Biliary atresia-specific deciduous pulp stem cells feature biliary deficiency

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, are pallia...

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Detalles Bibliográficos
Autores principales: Sonoda, Soichiro, Yoshimaru, Koichiro, Yamaza, Haruyoshi, Yuniartha, Ratih, Matsuura, Toshiharu, Yamauchi-Tomoda, Erika, Murata, Sara, Nishida, Kento, Oda, Yoshinao, Ohga, Shouichi, Tajiri, Tasturo, Taguchi, Tomoaki, Yamaza, Takayoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607730/
https://www.ncbi.nlm.nih.gov/pubmed/34809720
http://dx.doi.org/10.1186/s13287-021-02652-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607730/
https://www.ncbi.nlm.nih.gov/pubmed/34809720
http://dx.doi.org/10.1186/s13287-021-02652-8

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