- Transferrin D Protein Variants in the Diagnosis of Congenital Disorders of Glycosylation (CDG)2009 | First Faculty of Medicine
- Transferrin D Protein Variants in the Diagnosis of Congenital Disorders of Glycosylation (CDG) +12009 | Faculty of Medicine in Hradec Králové
- Ribosome-Mediated Attenuation of vga(A) Expression Is Shaped by the Antibiotic Resistance Specificity of Vga(A) Protein Variants2020 | Faculty of Science
- Ribosome-Mediated Attenuation of vga(A) Expression Is Shaped by the Antibiotic Resistance Specificity of Vga(A) Protein Variants (vol 64, e00666-20, 2020)Publication without faculty affiliation
- p19-targeted ABD-derived protein variants inhibit IL-23 binding and exert suppressive control over IL-23-stimulated expansion of primary human IL-17+T-cells2017 | Second Faculty of Medicine
- Microheterogeneity of some serum glycoproteins in neurodegenerative diseases2012 | Faculty of Medicine in Hradec Králové
- Subtype-specific gout susceptibility loci and enrichment of selection pressure on ABCG2 and ALDH2 identified by subtype genome-wide meta-analyses of clinically defined gout patients2020 | First Faculty of Medicine
- Serum transferrin microheterogeneity in cystis fibrosis2009 | Faculty of Medicine in Hradec Králové, First Faculty of Medicine, Faculty of Physical Education and Sport
- Our Experience with Diagnostics of Congenital Disorders of Glycosylation2004 | First Faculty of Medicine
- Ambiguous decoding of the CUG codon alters the functionality of the Candida albicans translation initiation factor 4E2010 | Faculty of Science
- Distinct recruitment of human eIF4E isoforms to processing bodies and stress granules2016 | Faculty of Science
- The C-type lectin-like receptor Nkrp1b: Structural proteomics reveals features affecting protein conformation and interactions2019 | Faculty of Science
- Localization of AML-related nucleophosmin mutant depends on its subtype and is highly affected by its interaction with wild-type NPM2017 | Central Library of Charles University
- Regulation of IL-24/IL-20R2 complex formation using photocaged tyrosines and UV light2023 | Faculty of Science, First Faculty of Medicine, Central Library of Charles University
- Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I2011 | First Faculty of Medicine
- IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients2019 | Second Faculty of Medicine
- Three subfamilies of exocyst EXO70 family subunits in land plants: early divergence and ongoing functional specialization2020 | Faculty of Science, Central Library of Charles University
- Redesigning Protein Cavities as a Strategy for Increasing Affinity in Protein-Protein Interaction: Interferon-gamma Receptor 1 as a Model2015 | Central Library of Charles University
- Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes2023 | First Faculty of Medicine
- Surveillance of invasive meningococcal disease based on whole genome sequencing (WGS), Czech Republic, 20152018 | Central Library of Charles University