Guc-Scekic M - Search Results

1

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

2

A complex rearrangement involving cryptic deletion of ETV6 and CDKN1B genes in a case of childhood acute lymphoblastic leukemia.

Krstic AD, Impera L, Guc-Scekic M, Lakic N, Djokic D, Slavkovic B, Storlazzi CT. Krstic AD, et al. Cancer Genet Cytogenet. 2009 Dec;195(2):125-31. doi: 10.1016/j.cancergencyto.2009.07.002. Cancer Genet Cytogenet. 2009. PMID: 19963112

3

Molecular diagnosis of childhood acute leukemia: Serbian experience.

Krstic AD, Micic D, Lakic N, Guc-Scekic M, Janic D. Krstic AD, et al. Pediatr Blood Cancer. 2010 Aug;55(2):394-5. doi: 10.1002/pbc.22571. Pediatr Blood Cancer. 2010. PMID: 20582960 No abstract available.

4

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.

5

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

6

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.

7

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

8

Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation.

Major T, Culjkovic B, Stojkovic O, Gucscekic M, Lakic A, Romac S. Major T, et al. J Neurogenet. 2003 Apr-Sep;17(2-3):223-30. doi: 10.1080/neg.17.2-3.223.230. J Neurogenet. 2003. PMID: 14668200

9

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.

10

[Primary myelodysplastic syndrome in children].

Kuzmanović M, Bunjevacki G, Rasović N, Vujić D, Mićić D, Guć-Sćekić M, Jovanović V. Kuzmanović M, et al. Srp Arh Celok Lek. 2001 May-Jun;129 Suppl 1:10-6. Srp Arh Celok Lek. 2001. PMID: 15637984 Serbian.

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