Researchers



Results 61-80 of 97
GodinaNaslovAutor(i)Tip rezultataMp-kat.
2021Genetic variants in TNFA, LTA, TLR2 and TLR4 genes and risk of sepsis in patients with severe trauma: nested case-control study in a level-1 trauma centre in SERBIAĐurić, Olivera ; Anđelković, Marina  ; Vreća, Miša ; Skakić, Anita  ; Pavlović, Sonja  ; Novaković, Ivana  ; Jovanović, Bojan  ; Škodrić-Trifunović, Vesna ; Marković-Denić, Ljiljana Article
21M21
2021Planar printed electrodes for electroporation with high EM field homogeneityIlić, Anđelija  ; Bukvić, Branko M  ; Stojiljković, Maja  ; Skakić, Anita  ; Pavlović, Sonja  ; Jovanović, Siniša P; Ilić, Milan M  Article
21M21
2020Correlation of expression of TLR7 and Mirna-146a genes and fibrosis in peripheral blood and skin samples of SSc patientsVesna Spasovski  ; Vreca Misa; Andjelkovic, Marina  ; Stojiljkovic, Maja  ; Skakic, Anita  ; Klaassen Kristel  ; Zekovic, Ana; Damjanov Nemanja; Pavlovic, Sonja  Conference Paper
Mp. category will be shown later
2020Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type IbSarajlija, Adrijan  ; Đorđević, Maja  ; Kecman, Božica; Skakić, Anita  ; Pavlović, Sonja  ; Pašić, Srđan  ; Stojiljković, Maja  Article
22M22
2019Genomski profil pacijenata dečijeg uzrasta sa hepatičnim glikogenozama: korelacija genotipa i fenotipa i funkcionalna karakterizacija novih varijantiSkakić, Anita  Doctoral theses
70M70
2019GENOMIC PROFILING OF GLYCOGEN STORAGE DISEASES: FROM THE NGS METHOD TO THE CRISPR/CAS9 TECHNOLOGYSkakić, Anita  ; Anđelković, Marina  ; Tošic, Nataša  ; Kristel Klaassen  ; Vesna Spasovski  ; Ristivojevic, Bojan  ; Đordjevic, Maja; Adrijan Sarajlija; Pavlović, Sonja  ; Stojiljković, Maja  Conference Paper
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2019HYPERPHENYLALANINEMIA: FROM COMPLEX GENETICS TO COMPLEX PHENOTYPESKristel Klaassen  ; Stojiljković, Maja  ; Đorđević, Maja; Skakić, Anita  ; Srzentić, Sanja  ; Drmanac, Radoje; Pavlović, Sonja  Conference Paper
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2019The importance of comprehensive genomic profiling in differential diagnosis and discovery of novel disease causing genetic variants in patients with pediatric lung diseasesAnđelković, Marina  ; Minić, Predrag ; Vreća, Miša ; Stojiljković, Maja  ; Skakić, Anita  ; Sovtić, Aleksandar  ; Rodić, M.; Škodrić-Trifunović, Vesna ; Marić, N.; Višekruna, J.;
Spasovski, Vesna  ; Pavlović, Sonja  ;
Conference Paper
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2019Differential diagnosis of patients with pediatric lung diseases and discovery of novel disease-causing genes and genetic variants by using next-generation sequencing technologyAnđelković, Marina  ; Vesna Spasovski  ; Minić, Predrag; Sovtić, Aleksandar; Stojiljković, Maja  ; Skakić, Anita  ; Pavlovic, Sonja  Conference Paper
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2019GENOMIC PROFILING AS A TOOL FOR DIFFERENTIAL DIAGNOSIS OF PATIENTS WITH PEDIATRIC LUNG DISEASES AND DISCOVERY OF NOVEL DISEASE-CAUSING GENES AND GENETIC VARIANTSAnđelković, Marina  ; Spasovski, Vesna  ; Minic, Predrag ; Sovtic, Aleksandar; Skakić, Anita  ; Pavlović, Sonja  Conference Paper
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2019Genomic profiling of glycogen storage diseasesSkakic, Anita  ; Anđelković, Marina  ; Tošic, Natasa  ; Kristel Klaassen  ; Spasovski, Vesna  ; Ristivojević, Bojan  ; Đorđević, Maja; Sarajlija, Adrijan; Pavlović, Sonja  ; Stojiljković, Maja  Conference Paper
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2019Genomic profiling of glycogen storage diseases: from NGS method to the CRISPR/Cas9 technologySkakić, Anita  ; Anđelković, Marina  ; Tošić, Nataša  ; Kristel Klaassen  ; Spasovski, Vesna  ; Đorđević, Maja; Sarajlija, Adrijan; Pavlović, Sonja  ; Stojiljković, Maja  Conference Paper
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2019CRISPR/Cas9 genome editing of SLC37A4 gene elucidates the role of molecular markers of endoplasmic reticulum stress and apoptosis in renal involvement in glycogen storage disease type IbSkakic, Anita  ; Andjelkovic, Marina  ; Tošić, Nataša  ; Klaassen, Kristel  ; Djordjevic, Maja; Pavlović, Sonja  ; Stojiljković, Maja  Article
22M22
2018Genomic profiling supports the diagnosis of primary ciliary dyskinesia and reveals novel candidate genes and genetic variantsAnđelković, Marina  ; Minić, Predrag ; Vreća, Miša ; Stojiljković, Maja  ; Skakić, Anita  ; Sovtić, Aleksandar  ; Rodić, Milan; Škodrić-Trifunović, Vesna  ; Marić, Nina; Višekruna, Jelena;
Spasovski, Vesna  ; Pavlović, Sonja  ;
Article
21M21
2018Functional Characterization of Novel Phenylalanine Hydroxylase p.Gln226Lys Mutation Revealed Its Non-responsiveness to Tetrahydrobiopterin Treatment in Hepatoma Cellular ModelKlaassen, Kristel  ; Djordjevic, Maja; Skakić, Anita  ; Desviat, Lourdes R.; Pavlović, Sonja  ; Perez, Belen; Stojiljković, Maja  Article
22M22
2018Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variantsSkakić, Anita  ; Đorđević, M.; Sarajlija, A.  ; Klaassen, Kristel  ; Tošić, Nataša  ; Kecman, B.; Ugrin, Milena  ; Spasovski, Vesna  ; Pavlović, Sonja  ; Stojiljković, Maja  Article
21M21
2018Nivoi ekspresije miR-146a i njenog targeta IRAK1 gena kao potencijalno novi biomarkeri u sistemskoj skleroziVreca, M; Andjelkovic, M; Tosic, Natasa  ; Skakic, A  ; Jovana Komazec  ; Spasovski, V  ; Pavlovic, SConference Paper
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2017Genetic modifiers of beta-thalassemia: a rise of a novel therapy approaches.Milena Ugrin  ; Stojiljkovic, Maja  ; Zukić, Branka  ; Kristel Klaassen  ; Jovana Komazec  ; Skakic, Anita  ; Dokmanovic, Lidija; Janic, Dragana; George Patrinos; Pavlovic, Sonja  Conference Paper
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2017Genetic modifiers of -thalassemia: a rise of a novel therapy approachesUgrin M.  ; Stojiljković M.; Zukić B.  ; Klaassen K.  ; Jovana Komazec  ; Skakić A.  ; Dokmanović, L.; Janić D.; Patrinos GP.; Pavlović S.Conference Paper
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2017Molecular genetic strategy for diagnosis of congenital adrenal hyperplasia in SerbiaUgrin, Milena  ; Milačić, Iva; Skakić, Anita  ; Klaassen, Kristel  ; Komazec, Jovana  ; Pavlović, Sonja  ; Stojiljković, Maja  Article
23M23