4.3 Article

Alcohol and fat promote steatohepatitis: a critical role for fat-specific protein 27/CIDEC

期刊

JOURNAL OF INVESTIGATIVE MEDICINE
卷 64, 期 6, 页码 1078-1081

出版社

BMJ PUBLISHING GROUP
DOI: 10.1136/jim-2016-000204

关键词

Liver Diseases; Alcoholic; Fatty Liver

资金

  1. National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health
  2. VA Merit Award [1I01CX000361]
  3. NIH [U01AA021840]
  4. US DOD [W81XWH-12-1-0497]

向作者/读者索取更多资源

Alcoholic liver disease (ALD) is a major public health problem worldwide and is the leading cause of end-stage liver disease. While the ultimate control of ALD will require the prevention of alcohol abuse, better understanding of the mechanisms of alcohol-induced liver injury may lead to treatments of fatty liver, alcoholic hepatitis, and prevention or delay of occurrence of cirrhosis. The elucidation and the discovery of several new concepts in ALD pathogenesis have raised our understanding on the complex mechanisms and the potential in developing the new strategies for therapeutic benefits. In this review, we provide the most up-to-date information on the basic molecular mechanisms focusing on the role of fat-specific protein 27/CIDEC in the pathogenesis of ALD.

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