List of works - Petr Slominsky

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 novel mutation in the GTP cyclohydrolase I gene associated with a broad range of clinical presentations in a family with autosomal dominant dopa-responsive dystonia

scientific article published on 01 September 1999

A polymorphism within the connective tissue growth factor (CTGF) gene has no effect on non-invasive markers of beta-cell area and risk of type 2 diabetes

scientific article published on January 2011

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 expansion of the triplet repeat (CTG)n in myotonic dystrophy patients from Bashkir

scientific article published on 01 June 2000

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

scientific article published in March 2004

Apolipoprotein B 3'-VNTR polymorphism in the Udmurt population

scientific article published on 01 July 2000

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

Associations between chronotype, road accidents and polymorphisms in genes linked with biological clock and dopaminergic system

scientific article published in January 2017

Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophy.

scientific article published in December 1996

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

Connection between p53 gene Bam HI RFLP polymorphism with the volume of brain infarction in patients with carotid atherothrombotic ischemic stroke

scientific article published on 01 January 2004

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

Differences in relative levels of 88 microRNAs in various regions of the normal adult human brain.

scientific article published on 19 May 2017

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

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 changes caused by the peptide semax in the intracellular signal pathway genes in rat hippocamp

scientific article published on 01 November 2007

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

scientific article published on May 24, 2011

GABA, Selank, and Olanzapine Affect the Expression of Genes Involved in GABAergic Neurotransmission in IMR-32 Cells.

scientific article

GSTM1 copy number variation in the context of single nucleotide polymorphisms in the human GSTM cluster.

scientific article published on 19 April 2016

Genetic Analysis of BDNF, GNB3, MTHFR, ACE and APOE Variants in Major and Recurrent Depressive Disorders in Russia

scientific article published on 08 December 2016

Genetic risk factors for recurrence-free urolithiasis in the russian population

scientific article published in August 2016

Heterogeneity of beta-thalassemia in Azerbaidzhan

scientific article published on 01 January 1984

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

Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism

scientific article published on 01 August 2003

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

scientific article published in January 2003

Peptide Selank Enhances the Effect of Diazepam in Reducing Anxiety in Unpredictable Chronic Mild Stress Conditions in Rats

scientific article published on 09 February 2017

Peptides semax and selank affect the behavior of rats with 6-OHDA induced PD-like parkinsonism

scientific article

Polymorphism of glutathione S-transferases M1 and T1 in several populations of Russia

scientific article published in February 2002

Polymorphism of trinucleotide repeats in loci DM, DRPLA and SCA1 in East European populations

scientific article published on 01 November 2001

Polymorphisms at locus D1S80 and other hypervariable regions in the analysis of Eastern European ethnic group relationships

article

Possible involvement of neuronal nicotinic acetylcholine receptors in compensatory brain mechanisms at early stages of Parkinson's disease

scientific article published in May 2017

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

scientific article published on 21 September 2015

Role of missense mutation (M235T) in the angiotensinogen gene in development of cerebral ischemia

scientific article published in January 2003

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

Spinocerebellar ataxia type 1 in Russia

scientific article published on 01 July 1996

The GTP cyclohydrolase I gene in Russian families with dopa-responsive dystonia

scientific article published on 01 June 1998

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

scientific article

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

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

scientific article

[A simple and rapid method for detection of the 106Gln mutation in Wilson-Konovalov disease]

scientific article

[ACE gene polymorphism in patients with ischemic brain disease]

scientific article published on 01 January 2001

[Analysis association of acute ischemic stroke and DNA markers in Russian and Moldavian populations]

scientific article published on 01 October 2011

[Analysis of deletion mutations in the PARK2 gene in idiopathic Parkinson's disease]

scientific article published on 01 February 2003

[Analysis of mutations in patients with suspected autosomal dominant form of the Parkinson disease]

scholarly article by E V Filatova et al published 1 January 2014 in Molekuliarnaia Genetika, Mikrobiologiia i Virusologiia

[Analysis of polymorphic variants of renin-angiotensin system genes in polymetabolic syndrome and non-insulin-dependent diabetes]

scientific article published on 01 October 2001

[Analysis of polymorphism of CTG repetitive sequences in the gene of myotonic dystrophy in human populations of the Volga-Ural region]

scientific article published on 01 July 1999

[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 single nucleotide polymorphism rs415430 in the WNT3 gene in the Russian population with the Parkinson disease]

scientific article published on 01 January 2011

[Analysis of the genetic heterogeneity of homozygous beta+- thalassemia in the Azerbaijan SSR]

scientific article published on 01 October 1985

[Analysis of the polymorphic variants of the PDE4D gene in patients with acute stroke in the Moldavian population]

scientific article published on 01 January 2011

[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 between Bam HI RFLP p53 gene polymorphism and brain infarction volume in patients with atherothrombotic ischemic stroke]

scientific article published on 01 January 2003

[Association between insertion-deletion polymorphism of the angiotensin-converting enzyme gene and development of angiopathies in patients with non-insulin dependent diabetes mellitus from the Chuvash Republic]

scientific article published on 01 January 2001

[Association of cerebral stroke with a phosphodiesterase 4D (PDE4D) gene polymorphism in the Moscow population]

scientific article published on 01 January 2011

[Association of insulinase gene polymorphisms with type 2 diabetes mellitus in patients from the Moscow population]

scientific article published on 01 January 2009

[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 rs10912745 and rs4916375 polymorphisms located in the cluster of flavin-containing monooxygenase genes, with ischaemic cardioembolic stroke]

scientific article published on 01 May 2012

[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

[Association study of polymorphic markers of F12, PON1, PON2, NOS2, PDE4D, HIF1a, GPIba, CYP11B2 genes with ischemic stroke in Russian patients]

scientific article published on 01 January 2012

[Association study of renin-angiotensin system genes and hemostasis system genes with ischemic stroke among Russians of Central Russia]

scientific article published on 01 March 2012

[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

[Changes in the frequency of alleles and genotypes of insertional-deletional polymorphism of the angiotensin-converting enzyme gene, dependent on age]

scientific article published on 01 January 2002

[Clinical and genetic analysis of juvenile parkinsonism in Russia]

scientific article published on 01 January 2004

[Comparative analysis of associations of polymorphic genes F2, F5, GP1BA and ACE with the risk of stroke development in Russian and Ukrainian populations]

scientific article published in January 2013

[Distribution of the 32 bp deletion in the CCR5 chemokine receptor gene in populations of the Volga-Ural region]

scientific article published on 01 August 1998

[Expansion and mutation rate in CTG repeats in the myotonic dystrophy gene]

scientific article published on 01 October 2000

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

scientific article

[Genetic risk factors of thyroid gland pathology]

scientific article published on 01 January 2005

[Genome-wide scanning in the study of risk for cerebral stroke]

scientific article published on 01 January 2009

[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 new nuclear protein specifically binding with M13-type minisatellite]

scientific article published on 01 April 1995

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

scientific article published on 01 January 1997

[Mapping of the gene for autosomal-recessive progressive muscular dystrophy in an isolate from a highland region of Dagestan to chromosome 2-13]

scientific article published on 01 November 1997

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

scientific article published on 01 September 2008

[Molecular causes of thalassemia. III. Molecular genetic variants of beta-thalassemia in Azerbaijan]

scientific article published on 01 July 1982

[Molecular genetic studies of beta-thalassemia heterogeneity]

scientific article published on 01 June 1983

[Molecular genetics of Parkinson's disease]

scientific article published on 01 August 2006

[Molecular-genetic analysis of hereditary neurological diseases]

scientific article published on 01 January 1999

[Moleculo-genetic study of beta-thalassemia heterogenity in the USSR]

scientific article published on 01 May 1983

[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

[Phosphodiesterase 4D (PDE4D) gene polymorphism in patients with acute stroke from Moscow]

scientific article published on 01 June 2010

[Polymorphic markers for the angiotensinogen and angiotensin-converting enzyme in Yakuts. Lack of association with blood pressure level]

scientific article published on 01 May 2001

[Polymorphic variants of ALOX5AP gene and the risk of acute stroke development in the Russian population]

scientific article published on 01 April 2011

[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

[Polymorphism of the STR-locus of Y chromosomes in Eastern Slavs in three populations from Belorussia, Russia and the Ukraine]

scientific article published on 01 January 2002

[Presymptomatic DNA diagnosis of spinocerebellar ataxia type 1]

scientific article published on 01 May 1997

[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

[The association between the DNA marker rs1842993 and risk for cardioembolic stroke in the Slavic population]

scientific article published on 01 January 2012

[The possible role of genetic factors in the cholesterol high density lipoprotein level in the Moscow population]

scientific article published on 01 October 2000

[The role of polymorphic variants of gene of inducible NO-synthase NOS2 in brain infarction in patients with acute ischemic stroke]

scientific article published on 01 January 2010

[The role of polymorphic variants of renin-angiotensin system genes in the development of ischemic stroke in Moscow population]

scientific article published on 01 January 2003

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

List of works by Petr Slominsky

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

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

A novel mutation in the GTP cyclohydrolase I gene associated with a broad range of clinical presentations in a family with autosomal dominant dopa-responsive dystonia

A polymorphism within the connective tissue growth factor (CTGF) gene has no effect on non-invasive markers of beta-cell area and risk of type 2 diabetes

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

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

Analysis of expansion of the triplet repeat (CTG)n in myotonic dystrophy patients from Bashkir

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

Apolipoprotein B 3'-VNTR polymorphism in the Udmurt population

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

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

Associations between chronotype, road accidents and polymorphisms in genes linked with biological clock and dopaminergic system

Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophy.

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

Connection between p53 gene Bam HI RFLP polymorphism with the volume of brain infarction in patients with carotid atherothrombotic ischemic stroke

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

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

Differences in relative levels of 88 microRNAs in various regions of the normal adult human brain.

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

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

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

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

Expression changes caused by the peptide semax in the intracellular signal pathway genes in rat hippocamp

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

GABA, Selank, and Olanzapine Affect the Expression of Genes Involved in GABAergic Neurotransmission in IMR-32 Cells.

GSTM1 copy number variation in the context of single nucleotide polymorphisms in the human GSTM cluster.

Genetic Analysis of BDNF, GNB3, MTHFR, ACE and APOE Variants in Major and Recurrent Depressive Disorders in Russia

Genetic risk factors for recurrence-free urolithiasis in the russian population

Heterogeneity of beta-thalassemia in Azerbaidzhan

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

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

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

Molecular genetic analysis of hereditary neurodegenerative diseases

Molecular mechanisms of pathogenesis of Parkinson's disease.

Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism

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

Peptide Selank Enhances the Effect of Diazepam in Reducing Anxiety in Unpredictable Chronic Mild Stress Conditions in Rats

Peptides semax and selank affect the behavior of rats with 6-OHDA induced PD-like parkinsonism

Polymorphism of glutathione S-transferases M1 and T1 in several populations of Russia

Polymorphism of trinucleotide repeats in loci DM, DRPLA and SCA1 in East European populations

Polymorphisms at locus D1S80 and other hypervariable regions in the analysis of Eastern European ethnic group relationships

Possible involvement of neuronal nicotinic acetylcholine receptors in compensatory brain mechanisms at early stages of Parkinson's disease

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

Role of missense mutation (M235T) in the angiotensinogen gene in development of cerebral ischemia

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

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

Spinocerebellar ataxia type 1 in Russia

The GTP cyclohydrolase I gene in Russian families with dopa-responsive dystonia

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

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

Transcranial sonography in Parkinson's disease

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

Transcriptome alteration in hippocampus under the treatment of tuftsin analog Selank

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

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

[A simple and rapid method for detection of the 106Gln mutation in Wilson-Konovalov disease]

[ACE gene polymorphism in patients with ischemic brain disease]

[Analysis association of acute ischemic stroke and DNA markers in Russian and Moldavian populations]

[Analysis of deletion mutations in the PARK2 gene in idiopathic Parkinson's disease]

[Analysis of mutations in patients with suspected autosomal dominant form of the Parkinson disease]

[Analysis of polymorphic variants of renin-angiotensin system genes in polymetabolic syndrome and non-insulin-dependent diabetes]

[Analysis of polymorphism of CTG repetitive sequences in the gene of myotonic dystrophy in human populations of the Volga-Ural region]

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

[Analysis of single nucleotide polymorphism rs415430 in the WNT3 gene in the Russian population with the Parkinson disease]

[Analysis of the genetic heterogeneity of homozygous beta+- thalassemia in the Azerbaijan SSR]

[Analysis of the polymorphic variants of the PDE4D gene in patients with acute stroke in the Moldavian population]

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

[Association between Bam HI RFLP p53 gene polymorphism and brain infarction volume in patients with atherothrombotic ischemic stroke]

[Association between insertion-deletion polymorphism of the angiotensin-converting enzyme gene and development of angiopathies in patients with non-insulin dependent diabetes mellitus from the Chuvash Republic]

[Association of cerebral stroke with a phosphodiesterase 4D (PDE4D) gene polymorphism in the Moscow population]

[Association of insulinase gene polymorphisms with type 2 diabetes mellitus in patients from the Moscow population]

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

[Association of rs10912745 and rs4916375 polymorphisms located in the cluster of flavin-containing monooxygenase genes, with ischaemic cardioembolic stroke]

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

[Association study of polymorphic markers of F12, PON1, PON2, NOS2, PDE4D, HIF1a, GPIba, CYP11B2 genes with ischemic stroke in Russian patients]

[Association study of renin-angiotensin system genes and hemostasis system genes with ischemic stroke among Russians of Central Russia]

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

[Changes in the frequency of alleles and genotypes of insertional-deletional polymorphism of the angiotensin-converting enzyme gene, dependent on age]

[Clinical and genetic analysis of juvenile parkinsonism in Russia]