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Drakulić, Danijela


Results 21-40 of 108
Issue DateTitleAuthor(s)TypeМp-cat.
2024mir-219 as a potential radiosensitier in glioblastoma cellsPetrović, Maja  ; Stanojković, Tatjana  ; Drakulić, Danijela  ; Stanisavljević Ninković, Danijela  Conference Paper
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2024CHARACTERIZATION OF INDUCED PLURIPOTENT STEM CELLS FROM PATIENTS WITH 22Q11.2 DUPLICATION SYNDROMEKostić, Jovana  ; Cuturilo, Goran; Drakulić, Danijela  ; Petter, Olena; Perić, Mina  ; Simeunović, Ivana  ; Stanisavljević Ninković, Danijela  ; Harwood J., Adrian; Stevanović, Milena  ; Kovačević-Grujicić, Nataša  Conference Paper
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2024Chemical profiling of Anthriscus cerefolium (L.) Hoffm., biological potential of the herbal extract, molecular modeling and KEGG pathway analysisStojković, Dejan  ; Gašić, Uroš  ; Uba, Abdullahi Ibrahim; Zengin, Gokhan; Rajaković, Mladen  ; Stevanović, Milena  ; Drakulić, Danijela  Article
22M22
2024Generation of induced pluripotent stem cells from patients with 22q11.2 Duplication Syndrome as an in vitro model system for exploring neurodevelopmental disordersKostić, Jovana  ; Čuturilo, Goran; Drakulić, Danijela  ; Petter, Olena; Perić, Mina  ; Simeunović, Ivana  ; Stanisavljević Ninković, Danijela  ; Harwood, Adrian J.; Stevanović, Milena  ; Kovačević-Grujicić, Nataša  Conference Paper
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2024Different roles of SOX genes in promotion of malignant behavior of glioblastoma cellsDrakulić, Danijela  Conference Paper
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2024Establishment of induced pluripotent stem cells derived from patients with 22q11.2 microdeletion as a tool for studying neurodevelopmental disordersSimeunović, Ivana  ; Čuturilo, Goran; Kovačević-Grujičić, Nataša  ; Petter, Olena; Perić, Mina  ; Kostić, Jovana  ; Stanisavljević Ninković, Danijela  ; Harwood, Adrian; Stevanović, Milena  ; Drakulić, Danijela  Conference Paper
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2024ESTABLISHMENT OF A MODEL SYSTEM FOR STUDYING NEURODEVELOPMENTAL DISORDERS USING INDUCED PLURIPOTENT STEM CELLS DERIVED FROM PATIENTS WITH 22Q11.2 DELETION SYNDROMEDrakulić, Danijela  ; Harwood, Adrian; Petrakis, Spyros; Linden, David; Stevanović, Milena  Conference Paper
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2024Speech Sounds Production, Narrative Skills, and Verbal Memory of Children with 22q11.2 MicrodeletionRakonjac, Marijana; Cuturilo, Goran; Kovačević-Grujičić, Nataša  ; Simeunović, Ivana  ; Kostić, Jovana  ; Stevanović, Milena  ; Drakulić, Danijela  Article
21M21
2023Detection rate of 22q11.2 microdeletion using strict diagnostic criteriaDrakulić, Danijela  ; Cuturilo, Goran; Jovanović, Ida; Krstić, Aleksandar; Milivojević, Milena  ; Stevanović, Milena  Conference Paper
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2023Generation of induced pluripotent stem cells derived from patients with 22q11.2 deletion syndrome as a tool for studying neurodevelopmental disordersSimeunović, Ivana  ; Čuturilo, Goran; Kovačević-Grujičić, Nataša  ; Petter, Olena; Perić, Mina  ; Kostić, Jovana  ; Harwood J., Adrian; Stevanović, Milena  ; Drakulić, Danijela  Conference Paper
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202322q11.2 Deletion syndrome as a tool for modelling and research of neurodevelopmental disordersLazić, Adrijana; Drakulić, Danijela  ; Kovačević-Grujičić, Nataša  ; Perić, Mina  ; Petrakis, Spyros; Linden, David; Harwood, Adrian; Stevanović, Milena  Conference Paper
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2023"Mindds-Connect" - Federated Data Sharing Platform for Neurodevelopmental Disorders and Rare Genetic MutationsMihaljevic, Marina; Huremagic, Benjamin; Harwood, Janet; Jorge, Paola; Teles, Natalia; Novakowska, Beata; Vandeweyer, Geert; Drakulic, Danijela  ; Van, Amelsvoort Therese; Linden, David;
Straccia, Marco; Vermeersch, Joris; Harwood, Adrian;
Conference Paper
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2023A Machine-Learning-Based Approach to Prediction of Biogeographic Ancestry within EuropeKloska, Anna; Giełczyk, Agata; Grzybowski, Tomasz; Płoski, Rafał; Kloska, Sylwester M.; Marciniak, Tomasz; Pałczyński, Krzysztof; Rogalla-Ładniak, Urszula; Malyarchuk, Boris A.; Derenko, Miroslava V.;
Kovačević-Grujičić, Nataša  ; Stevanović, Milena  ; Drakulić, Danijela  ; Davidović, Slobodan  ; Spólnicka, Magdalena; Zubańska, Magdalena; Woźniak, Marcin;
Article
21M21
2023Application of principal component analysis (PCA) and analytical hierarchy process (AHP) in analysis of articulatory characteristics of phonemes of children with 22q11.2 Deletion SyndromeDrakulić, Danijela  ; Rakonjac, Marijana; Cuturilo, Goran; Kovačević-Grujičić, Nataša  ; Kušić-Tišma, Jelena  ; Morić, Ivana  ; Zukić, Branka  ; Stevanović, Milena  Conference Paper
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2023Genomic and clinical findings in patients with 22q11.2 duplication syndromeKostić, Jovana  ; Drakulić, Danijela  ; Cuturilo, Goran; Kovačević-Grujičić, Nataša  ; Simeunović, Ivana  ; Stevanović, Milena  Conference Paper
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2023Establishment of induced pluripotent stem cells from patients with 22q11.2 duplication syndrome as a model system for studying neurodevelopmental disordersKostić, Jovana  ; Drakulić, Danijela  ; Čuturilo, Goran; Petter, Olena; Perić, Mina  ; Simeunović, Ivana  ; Harwood J., Adrian; Stevanović, Milena  ; Kovačević-Grujičić, Nataša  Conference Paper
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202322q11.2 microdeletion is the most common genomic abnormality in Serbian newborns with critical congenital heart disease and could be rapidly detected by Multiplex ligation probe amplification analysisMiletić, Aleksandra; Cuturilo, Goran; Ruml Stojanović, Jelena; Drakulić, Danijela  ; Mijović, Marija; Bosankić, Brankica; Petrović, Hristina; Stevanović, Milena  Conference Paper
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2023Analysis of cohort of patients with 22q11.2 deletion syndrome - a single-center experience from SerbiaSimeunović, Ivana  ; Drakulić, Danijela  ; Cuturilo, Goran; Kovačević-Grujičić, Nataša  ; Kostić, Jovana  ; Stevanović, Milena  Conference Paper
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2023EP06.016 22q11.2 microdeletion is the most common genomic abnormality in Serbian newborns with critical congenital heart disease and could be rapidly detected by Multiplex ligation probe amplification analysisMiletić, Aleksandra; Cuturilo, Goran; Ruml Stojanović, Jelena; Drakulić, Danijela  ; Mijović, Marija; Bosankić, Brankica; Petrović, Hristina; Stevanović, Milena  Conference Paper
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2023Crosstalk between SOX Genes and Long Non-Coding RNAs in GlioblastomaStevanović, Milena  ; Kovačević-Grujičić, Nataša  ; Petrović, Isidora  ; Drakulić, Danijela  ; Milivojević, Milena  ; Mojsin, Marija  Article
21M21