Publications by authors named "Alexander Bondar"

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The c.644 G > A p.(Trp215*) founder variant in the CLIC5 gene causes progressive autosomal recessive deafness 103 (DFNB103) in Eastern Siberia.
Vera G Pshennikova, Fedor M Teryutin, Tuyara V Borisova, Georgii P Romanov, Alexandra M Cherdonova, Alexander A Bondar

J Hum Genet· January 2026

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The Use of Heterologous Antigens for Biopanning Enables the Selection of Broadly Neutralizing Nanobodies Against SARS-CoV-2.
Vazirbek S Aripov, Anna V Zaykovskaya, Ludmila V Mechetina, Alexander M Najakshin, Alexander A Bondar

Antibodies (Basel)· March 2025

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Fast and Simple Protocol for N-Glycome Analysis of Human Blood Plasma Proteome.
Denis E Maslov, Anna N Timoshchuk, Alexander A Bondar, Maxim P Golubev, Anna G Soplenkova

Biomolecules· December 2024

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Phage Display Revealed the Complex Structure of the Epitope of the Monoclonal Antibody 10H10.
Daniil V Shanshin, Sophia S Borisevich, Olga N Shaprova, Valentina S Nesmeyanova, Alexander A Bondar

Int J Mol Sci· September 2024

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High prevalence of m.1555A > G in patients with hearing loss in the Baikal Lake region of Russia as a result of founder effect.
Tuyara V Borisova, Aleksandra M Cherdonova, Vera G Pshennikova, Fedor M Teryutin, Igor V Morozov, Alexander A Bondar

Sci Rep· July 2024

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Biochemical Properties of a Promising Milk-Clotting Enzyme, Moose () Recombinant Chymosin.
Dina V Balabova, Ekaterina A Belash, Svetlana V Belenkaya, Dmitry N Shcherbakov, Alexander N Belov, Alexander A Bondar

Foods· October 2023

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The (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia).
Vera G Pshennikova, Fedor M Teryutin, Alexandra M Cherdonova, Tuyara V Borisova, Aisen V Solovyev, Alexander A Bondar

Genes (Basel)· April 2023

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Can Modern Molecular Modeling Methods Help Find the Area of Potential Vulnerability of Flaviviruses?
Daniil V Shanshin, Sophia S Borisevich, Alexander A Bondar, Yuri B Porozov, Elena A Rukhlova

Int J Mol Sci· July 2022

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Different Rates of the -Related Hearing Loss in Two Indigenous Peoples of Southern Siberia (Russia).
Valeriia Yu Danilchenko, Marina V Zytsar, Ekaterina A Maslova, Marita S Bady-Khoo, Nikolay A Barashkov, Alexander A Bondar

Diagnostics (Basel)· December 2021

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Phage MD8: Genetic Mosaicism and Challenges of Taxonomic Classification of Lambdoid Bacteriophages.
Peter Evseev, Anna Lukianova, Nina Sykilinda, Anna Gorshkova, Alexander Bondar

Int J Mol Sci· September 2021

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Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene.
Nikolay A Barashkov, Fedor A Konovalov, Tuyara V Borisova, Fedor M Teryutin, Aisen V Solovyev, Alexander A Bondar

Eur J Hum Genet· June 2021

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High Rates of Three Common Mutations c.516G>C, c.-23+1G>A, c.235delC in Deaf Patients from Southern Siberia Are Due to the Founder Effect.
Marina V Zytsar, Marita S Bady-Khoo, Valeriia Yu Danilchenko, Ekaterina A Maslova, Nikolay A Barashkov, Alexander A Bondar

Genes (Basel)· July 2020

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A rare case of Waardenburg syndrome with unilateral hearing loss caused by nonsense variant c.772C>T (p.Arg259*) in the gene in Yakut patient from the Eastern Siberia (Sakha Republic, Russia).
Nikolay A Barashkov, Georgii P Romanov, Uigulaana P Borisova, Aisen V Solovyev, Vera G Pshennikova, Alexander A Bondar

Int J Circumpolar Health· December 2019

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Comparison of Predictive Tools on Missense Variants in , , and Genes Associated with Autosomal Recessive Deafness 1A (DFNB1A).
Vera G Pshennikova, Nikolay A Barashkov, Georgii P Romanov, Fedor M Teryutin, Aisen V Solov'ev, Alexander A Bondar

ScientificWorldJournal· September 2019

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Unique Mutational Spectrum of the Gene and its Pathogenic Contribution to Deafness in Tuvinians (Southern Siberia, Russia): A High Prevalence of Rare Variant c.516G>C (p.Trp172Cys).
Olga L Posukh, Marina V Zytsar, Marita S Bady-Khoo, Valeria Yu Danilchenko, Ekaterina A Maslova, Alexander A Bondar

Genes (Basel)· June 2019

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Prompt apoptotic response to high glucose in SGLT-expressing renal cells.
Linnéa M Nilsson, Liang Zhang, Alexander Bondar, Daniel Svensson, Annika Wernerson

Am J Physiol Renal Physiol· May 2019

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Benign Pleural Mesothelial Cells Have Higher Osmotic Water Permeability than Malignant Pleural Mesothelioma Cells and Differentially Respond to Hyperosmolality.
Liubov E Katkova, Galina S Baturina, Alexander A Bondar, Rajesh M Jagirdar, Chrissi Hatzoglou

Cell Physiol Biochem· April 2019

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A family of silicon transporter structural genes in a pennate diatom Synedra ulna subsp. danica (Kütz.) Skabitsch.
Artyom M Marchenkov, Darya P Petrova, Alexey A Morozov, Yulia R Zakharova, Michael A Grachev, Alexander A Bondar

PLoS One· February 2019

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Bioluminescent SNP genotyping technique: Development and application for detection of melanocortin 1 receptor gene polymorphisms.
Eugenia E Bashmakova, Vasilisa V Krasitskaya, Alexander A Bondar, Ekaterina N Eremina, Eugene V Slepov

Talanta· November 2018

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Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia.
Marina V Zytsar, Nikolay A Barashkov, Marita S Bady-Khoo, Olga A Shubina-Olejnik, Nina G Danilenko, Alexander A Bondar

BMC Med Genet· August 2018

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Regulation of Neuronal Na,K-ATPase by Extracellular Scaffolding Proteins.
Thomas Liebmann, Nicolas Fritz, Markus Kruusmägi, Linda Westin, Kristoffer Bernhem, Alexander Bondar

Int J Mol Sci· July 2018

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A novel pathogenic variant c.975G>A (p.Trp325*) in the POU3F4 gene in Yakut family (Eastern Siberia, Russia) with the X-linked deafness-2 (DFNX2).
Nikolay A Barashkov, Leonid A Klarov, Fedor M Teryutin, Aisen V Solovyev, Vera G Pshennikova, Alexander A Bondar

Int J Pediatr Otorhinolaryngol· January 2018

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Spectrum and Frequency of the GJB2 Gene Pathogenic Variants in a Large Cohort of Patients with Hearing Impairment Living in a Subarctic Region of Russia (the Sakha Republic).
Nikolay A Barashkov, Vera G Pshennikova, Olga L Posukh, Fedor M Teryutin, Aisen V Solovyev, Alexander A Bondar

PLoS One· July 2017

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Opinions of hearing parents about the causes of hearing impairment of their children with biallelic GJB2 mutations.
Aisen V Solovyev, Lilya U Dzhemileva, Olga L Posukh, Nikolay A Barashkov, Marita S Bady-Khoo, Alexander A Bondar

J Community Genet· July 2017

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AT-receptor response to non-saturating Ang-II concentrations is amplified by calcium channel blockers.
Kristoffer Bernhem, Kalaiselvan Krishnan, Alexander Bondar, Hjalmar Brismar, Anita Aperia

BMC Cardiovasc Disord· May 2017

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