Researchers
Skakić, Anita
Results 41-60 of 97
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 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 | 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 | 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 | Differential expression of TLR7 and miRNA-146a genes in peripheral blood and skin samples of patients with systemic sclerosis![]() | Spasovski, Vesna M | 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 | Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier![]() | Kristel Klaassen | Conference Paper | Mp. category will be shown later |
| 2022 | Retke bolesti u eri genomike | Stojiljković, Maja | Conference Paper | Mp. category will be shown later |
| 2022 | Dizajniranje jedinstvenih smernica za standardizaciju analize NGS podataka kod pacijenata sa retkim plućnim bolestima | Anđelković, Marina | Conference Paper | Mp. category will be shown later |
| 2022 | Молекуларна дијагностика гликогеноза : од методе NGS до технологије CRISP/Cas9![]() | Скакић, Анита | 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 |
| 2022 | Molekularna dijagnostika Fabrijeve bolesti kod pacijenata sa hroničnom bubrežnom insuficijencijom nepoznate etiologije![]() | Parezanović, Marina | Conference Paper | Mp. category will be shown later |
| 2022 | Диференцијална дијагноза педијатријских болесника са болестима плућа коришћењем секвенцирања нове генерације![]() | Анђелковић, Марина | Conference Paper | Mp. category will be shown later |
| 2022 | High risk population screening for Fabry disease in hemodialysis patients in Vojvodina: Pilot study![]() | Ćelić, Dejan | Article | 23M23 |
| 2022 | Crosstalk between Glycogen-Selective Autophagy, Autophagy and Apoptosis as a Road towards Modifier Gene Discovery and New Therapeutic Strategies for Glycogen Storage Diseases![]() | Anđelković, Marina | Article | 21M21 |
| 2021 | Genetic variants in TNFA, LTA, TLR2 and TLR4 genes and risk of sepsis in patients with severe trauma: nested case-control study in a level-1 trauma centre in SERBIA![]() | Đurić, Olivera | Article | 21M21 |
| 2021 | Association of Vitamin D, Zinc and Selenium Related Genetic Variants With COVID-19 Disease Severity![]() | Kotur, Nikola | Article | 21aM21a |
| 2021 | Planar printed electrodes for electroporation with high EM field homogeneity | Ilić, Anđelija | Article | 21M21 |
| 2021 | A novel 9 bp deletion (c.1271_1279delGTGCCCGCG) in exon 10 of CYP21A2 gene causing severe congenital adrenal hyperplasia![]() | Anastasovska, Violeta; Kocova, Mirjana; Zdraveska, Nikolina; Stojiljković, Maja | Article | 22M22 |
| 2021 | Primena crISPr/cas9 tehnologije u otkrivanju novih molekularnih terapeutika | Skakić, Anita | Book parts | Mp. category will be shown later |
| 2021 | Планарна биомедицинска електрода у технологији штампаних плоча са високом хомогеношћу електричног поља за електропорацију![]() | Ilić, Anđelija Ž. | Patent | Mp. category will be shown later |
