Researchers
Stojiljković, Maja
Results 121-138 of 138
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2012 | 6-mercaptopurine influences TPMT gene transcription in a TPMT gene promoter variable number of tandem repeats-dependent manner![]() | Kotur, Nikola | Article | 21M21 |
| 2011 | Clinical Applicability of Sequence Variations in Genes Related to Drug Metabolism | Stojiljković, Maja | Article | 21aM21a |
| 2011 | Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach![]() | Giardine, Belinda; Borg, Joseph; Higgs, Douglas R; Peterson, Kenneth R; Philipsen, Sjaak; Maglott, Donna; Singleton, Belinda K; Anstee, David J; Basak, A Nazli; Clark, Barnaby;
Costa, Flavia C; Faustino, Paula; Fedosyuk, Halyna; Felice, Alex E; Francina, Alain; Galanello, Renzo; Gallivan, Monica V E; Georgitsi, Marianthi; Gibbons, Richard J; Giordano, Piero C; Harteveld, Cornelis L; Hoyer, James D; Jarvis, Martin; Joly, Philippe; Kanavakis, Emmanuel; Kollia, Panagoula; Menzel, Stephan; Miller, Webb; Moradkhani, Kamran; Old, John; Papachatzopoulou, Adamantia; Papadakis, Manoussos N; Papadopoulos, Petros; Pavlović, Sonja
| Article | 21a+M21a+ |
| 2010 | Uloga sistema FasR/FasL u patogenezi mijeloproliferativnih neoplazija | Spasovski, Vesna | Article | 23M23 |
| 2010 | Functional analysis of the role of the TPMT gene promoter VNTR polymorphism in TPMT gene transcription![]() | Zukić, Branka | Article | 21M21 |
| 2010 | Novel transcriptional regulatory element in the phenylalanine hydroxylase gene intron 8 | Stojiljković, Maja | Article | 21M21 |
| 2010 | Pku mutation update and assessment of the potential benefit from BH4 supplementation therapy in Serbia | Stojiljković, Maja | Conference Paper | Mp. category will be shown later |
| 2010 | Thalassemia syndromes in Serbia: an update![]() | Radmilović Milena | Article | 23M23 |
| 2010 | VNTR polymorphisms in tpmt gene promoter: potential tool for thiopurine-guided therapy | Radmilović, M. | Conference Paper | Mp. category will be shown later |
| 2009 | New transcriptional regulatory element within the intron of phenylalanine hydroxylase gene | Stojiljković, Maja | Conference Paper | Mp. category will be shown later |
| 2009 | The Missense p.S231F Phenylalanine Hydroxylase Gene Mutation Causes Complete Loss of Enzymatic Activity In Vitro | Stojiljković, Maja | Article | 23M23 |
| 2009 | Molekularna dijagnoza fenilketonurije - od promena u proteinu do mutacija u genu | Pavlović, Sonja | Conference Paper | Mp. category will be shown later |
| 2009 | Acute myeloid leukemia with NUP98-HOXC13 fusion and FLT3 internal tandem duplication mutation: case report and literature review | Tošić, Nataša | Article | 22M22 |
| 2009 | Molecular characterization of rare translocation t(11;12)(pis;q13) generating nup98-hoxc13 fusion in the case of de novo flt3-itd positive acute myeloid leukemia | Pavlović, Sonja | Conference Paper | Mp. category will be shown later |
| 2008 | Functional analysis and phenotypic outcome of S231F mutation in phenylalanine hydroxylase gene | Stojiljković, Maja | Conference Paper | Mp. category will be shown later |
| 2007 | Molecular and phenotypic characteristics of patients with phenylketonuria in Serbia and Montenegro | Stojiljković, Maja | Conference Paper | Mp. category will be shown later |
| 2007 | Mutacije u PAH genu - osnova za populaciono-genetičko istraživanje | Stojiljković, Maja | Article | Mp. category will be shown later |
| 2006 | Molekularna dijagnostika strukturnih hromozomskih aberacija u leukemijama | Pavlović, Sonja | Article | Mp. category will be shown later |
