Researchers
Skakić, Anita
Results 41-60 of 89
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 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 | 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 | 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 | PLANARNA BIOMEDICINSKA ELEKTRODA U TEHNOLOGIJI ŠTAMPANIH PLOČA SA VISOKOM HOMOGENOŠĆU ELEKTRIČNOG POLjA ZA ELEKTROPORACIJU![]() | 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 |
| 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 | 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 | Planar printed electrodes for electroporation with high EM field homogeneity | Ilić, Anđelija | Article | 21M21 |
| 2021 | Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier![]() | Klaassen, Kristel | Article | 22M22 |
| 2020 | Correlation of expression of TLR7 and Mirna-146a genes and fibrosis in peripheral blood and skin samples of SSc patients![]() | Vesna Spasovski | Conference Paper | Mp. category will be shown later |
| 2020 | Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type Ib![]() | Sarajlija, Adrijan | Article | 22M22 |
| 2019 | HYPERPHENYLALANINEMIA: FROM COMPLEX GENETICS TO COMPLEX PHENOTYPES![]() | Kristel Klaassen | Conference Paper | Mp. category will be shown later |
| 2019 | The importance of comprehensive genomic profiling in differential diagnosis and discovery of novel disease causing genetic variants in patients with pediatric lung diseases![]() | Anđelković, Marina | Conference Paper | Mp. category will be shown later |
| 2019 | Genomic profiling of glycogen storage diseases: from NGS method to the CRISPR/Cas9 technology![]() | Skakić, Anita | Conference Paper | Mp. category will be shown later |
| 2019 | GENOMIC PROFILING AS A TOOL FOR DIFFERENTIAL DIAGNOSIS OF PATIENTS WITH PEDIATRIC LUNG DISEASES AND DISCOVERY OF NOVEL DISEASE-CAUSING GENES AND GENETIC VARIANTS![]() | Anđelković, Marina | Conference Paper | Mp. category will be shown later |
