Drakulic D - Search Results

1

SOX2 overexpression affects neural differentiation of human pluripotent NT2/D1 cells.

Klajn A, Drakulic D, Tosic M, Pavkovic Z, Schwirtlich M, Stevanovic M. Klajn A, et al. Among authors: drakulic d. Biochemistry (Mosc). 2014 Nov;79(11):1172-82. doi: 10.1134/S0006297914110042. Biochemistry (Mosc). 2014. PMID: 25540002 Free article.

2

A rare association of interrupted aortic arch type C and microdeletion 22q11.2.

Cuturilo G, Drakulic D, Stevanovic M, Jovanovic I, Djukic M, Miletic-Grkovic S, Atanaskovic-Markovic M. Cuturilo G, et al. Among authors: drakulic d. Eur J Pediatr. 2008 Oct;167(10):1195-8. doi: 10.1007/s00431-007-0632-7. Epub 2007 Nov 27. Eur J Pediatr. 2008. PMID: 18040716

3

Pattern of trisomy 1q in hematological malignancies: a single institution experience.

Djordjević V, Dencić-Fekete M, Jovanović J, Drakulić D, Stevanović M, Janković G, Gotić M. Djordjević V, et al. Among authors: drakulic d. Cancer Genet Cytogenet. 2008 Oct;186(1):12-8. doi: 10.1016/j.cancergencyto.2008.05.003. Cancer Genet Cytogenet. 2008. PMID: 18786437

4

Detection of premature segregation of centromeres in persons exposed to ionizing radiation.

Jovicić D, Milacić S, Vukov TD, Rakić B, Stevanović M, Drakulić D, Rakić R, Bukvić N. Jovicić D, et al. Among authors: drakulic d. Health Phys. 2010 May;98(5):717-27. doi: 10.1097/HP.0b013e3181d26da1. Health Phys. 2010. PMID: 20386201

5

4q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome.

Cuturilo G, Menten B, Krstic A, Drakulic D, Jovanovic I, Parezanovic V, Stevanovic M. Cuturilo G, et al. Among authors: drakulic d. Eur J Pediatr. 2011 Nov;170(11):1465-70. doi: 10.1007/s00431-011-1533-3. Epub 2011 Jul 22. Eur J Pediatr. 2011. PMID: 21833498

6

Establishment and initial characterization of SOX2-overexpressing NT2/D1 cell clones.

Drakulic D, Krstic A, Stevanovic M. Drakulic D, et al. Genet Mol Res. 2012 May 15;11(2):1385-400. doi: 10.4238/2012.May.15.9. Genet Mol Res. 2012. PMID: 22653585 Free article.

7

The role of modern imaging techniques in the diagnosis of malposition of the branch pulmonary arteries and possible association with microdeletion 22q11.2.

Cuturilo G, Drakulic D, Krstic A, Gradinac M, Ilisic T, Parezanovic V, Milivojevic M, Stevanovic M, Jovanovic I. Cuturilo G, et al. Among authors: drakulic d. Cardiol Young. 2013 Apr;23(2):181-8. doi: 10.1017/S1047951112000571. Epub 2012 Apr 26. Cardiol Young. 2013. PMID: 22717372

8

The overexpression of SOX2 affects the migration of human teratocarcinoma cell line NT2/D1.

Drakulic D, Vicentic JM, Schwirtlich M, Tosic J, Krstic A, Klajn A, Stevanovic M. Drakulic D, et al. An Acad Bras Cienc. 2015 Mar;87(1):389-404. doi: 10.1590/0001-3765201520140352. Epub 2015 Mar 6. An Acad Bras Cienc. 2015. PMID: 25761220 Free article.

9

Crosstalk between SOXB1 proteins and WNT/β-catenin signaling in NT2/D1 cells.

Mojsin M, Topalovic V, Vicentic JM, Schwirtlich M, Stanisavljevic D, Drakulic D, Stevanovic M. Mojsin M, et al. Among authors: drakulic d. Histochem Cell Biol. 2015 Nov;144(5):429-41. doi: 10.1007/s00418-015-1352-0. Epub 2015 Aug 4. Histochem Cell Biol. 2015. PMID: 26239426

10

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 M, Cuturilo G, Stevanovic M, Jelicic L, Subotic M, Jovanovic I, Drakulic D. Rakonjac M, et al. Among authors: drakulic d. Res Dev Disabil. 2016 Aug;55:322-9. doi: 10.1016/j.ridd.2016.05.006. Epub 2016 May 25. Res Dev Disabil. 2016. PMID: 27235769

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