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- FOXP1-related intellectual disability syndrome: a recognisable entity2017 | 2. lékařská fakulta
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- Hyperphenylalaninemia in the Czech Republic: Genotype-phenotype correlations and in silico analysis of novel missense mutations2013 | 3. lékařská fakulta
- Valproic acid downregulates heme oxygenase-1 independently of Nrf2 by increasing ubiquitination and proteasomal degradation2017 | 1. lékařská fakulta
- What is new in HIES? Recent insights from the interface of primary immune deficiency and atopy2018 | 2. lékařská fakulta
- Flow cytometric immunobead assay for the detection of BCR-ABL fusion proteins in leukemia patients2009 | 2. lékařská fakulta
- A deficiency of the link protein Bral2 affects the size of the extracellular space in the thalamus of aged mice2018 | 2. lékařská fakulta
- Molecular evolution and depth-related adaptations of rhodopsin in the adaptive radiation of cichlid fishes in Lake Tanganyika2022 | Přírodovědecká fakulta
- Partial deficiency of HIF-1 alpha stimulates pathological cardiac changes in streptozotocin-induced diabetic mice2014 | 1. lékařská fakulta
- Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders2021 | 1. lékařská fakulta
- Transcript, protein, metabolite and cellular studies in skin fibroblasts demonstrate variable pathogenic impacts of NPC1 mutations2020 | 1. lékařská fakulta
- Protein methyltransferase 7 deficiency in Leishmania major increases neutrophil associated pathology in murine model2021 | Přírodovědecká fakulta