Guć-Šćekić M - Search Results

1

Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney Disease.

Schmidts M, Frank V, Eisenberger T, Al Turki S, Bizet AA, Antony D, Rix S, Decker C, Bachmann N, Bald M, Vinke T, Toenshoff B, Di Donato N, Neuhann T, Hartley JL, Maher ER, Bogdanović R, Peco-Antić A, Mache C, Hurles ME, Joksić I, Guć-Šćekić M, Dobricic J, Brankovic-Magic M, Bolz HJ, Pazour GJ, Beales PL, Scambler PJ, Saunier S, Mitchison HM, Bergmann C. Schmidts M, et al. Among authors: guc scekic m. Hum Mutat. 2013 May;34(5):714-24. doi: 10.1002/humu.22294. Hum Mutat. 2013. PMID: 23418020 Free PMC article.

2

Fanconi anemia is characterized by delayed repair kinetics of DNA double-strand breaks.

Leskovac A, Vujic D, Guc-Scekic M, Petrovic S, Joksic I, Slijepcevic P, Joksic G. Leskovac A, et al. Tohoku J Exp Med. 2010 May;221(1):69-76. doi: 10.1620/tjem.221.69. Tohoku J Exp Med. 2010. PMID: 20453460 Free article.

3

Dysfunctional telomeres in primary cells from Fanconi anemia FANCD2 patients.

Joksic I, Vujic D, Guc-Scekic M, Leskovac A, Petrovic S, Ojani M, Trujillo JP, Surralles J, Zivkovic M, Stankovic A, Slijepcevic P, Joksic G. Joksic I, et al. Among authors: guc scekic m. Genome Integr. 2012 Sep 14;3(1):6. doi: 10.1186/2041-9414-3-6. Genome Integr. 2012. PMID: 22980747 Free PMC article.

4

Radiation-induced mitotic catastrophe in FANCD2 primary fibroblasts.

Leskovac A, Petrovic S, Guc-Scekic M, Vujic D, Joksic G. Leskovac A, et al. Among authors: guc scekic m. Int J Radiat Biol. 2014 May;90(5):373-81. doi: 10.3109/09553002.2014.892224. Epub 2014 Mar 19. Int J Radiat Biol. 2014. PMID: 24512567

5

Gender-related differences in the oxidant state of cells in Fanconi anemia heterozygotes.

Petrovic S, Leskovac A, Kotur-Stevuljevic J, Joksic J, Guc-Scekic M, Vujic D, Joksic G. Petrovic S, et al. Biol Chem. 2011 Jul;392(7):625-32. doi: 10.1515/BC.2011.064. Epub 2011 May 28. Biol Chem. 2011. PMID: 21619480

6

Diagnosis of Fanconi's Anemia by Diepoxybutane Analysis in Children from Serbia.

Cirkovic S, Guc-Scekic M, Vujic D, Ilic N, Micic D, Skoric D, Jovanovic A. Cirkovic S, et al. Among authors: guc scekic m. Balkan J Med Genet. 2011 Dec;14(2):65-70. doi: 10.2478/v10034-011-0048-6. Balkan J Med Genet. 2011. PMID: 24052713 Free PMC article.

7

Chromosomal instability in patients with Fanconi anemia from Serbia.

Cirković S, Guć-Sćekić M, Vujić D, Mićić D, Skorić D. Cirković S, et al. Among authors: guc scekic m. Vojnosanit Pregl. 2014 Apr;71(4):368-72. doi: 10.2298/vsp1404368c. Vojnosanit Pregl. 2014. PMID: 24783417

8

Monitoring of pediatric patients with malignant hematological diseases after allogeneic HSCT: Serbian experience.

Krstic AD, Stojkovic O, Guc-Scekic M, Jevtic D, Zecevic Z, Vujic DS. Krstic AD, et al. Among authors: guc scekic m. J Pediatr Hematol Oncol. 2012 Aug;34(6):e253-7. doi: 10.1097/MPH.0b013e31824872bb. J Pediatr Hematol Oncol. 2012. PMID: 22543520

9

Molecular analysis of ring y chromosome in a 10-year-old boy with mixed gonadal dysgenesis and growth hormone deficiency.

Milenkovic T, Guc-Scekic M, Zdravkovic D, Topic V, Liehr T, Joksic G, Radivojevic D, Lakic N. Milenkovic T, et al. Among authors: guc scekic m. Balkan J Med Genet. 2011 Dec;14(2):71-6. doi: 10.2478/v10034-011-0049-5. Balkan J Med Genet. 2011. PMID: 24052714 Free PMC article.

10

Lower incidence of deletions in the survival of motor neuron gene and the neuronal apoptosis inhibitory protein gene in children with spinal muscular atrophy from Serbia.

Miskovic M, Lalic T, Radivojevic D, Cirkovic S, Vlahovic G, Zamurovic D, Guc-Scekic M. Miskovic M, et al. Tohoku J Exp Med. 2011 Nov;225(3):153-9. doi: 10.1620/tjem.225.153. Tohoku J Exp Med. 2011. PMID: 21971302 Free article.

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