Pretraga
Rezultati
Molecular defects underlying the Kell null phenotype [2001]
Lee, S; Russo, DCW; Reiner, AP; Lee, JH; Sy, MY; Telen, MJ; Judd, WJ; Simon, P; Rodrigues, MJ; Chabert, T;
Poole, Jacqueline L; Jovanovic-Srzentic, Snezana; Levene, C; Yahalom, V; Redman, CM;
The rat leukocyte-type 12-lipoxygenase exhibits an intrinsic hepoxilin A<sub>3</sub> synthase activity [2004]
Nigam, S; Patabhiraman, S; Ciccoli, R; Ishdorj, G; Schwarz, K; Petrucev, BCalcium-induced conformational changes in C-terminal tail of polycystin-2 are necessary for channel gating [2012]
Ćelić, AnđelkaC-terminal domain of chromogranin B regulates intracellular calcium signaling [2011]
Schmidt, Stefan; Mo, Michelle; Heidrich, Felix M.; Ćelić, AnđelkaFoxo3 is essential for the regulation of ataxia telangiectasia mutated and oxidative stress-mediated homeostasis of hematopoietic stem cells [2008]
Yalcin, Safak; Zhang, Xin; Luciano, Julia P.; Mungamuri, Sathish Kumar; Marinković, DraganSynergistic Anticancer Action of Lysosomal Membrane Permeabilization and Glycolysis Inhibition
[2016]
Kosić, Milica The Extracellular Domain Determines the Kinetics of Desensitization in Acid-sensitive Ion Channel 1
[2003]
Coric, Tatjana; Zhang, Ping; Todorovic, Natasa An exploration of bioactive peptides: My collaboration with Ervin G. Erdos [2018]
Igic, RajkoCharacterization of NCS1?InsP3R1 interaction and its functional significance [2019]
Nguyen, Lien D; Petri, Edward TActivity Map of the Escherichia coli RNA Polymerase Bridge Helix
[2011]
Jovanovic, Milija Filteri
Po tipu
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