Results 1 to 10 of about 3,751 (115)

COVID-Associated Cast-Forming Cholangiopathy: A Commentary on Disease Mechanism, Treatment, and Prognosis

open access: yesHepatic Medicine: Evidence and Research, 2023
Yara Sarkis,1 Nasir Saleem,2 Raj Vuppalanchi,2 Mark Gromski2 1Department of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA; 2Division of Gastroenterology and Hepatology, Department of Medicine, Indiana University School of ...
Nasir Saleem, Mark Gromski
exaly   +2 more sources

Mixed cholangiopathy with eosinophilic and autoimmune features: a case report [PDF]

open access: yesJournal of Medical Case Reports
Background Eosinophilic cholangitis and autoimmune cholangiopathy are two rare immune-mediated biliary disorders with distinct demographic, clinical, and histopathological features.
Henry Shen   +4 more
doaj   +2 more sources

COVID-19-Related Cholangiopathy: Histological Findings

open access: yesDiagnostics
Cholangiopathy has been described in survivors of severe COVID-19, presenting significant clinical parallels to the pre-pandemic condition of secondary sclerosing cholangitis in critically ill patients (SSC-CIP).
  +2 more
exaly   +3 more sources

Challenges in the diagnosis and treatment of genetic cholestasis in adultsKeypoints [PDF]

open access: yesJHEP Reports
Summary: Disorders of bile formation and bile flow along the intra- and extrahepatic bile ducts are summarised under the term cholestasis. Clinically, conditions resulting in retention of biliary constituents such as bile acids within hepatocytes (termed
Richard J. Thompson   +3 more
doaj   +2 more sources

The role of miRNAs in the development of cholangiopathies. Part 1

open access: yesZdorovʹe Rebenka, 2023
The role of miRNA in the development of cholangiopathies is given in the scientific review. This article discusses the role of miRNA in primary sclerosing cholangitis and primary biliary cho­langitis.
A.E. Abaturov, V.L. Babуch
doaj   +1 more source

A joint transcriptional regulatory network and protein activity inference analysis identifies clinically associated master regulators for biliary atresia

open access: yesFrontiers in Pediatrics, 2022
Biliary atresia (BA) is a devastating cholangiopathy in neonate. Transcription factors (TFs), a type of master regulators in biological processes and diseases, have been implicated in pathogenesis of BA. However, a global view of TFs and how they link to
Panpan Sun   +10 more
doaj   +1 more source

Current Concepts of Biliary Atresia and Matrix Metalloproteinase-7: A Review of Literature

open access: yesFrontiers in Medicine, 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 ...
Mark Nomden   +4 more
doaj   +1 more source

The role of miRNAs in the development of cholangiopathies. Part 2

open access: yesZdorovʹe Rebenka, 2023
The role of miRNA in the development of cho­langiopathies is considered in the scientific review. This article discusses the role of miRNA in biliary atresia, polycystic liver disease, and cholangiocarcinoma.
A.E. Abaturov, V.L. Babуch
doaj   +2 more sources

Combining ASBT inhibitor and FGF15 treatments enhances therapeutic efficacy against cholangiopathy in female but not male Cyp2c70 KO mice

open access: yesJournal of Lipid Research, 2023
Therapeutic reduction of hydrophobic bile acids exposure is considered beneficial in cholestasis. The Cyp2c70 KO mice lack hydrophilic muricholic acids and have a human-like hydrophobic bile acid pool resulting in hepatobiliary injury.
Mohammad Nazmul Hasan   +8 more
doaj   +1 more source

Reversine attenuates cholestatic ductular reaction in rats

open access: yesFEBS Open Bio, 2023
Ductular reaction (DR) is usually observed in biliary disorders or various liver disorders, including nonalcoholic fatty liver disease. Few studies have focused on interrupting the DR process in the cholestatic environment.
Di Huang   +8 more
doaj   +1 more source

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