Biliary atresia-specific deciduous pulp stem cells feature biliary deficiency

Biliary atresia-specific deciduous pulp stem cells feature biliary deficiency

Abstract Background Biliary atresia (BA) is a severe hepatobiliary disease in infants that ultimately results in hepatic failure; however, its pathological mechanism is poorly elucidated. Current surgical options, including Kasai hepatoportoenterostomy and orthotopic liver organ transplantations, ar...

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Autores principales: Soichiro Sonoda, Koichiro Yoshimaru, Haruyoshi Yamaza, Ratih Yuniartha, Toshiharu Matsuura, Erika Yamauchi-Tomoda, Sara Murata, Kento Nishida, Yoshinao Oda, Shouichi Ohga, Tasturo Tajiri, Tomoaki Taguchi, Takayoshi Yamaza
Formato: article
Lenguaje:EN
Publicado: BMC 2021
Materias:
Biliary atresia
Patient-derived human deciduous pulp stem cells
Bile duct regeneration
Medicine (General)
R5-920
Biochemistry
QD415-436
Acceso en línea:https://doaj.org/article/7b22fc97f6e549fbb812a425f2b9dd8b
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https://doaj.org/article/7b22fc97f6e549fbb812a425f2b9dd8b

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