Iskalni niz:
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išči po
išči po
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Jezik:
Št. zadetkov: 8
Izvirni znanstveni članek
Oznake: vodenje;stili vodenja;kombiniranje;zdravstvena nega;
Leto: 2023 Vir: Fakulteta za poslovne in upravne vede Novo mesto (FPUV NM)
Magistrsko delo
Oznake: sir;potvorbe sira;kravji sir;ovčji sir;mešani sir;molekularne tehnike;PCR v realnem času;kvantitativno določanje;
Ugotavljanje potvorb kozjih in ovčjih sirov s kravjim mlekom
Leto: 2015 Vir: Biotehniška fakulteta (UL BF)
Magistrsko delo
Oznake: figa;Ficus carica;načini sušenja;primarni metaboliti;sekundarni metaboliti;
Vpliv različnih načinov sušenja na vsebnost izbranih primarnih in sekundarnih metabolitov v plodovih fig (Ficus carica L.)
Leto: 2016 Vir: Biotehniška fakulteta (UL BF)
Izvirni znanstveni članek
Oznake: smokva;figa;sušenje;sladkorji;organske kisline;fenoli;
Effect of drying of figs (Ficus carica L.) on the content of sugars, organic acids and phenolic compounds
Leto: 2011 Vir: Biotehniška fakulteta (UL BF)
Izvirni znanstveni članek
Oznake: sekvencioniranje RNA;variante DNA;spajanje;RNA sequencing;DNA variant;splicing;
RNA sequencing is a promising technique for detecting normal and aberrant RNA isoforms. Here, we present a new single-gene, straightforward 1-day hands-on protocol for detection of splicing alterations with deep RNA sequencing from blood. We have validated our method%s accuracy by detecting previous ...
Leto: 2021 Vir: Onkološki inštitut Ljubljana (OI)
Izvirni znanstveni članek
Oznake: dedni raki;sekvencioniranje RNA;spajanje;geni;hereditary cancer;RNA sequencing;spliceogenic;
Pathogenic/likely pathogenic variants in susceptibility genes that interrupt RNA splicing are a well-documented mechanism of hereditary cancer syndromes development. However, if RNA studies are not performed, most of the variants beyond the canonical GT-AG splice site are characterized as variants o ...
Leto: 2022 Vir: Onkološki inštitut Ljubljana (OI)
Izvirni znanstveni članek
Oznake: BAP1;rak dojke;dedni raki;imunoterapija;breast cancer;hereditary cancer syndromes;immunotherapy;
BAP1 cancer syndrome is a rare and highly penetrant hereditary cancer predisposition. Uveal melanoma, mesothelioma, renal cell carcinoma (RCC) and cutaneous melanoma are considered BAP1 cancer syndrome core cancers, whereas association with breast cancer has previously been suggested but not confirm ...
Leto: 2022 Vir: Onkološki inštitut Ljubljana (OI)
Izvirni znanstveni članek
Oznake: BRCA;rak jajčnikov;genotip tumorja;HBOC;ovarian cancer;tumor genotyping;
Detection of germline and somatic pathogenic/likely pathogenic variants (PV/LPV) in BRCA genes is at the moment a prerequisite for use of PARP inhibitors in different treatment settings of different tumors. The aim of our study was to determine the most appropriate testing workflow in epithelial ova ...
Leto: 2022 Vir: Onkološki inštitut Ljubljana (OI)
Št. zadetkov: 8
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