Pretraga
Rezultati
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, MatijaCRISPR/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 PHACTR1 haplotypes are associated with carotid plaque presence and affect PHACTR1 mRNA expression in carotid plaque tissue
[2019]
Kuveljić, Jovana On the Bantu expansion
[2016]
Rowold, Daine J.; Perez-Benedico, David; Stojković, Oliver Functional characterization of the human SOX3 promoter: identification of transcription factors implicated in basal promoter activity
[2005]
Kovačević Grujičić, Nataša Filamentous phage infection-mediated gene expression: construction and propagation of the gIII deletion mutant helper phage R408d3 [1997]
Rakonjac, J; Jovanović, GoranAssociation between genetic variants in DICER1 and cancer risk: An updated meta-analysis
[2021]
Dobrijević, Zorana Genetic analysis and allele-specific expression of SMAD7 3′UTR variants in human colorectal cancer reveal a novel somatic variant exhibiting allelic imbalance
[2023]
Rosić, Jovana Association study of rs7799039, rs1137101 and rs8192678 gene variants with disease susceptibility/severity and corresponding LEP, LEPR and PGC1A gene expression in multiple sclerosis [2021]
Kolić, IvanaComplex transcriptional regulation of the BCL2L12 gene: Novel, active promoter in K562 cells [2020]
Nikčević, GordanaFilteri
Po tipu
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