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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
Sporadic ALS associated with the D90A Cu,Zn superoxide dismutase mutation in Russia.
Published in:
European Journal of Neurology, 2001, v. 8, n. 2, p. 167, doi. 10.1046/j.1468-1331.2001.00186.x
By:
- Skvortsova, V. I;
- Limborska, S. A;
- Slominsky, P. A;
- Levitskaya, N. I;
- Levitsky, G. N;
- Shadrina, M. I;
- Kondratyeva, E. A
Publication type:
Article
Transcriptomic response of rat hippocampus and spleen cells to single and chronic administration of the peptide selank.
Published in:
Doklady Biochemistry & Biophysics, 2010, v. 430, n. 1, p. 5, doi. 10.1134/S1607672910010023
By:
- Kolomin, T. A.;
- Shadrina, M. I.;
- Agniullin, Ya. V.;
- Shram, S. I.;
- Slominskii, P. A.;
- Limborska, S. A.;
- Myasoedov, N. F.
Publication type:
Article
Expression changes caused by the peptide semax in the intracellular signal pathway genes in rat hippocamp.
Published in:
Doklady Biochemistry & Biophysics, 2007, v. 417, n. 1, p. 334, doi. 10.1134/S1607672907060129
By:
- Agapova, T. Yu.;
- Agniullin, Ya. V.;
- Silachev, D. N.;
- Shadrina, M. I.;
- Slominsky, P. A.;
- Shram, S. I.;
- Limborskaya, S. A.;
- Myasoedov, N. F.
Publication type:
Article
Possible Involvement of Genes Related to Lysosomal Storage Disorders in the Pathogenesis of Parkinson's Disease.
Published in:
Molecular Biology, 2019, v. 53, n. 1, p. 24, doi. 10.1134/S002689331901014X
By:
- Rudenok, M. M.;
- Alieva, A. Kh.;
- Nikolaev, M. A.;
- Kolacheva, A. A.;
- Ugryumov, M. V.;
- Pchelina, S. N.;
- Slominsky, P. A.;
- Shadrina, M. I.
Publication type:
Article
Mitochondrial dysfunction and oxidative damage in the molecular pathology of Parkinson’s disease.
Published in:
Molecular Biology, 2008, v. 42, n. 5, p. 720, doi. 10.1134/S0026893308050099
By:
- Shadrina, M. I.;
- Slominsky, P. A.
Publication type:
Article
Association of Polymorphic Trinucleotide Repeat (GAA)n of the Frataxin Gene with Diabetes Mellitus Type 2 in the Moscow Population.
Published in:
Molecular Biology, 2002, v. 36, n. 1, p. 26, doi. 10.1023/A:1014234120518
By:
- Shadrina, M. I.;
- Miloserdova, O. V.;
- Slominskii, P. A.;
- Balabolkin, M. I.;
- Limborskaya, S. A.
Publication type:
Article
Common and Specific Genetic Risk Factors for Three Disorders with Depressive Symptoms.
Published in:
Russian Journal of Genetics, 2022, v. 58, n. 1, p. 65, doi. 10.1134/S1022795422010100
By:
- Rafikova, E. I.;
- Shibalev, D. V.;
- Shadrina, M. I.;
- Slominsky, P. A.;
- Guekht, A. B.;
- Ryskov, A. P.;
- Vasilyev, V. A.
Publication type:
Article
Influence of Polymorphic Gene Variants of the Dopaminergic System on the Risk of Disorders with Depressive Symptoms.
Published in:
Russian Journal of Genetics, 2021, v. 57, n. 8, p. 942, doi. 10.1134/S1022795421070115
By:
- Rafikova, E. I.;
- Shibalev, D. V.;
- Shadrina, M. I.;
- Slominsky, P. A.;
- Guekht, A. B.;
- Ryskov, A. P.;
- Vasilyev, V. A.
Publication type:
Article
Association of insulinase gene polymorphisms with type 2 diabetes mellitus in patients from the Moscow population.
Published in:
Russian Journal of Genetics, 2009, v. 45, n. 1, p. 113, doi. 10.1134/S1022795409010165
By:
- Slominsky, P. A.;
- Pivovarova, O. V.;
- Shadrina, M. I.;
- Artem’eva, A. V.;
- Pfaipffer, F. G.;
- Rudovich, N. N.;
- Agadghanyan, S. E.;
- Pronin, V. S.;
- Limborska, S. A.
Publication type:
Article
Molecular genetics of Parkinson’s disease.
Published in:
Russian Journal of Genetics, 2006, v. 42, n. 8, p. 858, doi. 10.1134/S1022795406080035
By:
- Shadrina, M. I.;
- Slominsky, P. A.
Publication type:
Article
Analysis of the possible involvement of the glutamate transporter gene EAAT2 and the glutamate receptor genes GRIA1 and GRIA2 in the pathogenesis of motor neuron disease in the Russian population.
Published in:
Russian Journal of Genetics, 2006, v. 42, n. 1, p. 89, doi. 10.1134/S1022795406010133
By:
- Zherebtsova, A. L.;
- Shadrina, M. I.;
- Semenova, E. V.;
- Levitsky, G. N.;
- Alekhin, A. V.;
- Slominsky, P. A.;
- Skvortsova, V. I.;
- Limborska, S. A.
Publication type:
Article
Analysis of the Glutathione S-Transferase P1 Gene Ile105Val Polymorphism in the Patients with Sporadic Motor Neuron Disease from Russia.
Published in:
Russian Journal of Genetics, 2004, v. 40, n. 6, p. 691, doi. 10.1023/B:RUGE.0000033319.46071.84
By:
- Zherebtsova, A. L.;
- Shadrina, M. I.;
- Levitsky, G. N.;
- Levitskaya, N. I.;
- Alekhin, A. V.;
- Slominsky, P. A.;
- Skvortsova, V. I.;
- Limborska, S. A.
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

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