Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Irina N Filippova"'
Autor:
Andrey V Khrunin, Denis V Khokhrin, Irina N Filippova, Tõnu Esko, Mari Nelis, Natalia A Bebyakova, Natalia L Bolotova, Janis Klovins, Liene Nikitina-Zake, Karola Rehnström, Samuli Ripatti, Stefan Schreiber, Andre Franke, Milan Macek, Veronika Krulišová, Jan Lubinski, Andres Metspalu, Svetlana A Limborska
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e58552 (2013)
Several studies examined the fine-scale structure of human genetic variation in Europe. However, the European sets analyzed represent mainly northern, western, central, and southern Europe. Here, we report an analysis of approximately 166,000 single
Externí odkaz:
https://doaj.org/article/e9a30dda50d04c20ac9017c9cc9c28dc
Publikováno v:
Управленец, Vol 13, Iss 6, Pp 15-29 (2023)
Geographic market definition is an important element of antitrust enforcement in the framework of countering monopolistic activities and M&A (mergers and acquisitions) control. Incorrectly defined geographic market can lead to false conclusions about
Externí odkaz:
https://doaj.org/article/88ccd969217449cd8adf2c0b49a51c3e
Autor:
Irina N. Filippova
Publikováno v:
Вестник Московского государственного областного университета, Iss 3 (2023)
Aim. To study approbation as a strategy of intersemiotic translation, evaluation of transformations and polymodal means of transmitting a conceptual picture of the world reflected in the original text - Pushkin’s fairy tale poem “Ruslan and Lyudm
Externí odkaz:
https://doaj.org/article/65d5a9b32623410d9108d6e41992e620
Publikováno v:
Bulletin of the Moscow State Regional University (Linguistics). :117-126
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b55f444e1005017c3fb8f36094d18ac2
https://doi.org/10.18384/2310-712x-2018-4-117-126
https://doi.org/10.18384/2310-712x-2018-4-117-126
Publikováno v:
Molecular Genetics, Microbiology and Virology. 29:53-57
In many human populations, from 16 to 60% of individuals are homozygotes for glutathione-S-transferase M1 gene deletion. In this study, we determined the correlation between GSTM1 gene deletion and the genetic diversity of the GSTM cluster (which inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b4226241e3a9f8519adaa0953a172f7
https://doi.org/10.3103/s0891416814020062
https://doi.org/10.3103/s0891416814020062
Autor:
Irina N. Filippova
Publikováno v:
Bulletin of the Moskow State Regional University.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9fa360919cb2e778e5d7580270d908c
https://doi.org/10.18384/2224-0209-2015-3-690
https://doi.org/10.18384/2224-0209-2015-3-690
Autor:
Irina N. Filippova
Publikováno v:
Bulletin of the Moskow State Regional University.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f80c31da52dc76954665d828c6281ba5
https://doi.org/10.18384/2224-0209-2013-4-476
https://doi.org/10.18384/2224-0209-2013-4-476
Publikováno v:
BMC Genetics, Vol 13, Iss 1, p 89 (2012)
BMC Genetics
BMC Genetics
Background Extensive genome-wide analyses of many human populations, using microarrays containing hundreds of thousands of single-nucleotide polymorphisms, have provided us with abundant information about global genomic diversity. However, these data
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86a55af0a0e30283a1960aafc658098a
https://doi.org/10.1186/1471-2156-13-89
https://doi.org/10.1186/1471-2156-13-89
Autor:
Petr Slominsky, Svetlana A. Limborska, Andrey Khrunin, Aydar M. Aliev, Irina N. Filippova, Tat’yana V. Tupitsina
Publikováno v:
Molecular Cytogenetics
Background GSTM1 gene deletion is one of the most known copy number polymorphisms in human genome. It is most likely caused by homologous recombination between the repeats flanking the gene. However, taking into account that the deletion has no cruci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b37b16a13e8378eb9e6dbb60a70a764e
Autor:
Andres Metspalu, Milan Macek, Samuli Ripatti, Liene Nikitina-Zake, Irina N. Filippova, Veronika Krulisova, Denis Khokhrin, Jan Lubinski, Stefan Schreiber, N. A. Bebyakova, Tõnu Esko, Mari Nelis, Natalia L. Bolotova, Karola Hannele Rehnström, Andre Franke, Janis Klovins, Andrey Khrunin, Svetlana A. Limborska
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 3, p e58552 (2013)
PLoS ONE, Vol 8, Iss 3, p e58552 (2013)
Several studies examined the fine-scale structure of human genetic variation in Europe. However, the European sets analyzed represent mainly northern, western, central, and southern Europe. Here, we report an analysis of approximately 166,000 single
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::048aeb57f9cc8a22f33b13b0408dab3d