Publikační okénko
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Revising pathogenesis of AP1S1-related MEDNIK syndrome: a missense variant in the AP1S1 gene as a causal genetic lesion. Rackova M, Mattera R, Svaton M, Fencl F, Kanderova V, Spicakova K, Park SY, Fabian O, Koblizek M, Fronkova E, Bonifacino JS, Skvarova Kramarzova K. J Mol Med (Berl). 2024 Sep 13. Online ahead of print. |
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Rewired glutamate metabolism diminishes cytostatic action of L-asparaginase. Hlozkova K, Vasylkivska M, Boufersaoui A, Marzullo B, Kolarik M, Alquezar-Artieda N, Shaikh M, Faradonbeh FA, Zaliova M, Zwyrtkova M, Bakardijeva-Mihaylova V, Alberich-Jorda M, Trka J, Tennant DA, Starkova J. Cancer Lett. 2024 Sep 11:217242. Online ahead of print. |
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Tviblindi algorithm identifies branching developmental trajectories of human B-cell development and describes abnormalities in RAG-1 and WAS patients. Bakardjieva M, Pelák O, Wentink M, Glier H, Novák D, Stančíková J, Kužílková D, Mejstříková E, Janowska I, Rizzi M, van der Burg M, Stuchlý J, Kalina T. Eur J Immunol. 2024 Sep 5:e2451004. Online ahead of print. |