- Two Photon-Induced Electron Injection From a Nanotrigger in Native Endothelial NO-Synthase2008 | First Faculty of Medicine
- TMEM70 protein - A novel ancillary factor of mammalian ATP synthase2009 | First Faculty of Medicine
- Nitric oxide synthase, typical flavohemoprotein and their complicated enzymology2006 | Faculty of Physical Education and Sport
- Relaxing effect of formaldoxime in the isolated rat aorta: implication of NO synthase-independent NO formation2001 | Faculty of Science
- Inherited disorders of mitochondrial ATP synthase2004 | Faculty of Physical Education and Sport
- Nitric Oxide Synthases Activation and Inhibition by Metallacarborane-Cluster-Based Isoform-Specific Affectors2012 | First Faculty of Medicine
- Association of the -344T/C aldosterone synthase gene variant with essential hypertension2009 | First Faculty of Medicine
- Cyclopropyl- and methyl-containing inhibitors of neuronal nitric oxide synthase2013 | First Faculty of Medicine
- Predictive Significance of Thymidylate Synthase Expression in Non-small Cell Lung Cancer2017 | Faculty of Medicine in Pilsen
- Mitochondrial membrane potential and ATP production in primary disorders of ATP synthase2004 | Publication without faculty affiliation
- Haplotype analysis of the endothelial nitric oxide synthase gene in asthma2008 | Second Faculty of Medicine
- Nitric oxide synthase inhibition in sepsis? Lessons learned from large-animal studies2005 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Dynamics of NO rebinding to the heme domain of NO synthase-like proteins from bacterial pathogens2006 | First Faculty of Medicine
- Enzymatic diagnosis of homocystinuria by determination of cystathionine-beta-synthase activity in plasma using LC-MS/MS2015 | First Faculty of Medicine
- Amaryllidaceae Alkaloids as Potential Glycogen Synthase Kinase-3 beta Inhibitors2018 | Publication without faculty affiliation
- Impaired heme binding and aggregation of mutant cystathionine beta-synthase subunits in homocystinuria2001 | First Faculty of Medicine
- Knockdown of human OXA1L impairs the biogenes of F(1)F(0)- ATP synthase and NADH2007 | First Faculty of Medicine
- Analogues of 2-aminopyridine-based selective inhibitors of neuronal nitric oxide synthase with increased bioavailability2009 | First Faculty of Medicine
- Recent therapeutic approaches to cystathionine beta-synthase-deficient homocystinuria2023 | First Faculty of Medicine
- Genetic Complementation of ATP Synthase Deficiency Due to Dysfunction of TMEM70 Assembly Factor in Rat2022 | First Faculty of Medicine, Faculty of Science
- Association between endothelial NO synthase polymorphism (rs3918226) and arterial properties2013 | Faculty of Medicine in Pilsen
- Mitochondrial Membrane Potential and ATP Production in Primary Disorders of ATP Synthase2004 | First Faculty of Medicine
- Effects of combining inducible nitric oxide synthase inhibitor and radical scavenger during porcine bacteremia2007 | Central Library of Charles University
- Association between endothelial NO synthase polymorphisms and arterial properties in the general population2015 | Faculty of Medicine in Pilsen
- Changes in activity of monoamine oxidase, citrate synthase and enzymes of respiratory chain induced by antidepressants and mood stabilizers2010 | First Faculty of Medicine
- Acute intermittent porphyria - impact of mutations found in the hydroxymethylbilane synthase gene on biochemical and enzymatic protein properties2009 | First Faculty of Medicine
- Synthesis and enzymatic evaluation of 2-and 4-aminothiazole-based inhibitors of neuronal nitric oxide synthase2009 | First Faculty of Medicine
- Characterization of two missense variants in the hydroxymethylbilane synthase gene in the Israeli population, which differ in their associations with acute intermittent porphyria2008 | First Faculty of Medicine
- Isoform-specific differences in the nitrite reductase activity of nitric oxide synthases under hypoxia2009 | First Faculty of Medicine
- Compensatory upregulation of respiratory chain complexes III and IV in isolated deficiency of ATP synthase due to TMEM70 mutation2012 | First Faculty of Medicine