Истраживачи
Ugrin, Milena
Results 41-60 of 100
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 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 |
| 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 | 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 | The Role of Autophagy and Apoptosis in Affected Skin and Lungs in Patients with Systemic Sclerosis![]() | Spasovski, Vesna | Article | 21M21 |
| 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 | The Significance of MGMT Promoter Methylation Status in Diffuse Glioma![]() | Jovanović, Nikola | Article | 21M21 |
| 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 | Geni-modifikatori β-talasemijskih sindroma – novi terapijski pristupi | Ugrin, Milena | Book parts | 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 | Молекуларна дијагностика дијабетеса адултног типа код младих (MODY)![]() | Комазец, Јована | 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 | Ekspresija gena BCL11A u hroničnoj limfocitnoj leukemiji![]() | Karan-Đurašević, Teodora | 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 |
| 2021 | Molekularna osnova monogenskog dijabetesa | Komazec, Jovana | Book parts | Mp. category will be shown later |
| 2021 | Bacterial Nanocellulose as a Scaffold for In Vitro Cell Migration Assay | Ugrin, Milena | Article | 21M21 |
| 2020 | EXPRESSION PATTERN AND PROGNOSTIC SIGNIFICANCE OF BCL11A GENE IN CHRONIC LYMPHOCYTIC LEUKEMIA![]() | Karan-Djurasevic, Teodora
Pavlović, Sonja; Tošić, Nataša;
| Conference Paper | Mp. category will be shown later |
| 2020 | Analysis of the promoter regions of disease-causing genes in maturity-onset diabetes of the young patients | Komazec, Jovana | Article | 22M22 |
| 2019 | The importance of combined NGS and MLPA genetic tests for differential diagnosis of maturity onset diabetes of the young![]() | Komazec, Jovana | Article | 23M23 |
