Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Fibropolycystic Liver Disease"'
Autor:
Chaobo Chen, Hanghang Wu, Hui Ye, Agustín Tortajada, Sandra Rodríguez-Perales, Raúl Torres-Ruiz, August Vidal, Maria Isabel Peligros, Johanna Reissing, Tony Bruns, Mohamed Ramadan Mohamed, Kang Zheng, Amaia Lujambio, Maria J. Iraburu, Leticia Colyn, Maria Ujue Latasa, María Arechederra, Maite G. Fernández-Barrena, Carmen Berasain, Javier Vaquero, Rafael Bañares, Leonard J. Nelson, Christian Trautwein, Roger J. Davis, Eduardo Martinez-Naves, Yulia A. Nevzorova, Alberto Villanueva, Matias A. Avila, Francisco Javier Cubero
Publikováno v:
Cancers
Dipòsit Digital de la UB
Universidad de Barcelona
Cancers, Vol 14, Iss 78, p 78 (2022)
Cancers; Volume 14; Issue 1; Pages: 78
Dadun. Depósito Académico Digital de la Universidad de Navarra
Consejo Superior de Investigaciones Científicas (CSIC)
Dipòsit Digital de la UB
Universidad de Barcelona
Cancers, Vol 14, Iss 78, p 78 (2022)
Cancers; Volume 14; Issue 1; Pages: 78
Dadun. Depósito Académico Digital de la Universidad de Navarra
Consejo Superior de Investigaciones Científicas (CSIC)
Simple Summary Polycystic liver disease (PLD) is a group of rare disorders that result from structural changes in the biliary tree development in the liver. In the present work, we studied alterations in molecular mechanisms and signaling pathways th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6483fc845531aaf67f238b004196fdc9
https://pubmed.ncbi.nlm.nih.gov/35008241
https://pubmed.ncbi.nlm.nih.gov/35008241
Autor:
Chen, C. (Chaobo), Wu, H. (Hanghang), Ye, H. (Hui), Tortajada, A. (Agustín), Rodriguez-Perales, S. (Sandra), Torres-Ruiz, R. (Raúl), Vidal, A. (August), Peligros, M.I. (María Isabel), Reissing, J. (Johanna), Bruns, T. (Tony), Zheng, K. (Kang), Mohamed, M.R. (Mohamed Ramadan), Lujambio, A. (Amaya), Iraburu-Elizalde, M.J. (María José), Colyn, L. (Leticia), Latasa, M.U. (María Ujué), Arechederra, M. (María), Fernández-Barrena, M.G. (Maite G.), Berasain, C. (Carmen), Vaquero, J. (Javier), Bañares, R. (Rafael), Nelson, L.J. (Leonard J.), Trautwein, C. (Christian), Davis, R.J. (Roger J.), Martínez-Naves, E. (Eduardo), Nevzorova, Y. (Yulia), Villanueva, A. (Alberto), Avila, M.A. (Matías Antonio), Cubero, F.J. (Francisco Javier)
Polycystic liver disease (PLD) is a group of rare disorders that result from structural changes in the biliary tree development in the liver. In the present work, we studied alterations in molecular mechanisms and signaling pathways that might be res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1111::9d2f1fa941d50f60d7ae30a626ba5970
https://hdl.handle.net/10171/63434
https://hdl.handle.net/10171/63434
Autor:
Mariangela Diamarco, Giuseppe Cutaia, Massimo Midiri, Dario Giambelluca, Roberto Cannella, Giovanni Caruana, Giuseppe Salvaggio
Congenital cystic lesions of the bile ducts represent a spectrum of liver and biliary system lesions, resulting from abnormal embryologic development of the ductal plate. These disorders include Caroli disease, choledochal cysts, autosomal dominant p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b687a9fe9a05c25f2f966a323628d857
https://hdl.handle.net/10447/588655
https://hdl.handle.net/10447/588655
Akademický článek
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Kniha
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Autor:
Kaffe, E, Fiorotto, R, Pellegrino, F, Mariotti, V, Amenduni, M, Cadamuro, M, Fabris, L, Strazzabosco, M, Spirli, C
Congenital Hepatic Fibrosis (CHF), a genetic disease caused by mutations in the PKHD1 gene, encoding for the protein fibrocystin (FPC), is characterized by biliary dysgenesis, progressive portal fibrosis, and by a PKA-mediated activating phosphorylat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::36cf314334409c6f5285e644829e5d8e
https://europepmc.org/articles/PMC5906178/
https://europepmc.org/articles/PMC5906178/