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Article: Svyaz' polimorfizmov gena serotoninovogo transportera SLC6A4 s depressiei.

Gafarov, V V / Gromova, E A / Gubina, M A / Gagulin, I V / Maksimov, V N / Gafarova, A V

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova

2024 Volume 124, Issue 2, Page(s) 135–139

Abstract: Objective: To study the relationship of polymorphic variants of the SLC6A4 gene with depression among people aged 25-44 years in Novosibirsk.: Material and methods: Under the WHO program «MONICA-psychosocial (MOPSY)», a random representative sample ... ...

Title translation	The association of polymorphisms of the serotonin transporter gene SLC6A4 with depression.
Abstract	Objective: To study the relationship of polymorphic variants of the SLC6A4 gene with depression among people aged 25-44 years in Novosibirsk. Material and methods: Under the WHO program «MONICA-psychosocial (MOPSY)», a random representative sample of people aged 25-44 years from the population of the Oktyabrsky district of Novosibirsk (men Results: The high level of depression among people aged 25-44 was 12.8% (for men 9.1%, for women - 15.92%); the average level of depression occurred in 24.5% of the population (among men in 21.24%, among women in 26.76%) (χ Conclusion: Associative links between polymorphic variants of the SLC6A4 gene and depression have been established.
MeSH term(s)	Male ; Humans ; Female ; Adult ; Middle Aged ; Depression/epidemiology ; Depression/genetics ; Serotonin Plasma Membrane Transport Proteins/genetics ; Polymorphism, Genetic ; Genotype ; Surveys and Questionnaires
Chemical Substances	Serotonin Plasma Membrane Transport Proteins ; SLC6A4 protein, human
Language	Russian
Publishing date	2024-03-11
Publishing country	Russia (Federation)
Document type	English Abstract ; Journal Article
ZDB-ID	1201462-x
ISSN	2309-4729 ; 1997-7298 ; 0044-4588
ISSN (online)	2309-4729
ISSN	1997-7298 ; 0044-4588
DOI	10.17116/jnevro2024124021135
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Article: Polymorphism of Mitochondrial DNA and Six Nuclear Genes in the Amur Evenk Population

Gubina, M. A. / Babenko, V. N. / Batsevich, V. A. / Leibova, N. A. / Zabiyako, A. P.

Russian journal of genetics. 2022 Feb., v. 58, no. 1

2022

Abstract: The polymorphism of six nuclear genes, ACE (I/D, rs1799752), NOS3 (4b/4a, rs61722009), ADRA2B (I/D, rs28365031), MTHFR (С677Т, rs1801133), TCF7L2 (rs7903146), and CSK (rs1378942), as well as mitochondrial DNA, was examined in the population of Amur ... ...

Abstract	The polymorphism of six nuclear genes, ACE (I/D, rs1799752), NOS3 (4b/4a, rs61722009), ADRA2B (I/D, rs28365031), MTHFR (С677Т, rs1801133), TCF7L2 (rs7903146), and CSK (rs1378942), as well as mitochondrial DNA, was examined in the population of Amur Evenks. It was demonstrated that among Evenks, Eastern Eurasian mtDNA haplogroups with the predominance of two of them, C and D (58%), were the most common. These haplogroups are most typical of the populations of North Asia and Siberia. Among West Eurasian haplogroups, the most common is haplogroup H (15%). The lowest statistically significant differences in mtDNA were found between Evenks, Turks, and Samoyeds, and the largest differences were with Finno-Ugric populations. The observed distribution of frequencies of loci for four genes in the studied population did not differ from the theoretically expected under the Hardy–Weinberg law, with the exception of TCF7L2 and CSK loci. Statistically significant association for gametic disequilibrium was observed between four pairs of genes (ACE and MTHFR, ACE and TCF7L2, NOS3 and CSK, ADRA2B and MTHFR). The distribution of allele associations at six loci was assessed using the maximum likelihood method. The number of associated alleles was calculated for each pseudohaplotype. It was demonstrated that the number of associated alleles proportionally increased with the decrease of pseudohaplotype frequency (R² = 0.5, R = 0.7, d.f. = 16, P < 0.001). It is suggested that the data obtained are characteristic not only of the studied population and also may reflect such processes as gametic disequilibrium (meiotic drive).
Keywords	Siberia ; alleles ; meiotic drive ; mitochondrial DNA ; statistical analysis
Language	English
Dates of publication	2022-02
Size	p. 42-56.
Publishing place	Pleiades Publishing
Document type	Article
ZDB-ID	1195858-3
ISSN	1608-3369 ; 1022-7954
ISSN (online)	1608-3369
ISSN	1022-7954
DOI	10.1134/S1022795422010033
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Article: Polymorphism of the Interleukin Genes IL-17A G197A and IL-17F A7488G in Patients with Gastric Cancer in the West Siberian Region

Gubina, M. A. / Solovieva, I. G. / Babenko, V. N. / Sokolov, A. V. / Gubina, E. Yu

Russian journal of genetics. 2022 July, v. 58, no. 7

2022

Abstract: The frequency of occurrence of alleles of the IL-17A G197A and IL-17F A7488G genes in 150 people with gastric cancer and 103 healthy people was analyzed. The frequencies of genotypes IL-17F A7488G in patients (AA—68.6, AG—25.3, and GG—6%) did not differ ... ...

Abstract	The frequency of occurrence of alleles of the IL-17A G197A and IL-17F A7488G genes in 150 people with gastric cancer and 103 healthy people was analyzed. The frequencies of genotypes IL-17F A7488G in patients (AA—68.6, AG—25.3, and GG—6%) did not differ significantly from those in the control (AA—77.7, AG—22.3, and GG—0.0%). Carriers of the GG genotype were found only in patients. There were no significant differences between patients and healthy people (χ² = 4.80, p < 0.09). The frequencies of genotypes IL-17A G197A in patients (GG—10.6, AG—48.7, and AA—40.7%) differed from the control (GG—11.7, AG—70.8, and AA—17.5%). The distribution of IL-17A genotypes G197A “case–control” showed that the frequency of occurrence of the AA genotype in a sample of patients with gastric cancer is two times higher than in a sample of healthy people. Significant differences between patients and healthy people were revealed (χ² = 15.79, p < 0.0003). Significant differences were found between sick and healthy women both in IL-17A G197A (χ² = 16.18, p < 0.0003) and in IL-17F A488G (χ² = 7.176, p < 0.027). No significant differences were found between the male samples. The results of our studies showed that only the A allele and the AA genotype of the IL-17A G197A gene are significantly more common in patients with gastric cancer than in healthy people, which may be a marker of the risk of developing gastric cancer in people living in the West Siberian region. Haplotypes characteristic only of patients with gastric cancer were identified. One of them (AAGG) is found with the same frequency in both men and women, and the second (AGGG) is most characteristic of women.
Keywords	alleles ; haplotypes ; interleukin-17 ; males ; risk ; stomach neoplasms
Language	English
Dates of publication	2022-07
Size	p. 823-828.
Publishing place	Pleiades Publishing
Document type	Article
ZDB-ID	1195858-3
ISSN	1608-3369 ; 1022-7954
ISSN (online)	1608-3369
ISSN	1022-7954
DOI	10.1134/S1022795422070067
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Article: Polymorphism of Mitochondrial DNA in Population of Siberian Tatars from Barabinsk Forest Steppe

Gubina, M. A / M. I. Voevoda / V. N. Babenko

Russian journal of genetics. 2018 June, v. 54, no. 6

2018

Abstract: The analysis of mtDNA polymorphism was carried out in the population of Siberian Tatars from the Barabinsk forest steppe living on the territory of Novosibirsk oblast (N = 199). As a result of the analysis of HVS I and HVS II nucleotide sequence, 101 ... ...

Abstract	The analysis of mtDNA polymorphism was carried out in the population of Siberian Tatars from the Barabinsk forest steppe living on the territory of Novosibirsk oblast (N = 199). As a result of the analysis of HVS I and HVS II nucleotide sequence, 101 haplotypes that refer to 22 mtDNA haplogroups were detected. The population of Baraba Tatars is represented by both East Eurasian (38.7%) and West Eurasian mtDNA lines (61.3%). H, T, U5, and J haplogroups prevail among West Eurasian haplogroups; C, D, G, M, and A haplogroups prevail among East Eurasian ones. According to the index of genetic diversity, Tatars from the Barabinsk forest steppe (0.9141) are the closest to Kazakhs (0.9108), Bashkirs (0.9165), and Tobol-Irtysh Tatars (0.9104). The greatest statistically significant interpopulation differences (FST) were detected between all studied samples; the smallest interpopulation differences were detected between all Tatar samples, as well as between Tatars and Komi, Mansi, Udmurts, Kazakhs, Chuvashes, and Bashkirs. The haplogroup H is the most common in populations that we studied. In the present study, was registered the haplotype 16126–16294 with the frequency of 4% (T cluster) previously found only in Caucasians. High frequency of haplogroups U4, U5, and H in the gene pool of Baraba Tatars brings them together not only with Samoyeds but also with Finno-Ugric populations. The highest intrapopulation genetic diversity was detected in Tatars from the Barabinsk forest steppe, Tobol-Irtysh Tatars, Kazakhs, and Bashkirs. The presence of the haplogroup B in the mitochondrial DNA genetic pool of Siberian Tatars brings them together with Turks that came from regions of Altai and Central Kazakhstan and inhabited the Western Siberian forest steppe in the 6th–9th centuries. The haplogroup U7, which is typical of populations of Jordan, Kuwait, Iran, and Saudi Arabia, could also have entered the territory of residence of Siberian Tatars in the middle of second millennium BC, when Iranian-speaking tribes entered Siberia.
Keywords	forest steppe ; gene pool ; genetic variation ; haplotypes ; mitochondrial DNA ; nucleotide sequences ; Whites ; Iran ; Jordan ; Kazakhstan ; Kuwait ; Saudi Arabia ; Siberia
Language	English
Dates of publication	2018-06
Size	p. 717-731.
Publishing place	Pleiades Publishing
Document type	Article
ZDB-ID	1195858-3
ISSN	1608-3369 ; 1022-7954
ISSN (online)	1608-3369
ISSN	1022-7954
DOI	10.1134/S1022795418060066
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Article: Signals of Directed Selection in the Indigenous Populations of Siberia

Kolesnikov, N. A. / Kharkov, V. N. / Zarubin, A. A. / Voevoda, M. I. / Gubina, M. A. / Shtygasheva, O. V. / Maksimova, N. R. / Sukhomyasova, A. L. / Stepanov, V. A.

Russian journal of genetics. 2022 Apr., v. 58, no. 4

2022

Abstract: The indigenous populations of Siberia are of significant interest for population genomics because of the specificity of their gene pools, which developed in various genetic and demographic conditions. Data on directional selection signals is an important ...

Abstract	The indigenous populations of Siberia are of significant interest for population genomics because of the specificity of their gene pools, which developed in various genetic and demographic conditions. Data on directional selection signals is an important addition to the existing data on the evolution of gene pools and the mechanisms of genetic adaptation of the population of Eurasia. We used genotype array of 1 779 819 SNPs in a group of 477 unrelated subjects, including 20 indigenous populations of Siberia, to search for directional selection signals using a test for extended homozygosity of haplotypes (nSL). The present study detected that all studied populations of Siberia strongly differ from each other in the composition of genes that demonstrate the effect of selection. The largest number of significant signals of natural selection was found in the populations of the Khanty, Koryaks, and Chukchi. The genes ADGRB3, ANO3, CDH13, CUEDC1, and PCDH15 are distinguished among the genomic loci carrying the most pronounced directional selection signals in the northern populations.
Keywords	Siberia ; genes ; haplotypes ; homozygosity ; metagenomics ; natural selection ; Eurasia
Language	English
Dates of publication	2022-04
Size	p. 473-477.
Publishing place	Pleiades Publishing
Document type	Article
ZDB-ID	1195858-3
ISSN	1608-3369 ; 1022-7954
ISSN (online)	1608-3369
ISSN	1022-7954
DOI	10.1134/S102279542204007X
Database	NAL-Catalogue (AGRICOLA)

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Article: Polymorphism of Human Thermoreceptor Genes TRPV1 and TRPA1 in Populations of the Altai-Sayan Region and the Far East

Gubina, M.A / P. S. Orlov / V. N. Babenko / A. P. Zabiyako / D. E. Ivanoschuk / M. I. Voevoda

Russian journal of genetics. 2018 Feb., v. 54, no. 2

2018

Abstract: Genotyping of TRPV1 and TRPA1 genes encoding thermoreceptors in the populations of the Altai-Sayan region and the Far East was conducted. The sample consisted of 15 populations comprising 1482 individuals. The analysis of TRPV1 rs222747 demonstrated that ...

Abstract	Genotyping of TRPV1 and TRPA1 genes encoding thermoreceptors in the populations of the Altai-Sayan region and the Far East was conducted. The sample consisted of 15 populations comprising 1482 individuals. The analysis of TRPV1 rs222747 demonstrated that the frequency of M315I was closest to East Asian populations only in Nanais and Koryaks (56 and 64%, respectively). Siberian Tatars, Yakuts, and Evenks were closest to European populations. All populations of the Altai-Sayan region reported an intermediate position between the Caucasoids and the Eastern Mongoloids on the basis of the frequency of M315I. No deviations from the Hardy–Weinberg distribution were observed. The observed heterozygosity exceeded the expected one in eight populations. The analysis of TRPA1 rs13268757 revealed that Chukchi, Yukaghir, Koryak, Tuvinian, Southern Altaian, and Telengit populations were closest to the East Asian populations on the basis of the frequency of R3C substitution (3–7%). At the same time, populations of Siberian Tatars, Nanais, Evenks, Yakuts, Shorians, Khakases, and Kazakhs were intermediate between the Caucasoids (18–23%) and the Mongoloids from East Asia (3–7%) on the basis of the frequency of this polymorphism. A deviation from the Hardy–Weinberg distribution was detected only in the Yukaghir population. The observed heterozygosity was higher than the expected one in nine populations. A trans-association of TRPA1 and TRPV1 gene polymorphisms was carried out in 14 populations via regression analysis. A negative correlation of–0.545 was determined, the number of degrees of freedom (df) was 13, and the P-value was 0.048. The data obtained indicate that the analyzed polymorphisms are correlated, which confirms an earlier conclusion of the TRPA1-dependent inhibition of TRPV1 function. The results may evidence in the co-evolution of analyzed genes.
Keywords	coevolution ; genes ; genetic polymorphism ; genotyping ; heterozygosity ; humans ; regression analysis ; sensory receptors ; East Asia ; Russia
Language	English
Dates of publication	2018-02
Size	p. 235-243.
Publishing place	Pleiades Publishing
Document type	Article
ZDB-ID	1195858-3
ISSN	1608-3369 ; 1022-7954
ISSN (online)	1608-3369
ISSN	1022-7954
DOI	10.1134/S1022795418020084
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Article: Features of the Genomic Distribution of Runs of Homozygosity in the Indigenous Population of Northern Eurasia at the Individual and Population Levels Based on High Density SNP Analysis

Kolesnikov, N. A. / Kharkov, V. N. / Zarubin, A. A. / Radzhabov, M. O. / Voevoda, M. I. / Gubina, M. A. / Khusnutdinova, E. K. / Litvinov, S. S. / Ekomasova, N. V. / Shtygasheva, O. V. / Maksimova, N. R. / Sukhomyasova, A. L. / Stepanov, V. A.

Russian journal of genetics. 2021 Nov., v. 57, no. 11

2021

Abstract: The genomic data analysis (~886 889 autosomal SNPs) allowed us to estimate the inbreeding level on the basis of the analysis of runs of homozygosity (FROH) in a sample of 1836 individuals, including 76 indigenous populations of Siberia, Dagestan, the ... ...

Abstract	The genomic data analysis (~886 889 autosomal SNPs) allowed us to estimate the inbreeding level on the basis of the analysis of runs of homozygosity (FROH) in a sample of 1836 individuals, including 76 indigenous populations of Siberia, Dagestan, the Caucasus, Volga-Ural region, Eastern Europe, and Central Asia. The data were obtained using the Infinium Multi-Ethnic Global-8 Kit. In the populations of Dagestan, within the Nakh-Daghestanian language family, representatives of several language groups can be distinguished, with the maximum FROH level for the Dido group (0.0727) and the Andean group (0.0378), which is similar in values to the populations speaking the Chukchi-Kamchatka and Nivkh languages of Siberia (0.0360). The Siberian populations are characterized by a greater value of the total length of short and medium runs of homozygosity per person. The total length of long ROHs is more variable and much larger in the most of the populations of Dagestan and Siberia compared to other populations of the Caucasus, Central Asia, Europe, and the Volga-Ural region.
Keywords	Siberia ; genomics ; homozygosity ; nationalities and ethnic groups ; Andes region ; Caucasus region ; Central Asia ; Eastern European region ; Eurasia
Language	English
Dates of publication	2021-11
Size	p. 1271-1284.
Publishing place	Pleiades Publishing
Document type	Article
ZDB-ID	1195858-3
ISSN	1608-3369 ; 1022-7954
ISSN (online)	1608-3369
ISSN	1022-7954
DOI	10.1134/S1022795421110053
Database	NAL-Catalogue (AGRICOLA)

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Article ; Online: Haplotype analysis of the HFE gene among populations of Northern Eurasia, in patients with metabolic disorders or stomach cancer, and in long-lived people.

Mikhailova, S V / Babenko, V N / Ivanoshchuk, D E / Gubina, M A / Maksimov, V N / Solovjova, I G / Voevoda, M I

BMC genetics

2016 Volume 17, Issue 1, Page(s) 83

Abstract: Background: Previously, it was shown that the HFE gene (associated with human hereditary hemochromatosis) has several haplotypes of intronic polymorphisms. Some haplotype frequencies are race specific and hence can be used in phylogenetic analysis. We ... ...

Abstract	Background: Previously, it was shown that the HFE gene (associated with human hereditary hemochromatosis) has several haplotypes of intronic polymorphisms. Some haplotype frequencies are race specific and hence can be used in phylogenetic analysis. We assumed that analysis of Caucasoid patients-living now in Western Siberia and having diseases associated with dietary habits and metabolic rate-will allow us to understand the processes of possible selection during settling of the northern part of Asia. Results: Haplotype analysis of Northern Eurasian native and recently settled ethnic groups was performed on polymorphisms rs1799945, rs1800730, rs1800562, rs2071303, rs1800708, rs1572982, rs2794719, rs807209, and rs2032451 of this gene. The CCA haplotype of the rs2071303, rs1800708, and rs1572982 was found to be associated with HLA-A2 (39 %) in Asian populations. Haplotype analysis for the rs1799945, rs1800730, rs1800562, rs2071303, rs1800708, and rs1572982 was performed on Russian patients with some metabolic disorders or stomach cancer and among long-lived people. Decreased frequencies of the TTA haplotype (T in rs2071303, T in rs1800708, and A in rs1572982) were observed in the groups of patients with diseases associated with overweight (fatty liver disease, type 2 diabetes mellitus, or metabolic syndrome + arterial hypertension) as compared with the control sample. We detected significant differences in this haplotype's frequency between the patients with type 2 diabetes mellitus and Russian adolescents, elderly citizens, and long-lived people (χ(2) P value = 0.003, 0.010, and 0.015, respectively). Conclusions: No significant differences in frequencies of the alleles with mutations in coding regions of the HFE gene (C282Y, H63D, and S65C) were detected between the analyzed patients (with stomach cancer, metabolic syndrome, fatty liver disease, or type 2 diabetes mellitus) and the control Caucasoid sample. Monophyletic origin of H63D (rs1799945) was confirmed in Caucasoids and Northern Asians. The reasons for a sharp increase in the frequency of CCA haplotype of HFE in the Asian race remain unclear.
MeSH term(s)	Adolescent ; Aged ; Aged, 80 and over ; Alleles ; Asia ; Environment ; European Continental Ancestry Group/genetics ; Evolution, Molecular ; HLA-A Antigens/genetics ; Haplotypes ; Hemochromatosis Protein/genetics ; Homozygote ; Humans ; Longevity/genetics ; Metabolic Diseases/genetics ; Middle Aged ; Selection, Genetic ; Stomach Neoplasms/genetics
Chemical Substances	HLA-A Antigens ; Hemochromatosis Protein
Language	English
Publishing date	2016-06-17
Publishing country	England
Document type	Journal Article
ISSN	1471-2156
ISSN (online)	1471-2156
DOI	10.1186/s12863-016-0396-z
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article: [The Dynamics of the Composition of mtDNA Haplotypes of the Ancient Population of the Altai Mountains from the Early Bronze Age (3rd Millennium BC) to the Iron Age (2nd-1st Centuries BC)].

Gubina, M A / Kulikov, I V / Babenko, V N / Chikisheva, T A / Romaschenko, A G / Voevoda, M I / Molodin, V I

Genetika

2016 Volume 52, Issue 1, Page(s) 106–119

Abstract: The mtDNA polymorphism in representatives of various archaeological cultures of the Developed Bronze Age, Early Scythian, and Hunnish-Sarmatian periods was analyzed (N = 34). It detected the dominance of Western-Eurasian haplotypes (70.6%) in mtDNA ... ...

Abstract	The mtDNA polymorphism in representatives of various archaeological cultures of the Developed Bronze Age, Early Scythian, and Hunnish-Sarmatian periods was analyzed (N = 34). It detected the dominance of Western-Eurasian haplotypes (70.6%) in mtDNA samples from the representatives of the ancient population of the Early Bronze Age--Iron Age on the territory of Altai Mountains. Since the 8th to the 7th centuries BC, a sharp increase was revealed in the Eastern-Eurasian haplogroups A, D, C, andZ (43.75%) as compared to previous cultures (16.7%). The presence of haplotype 223-242-290-319 of haplogroup A8 in Dolgans, Itelmens, Evens, Koryaks, and Yakuts indicates the possible long-term presence of its carriers in areas inhabited by these populations. The prevalence of Western-Eurasian haplotypes is observed not only in the Altai Mountains but also in Central Asia (Kazakhstan) and the South of the Krasnoyarsk Krai. All of the three studied samples from the Western-Eurasian haplogroups were revealed to contain U, H, T, and HV. The ubiquitous presence of haplotypes of haplogroup H and some haplogroups of cluster U (U5al, U4, U2e, and K) in the vast territory from the Yenisei River basin to the Atlantic Ocean may indicate the direction of human settlement, which most likely occurred in the Paleolithic Period from Central Asia.
MeSH term(s)	DNA, Mitochondrial/genetics ; Genetics, Population/history ; Haplotypes ; History, Ancient ; Humans ; Kazakhstan ; Mitochondria/genetics ; Paleontology ; Polymorphism, Genetic ; Russia
Chemical Substances	DNA, Mitochondrial
Language	Russian
Publishing date	2016-01
Publishing country	Russia (Federation)
Document type	English Abstract ; Historical Article ; Journal Article
ZDB-ID	216714-1
ISSN	0016-6758
ISSN	0016-6758
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Article: Polymorphism of mitochondrial DNA in old believers from Siberia

Gubina, M. A / Babenko, V. N / Damba, L. D / Ponomareva, M. N / Konovalova, N. A / Voevoda, M. I

Russian journal of genetics. 2014 June, v. 50, no. 6

2014

Abstract: The polymorphism of mtDNA was examined in populations of Old Believers (n = 104) and Russians from Novosibirsk oblast (n = 270). Most of the haplogroups identified belonged to West Eurasian lineages. The frequencies of these haplogroups constituted 96.6% ...

Abstract	The polymorphism of mtDNA was examined in populations of Old Believers (n = 104) and Russians from Novosibirsk oblast (n = 270). Most of the haplogroups identified belonged to West Eurasian lineages. The frequencies of these haplogroups constituted 96.6% in Russians from Novosibirsk and 93.2% in Old Believers from Tyumen oblast. The populations examined were characterized by a high mtDNA diversity level (h = 0.98) compared to other population samples of Russians from Russia. Among the West Eurasian haplogroups, the most common (a frequency of more than 10%) were haplogroups H, U, J, and T, the proportion of which constituted 77.9% in Old Believers and 83.1% in Russians from Novosibirsk. The Mongoloid admixture in Russians (3.3%) and Old Believers (6.7%) was represented by haplogroups A, D, Z, and C, D, M*, respectively. Statistically significant differences (P < 0.05) were revealed between the Old Believers examined and Bosnians, Czechs, Slovenes, and Russians from the cities of Nizhny Novgorod and Tula. The data obtained confirm the earlier hypothesized influence of the Finno-Ugric component on the East Slavic populations.
Keywords	cities ; mitochondrial DNA ; Siberia
Language	English
Dates of publication	2014-06
Size	p. 638-652.
Publishing place	Springer-Verlag
Document type	Article
ZDB-ID	1195858-3
ISSN	1608-3369 ; 1022-7954
ISSN (online)	1608-3369
ISSN	1022-7954
DOI	10.1134/S1022795414060040
Database	NAL-Catalogue (AGRICOLA)

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