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Olga L. Kardymon

Researcher at Engelhardt Institute of Molecular Biology

Publications -  9
Citations -  863

Olga L. Kardymon is an academic researcher from Engelhardt Institute of Molecular Biology. The author has contributed to research in topics: Biology & Computer science. The author has an hindex of 3, co-authored 3 publications receiving 434 citations.

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ROS Generation and Antioxidant Defense Systems in Normal and Malignant Cells

TL;DR: This review covers the current data on the mechanisms of ROS generation and existing antioxidant systems balancing the redox state in mammalian cells that can also be related to tumors.
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Mitochondrial dysfunction and oxidative stress in aging and cancer

TL;DR: This review focuses on the similarities between ageing-associated and cancer-associated oxidative stress and mitochondrial dysfunction as their common phenotype and suggests that the oxidative stress as a cause and/or consequence of the mitochondrial dysfunction is one of the main drivers of these processes.
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The Dysregulation of Polyamine Metabolism in Colorectal Cancer Is Associated with Overexpression of c-Myc and C/EBPβ rather than Enterotoxigenic Bacteroides fragilis Infection

TL;DR: Two mediators of metabolic reprogramming, inflammation, and cell proliferation c-Myc and C/EBPβ may serve as regulators of polyamine metabolism genes (SMOX, AZIN1, MTAP, SRM, ODC1, AMD1, and AGMAT) as they are overexpressed in tumors, have binding site according to ENCODE ChIP-Seq data, and demonstrate strong coexpression with their targets.
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SEMA: Antigen B-cell conformational epitope prediction using deep transfer learning

TL;DR: The transfer learning approach using pretrained deep learning models was applied to develop a model that predicts conformational B-cell epitopes based on the primary antigen sequence and tertiary structure called SEMA, which can quantitatively rank the immunodominant regions within the RBD domain of SARS-CoV-2.
Posted ContentDOI

Cell type–specific interpretation of noncoding variants using deep learning–based methods

TL;DR: It is shown here that available epigenetic characteristics of human cell types are extremely sparse, limiting those approaches that rely on specific epigenetic input and proposing a new neural network architecture, DeepCT, which can learn complex interconnections of epigenetic features and infer unmeasured data from any available input.