Works by Illarioshkin, S. N.

Results: 27

Effects of the Pharmabiotic U-21 under Conditions of a Combined Neuroinflammatory Model of Parkinson's Disease in Rats.

Published in:

Bulletin of Experimental Biology & Medicine, 2024, v. 177, n. 2, p. 225, doi. 10.1007/s10517-024-06161-5

By:

Stavrovskaya, A. V.;
Voronkov, D. N.;
Marsova, M. V.;
Olshansky, A. S.;
Gushchina, A. S.;
Danilenko, V. N.;
Illarioshkin, S. N.

Publication type:

Article

C9orf72 Gene Expression in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.

Published in:

Bulletin of Experimental Biology & Medicine, 2020, v. 169, n. 5, p. 673, doi. 10.1007/s10517-020-04952-0

By:

Shpilyukova, Yu. A.;
Fedotova, E. Yu.;
Abramycheva, N. Yu.;
Kochergin, I. A.;
Zakroyshchikova, I. V.;
Zakharova, M. N.;
Illarioshkin, S. N.

Publication type:

Article

Effect of Mutations in SOD1 and C9orf72 Genes on Autophagy in Lymphomonocytes in Myotrophic Lateral Sclerosis.

Published in:

Bulletin of Experimental Biology & Medicine, 2019, v. 167, n. 5, p. 667, doi. 10.1007/s10517-019-04595-w

By:

Kochergin, I. A.;
Shpilyukova, Yu. A.;
Lysogorskaia, E. V.;
Abramycheva, N. Yu.;
Zakharova, M. N.;
Illarioshkin, S. N.

Publication type:

Article

Effect of Mutations in SOD1 and C9orf72 Genes on Autophagy in Lymphomonocytes in Myotrophic Lateral Sclerosis.

Published in:

Bulletin of Experimental Biology & Medicine, 2019, v. 166, n. 6, p. 667, doi. 10.1007/s10517-019-04595-w

By:

Kochergin, I. A.;
Shpilyukova, Yu. A.;
Lysogorskaia, E. V.;
Abramycheva, N. Yu.;
Zakharova, M. N.;
Illarioshkin, S. N.

Publication type:

Article

Cytogenetic Analysis of the Results of Genome Editing on the Cell Model of Parkinson’s Disease.

Published in:

Bulletin of Experimental Biology & Medicine, 2018, v. 165, n. 3, p. 378, doi. 10.1007/s10517-018-4174-y

By:

Vetchinova, A. S.;
Simonova, V. V.;
Novosadova, E. V.;
Manuilova, E. S.;
Nenasheva, V. V.;
Tarantul, V. Z.;
Grivennikov, I. A.;
Khaspekov, L. G.;
Illarioshkin, S. N.

Publication type:

Article

Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophy.

Published in:

Brain: A Journal of Neurology, 1996, v. 119, n. 6, p. 1895, doi. 10.1093/brain/119.6.1895

By:

Illarioshkin, S. N.;
Ivanova-Smolenskaya, I. A.;
Tanaka, H.;
Vereshchagin, N. V.;
Markova, E. D.;
Poleshchuk, V. V.;
Lozhnikova, S. M.;
Sukhorukov, V. S.;
Limborska, S. A.;
Slominsky, P. A.;
Bulayeva, K. B.;
Tsuji, S.

Publication type:

Article

Clinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan.

Published in:

2000

By:

Illarioshkin, Sergei N.;
Ivanova-Smolenskaya, Irina A.;
Rahmonov, Rahmatullo A.;
Markova, Elena D.;
Stevanin, Giovanni;
Brice, Alexis;
Illarioshkin, S N;
Ivanova-Smolenskaya, I A;
Rahmonov, R A;
Markova, E D;
Stevanin, G;
Brice, A

Publication type:

journal article

A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in Russia.

Published in:

European Journal of Neurology, 2007, v. 14, n. 4, p. 413, doi. 10.1111/j.1468-1331.2007.01685.x

By:

Illarioshkin, S. N.;
Shadrina, M. I.;
Slominsky, P. A.;
Bespalova, E. V.;
Zagorovskaya, T. B.;
Bagyeva, G. Kh.;
Markova, E. D.;
Limborska, S. A.;
Ivanova-Smolenskaya, I. A.

Publication type:

Article

Development of a Panel of Biomarkers for Differential Diagnosis of Multiple Sclerosis.

Published in:

Doklady Biochemistry & Biophysics, 2024, v. 519, n. 1, p. 593, doi. 10.1134/S160767292460060X

By:

Ovchinnikova, L. A.;
Dzhelad, S. S.;
Simaniv, T. O.;
Zakharova, M. N.;
Lomakin, Y. A.;
Gabibov, A. G.;
Illarioshkin, S. N.

Publication type:

Article

Genetic Diversity in Frontotemporal Dementia.

Published in:

Molecular Biology, 2020, v. 54, n. 1, p. 13, doi. 10.1134/S0026893320010136

By:

Shpilyukova, Yu. A.;
Fedotova, E. Yu.;
Illarioshkin, S. N.

Publication type:

Article

Rare Forms of Autosomal Recessive Spinocerebellar Ataxia Associated with Mutations in the ANO10 (ATX-ANO10) and SYNE1 (ATX-SYNE1) Genes.

Published in:

Neuroscience & Behavioral Physiology, 2025, v. 55, n. 1, p. 139, doi. 10.1007/s11055-025-01764-5

By:

Nuzhnyi, E. P.;
Protopopova, A. O.;
Abramycheva, N. Yu.;
Protsenko, A. R.;
Illarioshkin, S. N.

Publication type:

Article

Cerebellar Degeneration Associated with HIV Infection.

Published in:

Neuroscience & Behavioral Physiology, 2023, v. 53, n. 8, p. 1391, doi. 10.1007/s11055-023-01532-3

By:

Nuzhnyi, E. P.;
Brsikyan, L. A.;
Fedotova, E. Yu.;
Illarioshkin, S. N.

Publication type:

Article

Epigenetic Regulation of the Clinical Signs of Friedreich's Disease.

Published in:

Neuroscience & Behavioral Physiology, 2020, v. 50, n. 8, p. 1000, doi. 10.1007/s11055-020-00998-9

By:

Nuzhny, E. P.;
Abramycheva, N. Yu.;
Nikolaeva, N. S.;
Ershova, M. V.;
Klyushnikov, S. A.;
Illarioshkin, S. N.;
Fedotova, E. Yu.

Publication type:

Article

Interhemisphere Asymmetry in the Structure of the Hippocampus in Men.

Published in:

Neuroscience & Behavioral Physiology, 2018, v. 48, n. 7, p. 899, doi. 10.1007/s11055-018-0646-9

By:

Bogolepova, I. N.;
Illarioshkin, S. N.;
Sveshnikov, A. V.;
Lovchitskaya, A. O.

Publication type:

Article

Methylation of MAPT Gene in Neurodegenerative Synucleinopathies.

Published in:

Russian Journal of Genetics, 2022, v. 58, n. 5, p. 576, doi. 10.1134/S1022795422050118

By:

Iakovenko, E. V.;
Abramycheva, N. Yu.;
Fedotova, E. Yu.;
Illarioshkin, S. N.

Publication type:

Article

Massive Parallel Sequencing and the Problem of Overlapping Phenotypes in Hereditary Spastic Paraplegias and Spinocerebellar Ataxias.

Published in:

Russian Journal of Genetics, 2022, v. 58, n. 4, p. 456, doi. 10.1134/S1022795422040111

By:

Nuzhnyi, E. P.;
Abramycheva, N. Yu.;
Safonov, D. G.;
Fedotova, E. Yu.;
Illarioshkin, S. N.

Publication type:

Article

The Role of Mitochondrial DNA Individuality in the Pathogenesis of Parkinson's Disease.

Published in:

Russian Journal of Genetics, 2020, v. 56, n. 4, p. 402, doi. 10.1134/S1022795420040146

By:

Sukhorukov, V. S.;
Voronkova, A. S.;
Litvinova, N. A.;
Baranich, T. I.;
Illarioshkin, S. N.

Publication type:

Article

DNA Methylation in Neurodegenerative Diseases.

Published in:

Russian Journal of Genetics, 2019, v. 55, n. 3, p. 271, doi. 10.1134/S1022795419030062

By:

Fedotova, E. Yu.;
Illarioshkin, S. N.

Publication type:

Article

Parkinson's Disease–Associated Changes in the Expression of Neurotrophic Factors and their Receptors upon Neuronal Differentiation of Human Induced Pluripotent Stem Cells.

Published in:

Journal of Molecular Neuroscience, 2020, v. 70, n. 4, p. 514, doi. 10.1007/s12031-019-01450-5

By:

Novosadova, E. V.;
Nenasheva, V. V.;
Makarova, I. V.;
Dolotov, O. V.;
Inozemtseva, L. S.;
Arsenyeva, E. L.;
Chernyshenko, S. V.;
Sultanov, R. I.;
Illarioshkin, S. N.;
Grivennikov, I. A.;
Tarantul, V. Z.

Publication type:

Article

Molecular Genetic Analysis of Hereditary Neurodegenerative Diseases.

Published in:

Russian Journal of Genetics, 2004, v. 40, n. 6, p. 663, doi. 10.1023/B:RUGE.0000033314.49573.db

By:

Illarioshkin, S. N.;
Ivanova-Smolenskaya, I. A.;
Markova, E. D.;
Shadrina, M. I.;
Klyushnikov, S. A.;
Zagorovskaya, T. B.;
Miklina, N. I.;
Slominsky, P. A.;
Limborska, S. A.

Publication type:

Article

Thymoquinone as a Potential Neuroprotector in Acute and Chronic Forms of Cerebral Pathology.

Published in:

Biochemistry (00062979), 2020, v. 85, n. 2, p. 167, doi. 10.1134/S0006297920020042

By:

Isaev, N. K.;
Chetverikov, N. S.;
Stelmashook, E. V.;
Genrikhs, E. E.;
Khaspekov, L. G.;
Illarioshkin, S. N.

Publication type:

Article

The Use of Human Induced Pluripotent Stem Cells for Testing Neuroprotective Activity of Pharmacological Compounds.

Published in:

Biochemistry (00062979), 2019, v. 84, n. 11, p. 1296, doi. 10.1134/S0006297919110075

By:

Novosadova, E. V.;
Arsenyeva, E. L.;
Antonov, S. A.;
Vanyushina, Y. N.;
Malova, T. V.;
Komissarov, A. A.;
Illarioshkin, S. N.;
Khaspekov, L. G.;
Andreeva, L. A.;
Myasoedov, N. F.;
Tarantul, V. Z.;
Grivennikov, I. A.

Publication type:

Article

Expression and Functional Properties of NMDA and GABA<sub>A</sub> Receptors during Differentiation of Human Induced Pluripotent Stem Cells into Ventral Mesencephalic Neurons.

Published in:

Biochemistry (00062979), 2019, v. 84, n. 3, p. 310, doi. 10.1134/S0006297919030131

By:

Antonov, S. A.;
Novosadova, E. V.;
Kobylyansky, A. G.;
Illarioshkin, S. N.;
Tarantul, V. Z.;
Grivennikov, I. A.

Publication type:

Article

A Platform for Studying Neurodegeneration Mechanisms Using Genetically Encoded Biosensors.

Published in:

Biochemistry (00062979), 2019, v. 84, n. 3, p. 299, doi. 10.1134/S000629791903012X

By:

Ustyantseva, E. I.;
Medvedev, S. P.;
Vetchinova, A. S.;
Minina, J. M.;
Illarioshkin, S. N.;
Zakian, S. M.

Publication type:

Article

Genetic Association between Alzheimer’s Disease Risk Variant of the PICALM Gene and Auditory Event-Related Potentials in Aging.

Published in:

Biochemistry (00062979), 2018, v. 83, n. 9, p. 1075, doi. 10.1134/S0006297918090092

By:

Ponomareva, N. V.;
Andreeva, T. V.;
Protasova, M. A.;
Filippova, Yu. V.;
Kolesnikova, E. P.;
Fokin, V. F.;
Illarioshkin, S. N.;
Rogaev, E. I.

Publication type:

Article

Genome Editing and the Problem of Tetraploidy in Cell Modeling of the Genetic Form of Parkinsonism.

Published in:

Biochemistry (00062979), 2018, v. 83, n. 9, p. 1040, doi. 10.1134/S0006297918090055

By:

Simonova, V. V.;
Vetchinova, A. S.;
Novosadova, E. V.;
Khaspekov, L. G.;
Illarioshkin, S. N.

Publication type:

Article

Molecular Pathogenesis in Huntington’s Disease.

Published in:

Biochemistry (00062979), 2018, v. 83, n. 9, p. 1030, doi. 10.1134/S0006297918090043

By:

Illarioshkin, S. N.;
Klyushnikov, S. A.;
Vigont, V. A.;
Seliverstov, Yu. A.;
Kaznacheyeva, E. V.

Publication type:

Article