Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Sander Barnhoorn"'
Autor:
Trisha V. Kers, Romain Tching Chi Yen, Martine L.M. Lamfers, Clemens M F Dirven, Stijn L.W. Koolen, Ioannis Ntafoulis, Pim J. French, César Payán-Gómez, Cassandra Verheul, E.A. Struys, Sander Barnhoorn, Pier G. Mastroberardino, Youri Hoogstrate, Sieger Leenstra
BackgroundMutations of the isocitrate dehydrogenase (IDH) gene occur in over 80% of low-grade gliomas and secondary glioblastomas. Despite considerable efforts, endogenous in vitro IDH-mutated glioma models remain scarce. Availability of these models
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e760ff32ce5e7dda6a29f7bb4a3fd1d
https://doi.org/10.1101/2021.04.09.435131
https://doi.org/10.1101/2021.04.09.435131
Autor:
Bert Callewaert, Christophe Casteleyn, Sander Barnhoorn, Andy Willaert, Marjolijn Renard, Annekatrien Boel, Ingrid van der Pluijm, Marine Vanhomwegen, Dieter P. Reinhardt, Paul Coucke, Jeroen Essers, Joyce Burger, Benedicte Descamps, Christian Vanhove, Aude Beyens
Arterial tortuosity syndrome (ATS) is a recessively inherited connective tissue disorder, mainly characterized by tortuosity and aneurysm formation of the major arteries. ATS is caused by loss-of-function mutations inSLC2A10, encoding the facilitativ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff8f00c59e5b885cdd5120b341664191