Zobrazeno 1 - 10
of 374
pro vyhledávání: '"Biliary fibrosis"'
Autor:
Zhao Jinyu, Yue Ping, Mi Ningning, Li Matu, Fu Wenkang, Zhang Xianzhuo, Gao Long, Bai Mingzhen, Tian Liang, Jiang Ningzu, Lu Yawen, Ma Haidong, Dong Chunlu, Zhang Yong, Zhang Hengwei, Zhang Jinduo, Ren Yanxian, Suzuki Azumi, Wong Peng F., Tanaka Kiyohito, Rerknimitr Rungsun, Junger Henrik H., Cheung Tan T., Melloul Emmanuel, Demartines Nicolas, Leung Joseph W., Yao Jia, Yuan Jinqiu, Lin Yanyan, Schlitt Hans J., Meng Wenbo
Publikováno v:
Medical Review, Vol 4, Iss 4, Pp 326-365 (2024)
Fibrosis resulting from pathological repair secondary to recurrent or persistent tissue damage often leads to organ failure and mortality. Biliary fibrosis is a crucial but easily neglected pathological feature in hepatobiliary disorders, which may p
Externí odkaz:
https://doaj.org/article/f00ec880e3164f95b5225644f4d94ec7
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology, Vol 17, Iss 4, Pp 553-565 (2024)
Biliary fibrosis is seen in cholangiopathies, including primary biliary cholangitis (PBC) and primary sclerosing cholangitis (PSC). In PBC and PSC, biliary fibrosis is associated with worse outcomes and histologic scores. Within the liver, both hepat
Externí odkaz:
https://doaj.org/article/882c26d77ba94919b409cf07aa2ef7c6
Publikováno v:
Cells, Vol 13, Iss 19, p 1650 (2024)
Primary sclerosing cholangitis (PSC) is a rare, chronic liver disease with no approved therapies. The ursodeoxycholic acid (UDCA) has been widely used, although there is no evidence that the use of UDCA delays the time to liver transplant or increase
Externí odkaz:
https://doaj.org/article/8c33c16252b149838b750ac30deaed77
Autor:
Trinh Van Le, Thanh Minh Dang, Huy Quang Do, Ai-Xuan Le Holterman, Hong-Thuy Phan-Thi, Thong Tan Tran, Nhung Hai Truong
Publikováno v:
Liver Research, Vol 7, Iss 1, Pp 90-98 (2023)
Background: Biliary atresia is a rare congenital bile duct disease that is the leading cause of liver fibrosis in neonates. Granulocyte colony-stimulating factor (GCSF) is a potential therapy for hepatocellular diseases, but data on GCSF for cholesta
Externí odkaz:
https://doaj.org/article/7cbdc1a4721e4ee588aa9ff53bb66aa1
Autor:
Chao Yan, Na Xu, Man Liu, Zhihua Jiang, Jing Wu, Stephane Koda, Yu Chen, Beibei Zhang, Qian Yu, Yin-Hai Xu, Jian-Lin Wu, Kui-Yang Zheng
Publikováno v:
Parasites & Vectors, Vol 15, Iss 1, Pp 1-9 (2022)
Abstract Background Clonorchiasis caused by Clonorchis sinensis is a zoonotic parasitic disease characterized by cholangitis, biliary proliferation, biliary fibrosis, and even cholangiocarcinoma. Our previous study showed that the expression of inter
Externí odkaz:
https://doaj.org/article/cc29c229725d4eac85a8ac018674e764
Autor:
Dingding Wang, Shen Yang, Yong Zhao, Yanan Zhang, Kaiyun Hua, Yichao Gu, Shuangshuang Li, Junmin Liao, Ting Yang, Jiawei Zhao, Jinshi Huang
Publikováno v:
Frontiers in Immunology, Vol 13 (2023)
BackgroundBiliary atresia (BA) is the most common form of severe neonatal obstructive jaundice. The etiology and pathogenesis of BA are multifactorial, and different factors may interact to produce heterogeneous pathological features and clinical out
Externí odkaz:
https://doaj.org/article/22751151a03143c49a14c959a7161a0e
Publikováno v:
Cells, Vol 12, Iss 5, p 792 (2023)
Biliary fibrosis is the driving pathological process in cholangiopathies such as primary biliary cholangitis (PBC) and primary sclerosing cholangitis (PSC). Cholangiopathies are also associated with cholestasis, which is the retention of biliary comp
Externí odkaz:
https://doaj.org/article/a0b7f108441c41eaa437150539ce9833
Akademický článek
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Publikováno v:
Frontiers in Medicine, Vol 7 (2020)
Biliary atresia (BA) is a rare cholangiopathy of infancy in which the bile ducts obliterate, leading to profound cholestasis and liver fibrosis. BA is hypothesized to be caused by a viral insult that leads to over-activation of the immune system. Pat
Externí odkaz:
https://doaj.org/article/67efd32b47204f469f295a7e19a05abd
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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