Researchers
Stevanović, Nina
Results 1-20 of 36
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2026 | Identification and Molecular Characterization of a Large-Scale Mitochondrial DNA Deletion in a Patient with Kearns–Sayre Syndrome![]() | Grujić, Kristina | Conference Paper | Mp. category will be shown later |
| 2026 | Implementation and clinical utility of the GATK gCNV pipeline for rare disease diagnostics using whole exome sequencing | Pavlović, Đorđe | Conference Paper | Mp. category will be shown later |
| 2026 | Pregled metaboličkih retkih bolesti detektovanih u Srbiji radi odabira najpogodnijih bolesti za pravljenje novog hepatičnog modela bolesti baziranog na iPSC | Grujić, Kristina | Conference Paper | Mp. category will be shown later |
| 2026 | Uticaj tretmana mikroRNK-34 familije na ciliogenezu u NHBE in vitro modelu humanog respiratornog epitela![]() | Stevanović, Nina | Conference Paper | Mp. category will be shown later |
| 2026 | Precision and recall in rare disease genomics: benchmarking the IMGGE whole genome sequencing pipeline | Stanković, Sara | Conference Paper | Mp. category will be shown later |
| 2026 | Development and validation of a reproducible RNA-seq pipeline for transcriptomic analysis | Jocić, Nikola | Conference Paper | Mp. category will be shown later |
| 2026 | Ispitivanje patofiziologije i terapijskih strategija za glikogenozu tip Ib upotrebom CRISPR/Cas9 i iPSC model sistema![]() | Parezanović, Marina | Conference Paper | Mp. category will be shown later |
| 2026 | Evaluation of Candidate Inhibitors of the Glucose-6-Phosphate Transporter in HepG2 Cells | Kaličanin, Milana; Grujić, Kristina | Conference Paper | Mp. category will be shown later |
| 2026 | Sekvenciranje kompletnog genoma dugim očitavanjima (LR-WGS) u cilju preciznije molekularno-genetičke dijagnoze kongenitalne adrenalne hiperplazije![]() | Jocić, Nikola | Conference Paper | Mp. category will be shown later |
| 2026 | Transkriptomski profil oštećenja neurona posredovanog fenilalaninom: novi uvidi u izmenjenu gensku ekspresiju u neuropatologiji PKU | Stanković, Sara | 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 | 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 | 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 |
| 2025 | Thalassemia syndromes in Serbia:the importance of genetic (re)analysis![]() | Ugrin, Milena | Conference Paper | Mp. category will be shown later |
| 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 | CRISPR/Cas9 and iPSC-based platforms to explore pathophysiology and therapeutic approaches in glycogen storage disease type Ib | Skakić, Anita | Conference Paper | Mp. category will be shown later |
| 2025 | Establishment of an insulin resistance model in HepG2 cells using combined high glucose and insulin treatment | Spasovski, Vesna | 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 |
