Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Bang-Yu Liou"'
Publikováno v:
Journal of the Formosan Medical Association, Vol 122, Iss 7, Pp 648-652 (2023)
Rotor syndrome is a rare, benign, inherited disorder that is commonly associated with mild hyperbilirubinemia. It is caused by bi-allelic pathological variants in both SLCO1B1 and SLCO1B3 genes, causing defective OATP1B1 and OATP1B3 in the sinusoidal
Externí odkaz:
https://doaj.org/article/04aa3c2c1eb343d1bf1d16d56a1eba78
Autor:
Che‐Ming Chiang, Yung‐Ming Jeng, Ming‐Chih Ho, Ming‐Wei Lai, Huei‐Ying Li, Pei‐Lung Chen, Ni‐Chung Lee, Jia‐Feng Wu, Yu‐Chun Chiu, Bang‐Yu Liou, Yen‐Hsuan Ni, Hong‐Yuan Hsu, Mei‐Hwei Chang, Huey‐Ling Chen
Publikováno v:
JGH Open, Vol 6, Iss 12, Pp 839-845 (2022)
Abstract Background and Aim Alagille syndrome (ALGS) is a multisystem disorder with variable clinical courses. This study investigated the clinical and genetic features of ALGS patients with different outcomes and analyzed the liver pathology at live
Externí odkaz:
https://doaj.org/article/c4fe4b8c39664be18f32bf07e6276ac7
Autor:
Ju-Yin Chen, Jia-Feng Wu, Akihiko Kimura, Hiroshi Nittono, Bang-Yu Liou, Chee-Seng Lee, Ho-Sheng Chen, Yu-Chun Chiu, Yen-Hsuan Ni, Steven Shinn-Forng Peng, Wang-Tso Lee, I-Jung Tsai, Mei-Hwei Chang, Huey-Ling Chen
Publikováno v:
Pediatrics and Neonatology, Vol 61, Iss 1, Pp 75-83 (2020)
Background: Inborn errors of bile acid metabolism (IEBAM) cause rare but treatable genetic disorders that can present as neonatal cholestasis or neurological diseases. Without timely primary bile acid treatment, patients may develop liver failure ear
Externí odkaz:
https://doaj.org/article/bc23a19a3e6d4a19a24bb123280ed82d
Autor:
Cheng-Ju Kuo, Ya-Chu Hsu, Sin-Tian Wang, Bang-Yu Liou, Serene Boon-Yuean Lim, Yi-Wei Chen, Chang-Shi Chen
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Enterohemorrhagic Escherichia coli (EHEC), a human pathogen, also infects Caenorhabditis elegans. We demonstrated previously that C. elegans activates the p38 MAPK innate immune pathway to defend against EHEC infection. However, whether a C. elegans
Externí odkaz:
https://doaj.org/article/8363141946e94543b4ab74cdbdc4ecb8
Publikováno v:
Journal of Biomedical Science, Vol 25, Iss 1, Pp 1-13 (2018)
Abstract Background Jaundice is a common symptom of inherited or acquired liver diseases or a manifestation of diseases involving red blood cell metabolism. Recent progress has elucidated the molecular mechanisms of bile metabolism, hepatocellular tr
Externí odkaz:
https://doaj.org/article/a8d098562f4f4b4594ea7193cb43bc4c
Autor:
Yu-Chun Chiu, Steven Shinn-Forng Peng, Ho-Sheng Chen, Hiroshi Nittono, Akihiko Kimura, Jia-Feng Wu, I-Jung Tsai, Yen-Hsuan Ni, Bang-Yu Liou, Mei-Hwei Chang, Huey-Ling Chen, Wang-Tso Lee, Ju-Yin Chen, Chee-Seng Lee
Publikováno v:
Pediatrics and Neonatology, Vol 61, Iss 1, Pp 75-83 (2020)
Background: Inborn errors of bile acid metabolism (IEBAM) cause rare but treatable genetic disorders that can present as neonatal cholestasis or neurological diseases. Without timely primary bile acid treatment, patients may develop liver failure ear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99513381bfb84dfacf6f1b34ce00cae0
https://doi.org/10.1016/j.pedneo.2019.06.009
https://doi.org/10.1016/j.pedneo.2019.06.009
Autor:
Jacob Shujui Hsu, Shang-Hsin Wu, Ming-Chih Ho, Yung-Ming Jeng, Hui-Ling Chen, Bang Yu Liou, Yen-Hsuan Ni, Jia-Feng Wu, Mei-Hwei Chang, Mu Ming Chien, Huey-Ling Chen, Pei-Lung Chen
Publikováno v:
Hepatology (Baltimore, Md.)References. 70(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0602b3450c267707fdc14f6b338e3cb
https://pubmed.ncbi.nlm.nih.gov/31269534
https://pubmed.ncbi.nlm.nih.gov/31269534
Autor:
Hui-Ling Chen, Yu-Hsuan Yang, Yu-Hua Hsu, Shang-Hsin Wu, Huey-Ling Chen, Bang-Yu Liou, Huei-Ying Li, Yen-Hsuan Ni, Mei-Hwei Chang, Jia-Feng Wu
Publikováno v:
The Journal of pediatrics. 205
Objective To test the application of a target enrichment next-generation sequencing (NGS) jaundice panel in genetic diagnosis of pediatric liver diseases. Study design We developed a capture-based target enrichment NGS jaundice panel containing 42 kn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4212e6de6b7c37c360eef340249496f
https://pubmed.ncbi.nlm.nih.gov/30366773
https://pubmed.ncbi.nlm.nih.gov/30366773
Autor:
Kah-Sin Loh, Chang Shi Chen, Ya-Luen Yang, Huan-Da Chen, Cheng-Ju Kuo, I-Hua Chu, Bang-Yu Liou
Publikováno v:
Experimental Gerontology. 48:371-379
Aging is a process of gradual functional decline leading to death. Reactive oxygen species (ROS) not only contribute to oxidative stress and cell damage that lead to aging but also serve as signaling molecules. Sestrins are evolutionarily conserved i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5eb93212066ba3da232c298fb4d87bda
https://doi.org/10.1016/j.exger.2012.12.011
https://doi.org/10.1016/j.exger.2012.12.011