Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Yingfu Chen has a total of 7 co-authors. Here are the top co-authors by number of shared publications:

  • Eva Katrin Wirth

    DZHK (German Centre for Cardiovascular Research), partner site Berlin, Berlin, Germany

    1 shared publication
  • Frank Tacke

    Department of Hepatology and Gastroenterology, Campus Virchow-Klinikum and Campus Charité Mitte, Charité - Universitätsmedizin Berlin, Berlin, Germany

    1 shared publication
  • Joachim Spranger

    Department of Endcrinology and Metabolism, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt Universität zu Berlin, Berlin, Germany

    1 shared publication
  • Josef Köhrle

    Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Institut für Experimentelle Endokrinologie, Berlin, Germany

    1 shared publication
  • Joshua Seifert

    Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Institut für Experimentelle Endokrinologie, 10115 Berlin, Germany

    1 shared publication
  • Knut Mai

    Department of Endocrinology and Metabolism, Charité—Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 10117 Berlin, Germany

    1 shared publication

Latest Publications

  • Open Access

    Hepatic Energy Metabolism under the Local Control of the Thyroid Hormone System

    by Joshua Seifert, Yingfu Chen, Wenzel Schöning, Knut Mai, Frank Tacke, Joachim Spranger, Josef Köhrle, Eva Katrin Wirth

    The energy homeostasis of the organism is orchestrated by a complex interplay of energy substrate shuttling, breakdown, storage, and distribution. Many of these processes are interconnected via the liver. Thyroid hormones (TH) are well known to provide signals for the regulation of energy homeostasis through direct gene regulation via their nuclear receptors acting as transcription factors. In this comprehensive review, we summarize the effects of nutritional intervention like fasting and diets on the TH system. In parallel, we detail direct effects of TH in liver metabolic pathways with regards to glucose, lipid, and cholesterol metabolism. This overview on hepatic effects of TH provides the basis for understanding the complex regulatory network and its translational potential with regards to currently discussed treatment options of non-alcoholic fatty liver disease (NAFLD) and non-alcoholic steatohepatitis (NASH) involving TH mimetics.