Pchelina SN - Search Results

1

Genetics variants and expression of the SCARB2 gene in the pathogenesis of Parkinson's disease in Russia.

Usenko TS, Bezrukova AI, Bogdanova DA, Kopytova AE, Senkevich KA, Gracheva EV, Timofeeva AA, Miliukhina IV, Zakharova EY, Emelyanov AK, Pchelina SN. Usenko TS, et al. Among authors: pchelina sn. Neurosci Lett. 2021 Jan 10;741:135509. doi: 10.1016/j.neulet.2020.135509. Epub 2020 Nov 20. Neurosci Lett. 2021. PMID: 33227372

2

G2019S LRRK2 mutation in familial and sporadic Parkinson's disease in Russia.

Pchelina SN, Yakimovskii AF, Ivanova ON, Emelianov AK, Zakharchuk AH, Schwarzman AL. Pchelina SN, et al. Mov Disord. 2006 Dec;21(12):2234-6. doi: 10.1002/mds.21134. Mov Disord. 2006. PMID: 17044089

3

Screening for LRRK2 mutations in patients with Parkinson's disease in Russia: identification of a novel LRRK2 variant.

Pchelina SN, Yakimovskii AF, Emelyanov AK, Ivanova ON, Schwarzman AL, Singleton AB. Pchelina SN, et al. Eur J Neurol. 2008 Jul;15(7):692-6. doi: 10.1111/j.1468-1331.2008.02149.x. Epub 2008 Apr 24. Eur J Neurol. 2008. PMID: 18435766

4

Glucocerebrosidase gene mutations are associated with Parkinson's disease in Russia.

Emelyanov A, Boukina T, Yakimovskii A, Usenko T, Drosdova A, Zakharchuk A, Andoskin P, Dubina M, Schwarzman A, Pchelina S. Emelyanov A, et al. Mov Disord. 2012 Jan;27(1):158-9. doi: 10.1002/mds.23950. Epub 2011 Sep 13. Mov Disord. 2012. PMID: 21915911 No abstract available.

5

Reduced content of α-synuclein in peripheral blood leukocytes of patients with LRRK2-associated Parkinson's disease.

Pchelina SN, Emelyanov AK, Yakimovskii AF, Miller DW, Shabalina IG, Drozdova AS, Schwarzman AL. Pchelina SN, et al. Bull Exp Biol Med. 2011 Apr;150(6):679-81. doi: 10.1007/s10517-011-1221-3. Bull Exp Biol Med. 2011. PMID: 22235415

6

[Apoptosis of peripheral blood lymphocytes in patients with LRRK2-assoctated Parkinson's disease].

Usenko TS, Emel'ianov AK, Iakimovskiĭ AF, Bogan'kova NA, Vavilova TV, Shvartsman AL, Pchelina SN. Usenko TS, et al. Among authors: pchelina sn. Tsitologiia. 2012;54(1):44-8. Tsitologiia. 2012. PMID: 22567899 Russian.

7

SNCA, LRRK2, MAPT polymorphisms and Parkinson's disease in Russia.

Emelyanov A, Andoskin P, Yakimovskii A, Usenko T, Nuzhnyi E, Nikolaev M, Pchelina S. Emelyanov A, et al. Parkinsonism Relat Disord. 2013 Nov;19(11):1064-5. doi: 10.1016/j.parkreldis.2013.06.003. Epub 2013 Jul 3. Parkinsonism Relat Disord. 2013. PMID: 23830801 No abstract available.

8

Increased plasma oligomeric alpha-synuclein in patients with lysosomal storage diseases.

Pchelina SN, Nuzhnyi EP, Emelyanov AK, Boukina TM, Usenko TS, Nikolaev MA, Salogub GN, Yakimovskii AF, Zakharova EY. Pchelina SN, et al. Neurosci Lett. 2014 Nov 7;583:188-93. doi: 10.1016/j.neulet.2014.09.041. Epub 2014 Sep 26. Neurosci Lett. 2014. PMID: 25265039

9

[Molecular basis of Parkinson's disease linked with mutations in the LRRK2 gene].

Pchelina SN, emel'ianov AK, Usenko TS. Pchelina SN, et al. Mol Biol (Mosk). 2014 Jan-Feb;48(1):3-14. Mol Biol (Mosk). 2014. PMID: 25842821 Free article. Review. Russian.

10

Plasma oligomeric alpha-synuclein is associated with glucocerebrosidase activity in Gaucher disease.

Nuzhnyi E, Emelyanov A, Boukina T, Usenko T, Yakimovskii A, Zakharova E, Pchelina S. Nuzhnyi E, et al. Mov Disord. 2015 Jun;30(7):989-91. doi: 10.1002/mds.26200. Epub 2015 May 12. Mov Disord. 2015. PMID: 25962734

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