Pretraga

Rezultati

Functional characterization of the human SOX3 promoter: identification of transcription factors implicated in basal promoter activity [2005]

Kovačević Grujičić, Nataša ; Mojsin, Marija ; Krstić, A; Stevanović, Milena

CRISPR/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 Ib [2019]

Skakic, Anita ; Andjelkovic, Marina ; Tošić, Nataša ; Klaassen, Kristel ; Djordjevic, Maja; Pavlović, Sonja ; Stojiljković, Maja

PHACTR1 haplotypes are associated with carotid plaque presence and affect PHACTR1 mRNA expression in carotid plaque tissue [2019]

Kuveljić, Jovana ; Đurić, Tamara ; Stanković, Aleksandra ; Končar, Igor ; Alavantić, Dragan ; Živković, Maja

Ancestral modal Y-STR haplotype shared among Romani and South Indian populations [2012]

Regueiro, Maria; Rivera, Luis; Chennakrishnaiah, Shilpa; Popović, Branka ; Andjus, Stefan ; Milašin, Jelena ; Herrera, Rene J.

The HACD4 haplotype as a risk factor for atherosclerosis in males [2018]

Životić, Ivan ; Đurić, Tamara ; Stanković, Aleksandra ; Ivančević, Ilija; Končar, Igor ; Milašinović, Dejan ; Stanković, Goran ; Alavantić, Dragan ; Živković, Maja

High levels of Paleolithic Y-chromosome lineages characterize Serbia [2012]

Regueiro, Maria; Rivera, Luis; Damnjanović, Tatjana ; Luković, Ljiljana ; Milašin, Jelena ; Herrera, Rene J.

Novel chromosomal translocation (17;22)(q12;q12) in a case of myelodisplastic syndrome characterized with signs of hemolytic anemia at presentation [2012]

Antić, Darko ; Impera, Luciana; Fekete, Marija Dencic; Djordjevic, Vesna ; Storlazzi, Clelia Tiziana; Elezovic, Ivo

The stress responsive gene ankrd1a is dynamically regulated during skeletal muscle development and upregulated following cardiac injury in border zone cardiomyocytes in adult zebrafish [2021]

Bošković, Srđan ; Juez, Ruben Marin; Stamenković, Nemanja; Radojković, Dragica ; Stainier, Didier Y. R.; Kojić, Snežana

The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency [2024]

Rupar, Nina; Selb, Julij; Kosnik, Mitja; Zidarn, Mihaela; Andrejevic, Sladjana B; Culav, Ljerka; Grivceva-Panovska, Vesna; Korosec, Peter; Rijavec, Matija

On the Bantu expansion [2016]

Rowold, Daine J.; Perez-Benedico, David; Stojković, Oliver ; Garcia-Bertrand, Ralph; Herrera, Rene J.