eNauka - pregled
Pregled prema Autor Bartsakoulia, Marina
Prikaz rezultata 1 do 5 od 5
| Godina | Naslov | Autor(i) | Tip rezultata | Mp-kat. |
|---|---|---|---|---|
| 2012 | A novel KLF1 gene promoter variant (g.-148 g gt a) is associated with hereditary persistence of fetal hemoglobin | Radmilović, M.   ; Zukić, Branka ; Stojiljković, Maja ; Kotur, Nikola ; Stanković, Biljana ; Karan-Đurašević, Teodora ; Dokmanović, Lidija ; Bartsakoulia, Marina; Georgitsi, M.; Hatzimichael, E.;
Koutsouka, F.; Briasoulis, E.; Patrinos, G.; Pavlović, Sonja
; | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2012 | A Novel Klf1 Gene Promoter Variant (G.-148 G > A) Is Associated with Hereditary Persistence of Fetal Hemoglobin | Radmilovic, Milena M; Zukic, Branka ; Stojiljkovic-Petrovic, Maja M; Kotur, Nikola M ; Stankovic, Biljana B ; Klaassen, Kristel M ; Dokmanovic, Lidija B ; Bartsakoulia, Marina; Georgitsi, Marianthi; Hatzimichael, E;
Koutsouka, F; Briasoulis, E; Partinos, George P; Pavlovic, Sonja T;
| Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2013 | Functional analysis of a novel KLF1 gene promoter variation associated with hereditary persistence of fetal hemoglobin | Radmilović Milena ; Zukić, Branka ; Stojiljković, Maja ; Bartsakoulia, Marina; Stanković, Biljana ; Kotur, Nikola ; Dokmanović, Lidija ; Georgitsi, Marianthi; Patrinos, George P.; Pavlović, Sonja | Naučni članak | 22M22 - Međunarodni časopis kategorije M22 |
| 2013 | Genomic variation in the MAP3K5 gene is associated with beta-thalassemia disease severity and hydroxyurea treatment efficacy | Tafrali, Christina; Paizi, Arsinoi; Borg, Joseph; Radmilović Milena ; Bartsakoulia, Marina; Giannopoulou, Emily; Giannakopoulou, Olga; Stojiljković, Maja ; Zukić, Branka ; Poulas, Konstantinos;
Stavrou, Eleana F; Lambropoulou, Polyxeni; Kourakli, Alexandra; Felice, Alexander E; Papachatzopoulou, Adamantia; Philipsen, Sjaak; Pavlović, Sonja
; Georgitsi, Marianthi; Patrinos, George P; | Naučni članak | 21M21 - Vodeći međunarodni časopis kategorije M21 |
| 2014 | Truncating and Missense Mutations in IGHMBP2 Cause Charcot-Marie Tooth Disease Type 2 | Cottenie, Ellen; Kochanski, Andrzej; Jordanova, Albena; Bansagi, Boglarka; Zimon, Magdalena; Horga, Alejandro; Jaunmuktane, Zane; Saveri, Paola; Milić-Rašić, Vedrana ; Baets, Jonathan;
Bartsakoulia, Marina; Ploski, Rafal; Teterycz, Pawel; Nikolić, Miloš
; Quinlivan, Ros; Laura, Matilde; Sweeney, Mary G.; Taroni, Franco; Lunn, Michael P.; Moroni, Isabella; Gonzalez, Michael; Hanna, Michael G.; Bettencourt, Conceicao; Chabrol, Elodie; Franke, Andre; von Au, Katja; Schilhabel, Markus; Kabzińska, Dagmara; Hausmanowa-Petrusewicz, Irena; Brandner, Sebastian; Lim, Siew Choo; Song, Haiwei; Choi, Byung-Ok; Horvath, Rita; Chung, Ki-Wha; Zuchner, Stephan; Pareyson, Davide; Harms, Matthew; Reilly, Mary M.; Houlden, Henry; | Naučni članak | 21a+M21a+ - Vodeći međunarodni časopis kategorije M21a+ |