Researchers
Skakić, Anita
Results 41-60 of 97
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2023 | Rare metabolic diseases in the genomics era | Stojiljković, Maja | 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 | Covid-19 disease severity associated with vitamin d related genetic Variants | Kotur, Nikola | 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 | 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 |
| 2022 | Молекуларна дијагностика гликогеноза : од методе NGS до технологије CRISP/Cas9![]() | Скакић, Анита | Conference Paper | Mp. category will be shown later |
| 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 |
| 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 | Funkcionalna karatkerizacija novootkrivenih varijanti u genu DNAI1 kod pacijenta sa primarnom cilijarnom diskinezijom | Stevanović, Nina | 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 | Molekularna dijagnostika Fabrijeve bolesti kod pacijenata sa hroničnom bubrežnom insuficijencijom nepoznate etiologije![]() | Parezanović, Marina | 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 | 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 | Retke bolesti u eri genomike | Stojiljković, Maja | Conference Paper | Mp. category will be shown later |
| 2021 | Primena crISPr/cas9 tehnologije u otkrivanju novih molekularnih terapeutika | Skakić, Anita | Book parts | Mp. category will be shown later |
| 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 | Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier![]() | Klaassen, Kristel | Article | 22M22 |
| 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 |
| 2021 | Identification and Classification of Novel Genetic Variants: En Route to the Diagnosis of Primary Ciliary Dyskinesia![]() | Stevanović, Nina | Article | 21M21 |
| 2021 | Association of Vitamin D, Zinc and Selenium Related Genetic Variants With COVID-19 Disease Severity![]() | Kotur, Nikola | Article | 21aM21a |
