High Mobility Group Box 1 Release by Cholangiocytes Governs Biliary Atresia Pathogenesis and Correlates With Increases in Afflicted Infants

BACKGROUND AND AIMS: Biliary atresia (BA) is a devastating cholangiopathy of infancy. Upon diagnosis, surgical reconstruction by Kasai hepatoportoenterostomy (HPE) restores biliary drainage in a subset of patients, but most patients develop fibrosis and progress to end‐stage liver disease requiring...

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Detalles Bibliográficos
Autores principales: Mohanty, Sujit K., Donnelly, Bryan, Temple, Haley, Ortiz‐Perez, Ana, Mowery, Sarah, Lobeck, Inna, Dupree, Phylicia, Poling, Holly M., McNeal, Monica, Mourya, Reena, Jenkins, Todd, Bansal, Ruchi, Bezerra, Jorge, Tiao, Greg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8349381/
https://www.ncbi.nlm.nih.gov/pubmed/33559243
http://dx.doi.org/10.1002/hep.31745

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8349381/
https://www.ncbi.nlm.nih.gov/pubmed/33559243
http://dx.doi.org/10.1002/hep.31745

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