Publications by authors named "Olga I Efimova"

Article Synopsis
  • Chromatin structure plays a crucial role in determining gene expression and cell identity, especially in neurons, through the action of polycomb group (PcG) proteins.
  • A study mapping the 3D genome in neuronal and non-neuronal cells from the Wernicke's area shows that neurons have less separation between active and inactive gene regions compared to other brain cells.
  • Neuronal cells display unique chromatin interactions, including a specific network of PcG contacts linked to genes that control development, with a distinct pattern of histone modifications that suggest a functional significance of these interactions for neuron identity.
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Background: Transcriptomic studies of the brains of schizophrenia (SZ) patients have produced abundant but largely inconsistent findings about the disorders pathophysiology. These inconsistencies might stem not only from the heterogeneous nature of the disorder, but also from the unbalanced focus on particular cortical regions and protein-coding genes. Compared to protein-coding transcripts, long intergenic non-coding RNA (lincRNA) display substantially greater brain region and disease response specificity, positioning them as prospective indicators of SZ-associated alterations.

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The present study focuses on the immobilization of the bacterial ribonuclease barnase (Bn) into submicron porous calcium carbonate (CaCO) particles. For encapsulation, we apply adsorption, freezing-induced loading and co-precipitation methods and study the effects of adsorption time, enzyme concentration and anionic polyelectrolytes on the encapsulation efficiency of Bn. We show that the use of negatively charged dextran sulfate (DS) and ribonucleic acid from yeast (RNA) increases the loading capacity (LC) of the enzyme on CaCO particles by about 3-fold as compared to the particles with Bn itself.

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Development of multimodal systems for therapy and diagnosis of neoplastic diseases is an unmet need in oncology. The possibility of simultaneous diagnostics, monitoring, and therapy of various diseases allows expanding the applicability of modern systems for drug delivery. We have developed hybrid particles based on biocompatible polymers containing magnetic nanoparticles (MNPs), photoacoustic (MNPs), fluorescent (Cy5 or Cy7 dyes), and therapeutic components (doxorubicin).

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