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Molecules (Basel, Switzerland)|February 25, 2023
Efficient Separation of the Methoxyfuranocoumarins Peucedanin, 8-Methoxypeucedanin, and Bergapten by Centrifugal Partition Chromatography (CPC)Magdalena BartnikCurrent Issues in Molecular Biology|January 26, 2024
Methoxyfuranocoumarins of Natural Origin-Updating Biological Activity Research and Searching for New Directions-A ReviewMagdalena BartnikJournal of Chromatographic Science|July 26, 2015
Isolation of Methoxyfuranocoumarins From Ammi majus by Centrifugal Partition ChromatographyMagdalena Bartnik, Anna Katarzyna MazurekActa Poloniae Pharmaceutica|April 3, 2003
Essential oil from fruit of Peucedanum tauricum BiebMagdalena Bartnik, Kazimierz Głowniak, Marek MardarowiczJournal of Pediatric Hematology/Oncology|November 27, 2018
Prevalence and Risk Factors for Arterial Hypertension Development in Childhood Acute Lymphoblastic Leukemia SurvivorsTomasz Ociepa, Magdalena Bartnik, Karolina Zielezińska, et al.International Journal of Molecular Sciences|November 14, 2023
Evaluation of the Biological Effect of Non-UV-Activated Bergapten on Selected Human Tumor Cells and the Insight into the Molecular Mechanism of Its ActionMagdalena Bartnik, Adrianna Sławińska-Brych, Magdalena Mizerska-Kowalska, et al.American Journal of Medical Genetics. Part A|February 3, 2016
Novel 14q11.2 microduplication including the CHD8 and SUPT16H genes associated with developmental delayMarta Smyk, Anna Poluha, Ilona Jaszczuk, et al.Phytochemistry|March 18, 2005
Secondary metabolites of Peucedanum tauricum fruitsHailemichael Tesso, Wilfried A König, Karl-Heinz Kubeczka, et al.Hypertension Research : Official Journal of the Japanese Society of Hypertension|March 4, 2016
Abnormal correlation of circulating endothelial progenitor cells and endothelin-1 concentration may contribute to the development of arterial hypertension in childhood acute lymphoblastic leukemia survivorsTomasz Ociepa, Magdalena Bartnik, Karolina Zielezinska, et al.Genes|January 8, 2025
A Novel Pathogenic Sense Variant in Exon 7 of the HK1 Gene in a Patient with Hexokinase Deficiency and Gilbert SyndromeMagdalena Bartnik, Weronika Pawlik, Beata Burzyńska, et al.Pageof 5