Stevanović, Milena
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Full Name
Stevanović, Milena
Main Affiliation
Email
milenastevanovic@imgge.bg.ac.rs
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Results 1-11 of 11 (Search time: 0.011 seconds).
| Issue Date | Title | Author(s) | Rank | |
|---|---|---|---|---|
| 1 | 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 |
| 2 | 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 |
| 3 | Dec-2017 | The Impact of 22q11.2 Microdeletion on Cardiac Surgery Postoperative Outcome | Cuturilo, Goran; Drakulic, Danijela; Jovanovic, Ida; Ilic, Slobodan; Kalanj, Jasna; Vulicevic, Irena; Raus, Misela; Skoric, Dejan; Mijovic, Marija; Medjo, Biljana; Rsovac, Snezana; Stevanović, Milena | |
| 4 | 8-Sep-2016 | Improving the diagnosis of children with 22q11.2 deletion syndrome: A single-center experience from Serbia | Cuturilo, Goran; Drakulic, Danijela; Jovanovic, Ida; Krstic, Aleksandar; Djukic, Milan; Skoric, Dejan; Mijovic, Marija; Stefanovic, Igor; Milivojevic, Milena; Stevanović, Milena | |
| 5 | Aug-2016 | Differences in speech and language abilities between children with 22q11.2 deletion syndrome and children with phenotypic features of 22q11.2 deletion syndrome but without microdeletion | Rakonjac, Marijana; Cuturilo, Goran; Stevanović, Milena ; Jelicic, Ljiljana; Subotic, Misko; Jovanovic, Ida; Drakulic, Danijela | |
| 6 | 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 | |
| 7 | Nov-2015 | Crosstalk between SOXB1 proteins and WNT/β-catenin signaling in NT2/D1 cells | Mojsin, Marija; Topalovic, Vladanka; Vicentic, Jelena Marjanovic; Schwirtlich, Marija; Stanisavljevic, Danijela; Drakulic, Danijela; Stevanović, Milena | |
| 8 | 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 | |
| 9 | 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 | |
| 10 | Nov-2011 | 4q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome | Cuturilo, Goran; Menten, Björn; Krstic, Aleksandar; Drakulic, Danijela; Jovanovic, Ida; Parezanovic, Vojislav; Stevanović, Milena | |
| 11 | 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 |