Search Results - "SCHWARZMAN, A. L"
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Screening for LRRK2 mutations in patients with Parkinson's disease in Russia: identification of a novel LRRK2 variant
Published in European journal of neurology (01-07-2008)“…Background and purpose: Mutations in LRRK2, encoding leucine‐rich repeat kinase 2 (or Dardarin), cause autosomal dominant Parkinson's disease (AdPD) and are…”
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Dendrimer D5 is a Vector for Peptide Transport to Brain Cells
Published in Bulletin of experimental biology and medicine (01-02-2011)“…Dendrimers are a new class of nonviral vectors for gene or drug transport. Dendrimer capacity to penetrate through the blood-brain barrier remaines little…”
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Modern genetic approaches to searching for targets for medicinal preparations
Published in Russian journal of genetics (01-07-2009)“…In spite of a vast number of drug preparations used in medicine, advances in treating most socially important human diseases remain modest. Historically, many…”
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Transthyretin Sequesters Amyloid β Protein and Prevents Amyloid Formation
Published in Proceedings of the National Academy of Sciences - PNAS (30-08-1994)“…The cardinal pathological features of Alzheimer disease are depositions of aggregated amyloid β protein (Aβ) in the brain and cerebrovasculature. However, the…”
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Transmission of pathogenic protein aggregates in Alzheimer’s disease
Published in Molecular biology (New York) (01-05-2017)“…Deposits of amyloid peptide Aβ and intracellular aggregates of hyperphosphorylated tau protein in the brain of patients are major neuropathological features of…”
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Prion Properties of Alpha-Synuclein
Published in Molecular biology (New York) (01-05-2019)“…— The prion properties of alpha-synuclein, a key aggregating protein involved in the pathogenesis of so-called synucleinopathies, including Parkinson’s disease…”
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High Level of α-Synuclein mRNA in Peripheral Lymphocytes of Patients with Alcohol Dependence Syndrome
Published in Bulletin of experimental biology and medicine (01-11-2008)“…The content of mRNA for α-synuclein (a key protein of the dopaminergic system) was elevated in the peripheral lymphocytes of patients with alcohol dependence…”
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Reduced Content of α-Synuclein in Peripheral Blood Leukocytes of Patients with LRRK2-Associated Parkinson’s Disease
Published in Bulletin of experimental biology and medicine (01-04-2011)“…Measurement of α-synuclein level in the peripheral blood was proposed as a diagnostic test for Parkinson’s disease. However, the results of these studies…”
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Role of the ABC transporters A1 and G1, key reverse cholesterol transport proteins, in atherosclerosis
Published in Molecular biology (New York) (01-03-2016)“…Atherosclerosis is one of the most common causes of death worldwide. Epidemiology studies firmly established an inverse relationship between atherogenesis and…”
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Studying the pathogenesis of Alzheimer's disease in a Drosophila melanogaster model: Human APP overexpression in the brain of transgenic flies leads to deficit of the synaptic protein synaptotagmin
Published in Russian journal of genetics (2009)“…Alzheimer's disease (AD) is a progressive neurodegenerative disease whose main pathomorphological sign is synapse degeneration in the cortex and hippocampus…”
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Endogenous Presenilin 1 Redistributes to the Surface of Lamellipodia upon Adhesion of Jurkat Cells to a Collagen Matrix
Published in Proceedings of the National Academy of Sciences - PNAS (06-07-1999)“…Most familial early-onset Alzheimer's disease cases are caused by mutations in the presenilin 1 (PS1) gene. Subcellular localization of the endogenous PS1 is…”
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Expression of human amyloid precursor protein in Drosophila melanogaster nerve cells causes a decrease in presynaptic gene mRNA levels
Published in Genetics and molecular research (10-08-2015)“…Amyloid precursor protein (APP) is a key player in Alzheimer's disease. The proteolytic cleavage of APP results in various short peptide fragments including…”
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Genetic variants of platelet ADP receptor P2Y12 associated with changed platelet functional activity and development of cardiovascular diseases
Published in Russian journal of genetics (01-02-2009)“…The key role in platelet aggregation is played by the platelet ADP receptor P2Y12, which is the target for antiaggregant drugs, clopidogrel and ticlopidine. At…”
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Protein transduction domain peptide mediates delivery to the brain via the blood-brain barrier in Drosophila melanogaster
Published in Biochemistry (Moscow). Supplement. Series B, Biomedical chemistry (01-06-2009)“…The phenomenon of protein transduction represents internalization of short peptides known as protein transduction domains (PTD) by cells. It is widely used in…”
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Association of polymorphisms in apolipoprotein A-I gene with plasma lipid profile in population of Saint-Petersburg
Published in Uchenye zapiski (Sankt-Peterburgskiĭ gosudarstvennyĭ medit͡s︡inskiĭ universitet im. akad. I.P. Pavlova) (30-03-2014)“…Apolipoprotein A-I is a key structure protein of antiatherogenic high density lipoproteins (HDL). The aim of the study was to investigate the relationship…”
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Human APP gene expression in nerve cells of Drosophila melanogaster causes alteration of synaptoptagmin 1 mRNA level
Published in Doklady. Biochemistry and biophysics (01-02-2012)“…According to the amyloid cascade hypothesis, hereditary forms of Alzheimer's disease (AD), caused by mutations in the amyloid peptide precursor (APP) gene,…”
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The study of the neuroprotective activity of the apolipoprotein E peptide mimetic Cog1410 in transgenic strains of Drosophila melanogaster
Published in Biochemistry (Moscow). Supplement. Series B, Biomedical chemistry (2014)“…The neuroprotective activity of peptide mimetic of apolipoprotein E (apoE) Cog1410, containing the amino acid sequence of the apoE receptor-binding domain, has…”
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ABCA1 gene expression in peripheral blood lymphocytes and macrophages in patients with atherosclerosis
Published in Molecular biology (New York) (01-04-2011)“…ABCA1 transporter is known to play an important role in cholesterol transport from peripheral tissues. However, its contribution to atherosclerosis development…”
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Ceruloplasmin gene defect associated with epilepsy in EL mice
Published in Nature genetics (01-04-1994)“…Epilepsy is a dominant trait in EL mice, a model for human complex partial seizures. We recently mapped the major gene, El-1, to chromosome 9 near the…”
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De novo mutation within the intron-exon junction in the PiZ allele of the alpha-1-antitrypsin gene
Published in Human genetics (01-09-1992)“…A proband homozygous for the PiZ allele of the alpha-1-antitrypsin gene was found to be a heterozygous carrier of the additional nucleotide substitution (C-T)…”
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