Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Lee Law"'
Autor:
Jo-Ann L. Stanton, Rory O'Brien, Richard J. Hall, Anastasia Chernyavtseva, Hye Jeong Ha, Lauren Jelley, Peter D. Mace, Alexander Klenov, Jackson M. Treece, John D. Fraser, Fiona Clow, Lewis Clarke, Yongdong Su, Harikrishnan M. Kurup, Vyacheslav V. Filichev, William Rolleston, Lee Law, Phillip M. Rendle, Lawrence D. Harris, James M. Wood, Thomas W. Scully, James E. Ussher, Jenny Grant, Timothy A. Hore, Tim V. Moser, Rhodri Harfoot, Blair Lawley, Miguel E. Quiñones-Mateu, Patrick Collins, Richard Blaikie
Publikováno v:
Frontiers in Public Health, Vol 9 (2022)
The rapid global rise of COVID-19 from late 2019 caught major manufacturers of RT-qPCR reagents by surprise and threw into sharp focus the heavy reliance of molecular diagnostic providers on a handful of reagent suppliers. In addition, lockdown and t
Externí odkaz:
https://doaj.org/article/c88caa11fedb42cf8990b491e7b3d6af
Autor:
Paula Olaizola, Pui Yuen Lee-Law, Maite G. Fernandez-Barrena, Laura Alvarez, Massimiliano Cadamuro, Mikel Azkargorta, Colm J. O’Rourke, Francisco J. Caballero-Camino, Irene Olaizola, Rocio I.R. Macias, Jose J.G. Marin, Marina Serrano-Maciá, Maria L. Martinez-Chantar, Matias A. Avila, Patricia Aspichueta, Diego F. Calvisi, Matthias Evert, Luca Fabris, Rui E. Castro, Felix Elortza, Jesper B. Andersen, Luis Bujanda, Pedro M. Rodrigues, Maria J. Perugorria, Jesus M. Banales
Publikováno v:
Olaizola, P, Lee-Law, P Y, Fernandez-Barrena, M G, Alvarez, L, Cadamuro, M, Azkargorta, M, O'Rourke, C J, Caballero-Camino, F J, Olaizola, I, Macias, R I R, Marin, J J G, Serrano-Maciá, M, Martinez-Chantar, M L, Avila, M A, Aspichueta, P, Calvisi, D F, Evert, M, Fabris, L, Castro, R E, Elortza, F, Andersen, J B, Bujanda, L, Rodrigues, P M, Perugorria, M J & Banales, J M 2022, ' Targeting NAE1-mediated protein hyper-NEDDylation halts cholangiocarcinogenesis and impacts on tumor-stroma crosstalk in experimental models ', Journal of Hepatology, vol. 77, no. 1, pp. 177-190 . https://doi.org/10.1016/j.jhep.2022.02.007
Addi. Archivo Digital para la Docencia y la Investigación
instname
Addi. Archivo Digital para la Docencia y la Investigación
instname
[EN] BACKGROUND & AIMS: Cholangiocarcinoma (CCA) comprises a heterogeneous group of malignant tumors associated with dismal prognosis. Alterations in post-translational modifications (PTMs), including NEDDylation, result in abnormal protein dynamics,
Lay summary Little is known about the role of post-translational modifications of proteins in cholangiocarcinoma development and progression. Herein, we show that protein NEDDylation is upregulated and hyperactivated in cholangiocarcinoma, promoting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f42870a83887ae8c170f353cb05bbd8
Akademický článek
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Autor:
Paula Olaizola, Irene Olaizola, Marta Fernández de Ara, Maite G. Fernández-Barrena, Laura Alvarez, Mikel Azkargorta, Colm J. O’Rourke, Pui-Yuen Lee-Law, Luiz Miguel Nova-Camacho, Jose J.G. Marin, Maria L. Martínez-Chantar, Matias A. Avila, Patricia Aspichueta, Felix Elortza, Jesper B. Andersen, Luis Bujanda, Pedro M. Rodrigues, Maria J. Perugorria, Jesus M. Bañales
Publikováno v:
Gastroenterología y Hepatología. 46:S210
Autor:
Pui Y. Lee-Law, María L. Martínez-Chantar, Marco Marzioni, Luis Bujanda, Mikel Azkargorta, Patricia Aspichueta, Francisco J. Caballero-Camino, Paula Olaizola, Maria J. Perugorria, Felix Elortza, Jesus M. Banales, Pedro M. Rodrigues, Laura Izquierdo-Sanchez, Joost P.H. Drenth
Publikováno v:
Addi. Archivo Digital para la Docencia y la Investigación
instname
United European Gastroenterology Journal
United European Gastroenterology Journal, 9, 848-59
United European Gastroenterology Journal, 9, 7, pp. 848-59
instname
United European Gastroenterology Journal
United European Gastroenterology Journal, 9, 848-59
United European Gastroenterology Journal, 9, 7, pp. 848-59
Background Polycystic liver diseases (PLDs) are genetic inherited disorders characterized by the progressive growth of numerous intrahepatic biliary cysts, which are the main cause of morbidity. Previous studies revealed that cystic cholangiocytes ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c40040aa1d16d65e8b27a34d8dadb91
https://hdl.handle.net/https://repository.ubn.ru.nl/handle/2066/244631
https://hdl.handle.net/https://repository.ubn.ru.nl/handle/2066/244631
Autor:
Joost P.H. Drenth, Luis Bujanda, Laura Izquierdo-Sanchez, Francisco J. Caballero-Camino, Maria J. Perugorria, Marco Marzioni, María L. Martínez-Chantar, Nicholas F. LaRusso, Felix Elortza, Jesus M. Banales, Pui Y. Lee-Law, Pedro M. Rodrigues, Alvaro Santos-Laso, Mikel Azkargorta, Patricia Aspichueta, Paula Olaizola
Publikováno v:
Journal of Hepatology, 74, 2, pp. 394-406
Journal of Hepatology, 74, 394-406
Addi. Archivo Digital para la Docencia y la Investigación
instname
Addi: Archivo Digital para la Docencia y la Investigación
Universidad del País Vasco
Journal of hepatology
Journal of Hepatology, 74, 394-406
Addi. Archivo Digital para la Docencia y la Investigación
instname
Addi: Archivo Digital para la Docencia y la Investigación
Universidad del País Vasco
Journal of hepatology
Background & Aims: Polycystic liver diseases (PLDs) are genetic disorders characterized by progressive development of multiple fluid-filled biliary cysts. Most PLD-causative genes participate in protein biogenesis and/or transport. Post-translational
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::709a9606d641ae9f2c976f09cbe38eec
https://hdl.handle.net/2066/231102
https://hdl.handle.net/2066/231102
Akademický článek
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Background & aims:polycystic liver diseases (PLDs) are genetic disorders characterized by progressive development of multiple fluid-filled biliary cysts. Most PLD-causative genes participate in protein biogenesis and/or transport. Post-translational
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33923d353e73b0084dcd6ad63070fd71
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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