Grupa za molekularnu biomedicinu
Најновије
-
Molecular profiling of rare thymoma using next-generation sequencing: meta-analysis
(Radiology and OncologyRadiology and Oncologythymomanext-generation sequencing (NGS)SNVs/InDelsmeta-analysis, 2023) -
A Comparison of MGMT Testing by MSP and qMSP in Paired Snap-Frozen and Formalin-Fixed Paraffin-Embedded Gliomas
(DiagnosticsDiagnostics, 2023) -
High-risk population screening for fabry disease in patients with chronic renal failure of unknown etiology
(Sarajevo : Institute for Genetic Engineering and Biotechnology, University of Sarajevo, 2023) -
The pharmacogenomics of vincristine-induced peripheral neuropathy in pediatric acute lymphoblastic leukemia patients in Serbia
(Sarajevo : Institute for Genetic Engineering and Biotechnology, University of Sarajevo, 2023) -
Pharmacogenomics and pharmacotranscriptomics of acute leukemia in children: a path to personalized medicine
(Sarajevo : Institute for Genetic Engineering and Biotechnology, University of Sarajevo, 2023) -
Covid-19 disease severity associated with vitamin d related genetic Variants
(Sarajevo : Institute for Genetic Engineering and Biotechnology, University of Sarajevo, 2023) -
Can Pharmacogenetic Variants in TPMT, MTHFR and SLCO1B1 Genes Be Used as Potential Markers of Outcome Prediction in Systemic Sclerosis Patients?
(International Journal of Molecular SciencesInternational Journal of Molecular Sciences, 2023) -
Signifi cance of molecular diagnosti cs in therapy of chronic lymphocytic leukemia
(Belgrade : Serbian Association on for Cancer Research, 2023) -
Improving the diagnostics of rare lung disorders using a uniquely designed pipeline for analysis of ngs data
(Sarajevo : Institute for Genetic Engineering and Biotechnology, University of Sarajevo, 2023) -
Genomics as a basis for precision medicine
(Sarajevo : Institute for Genetic Engineering and Biotechnology, University of Sarajevo, 2023) -
Pediatric acute myeloid leukemia: Insight into genetic landscape and novel targeted approaches
(Biochemical Pharmacology, 2023) -
PB2037: NEW TERT VARIANT IN A FAMILY WITH APLASTIC ANEMIA
(HemaSphere, 2023) -
Rare case of myelodysplastic syndrome with near-tetraploidy and TP53 mutation / Мијелодиспластични синдром са приближном тетраплоидијом удруженом са мутацијом гена TP53 – редак случај
(Srpski arhiv za celokupno lekarstvo, 2023) -
Micronutrients, genetics and COVID-19
(Current Opinion in Clinical Nutrition & Metabolic CareCurrent Opinion in Clinical Nutrition & Metabolic Care, 2023) -
Molecular basis of thalassemia syndromes in Serbia: an update
(Institute of Molecular Genetics and Genetic Engineering (IMGGE), University of Belgrade, 2023) -
Hybridosomes from spruce needle homogenate
(Serbian Society for Extracellular Vesicles (SrbEVs), Austrian Society for Extracellular Vesicles (ASEV), Hungarian Society for Extracellular Vesicles (HSEV), Slovenian Network for Extracellular Vesicles (SiN-EV), 2023)