Researchers
Ugrin, Milena
Type
Date issued
Results 81-89 of 89
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 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 | VNTR polymorphisms in tpmt gene promoter: potential tool for thiopurine-guided therapy | Radmilović, M. | Conference Paper | Mp. category will be shown later |
| 2010 | Thalassemia syndromes in Serbia: an update![]() | Radmilović Milena | Article | 23M23 |
| 2010 | Functional analysis of the role of the TPMT gene promoter VNTR polymorphism in TPMT gene transcription![]() | Zukić, Branka | 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 |
| 2009 | New transcriptional regulatory element within the intron of phenylalanine hydroxylase gene | Stojiljković, Maja | Conference Paper | Mp. category will be shown later |
| 2008 | Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and beta-thalassemia or Hb Sabine confirms the functional role of the A gamma-158 C gt T mutation in gamma-globin gene transcription | Kollia, Panagoula; Kalamaras, Angelos; Chassanidis, Christos; Samara, Maria; Vamvakopoulos, Nikolaos K.; Ugrin, Milena | Contribution to periodical | 22M22 |
| 2007 | Mutacije u PAH genu - osnova za populaciono-genetičko istraživanje | Stojiljković, Maja | Article | Mp. category will be shown later |
| 2007 | Elucidation of the origin of L48S PAH mutation in Serbian population | Stojiljković, Mojca; Stevanović, A.; Đorđević, M.; Petručev, Branka | Conference Paper | Mp. category will be shown later |
