Researchers
Savić-Pavićević, Dušanka
Results 41-60 of 310
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2024 | Whole exome sequencing in Serbian patients with hereditary spastic paraplegia![]() | Branković, Marija | Article | 22M22 |
| 2024 | Association between genetic variants in HSA-MIR-27A and HSA-MIR-146A genes and male infertility | Rajovski, Srećko; Milanović, Nikoleta | Article | 23M23 |
| 2024 | 469P Modal allele change as a predictor of skeletal muscle symptoms progression in myotonic dystrophy type 1 | Radovanović, Nemanja | Conference Paper | Mp. category will be shown later |
| 2024 | Our Journey from Individual Efforts to Nationwide Support: Implementing Newborn Screening for Spinal Muscular Atrophy in Serbia | Brkušanin, Miloš | Article | 21aM21a |
| 2024 | Main features and disease outcome of congenital myotonic dystrophy- experience from a single tertiary center![]() | Ostojić, Slavica B.; Kovačević, Gordana S. | Article | 22M22 |
| 2024 | CRISPR-Cas9 generated cell lines for myotonic dystrophy type 1 modeling![]() | Ninković, Anastasija | Conference Paper | Mp. category will be shown later |
| 2024 | Association between Cytotoxic T-Lymphocyte-Associated Antigen 4 (CTLA-4) Locus and Early-Onset Anti-acetylcholine Receptor-Positive Myasthenia Gravis in Serbian Patients![]() | Đorđević, Ivana; Garai, Nemanja | Article | 21M21 |
| 2023 | Dynamics of CTG repeat expansion in blood of Myotonic Dystrophy Type 1 patients over time | Radovanović, Nemanja | Conference Paper | Mp. category will be shown later |
| 2023 | EPR-210 Whole exome sequencing in Serbian patients with hereditary spastic paraplegia![]() | Ivanović, Vukan | Conference Paper | Mp. category will be shown later |
| 2023 | COMPARATIVE TRANSCRIPTOMIC ANALYSIS IMPLIES INNATE IMMUNE RESPONSE AND CELL CYCLE DISREGULATION IN PATIENT-DERIVED DM1 CELL MODELS | Stasuk, Mihajlo; Lazić, Dušan | Conference Paper | Mp. category will be shown later |
| 2023 | Sekvenciranje dugih fragmenata – sledeći nivo genomskih istraživanja![]() | Savić-Pavićević, Dušanka | Book parts | Mp. category will be shown later |
| 2023 | Mutation rates of 22 autosomal STR loci in a European population from Central Balkan, Republic of Serbia![]() | Nemanja Garai | Conference Paper | Mp. category will be shown later |
| 2023 | Generation of expanded CTG repeat plasmids in E. coli for myotonic dystrophy type 1 model systems![]() | Ninković, Anastasija | Conference Paper | Mp. category will be shown later |
| 2023 | The effect of epistatic interactions between genetic variants located in microRNA and silencing complex genes on prostate cancer progression risk![]() | Dobrijević, Zorana | Article | 22M22 |
| 2023 | Identification of potentally causal variants for myasthenia gravis: a bioinformatics-driven fine-mapping approach combined with genetic association study![]() | Garai, Nemanja | Conference Paper | Mp. category will be shown later |
| 2023 | Assesment of association between genetic variants in microRNA genes hsa-miR-146 and has-miR-27 and male infertility in North Macedocinan Population | Milanović, N.; Rajovski, S.; Matijašević Joković, Suzana | Conference Paper | Mp. category will be shown later |
| 2023 | Effect of enriched environment on serotonin and RNA editing of serotonin 2C receptor is specific for brain regions and mouse strains | Karanović, Jelena | Conference Paper | Mp. category will be shown later |
| 2023 | One year of newborn screening for spinal muscular atrophy – results of a Serbian pilot project | Brkušanin, Miloš | Conference Paper | Mp. category will be shown later |
| 2023 | ASSESSMENT OF ASSOCIATION BETWEEN GENETIC VARIANTS IN microRNA GENES hsa-miR-146a AND hsa-miR-27a AND MALE INFERTILITY IN NORTH MACEDONIAN POPULATION![]() | Milanović, Nikoleta; Srećko Rajovski; Joković, Matijašević Suzana; Radovanović, Nemanja; Savić-Pavićević, Dušanka | Conference Paper | Mp. category will be shown later |
| 2023 | Genetic risk factors in patients with Myasthenia gravis![]() | Garai Nemanja | Conference Paper | Mp. category will be shown later |
