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List of works by Maria Shadrina

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

scientific article published on 01 September 1999

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

scientific article published on 01 April 2007

A simple and rapid method for determining a 32-bp deletion in the gene for the chemokine receptor CCR5

scientific article

Analysis of PARK2 gene exon rearrangements in Russian patients with sporadic Parkinson's disease

scientific article published on 13 September 2011

Analysis of heavy neurofilament subunit gene polymorphism in Russian patients with sporadic motor neuron disease (MND).

scientific article published in March 2004

Association of homozygosity for short allele (S) of heavy neurofilament subunit gene with motor neuron disease and oxidative stress development

scientific article published in January 2003

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

scientific article published on 28 July 2006

Comparison of the temporary dynamics of NGF and BDNF gene expression in rat hippocampus, frontal cortex, and retina under Semax action.

scientific article published on 7 August 2009

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

scientific article published on 01 September 2000

Detoxication gene polymorphism and susceptibility to sporadic motor neuron disease in Russian population

scientific article published in January 2006

Effect of semax on the temporary dynamics of brain-derived neurotrophic factor and nerve growth factor gene expression in the rat hippocampus and frontal cortex

scientific journal article

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

scientific article

Effective simulations of gas diffusion through kinetically accessible tunnels in multisubunit proteins: O2 pathways and escape routes in T-state deoxyhemoglobin.

scientific article published on 26 June 2012

Expression analysis of genes of ubiquitin-proteasome protein degradation system in MPTP-induced mice models of early stages of Parkinson's disease.

scientific article published in May 2014

Expression analysis of suppression of tumorigenicity 13 gene in patients with Parkinson's disease.

scientific article published in March 2010

Expression of inflammation-related genes in mouse spleen under tuftsin analog Selank

scientific article published on May 24, 2011

ITPR1 gene p.Val1553Met mutation in Russian family with mild Spinocerebellar ataxia

scientific article published on 13 January 2016

Involvement of endocytosis and alternative splicing in the formation of the pathological process in the early stages of Parkinson's disease.

scientific article

MicroRNAs: possible role in pathogenesis of Parkinson's disease.

scientific article published on August 2012

Molecular genetic analysis of hereditary neurodegenerative diseases

scientific article published in June 2004

Molecular mechanisms of pathogenesis of Parkinson's disease.

scientific article published on January 2010

Peculiarities of sporadic motor neuron disease associated with D90A and G12R mutations in Russian population

scientific article published in January 2003

Potential Biomarkers of the Earliest Clinical Stages of Parkinson's Disease.

scientific article published on 21 September 2015

Second mutation in PARK2 is absent in patients with sporadic Parkinson's disease and heterozygous exonic deletions/duplications in parkin gene.

scientific article published on 31 October 2016

Selank Administration Affects the Expression of Some Genes Involved in GABAergic Neurotransmission

scientific article published on 18 February 2016

Simulated 18O kinetic isotope effects in enzymatic hydrolysis of guanosine triphosphate.

scientific article published in September 2009

Spinocerebellar ataxia type 1 in Russia

scientific article published on 01 July 1996

The spectrum of SDHD mutations in Russian patients with head and neck paraganglioma

scientific article published on 30 October 2018

The temporary dynamics of inflammation-related genes expression under tuftsin analog Selank action.

scientific article

Transcranial sonography in Parkinson's disease

scientific article published in January 2011

Transcriptome alteration in hippocampus under the treatment of tuftsin analog Selank

scientific article published in May 2013

Transcriptomic response of rat hippocampus and spleen cells to single and chronic administration of the peptide selank.

scientific article published in January 2010

VCP expression decrease as a biomarker of preclinical and early clinical stages of Parkinson's disease

scientific article published on 21 January 2020

[A PARK8 form of Parkinson's disease: a mutational analysis of the LRRK2 gene in Russian population].

scientific article

[Analysis of polymorphism of the 5'-terminal region of apolipoprotein B gene in patients with ischemic heard disease]

scientific article published on 01 August 1996

[Analysis of polymorphism of the angiotensin gene in patients with ischemic heart disease and in a random sample from the Moscow population]

scientific article published on 01 February 1998

[Analysis of the rs12720208 single-nucleotide polymorphism of the FGF20 gene in Russian patients with sporadic Parkinson's disease]

scientific article published on 01 December 2012

[Association of polymorphic trinucleotide repeat (GAA)n of the Frataxin gene with diabetes mellitus type 2 in the Moscow population]

scientific article published on 01 January 2002

[Association of the IVS9-675C > A polymorphism of the HIF-1alpha gene with acute ischemic stroke in the Moscow population]

scientific article published on 01 June 2006

[Changes in expression of the genes for chemokines, cytokines, and their receptors in response to selank and its fragments]

scientific article published on 01 May 2011

[Expression of GSK3B gene in peripheral blood in patient with Parkinson's disease].

scientific article

[Highly polymorphic regions of the genes for apolipoprotein B and angiotensin-converting enzyme in the Udmurt population]

scientific article published on 01 February 1997

[Isolation of a protein, specifically binding with a triplet repeat of the (CTG)n type]

scientific article published on 01 January 1997

[Mitochondrial dysfunction and oxidative damages in the molecular pathology of Parkinson's disease]

scientific article published on 01 September 2008

[Molecular genetics of Parkinson's disease]

scientific article published on 01 August 2006

[Normal polymorphism of the (CTG)n repeat in the myotonin protein kinase (DM) gene on chromosome 19q13.3 in Western European populations]

scientific article published on 01 July 2000

[PCR analysis of microsatellite DNA markers: possibility of erroneous determination of genotypes]

scientific article published on 01 June 1998

[Polymorphism of the (CTG)n repeat in the myotonin protein kinase (DM) gene in Belarussian populations: analysis of interethnic heterogeneity]

scientific article published on 01 July 1999

[Sporadic amyotrophic lateral sclerosis associated with Asp90Ala CuZn-superoxide dismutase mutations in Russia]

scientific article published on 01 January 2000

[The apolipoprotein AII gene is not a risk factor for development ischemic heart disease in the Moscow population]

scientific article published on 01 September 1997

miRNA expression is highly sensitive to a drug therapy in Parkinson's disease.

scholarly article by Anelya Alieva et al published 2015 in Parkinsonism and Related Disorders