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Marco Arrese

Researcher at Pontifical Catholic University of Chile

Publications -  276
Citations -  12354

Marco Arrese is an academic researcher from Pontifical Catholic University of Chile. The author has contributed to research in topics: Fatty liver & Medicine. The author has an hindex of 45, co-authored 225 publications receiving 8525 citations. Previous affiliations of Marco Arrese include University of Chile & Yale University.

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A new definition for metabolic dysfunction-associated fatty liver disease: An international expert consensus statement.

TL;DR: A panel of international experts from 22 countries propose a new definition of metabolic-dysfunction-associated fatty liver disease that is both comprehensive yet simple for the diagnosis of MAFLD and is independent of other liver diseases.
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Global Perspectives on Nonalcoholic Fatty Liver Disease and Nonalcoholic Steatohepatitis

TL;DR: The authors in this article examined the state of NAFLD among different regions and understand the global trajectory of this disease, an international group of experts came together during the 2017 American Association for the Study of Liver Diseases Global NASFLD Forum and provided a summary of this forum and an assessment of the current state of NASH worldwide.
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The rat canalicular conjugate export pump (Mrp2) is down-regulated in intrahepatic and obstructive cholestasis

TL;DR: Down-regulation of Mrp2 expression may explain impaired biliary excretion of amphiphilic anionic conjugates in these models of cholestasis.
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Triggering and resolution of inflammation in NASH.

TL;DR: The authors comprehensively discuss the key factors that trigger hepatic inflammation, as well as the pathways involved in inflammation resolution, which help to design targeted therapies able to halt or reverse disease progression in NASH.
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Bile acids and nonalcoholic fatty liver disease: Molecular insights and therapeutic perspectives

TL;DR: Current available data on the relationships of bile acids to NAFLD and the potential for therapeutically targeting bile‐acid‐related pathways to address this growing world‐wide disease are summarized.