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Items: 25

1.

Mutation analysis of Parkinson's disease genes in a Russian data set.

Emelyanov AK, Usenko TS, Tesson C, Senkevich KA, Nikolaev MA, Miliukhina IV, Kopytova AE, Timofeeva AA, Yakimovsky AF, Lesage S, Brice A, Pchelina SN.

Neurobiol Aging. 2018 Nov;71:267.e7-267.e10. doi: 10.1016/j.neurobiolaging.2018.06.027. Epub 2018 Jul 9.

PMID:
30146349
2.

Whole-Exome Sequencing in Searching for New Variants Associated With the Development of Parkinson's Disease.

Shulskaya MV, Alieva AK, Vlasov IN, Zyrin VV, Fedotova EY, Abramycheva NY, Usenko TS, Yakimovsky AF, Emelyanov AK, Pchelina SN, Illarioshkin SN, Slominsky PA, Shadrina MI.

Front Aging Neurosci. 2018 May 15;10:136. doi: 10.3389/fnagi.2018.00136. eCollection 2018.

3.

Enhanced human hematopoietic stem and progenitor cell engraftment by blocking donor T cell-mediated TNFα signaling.

Wang W, Fujii H, Kim HJ, Hermans K, Usenko T, Xie S, Luo ZJ, Ma J, Celso CL, Dick JE, Schroeder T, Krueger J, Wall D, Egeler RM, Zandstra PW.

Sci Transl Med. 2017 Dec 20;9(421). pii: eaag3214. doi: 10.1126/scitranslmed.aag3214.

PMID:
29263228
4.

Engineering the haemogenic niche mitigates endogenous inhibitory signals and controls pluripotent stem cell-derived blood emergence.

Rahman N, Brauer PM, Ho L, Usenko T, Tewary M, Zúñiga-Pflücker JC, Zandstra PW.

Nat Commun. 2017 May 25;8:15380. doi: 10.1038/ncomms15380.

5.

ITLN1, PPARg AND TNFa GENE EXPRESSION IN VISCERAL ADIPOSE TISSUE.

Usenko TS, Miroshnikova VV, Bazhenova EA, Nikolaev MA, Brovin DL, Kopytova AE, Panteleeva AA, He J, Semenova IA, Razgildina ND, Neimark AE, Berkovich OA, Belyaeva OD, Baranova EI, Pchelina SN.

Tsitologiia. 2017;59(1):27-33. English, Russian.

PMID:
30188100
6.

Oligomeric α-synuclein and glucocerebrosidase activity levels in GBA-associated Parkinson's disease.

Pchelina S, Emelyanov A, Baydakova G, Andoskin P, Senkevich K, Nikolaev M, Miliukhina I, Yakimovskii A, Timofeeva A, Fedotova E, Abramycheva N, Usenko T, Kulabukhova D, Lavrinova A, Kopytova A, Garaeva L, Nuzhnyi E, Illarioshkin S, Zakharova E.

Neurosci Lett. 2017 Jan 1;636:70-76. doi: 10.1016/j.neulet.2016.10.039. Epub 2016 Oct 22.

PMID:
27780739
7.

[Mutation del 1,02kb in the CLN3 gene and extrapyramidal syndrome].

Nuzhnyi EP, Yakimovskii AF, Timofeeva AA, Usenko TS, Nikolaev MA, Emelyanov AK, Amosov VI, Bubnova EV, Boukina AM, Zakharova EY, Pchelina SN.

Zh Nevrol Psikhiatr Im S S Korsakova. 2016;116(8):50-53. doi: 10.17116/jnevro20161168150-53. Russian.

PMID:
27635612
8.

[Regulation of ABCA1 and ABCG1 gene expression in the intraabdominal adipose tissue].

Miroshnikova VV, Panteleeva AA, Bazhenova EA, Demina EP, Usenko TS, Nikolaev MA, Semenova IA, Neimark AE, He J, Belyaeva OD, Berkovich OA, Baranova EI, Pchelina SN.

Biomed Khim. 2016 Mar;62(3):283-9. doi: 10.18097/PBMC20166203283. Russian.

PMID:
27420620
9.

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.

Lesage S, Drouet V, Majounie E, Deramecourt V, Jacoupy M, Nicolas A, Cormier-Dequaire F, Hassoun SM, Pujol C, Ciura S, Erpapazoglou Z, Usenko T, Maurage CA, Sahbatou M, Liebau S, Ding J, Bilgic B, Emre M, Erginel-Unaltuna N, Guven G, Tison F, Tranchant C, Vidailhet M, Corvol JC, Krack P, Leutenegger AL, Nalls MA, Hernandez DG, Heutink P, Gibbs JR, Hardy J, Wood NW, Gasser T, Durr A, Deleuze JF, Tazir M, Destée A, Lohmann E, Kabashi E, Singleton A, Corti O, Brice A; French Parkinson's Disease Genetics Study (PDG); International Parkinson's Disease Genomics Consortium (IPDGC).

Am J Hum Genet. 2016 Mar 3;98(3):500-513. doi: 10.1016/j.ajhg.2016.01.014.

10.

A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal-Recessive Juvenile-Onset Parkinson's Disease.

Elsayed LE, Drouet V, Usenko T, Mohammed IN, Hamed AA, Elseed MA, Salih MA, Koko ME, Mohamed AY, Siddig RA, Elbashir MI, Ibrahim ME, Durr A, Stevanin G, Lesage S, Ahmed AE, Brice A.

Ann Neurol. 2016 Feb;79(2):335-7. doi: 10.1002/ana.24591. Epub 2016 Jan 19. No abstract available.

PMID:
26703368
11.

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.

Mov Disord. 2015 Jun;30(7):989-91. doi: 10.1002/mds.26200. Epub 2015 May 12.

PMID:
25962734
12.

Leukemogenic Ptpn11 allele causes defective erythropoiesis in mice.

Usenko T, Chan G, Torlakovic E, Klingmüller U, Neel BG.

PLoS One. 2014 Oct 7;9(10):e109682. doi: 10.1371/journal.pone.0109682. eCollection 2014.

13.

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.

Neurosci Lett. 2014 Nov 7;583:188-93. doi: 10.1016/j.neulet.2014.09.041. Epub 2014 Sep 26.

PMID:
25265039
14.

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

Pchelina SN, emel'ianov AK, Usenko TS.

Mol Biol (Mosk). 2014 Jan-Feb;48(1):3-14. Review. Russian.

15.

Blood stem cell fate regulation by Delta-1-mediated rewiring of IL-6 paracrine signaling.

Csaszar E, Wang W, Usenko T, Qiao W, Delaney C, Bernstein ID, Zandstra PW.

Blood. 2014 Jan 30;123(5):650-8. doi: 10.1182/blood-2013-08-520445. Epub 2013 Nov 15.

16.

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

Emelyanov A, Andoskin P, Yakimovskii A, Usenko T, Nuzhnyi E, Nikolaev M, Pchelina S.

Parkinsonism Relat Disord. 2013 Nov;19(11):1064-5. doi: 10.1016/j.parkreldis.2013.06.003. Epub 2013 Jul 3. No abstract available.

PMID:
23830801
17.

[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.

Tsitologiia. 2012;54(1):44-8. Russian.

PMID:
22567899
18.

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.

Mov Disord. 2012 Jan;27(1):158-9. doi: 10.1002/mds.23950. Epub 2011 Sep 13. No abstract available.

PMID:
21915911
19.

Enrichment of Sca1+ hematopoietic progenitors in polycythemic mice inhibits leukemogenesis.

Usenko T, Li YJ, Haeri M, Li Y, Vecchiarelli-Federico LM, Zhao X, Prchal JT, Ben-David Y.

Blood. 2009 Aug 27;114(9):1831-41. doi: 10.1182/blood-2008-11-187419. Epub 2009 Jul 7.

PMID:
19584401
20.

Leukemogenic Ptpn11 causes fatal myeloproliferative disorder via cell-autonomous effects on multiple stages of hematopoiesis.

Chan G, Kalaitzidis D, Usenko T, Kutok JL, Yang W, Mohi MG, Neel BG.

Blood. 2009 Apr 30;113(18):4414-24. doi: 10.1182/blood-2008-10-182626. Epub 2009 Jan 29.

21.

Overexpression of SOCS-2 and SOCS-3 genes reverses erythroid overgrowth and IGF-I hypersensitivity of primary polycythemia vera (PV) cells.

Usenko T, Eskinazi D, Correa PN, Amato D, Ben-David Y, Axelrad AA.

Leuk Lymphoma. 2007 Jan;48(1):134-46.

PMID:
17325857
22.

Enhanced natural-killer cell and erythropoietic activities in VEGF-A-overexpressing mice delay F-MuLV-induced erythroleukemia.

Cervi D, Shaked Y, Haeri M, Usenko T, Lee CR, Haigh JJ, Nagy A, Kerbel RS, Yefenof E, Ben-David Y.

Blood. 2007 Mar 1;109(5):2139-46. Epub 2006 Oct 19.

23.

Transient expression of E1A and Ras oncogenes causes downregulation of c-fos gene transcription in nontransformed REF52 cells.

Usenko T, Kukushkin A, Pospelova T, Pospelov V.

Oncogene. 2003 Oct 23;22(48):7661-6.

PMID:
14576829
24.

[Transformation with the E1A + cHa-ras oncogenes enhances the trans-repressor function of the Elk-1 transcription factor].

Usenko TN, Pospelova TV, Pospelov VA.

Mol Biol (Mosk). 2002 Sep-Oct;36(5):825-32. Russian.

PMID:
12391846
25.

Neutrophil antiserum response to decrease in proteolytic activity in loaded rat muscle.

Morozov VI, Usenko TN, Rogozkin VA.

Eur J Appl Physiol. 2001 Mar;84(3):195-200.

PMID:
11320635

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