Browsing by Author Drakulic, Danijela

Showing results 1 to 11 of 11
Issue DateTitleAuthor(s)Rank
Nov-20114q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndromeCuturilo, Goran; Menten, Björn; Krstic, Aleksandar; Drakulic, Danijela; Jovanovic, Ida; Parezanovic, Vojislav; Stevanović, Milena 
Nov-2015Crosstalk between SOXB1 proteins and WNT/β-catenin signaling in NT2/D1 cellsMojsin, Marija; Topalovic, Vladanka; Vicentic, Jelena Marjanovic; Schwirtlich, Marija; Stanisavljevic, Danijela; Drakulic, Danijela; Stevanović, Milena 
Aug-2016Differences in speech and language abilities between children with 22q11.2 deletion syndrome and children with phenotypic features of 22q11.2 deletion syndrome but without microdeletionRakonjac, Marijana; Cuturilo, Goran; Stevanović, Milena ; Jelicic, Ljiljana; Subotic, Misko; Jovanovic, Ida; Drakulic, Danijela
Dec-2017The Impact of 22q11.2 Microdeletion on Cardiac Surgery Postoperative OutcomeCuturilo, Goran; Drakulic, Danijela; Jovanovic, Ida; Ilic, Slobodan; Kalanj, Jasna; Vulicevic, Irena; Raus, Misela; Skoric, Dejan; Mijovic, Marija; Medjo, Biljana; Rsovac, Snezana; Stevanović, Milena 
8-Sep-2016Improving the diagnosis of children with 22q11.2 deletion syndrome: A single-center experience from SerbiaCuturilo, Goran; Drakulic, Danijela; Jovanovic, Ida; Krstic, Aleksandar; Djukic, Milan; Skoric, Dejan; Mijovic, Marija; Stefanovic, Igor; Milivojevic, Milena; Stevanović, Milena 
Mar-2015The overexpression of SOX2 affects the migration of human teratocarcinoma cell line NT2/D1Drakulic, Danijela; Vicentic, Jelena Marjanovic; Schwirtlich, Marija; Tosic, Jelena; Krstic, Aleksandar; Klajn, Andrijana; Stevanović, Milena 
Oct-2008A rare association of interrupted aortic arch type C and microdeletion 22q11.2Cuturilo, Goran; Drakulic, Danijela; Stevanović, Milena ; Jovanovic, Ida; Djukic, Milan; Miletic-Grkovic, Slobodanka; Atanaskovic-Markovic, Marina
Apr-2013The role of modern imaging techniques in the diagnosis of malposition of the branch pulmonary arteries and possible association with microdeletion 22q11.2Cuturilo, Goran; Drakulic, Danijela; Krstic, Aleksandar; Gradinac, Marija; Ilisic, Tamara; Parezanovic, Vojislav; Milivojevic, Milena; Stevanović, Milena ; Jovanovic, Ida
2021SOX Transcription Factors as Important Regulators of Neuronal and Glial Differentiation During Nervous System Development and Adult NeurogenesisStevanović, Milena ; Drakulic, Danijela; Lazic, Andrijana; Ninkovic, Danijela Stanisavljevic; Schwirtlich, Marija; Mojsin, MarijaM21
Feb-2019SOX3 can promote the malignant behavior of glioblastoma cellsMarjanovic Vicentic, Jelena; Drakulic, Danijela; Garcia, Idoia; Vukovic, Vladanka; Aldaz, Paula; Puskas, Nela; Nikolic, Igor; Tasic, Goran; Raicevic, Savo; Garros-Regulez, Laura; Sampron, Nicolas; Atkinson, Michael J.; Anastasov, Natasa; Matheu, Ander; Stevanović, Milena M21a
2016Speech and language abilities of children with the familial form of 22Q11.2 deletion syndromeRakonjac, Marijana; Cuturilo, Goran; Stevanović, Milena ; Jovanovic, Ida; Dobrijevic, Ljiljana Jelicic; Mijovic, Marija; Drakulic, Danijela