Search Results - "Danilov, Lavrentii G"
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Identification of New FG-Repeat Nucleoporins with Amyloid Properties
Published in International journal of molecular sciences (10-05-2023)“…Amyloids are fibrillar protein aggregates with a cross-β structure. More than two hundred different proteins with amyloid or amyloid-like properties are…”
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Gene Expression Analysis of Yeast Strains with a Nonsense Mutation in the eRF3-Coding Gene Highlights Possible Mechanisms of Adaptation
Published in International journal of molecular sciences (07-06-2024)“…In yeast , there are two translation termination factors, eRF1 (Sup45) and eRF3 (Sup35), which are essential for viability. Previous studies have revealed that…”
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Does Background Matter? A Comparative Characterization of Mouse Models of Autosomal Retinitis Pigmentosa rd1 and Pde6b-KO
Published in International journal of molecular sciences (06-12-2023)“…Many retinal degenerative diseases result in vision impairment or permanent blindness due to photoreceptor loss or dysfunction. It has been observed that Pde6b…”
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Clinical and Genetic Characteristics of Pediatric Patients with Hypophosphatasia in the Russian Population
Published in International journal of molecular sciences (26-10-2022)“…(1) Hypophosphatasia (HPP) is a rare inherited disease caused by mutations (pathogenic variants) in the ALPL gene which encodes tissue-nonspecific alkaline…”
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Processing of Fluorescent Proteins May Prevent Detection of Prion Particles in [ PSI + ] Cells
Published in Biology (Basel, Switzerland) (22-11-2022)“…Yeast is a convenient model for studying protein aggregation as it is known to propagate amyloid prions. [ ] is the prion form of the release factor eRF3…”
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Chromosome-level genome assembly and structural variant analysis of two laboratory yeast strains from the Peterhof Genetic Collection lineage
Published in G3 : genes - genomes - genetics (01-04-2021)“…Thousands of yeast genomes have been sequenced with both traditional and long-read technologies, and multiple observations about modes of genome evolution for…”
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Species-Specific Proteins in the Oviducts of Snail Sibling Species: Proteotranscriptomic Study of Littorina fabalis and L. obtusata
Published in Biology (Basel, Switzerland) (22-10-2021)“…Genus Littorina subgenus Neritrema (Mollusca, Caenogastropoda) includes the “obtusata” group of closely related species (Littorina obtusata and L. fabalis)…”
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Data on RNA-seq analysis of the oviducts of five closely related species genus Littorina (Mollusca, Caenogastropoda): L. saxatilis, L. arcana, L. compressa, L. obtusata, L. fabalis
Published in Data in brief (01-06-2022)“…In the evolution of invertebrates, the transition from egg-layers to brooders occurred many times. However, the molecular mechanisms underlying this transition…”
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The Human NUP58 Nucleoporin Can Form Amyloids In Vitro and In Vivo
Published in Biomedicines (13-10-2021)“…Amyloids are fibrillar protein aggregates with a cross-β structure and unusual features, including high resistance to detergent or protease treatment. More…”
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Evaluation of Gut Microbiota in Healthy Persons and Type 1 Diabetes Mellitus Patients in North-Western Russia
Published in Microorganisms (Basel) (01-07-2023)“…Bacterial microbiota in stool may vary over a wide range, depending on age, nutrition, etc. The purpose of our work was to discriminate phyla and genera of…”
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Design of a New [ PSI + ]-No-More Mutation in SUP35 With Strong Inhibitory Effect on the [ PSI + ] Prion Propagation
Published in Frontiers in molecular neuroscience (19-11-2019)“…A number of [ ]-no-more (PNM) mutations, eliminating [ ] prion, were previously described in . In this study, we designed and analyzed a new PNM mutation based…”
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De novo transcriptome assembly and annotation of parthenogenetic lizard Darevskia unisexualis and its parental ancestors Darevskia valentini and Darevskia raddei nairensis
Published in Data in brief (01-12-2021)“…Darevskia rock lizards include 29 sexual and seven parthenogenetic species of hybrid origin distributed in the Caucasus. All seven parthenogenetic species of…”
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The Benefits of Whole-Exome Sequencing in the Differential Diagnosis of Hypophosphatasia
Published in International journal of molecular sciences (01-11-2024)“…Hypophosphatasia (HPP) is a rare inherited disorder characterized by the decreased activity of tissue-nonspecific alkaline phosphatase (TNSALP), caused by…”
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The Telomeric Repeats of HHV-6A Do Not Determine the Chromosome into Which the Virus Is Integrated
Published in Genes (18-02-2023)“…Human herpes virus 6A (HHV-6A) is able to integrate into the telomeric and subtelomeric regions of human chromosomes representing chromosomally integrated…”
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