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Annals of Clinical and Laboratory Science|May 16, 2012
Reversal of FLT3 mutational status and sustained expression of NPM1 mutation in paired presentation, and relapse samples in a patient with acute myeloid leukemiaMilica Radojkovic, Natasa Tosic, Natasa Colovic, et al.Journal of Thoracic Disease|January 15, 2021
Correlation of genomic alterations and PD-L1 expression in thymomaDragana Jovanovic, Jelena Markovic, Vesna Ceriman, et al.Genes|March 6, 2019
Pharmacogenomic and Pharmacotranscriptomic Profiling of Childhood Acute Lymphoblastic Leukemia: Paving the Way to Personalized TreatmentSonja Pavlovic, Nikola Kotur, Biljana Stankovic, et al.Journal of Child Neurology|July 11, 2007
Arterial ischemic stroke in a child with beta-thalassemia trait and methylentetrahydrofolate reductase mutationVesna Brankovic-Sreckovic, Vedrana Milic Rasic, Valentina Djordjevic, et al.Genes|September 28, 2021
Machine Learning Modeling from Omics Data as Prospective Tool for Improvement of Inflammatory Bowel Disease Diagnosis and Clinical ClassificationsBiljana Stankovic, Nikola Kotur, Gordana Nikcevic, et al.Journal of Clinical Medicine|July 13, 2024
Seven-Year Longitudinal Study: Clinical Evaluation of Knee Osteoarthritic Patients Treated with Mesenchymal Stem CellsDusko Spasovski, Vesna Spasovski, Zoran Bascarevic, et al.The Protein Journal|July 25, 2009
The Missense p.S231F phenylalanine hydroxylase gene mutation causes complete loss of enzymatic activity in vitroMaja Stojiljkovic, Belén Pérez, Lourdes R Desviat, et al.Life (Basel, Switzerland)|November 11, 2022
Diagnostic and Therapeutic Implications of Long Non-Coding RNAs in LeukemiaVladimir Gasic, Teodora Karan-Djurasevic, Djordje Pavlovic, et al.Therapeutic Drug Monitoring|December 14, 2006
Analysis of thiopurine S-methyltransferase polymorphism in the population of Serbia and Montenegro and mercaptopurine therapy tolerance in childhood acute lymphoblastic leukemiaLidija Dokmanovic, Jelena Urosevic, Dragana Janic, et al.International Journal of Molecular Sciences|August 27, 2021
Identification and Classification of Novel Genetic Variants: En Route to the Diagnosis of Primary Ciliary DyskinesiaNina Stevanovic, Anita Skakic, Predrag Minic, et al.Pageof 14