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I-Chin Wu
Researcher at National Cheng Kung University
Publications - 32
Citations - 536
I-Chin Wu is an academic researcher from National Cheng Kung University. The author has contributed to research in topics: Hepatitis B virus & HBeAg. The author has an hindex of 13, co-authored 32 publications receiving 437 citations.
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Journal ArticleDOI
Apolipoprotein J, a glucose-upregulated molecular chaperone, stabilizes core and NS5A to promote infectious hepatitis C virus virion production
Chun Chieh Lin,Peiju Tsai,Hung Yu Sun,Mei Chi Hsu,Jin-Ching Lee,I-Chin Wu,Chiung Wen Tsao,Ting-Tsung Chang,Kung Chia Young +8 more
TL;DR: The interplay between glucose, ApoJ and HCV virion production is investigated, which facilitates infectious HCV particle production via stabilization of core/NS5A, which might surround LDs at the ER-Golgi membrane contact site.
Journal ArticleDOI
Efficacy of entecavir in chronic hepatitis B patients with mildly elevated alanine aminotransferase and biopsy‐proven histological damage
I-Chin Wu,Ching-Lung Lai,Steven-Huy B. Han,Kwang-Hyup Han,Stuart C Gordon,You-Chen Chao,Chee-Kiat Tan,William Sievert,Tawesak Tanwandee,Dong Xu,Boon-Leong Neo,Ting-Tsung Chang +11 more
TL;DR: This retrospective analysis demonstrated that HBeAg‐negative CHB patients treated with entecavir responded similarly irrespective of baseline ALT level, however, H beAg‐positive patients with mildly elevated ALT responded less well to treatment with entECavir than did those with ALT greater than 2 × ULN.
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Very low-density lipoprotein/lipo-viro particles reverse lipoprotein lipase-mediated inhibition of hepatitis C virus infection via apolipoprotein C-III
Hung Yu Sun,Chun Chieh Lin,Jin-Ching Lee,Shainn Wei Wang,Pin-Nan Cheng,I-Chin Wu,Ting-Tsung Chang,Ming Derg Lai,Dar-Bin Shieh,Kung Chia Young +9 more
TL;DR: This study reveals that LPL is an anti-HCV factor, and that apoC-III in VLDL and LVPs reduces the LPL-mediated inhibition of HCV infection.
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Association of intrahepatic cccDNA reduction with the improvement of liver histology in chronic hepatitis B patients receiving oral antiviral agents.
TL;DR: Although one‐year ETV or ADV treatment is insufficient for cccDNA eradication, oral antiviral therapies may improve liver histology, probably by suppressing intrahepatic ccc DNA.
Journal ArticleDOI
Aberrant Serum Immunoglobulin G Glycosylation in Chronic Hepatitis B Is Associated With Histological Liver Damage and Reversible by Antiviral Therapy
Cheng-Hsun Ho,Rong-Nan Chien,Pin-Nan Cheng,Jia-Huei Liu,Cheng-Kun Liu,Chih-Sheng Su,I-Chin Wu,I-Chen Li,Hung Wen Tsai,Shiaw-Lin Wu,Wen-Chun Liu,Shu Hui Chen,Ting-Tsung Chang +12 more
TL;DR: Aberrant serum IgG-Fc glycosylation in CHB, which is highly associated with histological liver damage, affects IgG opsonizing activity and can be reversed by antiviral therapy.