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PhD theses (1)
Jasna Grželj:
Farmakogenetski dejavniki odziva na metotreksat pri bolnikih z luskavico
MSc theses (12)
Ida Lesar:
Vpliv polimorfizmov v genih za encime folatnega cikla na pojavnost prirojenih srčnih napak v slovenski populaciji
Kaja Štrigl:
Analiza izražanja genov proteasoma in imunoproteasoma v različnih celičnih modelih
Tina Štruc:
Vloga polimorfizmov v genih za izbrane metiltransferaze pri nastanku orofacialnih shiz
Urška Erklavec:
Vpliv selenita na aktivnost tiopurin S-metiltransferaze
Katarina Nemec:
Preučevanje vloge prostaglandinskega receptorja EP4 pri bolnikih s kronično limfocitno levkemijo
Ines Čadež:
Vpliv materinih genotipov TPMT in MTHFR na oksidativni status matere in otroka v drugem trimesečju ter s tem povezane izide nosečnosti
Ana Škapin:
Vloga polimorfizmov v genih za izbrane metiltransferaze pri nastanku prirojenih srčnih napak
Jacqueline Kajtna:
Analiza izražanja genov podenot proteasoma in imunoproteasoma v celicah mišjega modela sistemskega lupusa eritematozusa
Tanja Ramovš:
Vrednotenje izražanja genov za katalitične podenote proteasomov v limfoblastoidnih celičnih linijah
Valentina Matek:
Analiza sprememb nukleotidnega zapiredja gena IRF6 v družinah z orofacialnimi shizami
Katja Vozelj:
Analiza izražanja katalitično aktivnih proteasomskih podenot v limfoblastoidnh celičnih linijah na nivoju določanja proteinov
Marjetka Glavič:
Vpliv polimorfizma rs642961 v regulatorni regiji gena IRF6 na nastanek orofacialnih shiz in prirojenih srčnih napak v slovenski populaciji
Other documents (12)
Maša Vidmar, Jurij Trontelj, Ksenija Geršak, Irena Mlinarič-Raščan, Alenka Šmid:
Simultaneous quantification of intracellular concentrations of clinically important metabolites of folate-homocysteine cycle by LC-MS/MS
Eva Rajh, Tina Šket, Arne Praznik, Petra Sušjan-Leite, Alenka Šmid, Dunja Urbančič, Irena Mlinarič-Raščan, Polona Kogovšek, Tina Demšar, Mojca Milavec, Katarina Prosenc Trilar, Žiga Jensterle, Mihaela Zidarn, Viktorija Tomič, Gabriele Turel, Tatjana Lejko-Zupanc, Roman Jerala, Mojca Benčina:
Robust saliva-based RNA extraction-free one-step nucleic acid amplification test for mass SARS-CoV-2 monitoring
Jasna Grželj, Maruška Marovt, Pij B. Marko, Irena Mlinarič-Raščan, Tanja Gmeiner, Alenka Šmid:
Polymorphism in gene for ABCC2 transporter predicts methotrexate drug survival in patients with psoriasis
Dunja Urbančič, Anita Kotar, Alenka Šmid, Marko Jukič, Stanislav Gobec, Lars Martensson, Janez Plavec, Irena Mlinarič-Raščan:
Methylation of selenocysteine catalysed by thiopurine S-methyltransferase
Jasna Grželj, Irena Mlinarič-Raščan, Pij B. Marko, Maruška Marovt, Tanja Gmeiner, Alenka Šmid:
Polymorphisms in GNMT and DNMT3b are associated with methotrexate treatment outcome in plaque psoriasis
Maša Vidmar, Alenka Šmid, Nataša Karas Kuželički, Jurij Trontelj, Ksenija Geršak, Irena Mlinarič-Raščan:
Folate insufficiency due to MTHFR deficiency is bypassed by 5-methyltetrahydrofolate
Aida Zečkanović, Marko Kavčič, Tomaž Prelog, Alenka Šmid, Janez Jazbec:
Micronized, microencapsulated ferric iron supplementation in the form of >Your< Iron Syrup improves hemoglobin and ferritin levels in iron-deficient children
Mojca Zupanc, Martin Petkovšek, Jure Zevnik, Gregor Kozmus, Alenka Šmid, Matevž Dular:
Anomalies detected during hydrodynamic cavitation when using salicylic acid dosimetry to measure radical production
Nataša Karas Kuželički, Alenka Šmid, Maša Vidmar, Tina Kek, Borut Geršak, Uroš Mazić, Irena Mlinarič-Raščan, Ksenija Geršak:
A common polymorphism in the MTHFD1 gene is a modulator of risk of congenital heart disease
Martin Petkovšek, Andrej Kržan, Alenka Šmid, Ema Žagar, Mojca Zupanc:
Degradation of water soluble poly(vinyl alcohol) with acoustic and hydrodynamic cavitation
Dunja Urbančič, Flaka Pasha, Alenka Šmid, Irena Mlinarič-Raščan:
Personalization of thiopurine therapy
Nataša Karas Kuželički, Alenka Šmid, Maša Vidmar, Tina Kek, Andreja Eberlinc, Borut Geršak, Uroš Mazić, Irena Mlinarič-Raščan, Ksenija Geršak:
Higher incidence of common polymorphisms in the genes of folate and methionine cycles in children with orofacial clefs and congenital heart defects compared to their unaffected siblings