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European Journal of Medicinal Chemistry|March 15, 2021
Developing novel classes of protein kinase CK1δ inhibitors by fusing [1,2,4]triazole with different bicyclic heteroaromatic systemsIlenia Grieco, Maicol Bissaro, Davide Benedetto Tiz, et al.
Oncogene|September 22, 2018
Development of a yeast-based system to identify new hBRAFV600E functional interactorsSimone Lubrano, Laura Comelli, Chiara Piccirilli, et al.
Redox Biology|October 2, 2019
Insight into the mechanism of ferroptosis inhibition by ferrostatin-1Giovanni Miotto, Monica Rossetto, Maria Luisa Di Paolo, et al.
The Biochemical Journal|May 13, 2009
Quinalizarin as a potent, selective and cell-permeable inhibitor of protein kinase CK2Giorgio Cozza, Marco Mazzorana, Elena Papinutto, et al.
Biomacromolecules|January 30, 2019
Stealth Iron Oxide Nanoparticles for Organotropic Drug TargetingMassimiliano Magro, Davide Baratella, Emanuela Bonaiuto, et al.
EMBO Reports|May 13, 2018
TG2 regulates the heat-shock response by the post-translational modification of HSF1Federica Rossin, Valeria Rachela Villella, Manuela D'Eletto, et al.
Molecular Cancer|April 30, 2017
The landscape of BRAF transcript and protein variants in human cancerAndrea Marranci, Zhijie Jiang, Marianna Vitiello, et al.
The EMBO Journal|December 1, 2018
A pathogenic role for cystic fibrosis transmembrane conductance regulator in celiac diseaseValeria R Villella, Andrea Venerando, Giorgio Cozza, et al.
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