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Pregled prema Autor Kolić, Ivana

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GodinaNaslovAutor(i)Tip rezultataMp-kat.
2024A preliminary study of the miRNA restitution effect on CNV-induced miRNA downregulation in CAKUTMitrović, Kristina  ; Životić, Ivan  ; Kolić, Ivana  ; Žakula, Jelena  ; Živković, Maja  ; Stanković, Aleksandra  ; Jovanović, Ivan  Naučni članak
21M21 - Vodeći međunarodni časopis kategorije M21
2022Are miR-548 family members potential genetic drivers of CAKUTMitrović, Kristina  ; Kolić, Ivana  ; Životić, Ivan  ; Filipović Tričković, Jelena G.  ; Đorđević, Ana  ; Živković, Maja  ; Stanković, Aleksandra  ; Jovanović, Ivan G.  Konferencijski rad
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2022Assessing the burden of rare CNVs on miRNA genes in CAKUTKolić, Ivana  ; Mitrović, Kristina  ; Životić, Ivan  ; Đorđević, Ana  ; Filipović-Tričković, Jelena  ; Živković, Maja  ; Stanković, Aleksandra  ; Jovanović, Ivan  Konferencijski rad
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2019Association of ACE I/D, AGTR1 +1166A/C and AGTR2 -1332A/G gene variants with autonomous nervous system function in Serbian syncope patientsKolić, Ivana Z.  ; Životić, Ivan R.  ; Đurić, Tamara M.  ; Živković, Maja D.  ; Alavantić, Dragan  ; Jovanović, Dušica; Milovanović, Branislav M.  ; Stanković, Aleksandra D.  Konferencijski rad
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2017Association of allelic variant rs1137101 in LEPR gene with susceptibility and clinical course of multiple sclerosis, Preliminary resultsKolić, Ivana Z.  ; Stojković, Ljiljana S.  ; Živković, Maja D.  ; Dincic Evica; Alavantić, Dragan R.  ; Stanković, Aleksandra D.  Konferencijski rad
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2018Association of angiotensin-converting enzyme I/D gene variant rs1799752 and autonomic dysfunction with cardiovascular profile in syncope patientsGligorijevic Tatjana; Kolić, Ivana Z.  ; Živković, Maja D.  ; Milovanovic Branislav; Hinic S; Stanković, Aleksandra D.  Konferencijski rad
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2025Association of TGFB1 and IFNB1 expression levels in peripheral blood mononuclear cells with multiple sclerosis with respect to proximal rs1800469 and rs2275888 eQTLsŽivotić, Ivan  ; Kolić, Ivana  ; Stefanović, Milan  ; Stefanović Mačak, Nataša; Dinčić, Evica; Stanković, Aleksandra  ; Živković, Maja  Article
22M22
2016Association study of dopamine β-hydroxyIase (DBH) gene variants -1021C/T (rs1611115) and DBH5-I/D with cardiovascular profiles in vasovagal syncope (VVS) patientsKolić, Ivana  ; Životić, Ivan  ; Milovanović, Branislav  ; Đurić-Delić, Tamara  ; Živković, Maja  ; Stanković, Aleksandra  Conference Paper
Mp. category will be shown later
2021Association study of rs7799039, rs1137101 and rs8192678 gene variants with disease susceptibility/severity and corresponding LEP, LEPR and PGC1A gene expression in multiple sclerosisKolić, Ivana  ; Stojković, Ljiljana S.  ; Stanković, Aleksandra  ; Stefanović, Milan  ; Dinčić, Evica; Živković, Maja  Article
21M21
2024Cargo of circulating extracellular vesicles regulates CDKN1A gene expression according to the MS disease severityJovanović, Ivan; Seke, Mariana  ; Kolić, Ivana  ; Filipović Tričković, Jelena  ; Dinčić, Evica; Stanković, Aleksandra  ; Živković, Maja  Conference Paper
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2024Copy number variation analysis identifies MIR9-3 and MIR1299 as novel miRNA candidate genes for CAKUTŽivotić, Ivan  ; Kolić, Ivana  ; Cvetković, Mirjana; Spasojević-Dimitrijeva, Brankica; Živković, Maja  ; Stanković, Aleksandra  ; Jovanović, Ivan  Article
21M21
2024Endogenous IFNb1 mRNA level associates with the course of multiple sclerosisŽivotić, Ivan  ; Kolić, Ivana  ; Stefanović, Milan  ; Stojković, Ljiljana  ; Dinčić, Evica; Đurić, Tamara  ; Živković, Maja  Conference Paper
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2020Expression of LEP, LEPR and PGC1A genes is altered in peripheral blood mononuclear cells of patients with relapsing-remitting multiple sclerosisKolić, Ivana  ; Stojković, Ljiljana S.  ; Dinčić, Evica; Jovanović, Ivan G.  ; Stanković, Aleksandra  ; Živković, Maja  Article
22M22
2014Genetic polymorphism SCN5A-H558R as potential target for future therapies of trafficking defect associated with cardiac sodium channel mutations: S216L, V1951L and R282HStanković, Aleksandra  ; Kolić, Ivana  ; Živković, Maja  Conference Paper
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2022Identification and functional interpretation of miRNAs affected by rare CNVs in CAKUTMitrović, Kristina  ; Životić, Ivan  ; Kolić, Ivana  ; Đorđević, Ana  ; Žakula, Jelena  ; Filipović Tričković, Jelena G.  ; Živković, Maja  ; Stanković, Aleksandra  ; Jovanović, Ivan G.  Article
21aM21a
2023Identification of micro RNA from common copy number variants as risk factors for CAKUTŽivotić, Ivan  ; Mitrović, Kristina  ; Kolić, Ivana  ; Seke, Mariana  ; Živković, Maja  ; Stanković, Aleksandra  ; Jovanović, Ivan  Conference Paper
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2017Insulin resistance in drug naive patients with multiple sclerosisKostić, Smiljana  ; Kolić, Ivana  ; Raičević, Ranko  ; Stojanović, Zvezdana  ; Kostić, Dejan  ; Dinčić, Evica  Article
23M23
2018Leptin receptor gene variant rs1137101 is associated with multiple sclerosis onset ageKolić, Ivana Z.  ; Živković, Maja D.  ; Stanković, Aleksandra D.  ; Dincic Evica; Alavantić, Dragan R.  ; Stojković, Ljiljana S.  Conference Paper
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2019Leptin receptor gene variant rs1137101 is associated with multiple sclerosis onset ageKolic, Ivana Z  ; Zivkovic, Maja D  ; Stankovic, Aleksandra D  ; Dincic, Evica R; Alavantic, Dragan  ; Stojkovic, Ljiljana  Conference Paper
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2023Leptin signalling genetic variants and insulin resistance in multiple sclerosis patientsŽivković, Maja  ; Kostić, Smiljana; Stojković, Ljiljana  ; Kolić, Ivana  ; Stanković, Aleksandra  ; Dinčić, EvicaConference Paper
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