Researchers
Stevanović, Nina
Results 1-20 of 24
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2025 | Phenylbutyric Acid Modulates Apoptosis and ER Stress-Related Gene Expression in Glycogen Storage Disease Type Ib In Vitro Model | Parezanovic, Marina V | Article | 22M22 |
| 2025 | ESTABLISHMENT OF AN IN VITRO INSULIN RESISTANCE MODEL IN HepG2 CELLS THROUGH GLUCOSE AND INSULIN COTREATMENT | Spasovski, Vesna | Conference Paper | Mp. category will be shown later |
| 2025 | PULMONARY IN VITRO MODEL SYSTEM ENABLES EXPLORATION OF INNOVATIVE TREATMENT STRATEGIES FOR RARE RESPIRATORY DISEASES | Stevanović, Nina | Conference Paper | Mp. category will be shown later |
| 2025 | Thalassemia syndromes in Serbia:the importance of genetic (re)analysis | Ugrin, Milena M; Komazec, Jovana; Klaassen, Kristel M; Skakic, Anita G
Pavlovic, Sonja T; Stojiljkovic, Maja M;
| Conference Paper | Mp. category will be shown later |
| 2025 | ESTABLISHING IN VITRO MODELS FOR GLYCOGEN STORAGE DISEASE TYPE IB: A PLATFORM FOR THERAPEUTIC INVESTIGATIONS![]() | Jocić, Nikola | Conference Paper | Mp. category will be shown later |
| 2024 | Genetic landscape of phenylketonuria in Serbia![]() | Klaassen, Kristel | Conference Paper | Mp. category will be shown later |
| 2024 | INVESTIGATING THE GENETIC COMPLEXITY OF NEUTROPENIA IN PEDIATRIC PATIENTS WITH GLYCOGEN STORAGE DISEASE IB: A MODIFIER GENE PERSPECTIVE | Skakić, Anita | Conference Paper | Mp. category will be shown later |
| 2023 | High-risk population screening for fabry disease in patients with chronic renal failure of unknown etiology![]() | Parezanović, Marina | Conference Paper | Mp. category will be shown later |
| 2023 | Functional characterization of novel variants in the dnai1 gene in a patient with primary ciliary dyskinesia![]() | Skakić, Anita | Conference Paper | Mp. category will be shown later |
| 2023 | PHENYLBUTYRIC ACID REDUCES MOLECULAR MARKERS OF ER STRESS-INDUCED APOPTOSIS IN GLYCOGEN STORAGE DISEASE TYPE IB IN VITRO MODEL SYSTEM![]() | Parezanović, Marina | Conference Paper | Mp. category will be shown later |
| 2023 | Unique pipeline for the assessment of novel genetic variants leads to confirmation of PCD diagnosis | Stevanović, Nina | Conference Paper | Mp. category will be shown later |
| 2023 | Investigation of the role of the glucose-6-phosphate translocase in the activation of autophagy and glycogen-selective autophagy in glycogen storage disease type IB patients![]() | Jocić, Nikola | Conference Paper | Mp. category will be shown later |
| 2023 | Molecular basis of phenylketonuria in Serbia: an update![]() | Klaassen, Kristel | Conference Paper | Mp. category will be shown later |
| 2023 | Molecular basis of thalassemia syndromes in Serbia: an update![]() | Ugrin, Milena | Conference Paper | Mp. category will be shown later |
| 2023 | Molecular diagnosis of Fabry disease in patients with chronic renal failure of unknown etiology![]() | Parezanović, Marina | Conference Paper | Mp. category will be shown later |
| 2023 | Improving the diagnostics of rare lung disorders using a uniquely designed pipeline for analysis of ngs data | Anđelković, Marina | Conference Paper | Mp. category will be shown later |
| 2023 | Application of CRISPR/cas9 technology for in vitro disease modelling in glycogen storage disease type IB![]() | Parezanović, Marina | Conference Paper | Mp. category will be shown later |
| 2023 | The role of MIR-34 family members on the mucociliary process in the cellular respiratory model system![]() | Stevanović, Nina | Conference Paper | Mp. category will be shown later |
| 2022 | Molekularna dijagnostika Fabrijeve bolesti kod pacijenata sa hroničnom bubrežnom insuficijencijom nepoznate etiologije![]() | Parezanović, Marina | Conference Paper | Mp. category will be shown later |
| 2022 | Funkcionalna karatkerizacija novootkrivenih varijanti u genu DNAI1 kod pacijenta sa primarnom cilijarnom diskinezijom | Stevanović, Nina | Conference Paper | Mp. category will be shown later |
