M I Shadrina - JoVE Visualize

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Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|February 7, 2006

[Detoxication gene polymorphism and susceptibility to sporadic motor neuron disease in Russian population]V I Skvortsova, P A Slominskiĭ, M I Shadrina, et al.

Genetika|February 26, 2009

[Association of insulinase gene polymorphisms with type 2 diabetes mellitus in patients from the Moscow population]P A Slominskiĭ, O V Pivovarova, M I Shadrina, et al.

Molecular Genetics and Metabolism Reports|April 14, 2020

Expression analysis of genes involved in mitochondrial biogenesis in mice with MPTP-induced model of Parkinson's diseaseM M Rudenok, A Kh Alieva, J S Starovatykh, et al.

Cerebellum & Ataxias|January 16, 2016

ITPR1 gene p.Val1553Met mutation in Russian family with mild Spinocerebellar ataxiaM I Shadrina, M V Shulskaya, S A Klyushnikov, et al.

Genetika|September 3, 2004

[Molecular genetic analysis of hereditary neurodegenerative diseases]S N Illarioshkin, I A Ivanova-Smolenskaia, E D Markova, et al.

European Journal of Neurology|March 29, 2007

A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in RussiaS N Illarioshkin, M I Shadrina, P A Slominsky, et al.

Biomeditsinskaia Khimiia|August 8, 2017

[Possible involvement of neuronal nicotinic acetylcholine receptors in compensatory brain mechanisms at early stages of Parkinson's disease]E V Kryukova, I V Shelukhina, A A Kolacheva, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|April 2, 2008

[A PARK8 form of Parkinson's disease: a mutational analysis of the LRRK2 gene in Russian population]M I Shadrina, S N Illarioshkin, G Kh Bagyeva, et al.

Genetika|September 20, 2000

[Normal polymorphism of the (CTG)n repeat in the myotonin protein kinase (DM) gene on chromosome 19q13.3 in Western European populations]P A Slominskiĭ, S N Popova, M I Shadrina, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|December 20, 2003

[Peculiarities of sporadic motor neuron disease associated with D90A and G12R mutations in Russian population]V I Skvortsova, S A Limborskaia, P A Slominskiĭ, et al.

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Showing results (41-50 of 51) with videos related to

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Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|February 7, 2006

[Detoxication gene polymorphism and susceptibility to sporadic motor neuron disease in Russian population]V I Skvortsova, P A Slominskiĭ, M I Shadrina, et al.

Genetika|February 26, 2009

[Association of insulinase gene polymorphisms with type 2 diabetes mellitus in patients from the Moscow population]P A Slominskiĭ, O V Pivovarova, M I Shadrina, et al.

Molecular Genetics and Metabolism Reports|April 14, 2020

Expression analysis of genes involved in mitochondrial biogenesis in mice with MPTP-induced model of Parkinson's diseaseM M Rudenok, A Kh Alieva, J S Starovatykh, et al.

Cerebellum & Ataxias|January 16, 2016

ITPR1 gene p.Val1553Met mutation in Russian family with mild Spinocerebellar ataxiaM I Shadrina, M V Shulskaya, S A Klyushnikov, et al.

Genetika|September 3, 2004

[Molecular genetic analysis of hereditary neurodegenerative diseases]S N Illarioshkin, I A Ivanova-Smolenskaia, E D Markova, et al.

European Journal of Neurology|March 29, 2007

A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in RussiaS N Illarioshkin, M I Shadrina, P A Slominsky, et al.

Biomeditsinskaia Khimiia|August 8, 2017

[Possible involvement of neuronal nicotinic acetylcholine receptors in compensatory brain mechanisms at early stages of Parkinson's disease]E V Kryukova, I V Shelukhina, A A Kolacheva, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|April 2, 2008

[A PARK8 form of Parkinson's disease: a mutational analysis of the LRRK2 gene in Russian population]M I Shadrina, S N Illarioshkin, G Kh Bagyeva, et al.

Genetika|September 20, 2000

[Normal polymorphism of the (CTG)n repeat in the myotonin protein kinase (DM) gene on chromosome 19q13.3 in Western European populations]P A Slominskiĭ, S N Popova, M I Shadrina, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|December 20, 2003

[Peculiarities of sporadic motor neuron disease associated with D90A and G12R mutations in Russian population]V I Skvortsova, S A Limborskaia, P A Slominskiĭ, et al.

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