Претрага

Резултати

PHACTR1 mRNA expression is affected by rs9349379 in PBMC of patients six months after the first MI [2020]

Kuveljić, Jovana ; Đurić, Tamara M. ; Dekleva, Milica N. ; Marković-Nikolić, Nataša S. ; Stanković, Aleksandra D. ; Alavantić, Dragan ; Živković, Maja D.

Deletion and duplication screening in the DMD gene using MLPA [2005]

Lalic, Tanja; Vossen, RH; Coffa, J; Schouten, JP; Guc-Scekic, Marija P; Radivojevic, Danijela; Djurisic, Marina; Breuning, MH; White, SJ; den, Dunnen JT

NOTCH3 mutations in Serbian CADASIL patients [2019]

Janković, Milena Z. ; Dobričić, Valerija S. ; Marjanović, Ana ; Branković, Marija ; Pavlovic, Aleksandra M. ; Dujmović, Irena ; Mijajlović, Milija D. ; Novaković, Ivana V. ; Kostić, Vladimir S.

Analysis of the association between MMP-8 gene polymorphisms and the occurrence of adverse effects after acute ischemic stroke treated with recombinant tissue plasminogen activator [2024]

Dušanović-Pjević, Marija G. ; Grk, Milka B. ; Vojvodić, Ljubica M.; Rašić, Milica ; Perović, Dijana ; Damnjanović, Tatjana M. ; Pešić, Milica ; Jekić, Biljana B.

Gene expression analysis in cortical neurons differentiated from 32 induced pluripotent stem cell (iPSC) lines of THAP1 mutation carriers and controls [2019]

Baumann, Hauke; Trilck-Winkler, Michaela; Grosse, M; Munchau, Alexander; Kostic, Vladimir S; Klein, Christine; Kaiser, Frank J; Seibler, Philip; Lohmann, Katja

Novel mosaic CREBBP mutation in a patient with overlapping clinical features of Rubinstein-Taybi syndrome and Floating-Harbor syndrome [2019]

Ruml-Stojanovic, Jelena; Mijovic, Marija; Miletic, Aleksandra; Dimitrijevic, Brankica; Peterlin, Borut; Maver, Ales; Cuturilo, Goran

PHACTR1 mRNA expression is affected by rs9349379 in PBMC of patients six months after the first MI [2020]

Deletion and duplication screening in the DMD gene using MLPA [2005]

NOTCH3 mutations in Serbian CADASIL patients [2019]

Analysis of the association between MMP-8 gene polymorphisms and the occurrence of adverse effects after acute ischemic stroke treated with recombinant tissue plasminogen activator [2024]

Gene expression analysis in cortical neurons differentiated from 32 induced pluripotent stem cell (iPSC) lines of THAP1 mutation carriers and controls [2019]

Novel mosaic CREBBP mutation in a patient with overlapping clinical features of Rubinstein-Taybi syndrome and Floating-Harbor syndrome [2019]

De novo dominant variants affecting the motor domain of KIF1A are a cause of PEHO syndrome [2015]

Association of ADARB1 gene with suicide attempt risk in patients with major psychiatric disorders [2015]

Oncogenic miR-21 and miR-31 clinical relevance in oral cancer: tissue specimens vs. exosomes [2024]

A rare case of prenatal Stuve-Wiedemann syndrome presenting with asymmetric femoral involvement [2025]

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