ℹ️
🇬🇧
Search
Search for people relevant for "Dědičná onemocnění"
Dědičná onemocnění
Person
Class
Person
Publication
Programmes
Mgr. Václava Škopová
External person at First Faculty of Medicine
15 publications
Publications
publication
Biochemical and Structural Analysis of 14 Mutant ADSL Enzyme Complexes and Correlation to Phenotypic Heterogeneity of Adenylosuccinate Lyase Deficiency
2010 |
First Faculty of Medicine
publication
Improved diagnostics of purine and pyrimidine metabolism disorders using LC-MS/MS and its clinical application
2023 |
First Faculty of Medicine
publication
Pathway-specific effects of ADSL deficiency on neurodevelopment
2022 |
First Faculty of Medicine
publication
Metabolites of De Novo Purine Synthesis: Metabolic Regulators and Cytotoxic Compounds
2022 |
First Faculty of Medicine
publication
Metabolic Tools for Identification of New Mutations of Enzymes Engaged in Purine Synthesis Leading to Neurological Impairment
2019 |
First Faculty of Medicine
publication
PAICS deficiency, a new defect of de novo purine synthesis resulting in multiple congenital anomalies and fatal outcome
2019 |
First Faculty of Medicine
publication
Clinical manifestations and molecular aspects of phosphoribosylpyrophosphate synthetase superactivity in females
2018 |
First Faculty of Medicine
publication
Study of purinosome assembly in cell-based model systems with de novo purine synthesis and salvage pathway deficiencies
2018 |
First Faculty of Medicine
publication
Mass spectrometric analysis of purine de novo biosynthesis intermediates
2018 |
First Faculty of Medicine
publication
CRISPR-Cas9 induced mutations along de novo purine synthesis in HeLa cells result in accumulation of individual enzyme substrates and affect purinosome formation
2016 |
First Faculty of Medicine
Load more publications (5)
Loading network view...