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IMAGINE - Репозиторијум Института за молекуларну генетику и генетичко инжењерство
Институт за молекуларну генетику и генетичко инжењерство
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Преглед наслова
IMAGINE
Institut za molekularnu genetiku i genetičko inženjerstvo
Grupa za istraživanje retkih bolesti i razvoj terapeutika 02
Преглед наслова
IMAGINE
Institut za molekularnu genetiku i genetičko inženjerstvo
Grupa za istraživanje retkih bolesti i razvoj terapeutika 02
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Наслови
Assessment of Small Cellular Particles from Four Different Natural Sources and Liposomes by Interferometric Light Microscopy
[1]
Autologous Platelet and Extracellular Vesicle-Rich Plasma as Therapeutic Fluid: A Review
[1]
Can Pharmacogenetic Variants in TPMT, MTHFR and SLCO1B1 Genes Be Used as Potential Markers of Outcome Prediction in Systemic Sclerosis Patients?
[1]
Characterization of Nanohybridosomes from Lipids and Spruce Homogenate Containing Extracellular Vesicles
[1]
Covid-19 disease severity associated with vitamin d related genetic Variants
[1]
Expression of BCL11A in chronic lymphocytic leukaemia
[1]
Expression Pattern and Prognostic Significance of the Long Non-Coding RNA Metastasis-Associated Lung Adenocarcinoma Transcript 1 in Chronic Lymphocytic Leukemia
[1]
Extracellular vesicles from blood plasma as mediators of anti-inflammatory effects, oxidative stress and angiogenesis in HUVEC
[1]
Functional characterization of novel variants in the dnai1 gene in a patient with primary ciliary dyskinesia
[1]
Genome sequence diversity of SARS-CoV-2 in Serbia: insights gained from a 3-year pandemic study
[1]
Germline Variants in Cancer Predisposition Genes in Pediatric Patients with Central Nervous System Tumors
[1]
High-risk population screening for fabry disease in patients with chronic renal failure of unknown etiology
[1]
Improving the diagnostics of rare lung disorders using a uniquely designed pipeline for analysis of ngs data
[1]
Molecular basis of thalassemia syndromes in Serbia: an update
[1]
Molecular Biomarkers in Perthes Disease: A Review
[1]
Molecular diagnosis of Fabry disease in patients with chronic renal failure of unknown etiology
[1]
PB2037: NEW TERT VARIANT IN A FAMILY WITH APLASTIC ANEMIA
[1]
PHENYLBUTYRIC ACID REDUCES MOLECULAR MARKERS OF ER STRESS-INDUCED APOPTOSIS IN GLYCOGEN STORAGE DISEASE TYPE IB IN VITRO MODEL SYSTEM
[1]
Small Cellular Particles from European Spruce Needle Homogenate
[1]
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach
[1]
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