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期刊名:Seminars in liver disease

缩写:SEMIN LIVER DIS

ISSN:0272-8087

e-ISSN:1098-8971

IF/分区:4.0/Q2

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共收录本刊相关文章索引708条
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Martin Wagner,Gernot Zollner,Michael Trauner Martin Wagner
Although hereditary or acquired defects in hepatobiliary transporter systems cause or predispose to cholestasis, adaptive bile acid transporter changes can counteract cholestasis by reducing hepatocellular and systemic concentrations of ret...
Christiane Pauli-Magnus,Peter J Meier,Bruno Stieger Christiane Pauli-Magnus
Intrahepatic cholestasis of pregnancy and drug-induced cholestasis are two clinically important forms of acquired cholestatic liver disease. The understanding of the underlying mechanisms of acquired cholestasis has recently made considerab...
Anne Davit-Spraul,Emmanuel Gonzales,Christiane Baussan et al. Anne Davit-Spraul et al.
Class III multidrug resistance P-glycoproteins, Mdr2 in mice and MDR3 in human, are canalicular phospholipid translocators involved in biliary phospholipid (phosphatidylcholine) excretion. The role of an ABCB4 gene defect in liver disease h...
Ping Lam,Carol J Soroka,James L Boyer Ping Lam
The primary transporter responsible for bile salt secretion is the bile salt export pump (BSEP, ABCB11), a member of the ATP-binding cassette (ABC) superfamily, which is located at the bile canalicular apical domain of hepatocytes. In human...
Coen C Paulusma,Ronald P J Oude Elferink,Peter L M Jansen Coen C Paulusma
Progressive familial intrahepatic cholestasis type 1 is a rare genetic liver disease that presents in the first year of life. Bile salts are elevated and these patients are often jaundiced. Despite the cholestasis, serum gamma-glutamyltrans...
Qian Zhao,Chang-Qing Su,Hui Dong et al. Qian Zhao et al.
The authors present the case of a 48-year-old man with hepatitis B cirrhosis, who developed two primary malignant liver tumors that were morphologically distinct from each other. The first tumor was a hepatocellular carcinoma and the second...
Sherry X Hsu,Abby B Siegel,Paul D Berk Sherry X Hsu
The incidence of hepatocellular carcinoma (HCC) is growing dramatically in the Western world. It is currently the fifth most common cancer worldwide, and the third most common cause of death from cancer. Studies clearly demonstrate that sur...
Nelson Fausto,Jean S Campbell Nelson Fausto
The etiology of liver cancer is well known, but despite recent progress in the application of molecular techniques for the analysis of the development of these tumors, we still lack precise knowledge about pathogenesis of hepatocellular car...
Sandrine Imbeaud,Yannick Ladeiro,Jessica Zucman-Rossi Sandrine Imbeaud
Identification of novel oncogenes and tumor suppressors in hepatocellular carcinoma (HCC) is challenging, both because of the tumor complexity and the difficulty in integrating the very large amount of data provided by different approaches....