Hepatic STAMP2 mediates recombinant FGF21‐induced improvement of hepatic iron overload in nonalcoholic fatty liver disease-Reference-Cited by-同舟云学术

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Hepatic STAMP2 mediates recombinant FGF21‐induced improvement of hepatic iron overload in nonalcoholic fatty liver disease

Published:2020-07-28 Issue:9 Volume:34 Page:12354-12366
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:FASEB j.

Author:

Kim Hye Young¹,Kwon Woo Young¹,Park Joon Beom¹,Lee Mi Hwa¹,Oh Yoo Jin¹,Suh SungHwan²,Baek Yang Hyun³,Jeong Jin Sook⁴,Yoo Young Hyun¹

Affiliation:

1. Department of Anatomy and Cell Biology Dong‐A University College of Medicine Busan South Korea

2. Department of Endocrinology Dong‐A University College of Medicine Busan South Korea

3. Department of Gastroenterology Dong‐A University College of Medicine Busan South Korea

4. Department of Pathology Dong‐A University College of Medicine Busan South Korea

Funder

National Research Foundation of Korea

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.202000790R

Reference48 articles.

1. Nonalcoholic fatty liver disease and hepatocellular carcinoma: A weighty connection

2. Nonalcoholic fatty liver disease: From steatosis to cirrhosis

3. Non-alcoholic fatty liver disease – A global public health perspective

4. FGF21 ameliorates nonalcoholic fatty liver disease by inducing autophagy

5. FGF21 treatment ameliorates alcoholic fatty liver through activation of AMPK-SIRT1 pathway

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