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12. Vpliv izbranih polimorfizmov na stopnjo izražanja astme pri otrocihMateja Žavbi, 2010, undergraduate thesis Keywords: astma, otroške bolezni, bolezni dihal, polimorfizem, genotip, geni, genetika, nukleotidi, razvoj astme Full text (file, 1,30 MB) |
13. Gene expression levels of the prolyl hydroxylase domain proteins PHD1 and PHD2 but not PHD3 are decreased in primary tumours and correlate with poor prognosis of patients with surgically resected non-small-cell lung cancerAna Koren, Matija Rijavec, Tomaž Krumpestar, Izidor Kern, Aleksander Sadikov, Tanja Čufer, Peter Korošec, 2021, original scientific article Keywords: non-small-cell lung cancer, mRNA expression, prolyl hydroxylase domain proteins, carcinoma, prognosis Full text (file, 754,45 KB) This document has more files! More... |
14. Clonal mast cell disorders and hereditary α-tryptasemia as risk factors for anaphylaxisMark Kačar, Matija Rijavec, Julij Šelb, Peter Korošec, 2023, review article Keywords: anaphylaxis, venom, food, drugs, tryptase, mast cells, KIT p.D816V, hereditary α-tryptasemia, hypersensitivity, diagnosis, food hypersensitivity, drug hypersensitivity Full text (file, 3,53 MB) This document has more files! More... |
15. Ara h 2-specific IgE epitope-like peptides inhibit the binding of IgE to Ara h 2 and suppress lgE-dependent effector cell activationPeter Korošec, Ana Koren, Jerneja Debeljak, Abida Zahirović, Maja Skerbinjek-Kavalar, Vojko Berce, Luka Dejanović, Jernej Luzar, Borut Štrukelj, Mojca Lunder, 2023, original scientific article Keywords: Ara h 2, ImmunoCAP inhibition, basophil activation test, epitopes, mast cell activation test, paratopes, peanut allergy, peptides, specific IgE Full text (file, 8,31 MB) This document has more files! More... |
16. Integrative transcriptomic analysis in human and mouse model of anaphylaxis identifies gene signatures associated with cell movement, migration and neuroinflammatory signallingMatija Rijavec, Aleš Maver, Paul J. Turner, Keli Hočevar, Mitja Košnik, Amnah Yamani, Simon P. Hogan, Adnan Custovic, Borut Peterlin, Peter Korošec, 2022, original scientific article Keywords: transcriptome analysis, cell movement, migration, neuroinflammatory signaling, lipid activating nuclear receptors signaling, anaphylaxis, diagnosis, mast cells, basophils, neutrophils Full text (file, 4,89 MB) This document has more files! More... |
17. The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiencyNina Rupar, Julij Šelb, Mitja Košnik, Mihaela Zidarn, Slađana Andrejević, Ljerka Čulav, Vesna Grivčeva-Panovska, Peter Korošec, Matija Rijavec, 2024, original scientific article Keywords: hereditary angioedema, C1 inhibitor deficiency, genetic modifiers, clinical phenotype, genotype-phenotype correlation, genetic variant, SERPING1, CC2D2B Full text (file, 4,80 MB) This document has more files! More... |
18. Pathology of the placenta in singletons after assisted reproductive technology compared to singletons after spontaneous conceptionUrška Belak, Bojana Pinter, Helena Ban, Mojca Velikonja, Sara Korošec, 2023, review article Keywords: placenta, pathology, assisted reproductive technology, embryo transfer, in vitro fertilization Full text (file, 1,04 MB) This document has more files! More... |