Browsing by Author Drakulic, Danijela
Showing results 6 to 11 of 11
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| Issue Date | Title | Author(s) | Rank |
|---|---|---|---|
| Mar-2015 | The overexpression of SOX2 affects the migration of human teratocarcinoma cell line NT2/D1 | Drakulic, Danijela; Vicentic, Jelena Marjanovic; Schwirtlich, Marija; Tosic, Jelena; Krstic, Aleksandar; Klajn, Andrijana; Stevanović, Milena | |
| Oct-2008 | A rare association of interrupted aortic arch type C and microdeletion 22q11.2 | Cuturilo, Goran; Drakulic, Danijela; Stevanović, Milena ; Jovanovic, Ida; Djukic, Milan; Miletic-Grkovic, Slobodanka; Atanaskovic-Markovic, Marina | |
| Apr-2013 | The role of modern imaging techniques in the diagnosis of malposition of the branch pulmonary arteries and possible association with microdeletion 22q11.2 | Cuturilo, Goran; Drakulic, Danijela; Krstic, Aleksandar; Gradinac, Marija; Ilisic, Tamara; Parezanovic, Vojislav; Milivojevic, Milena; Stevanović, Milena ; Jovanovic, Ida | |
| 2021 | SOX Transcription Factors as Important Regulators of Neuronal and Glial Differentiation During Nervous System Development and Adult Neurogenesis | Stevanović, Milena ; Drakulic, Danijela; Lazic, Andrijana; Ninkovic, Danijela Stanisavljevic; Schwirtlich, Marija; Mojsin, Marija | M21 |
| Feb-2019 | SOX3 can promote the malignant behavior of glioblastoma cells | Marjanovic 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 |
| 2016 | Speech and language abilities of children with the familial form of 22Q11.2 deletion syndrome | Rakonjac, Marijana; Cuturilo, Goran; Stevanović, Milena ; Jovanovic, Ida; Dobrijevic, Ljiljana Jelicic; Mijovic, Marija; Drakulic, Danijela |