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MicroRNAs: Possible role in pathogenesis of Parkinson's disease.
Published in:
Biochemistry (00062979), 2012, v. 77, n. 8, p. 813, doi. 10.1134/S0006297912080020
By:
- Filatova, E.;
- Alieva, A.;
- Shadrina, M.;
- Slominsky, P.
Publication type:
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
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
Expression analysis of genes of ubiquitin-proteasome protein degradation system in MPTP-induced mice models of early stages of Parkinson's disease.
Published in:
Doklady Biochemistry & Biophysics, 2014, v. 456, n. 1, p. 116, doi. 10.1134/S1607672914030107
By:
- Filatova, E.;
- Shadrina, M.;
- Alieva, A.;
- Kolacheva, A.;
- Slominsky, P.;
- Ugrumov, M.
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
Polymorphism of trinucleotide repeats in loci DM, DRPLA and SCA1 in East European populations.
Published in:
European Journal of Human Genetics, 2001, v. 9, n. 11, p. 829, doi. 10.1038/sj.ejhg.5200716
By:
- Popova, Svetlana N;
- Slominsky, P A;
- Pocheshnova, E A;
- Balanovskaya, E V;
- Tarskaya, L A;
- Bebyakova, N A;
- Bets, L V;
- Ivanov, V P;
- Livshits, L A;
- Khusnutdinova, E K;
- Spitcyn, V A;
- Limborska, S A
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
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
Expression of GSK3B in peripheral blood of patients with Parkinson's disease.
Published in:
Molecular Biology, 2011, v. 45, n. 3, p. 417, doi. 10.1134/S0026893311020063
By:
- Filatova, E.;
- Shadrina, M.;
- Karabanov, A.;
- Slominsky, P.;
- Illarioshkin, S.;
- Ivanova-Smolenskaya, I.;
- Limborska, S.
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
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
Analysis of the rs12720208 single-nucleotide polymorphism of the FGF20 gene in Russian patients with sporadic Parkinson's disease.
Published in:
Russian Journal of Genetics, 2012, v. 48, n. 12, p. 1257, doi. 10.1134/S1022795412090086
By:
- Ustinova, V.;
- Shadrina, M.;
- Fedotova, E.;
- Illarioshkin, S.;
- Limborska, S.;
- Slominsky, P.
Publication type:
Article
Association of rs10912745 and rs4916375 polymorphisms located in the cluster of flavin-containing monooxygenase genes, with ischaemic cardioembolic stroke.
Published in:
Russian Journal of Genetics, 2012, v. 48, n. 5, p. 572, doi. 10.1134/S1022795412040138
By:
- Tupitsyna, T.;
- Bondarenko, E.;
- Slominsky, P.;
- Shetova, I.;
- Shamalov, N.;
- Timofeev, D.;
- Skvortsova, V.;
- Limborska, S.
Publication type:
Article
Analysis of acute ischemic stroke DNA markers in Russian and Moldavian populations.
Published in:
Russian Journal of Genetics, 2011, v. 47, n. 10, p. 1240, doi. 10.1134/S1022795411100048
By:
- Bondarenko, E.;
- Shetova, I.;
- Shamalov, N.;
- Mocan, E.;
- Barbacar, N.;
- Kurochkin, G.;
- Protopop, S.;
- Lysyi, L.;
- Slominsky, P.;
- Limborska, S.;
- Skvortsova, V.
Publication type:
Article
Polymorphic variants of ALOX5 AP gene and the risk of acute stroke development in the Russian population.
Published in:
Russian Journal of Genetics, 2011, v. 47, n. 4, p. 500, doi. 10.1134/S102279541104003X
By:
- Bondarenko, E.;
- Slominsky, P.;
- Limborska, S.;
- Shetova, I.;
- Timofeev, D.;
- Skvortsova, V.
Publication type:
Article
Changes in expression of the genes for chemokines, cytokines, and their receptors in response to selank and its fragments.
Published in:
Russian Journal of Genetics, 2011, v. 47, n. 5, p. 629, doi. 10.1134/S1022795411050103
By:
- Kolomin, T.;
- Shadrina, M.;
- Slominsky, P.;
- Limborska, S.;
- Myasoedov, N.
Publication type:
Article
Phosphodiesterase 4D ( PDE4D) gene polymorphism in patients with acute stroke from Moscow.
Published in:
Russian Journal of Genetics, 2010, v. 46, n. 6, p. 765, doi. 10.1134/S1022795410060189
By:
- Bondarenko, E. A.;
- Tupitsina, T. V.;
- Slominsky, P. A.;
- Shetova, I. M.;
- Shamalov, N. A.;
- Botsina, A. Yu.;
- Skvortsova, V. I.;
- Limborska, S. 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
Association of the IVS9-675C > A polymorphism of the HIF-1α gene with acute ischemic stroke in the Moscow population.
Published in:
Russian Journal of Genetics, 2006, v. 42, n. 6, p. 703, doi. 10.1134/S1022795406060172
By:
- Tupitsina, T.;
- Slominsky, P.;
- Shadrina, M.;
- Shetova, I.;
- Skvortsova, V.;
- Limborska, S.
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
Analysis of Deletion Mutations in the PARK2 Gene in Idiopathic Parkinson's Disease.
Published in:
Russian Journal of Genetics, 2003, v. 39, n. 2, p. 166, doi. 10.1023/A:1022427708736
By:
- Slominsky, P. A.;
- Miloserdova, O. V.;
- Popova, S. N.;
- Gilyazova, I. R.;
- Khidiyatova, I. V.;
- Magzhanov, R. V.;
- Khusnutdinova, E. K.;
- Limborska, S. A.
Publication type:
Article

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