Researchers
Klaassen Ljubičić, Kristel
Results 21-40 of 80
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2023 | Molecular basis of phenylketonuria in Serbia: an update![]() | Klaassen, Kristel | 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 | 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 | Covid-19 disease severity associated with vitamin d related genetic Variants | Kotur, Nikola | 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 |
| 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 | Improving the diagnostics of rare lung disorders using a uniquely designed pipeline for analysis of ngs data | Anđelković, Marina | Conference Paper | Mp. category will be shown later |
| 2023 | THE IMPACT OF NEXT-GENERATION SEQUENCING ON DIAGNOSIS AND TREATMENT OF RARE DISEASES | Stojiljković, Maja | 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 | Диференцијална дијагноза педијатријских болесника са болестима плућа коришћењем секвенцирања нове генерације![]() | Анђелковић, Марина | 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 | Functional prediction and comparative population analysis of variants in genes for proteases and innate immunity related to SARS-CoV-2 infection![]() | Klaassen, Kristel | 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 | 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 | The first insight into the genetic structure of the population of modern Serbia![]() | Drljača, Tamara | Article | 21aM21a |
