Shadrina MI - Search Results

1

Transcriptome Profile Changes in Mice with MPTP-Induced Early Stages of Parkinson's Disease.

Alieva AK, Filatova EV, Kolacheva AA, Rudenok MM, Slominsky PA, Ugrumov MV, Shadrina MI. Alieva AK, et al. Among authors: shadrina mi. Mol Neurobiol. 2017 Nov;54(9):6775-6784. doi: 10.1007/s12035-016-0190-y. Epub 2016 Oct 18. Mol Neurobiol. 2017. PMID: 27757834

2

Spinocerebellar ataxia type 1 in Russia.

Illarioshkin SN, Slominsky PA, Ovchinnikov IV, Markova ED, Miklina NI, Klyushnikov SA, Shadrina M, Vereshchagin NV, Limborskaya SA, Ivanova-Smolenskaya IA. Illarioshkin SN, et al. J Neurol. 1996 Jul;243(7):506-10. doi: 10.1007/BF00886871. J Neurol. 1996. PMID: 8836939

3

A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystonia.

Slominsky PA, Markova ED, Shadrina MI, Illarioshkin SN, Miklina NI, Limborska SA, Ivanova-Smolenskaya IA. Slominsky PA, et al. Among authors: shadrina mi. Hum Mutat. 1999 Sep 19;14(3):269. doi: 10.1002/(SICI)1098-1004(1999)14:3<269::AID-HUMU12>3.0.CO;2-9. Hum Mutat. 1999. PMID: 10477437

4

CuZn-superoxide dismutase gene in sporadic amyotrophic lateral sclerosis patients from Russia: Asp90Ala (D90A) mutation and novel rare polymorphism IVS3+35 A>C.

Slominsky PA, Shadrina MI, Kondratyeva EA, Tupitsina TV, Levitsky GN, Skvortsova VI, Limborska SA. Slominsky PA, et al. Among authors: shadrina mi. Hum Mutat. 2000 Sep;16(3):277-8. doi: 10.1002/1098-1004(200009)16:3<277::AID-HUMU27>3.0.CO;2-P. Hum Mutat. 2000. PMID: 10980551 No abstract available.

5

Sporadic ALS associated with the D90A Cu,Zn superoxide dismutase mutation in Russia.

Skvortsova VI, Limborska SA, Slominsky PA, Levitskaya NI, Levitsky GN, Shadrina MI, Kondratyeva EA. Skvortsova VI, et al. Among authors: shadrina mi. Eur J Neurol. 2001 Mar;8(2):167-72. doi: 10.1046/j.1468-1331.2001.00186.x. Eur J Neurol. 2001. PMID: 11284995 Review.

6

Rapid induction of neurotrophin mRNAs in rat glial cell cultures by Semax, an adrenocorticotropic hormone analog.

Shadrina MI, Dolotov OV, Grivennikov IA, Slominsky PA, Andreeva LA, Inozemtseva LS, Limborska SA, Myasoedov NF. Shadrina MI, et al. Neurosci Lett. 2001 Aug 3;308(2):115-8. doi: 10.1016/s0304-3940(01)01994-2. Neurosci Lett. 2001. PMID: 11457573

7

Association study of sporadic Parkinson's disease genetic risk factors in patients from Russia by APEX technology.

Shadrina M, Nikopensius T, Slominsky P, Illarioshkin S, Bagyeva G, Markova E, Ivanova-Smolenskaia I, Kurg A, Limborska S, Metspalu A. Shadrina M, et al. Neurosci Lett. 2006 Sep 25;405(3):212-6. doi: 10.1016/j.neulet.2006.06.066. Epub 2006 Jul 28. Neurosci Lett. 2006. PMID: 16876316

8

Effective quantitative real-time polymerase chain reaction analysis of the parkin gene (PARK2) exon 1-12 dosage.

Shadrina MI, Semenova EV, Slominsky PA, Bagyeva GH, Illarioshkin SN, Ivanova-Smolenskaia II, Limborska SA. Shadrina MI, et al. BMC Med Genet. 2007 Feb 26;8:6. doi: 10.1186/1471-2350-8-6. BMC Med Genet. 2007. PMID: 17324265 Free PMC article.

9

Neurotrophin gene expression in rat brain under the action of Semax, an analogue of ACTH 4-10.

Agapova TY, Agniullin YV, Shadrina MI, Shram SI, Slominsky PA, Lymborska SA, Myasoedov NF. Agapova TY, et al. Among authors: shadrina mi. Neurosci Lett. 2007 May 1;417(2):201-5. doi: 10.1016/j.neulet.2007.02.042. Epub 2007 Feb 20. Neurosci Lett. 2007. PMID: 17353092

10

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

Illarioshkin SN, Shadrina MI, Slominsky PA, Bespalova EV, Zagorovskaya TB, Bagyeva GKh, Markova ED, Limborska SA, Ivanova-Smolenskaya IA. Illarioshkin SN, et al. Among authors: shadrina mi. Eur J Neurol. 2007 Apr;14(4):413-7. doi: 10.1111/j.1468-1331.2007.01685.x. Eur J Neurol. 2007. PMID: 17388990

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