Publications by authors named "Alexey Spiridonov"

Study Design: This was a prospective multicenter study.

Background: Adjacent segment degenerative disease (ASDd) is a common complication of open transforaminal lumbar interbody fusion (O-TLIF), the leading cause of which is initial adjacent segment degeneration (ASD). To date, various surgical techniques for the prevention of ASDd have been developed, such as, simultaneous use of interspinous stabilization (IS) and preventive rigid stabilization of the adjacent segment.

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The majority of mammalian genes produce multiple transcripts resulting from alternative splicing (AS) and/or alternative transcription initiation (ATI) and alternative transcription termination (ATT). Comparative analysis of the number of alternative nucleotides, isoforms, and introns per locus in genes with different types of alternative events suggests that ATI and ATT contribute to the diversity of human and mouse transcriptome even more than AS. There is a strong negative correlation between AS and ATI in 5' untranslated regions (UTRs) and AS in coding sequences (CDSs) but an even stronger positive correlation between AS in CDSs and ATT in 3' UTRs.

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Article Synopsis
  • Developing effective oligonucleotides for RNA interference (RNAi) is complex due to variable results and the need for significant computational support in building genome-wide RNAi libraries.
  • The authors introduce a quick and practical algorithm for designing short hairpin RNAs (shRNAs) by analyzing thousands of RNAi experiments, identifying key parameters, specifically terminal duplex asymmetry and duplex stability, that correlate with higher silencing efficiency.
  • Testing their predictions, the researchers designed 83 shRNAs demonstrating that slight adjustments in duplex stability can significantly impact silencing efficiency, achieving results comparable to the best existing prediction methods in RNAi design.
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Article Synopsis
  • Intronless genes in mammals are expressed at lower levels, are often tissue-specific, and evolve faster than intron-containing genes.
  • Both monomorphic spliced genes and polymorphic alternatively spliced genes exhibit similar expression and evolutionary patterns, indicating no major differences between them.
  • Alternative splicing is prevalent in ancient genes, while intronless genes are relatively newer, suggesting a connection between gene expression processes and the evolution of new tissue-specific functions.
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Catechol-O-methyltransferase (COMT) is an enzyme that plays a key role in the modulation of catechol-dependent functions such as cognition, cardiovascular function, and pain processing. Three common haplotypes of the human COMT gene, divergent in two synonymous and one nonsynonymous (val(158)met) position, designated as low (LPS), average (APS), and high pain sensitive (HPS), are associated with experimental pain sensitivity and risk of developing chronic musculoskeletal pain conditions. APS and HPS haplotypes produce significant functional effects, coding for 3- and 20-fold reductions in COMT enzymatic activity, respectively.

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Background: Small interfering RNAs (siRNAs) have become an important tool in cell and molecular biology. Reliable design of siRNA molecules is essential for the needs of large functional genomics projects.

Results: To improve the design of efficient siRNA molecules, we performed a comparative, thermodynamic and correlation analysis on a heterogeneous set of 653 siRNAs collected from the literature.

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Objective: Operation for aortic recoarctation and/or residual hypoplastic arch represents a surgical challenge because of surrounding scar tissue in the coarctation area, hazard of spinal cord ischemia due to aortic cross-clamping, laceration of the recurrent nerve, and the choice of the best approach. We demonstrate the results of 52 operations of an extra anatomically bypass technique via right thoracotomy approach without establishment of cardiopulmonary bypass.

Methods: Since 1987, 52 patients underwent extra anatomically positioned ascending-descending bypass grafting.

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Prokaryotic genomes are considered to be 'wall-to-wall' genomes, which consist largely of genes for proteins and structural RNAs, with only a small fraction of the genomic DNA allotted to intergenic regions, which are thought to typically contain regulatory signals. The majority of bacterial and archaeal genomes contain 6-14% non-coding DNA. Significant positive correlations were detected between the fraction of non-coding DNA and inter- and intra-operonic distances, suggesting that different classes of non-coding DNA evolve congruently.

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In overlapping genes, the same DNA sequence codes for two proteins using different reading frames. Analysis of overlapping genes can help in understanding the mode of evolution of a coding region from noncoding DNA. We identified 71 pairs of convergent genes, with overlapping 3' ends longer than 15 nucleotides, that are conserved in at least two prokaryotic genomes.

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