差异调节原代大鼠肝细胞和肝癌细胞的增殖。
4. Anti-hepatocarcinoma effects of resveratrol nanoethosomes against human HepG2 cells [C] . Xiang-Ping Meng, Zhen Zhang, Tong-sheng Chen, Biophotonics and immune responses XII . 2017

机译：白藜芦醇纳米脂质体对人HepG2细胞的抗肝癌作用
5. Resveratrol-induced activation of the SIRT1/AMPK axis in human CD4 T cells triggers replicative stress and an ATR-dependent cell cycle arrest [D] . Craveiro, Marco Filipe Marques 2013

机译：白藜芦醇诱导人CD4 T细胞中SIRT1 / AMPK轴的激活触发复制应激和ATR依赖性细胞周期阻滞
6. Resveratrol differentially regulates NAMPT and SIRT1 in hepatocarcinoma cells and primary human hepatocytes [O] . Susanne Schuster, Melanie Penke, Theresa Gorski, 2014

机译：白藜芦醇在肝癌细胞和原代人肝细胞中差异调节NAMPT和SIRT1
7. Resveratrol differentially regulates NAMPT and SIRT1 in hepatocarcinoma cells and primary human hepatocytes [O] . Susanne Schuster, Melanie Penke, Theresa Gorski, 2014

机译：白藜芦醇在肝癌细胞和原代人肝细胞中差异调节NAMPT和SIRT1

Resveratrol differentially regulates NAMPT and SIRT1 in Hepatocarcinoma cells and primary human hepatocytes.

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