Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Maria I. Churkina"'
Autor:
Elena N. Voropaeva, Yuriy L. Orlov, Tatiana I. Pospelova, Anna A. Gurageva, Mikhail I. Voevoda, Vladimir N. Maksimov, Olga B. Seregina, Maria I. Churkina
Publikováno v:
PeerJ, Vol 8, p e10335 (2020)
Background Rare single nucleotide polymorphisms (SNPs) are likely to be a crucial genetic factor for human diseases, including cancer. rs78378222 is rare SNP in 3′-untranslated region (UTR) of TP53 gene leading to disturbance of 3′-end mRNA proce
Externí odkaz:
https://doaj.org/article/c1a93b0d6aa0467ea22b4ae993435667
Autor:
Elena N. Voropaeva, Tatjana I. Pospelova, Yuriy L. Orlov, Maria I. Churkina, Olga V. Berezina, Anna A. Gurazheva, Tatjana A. Ageeva, Olga B. Seregina, Vladimir N. Maksimov
Publikováno v:
Genes; Volume 13; Issue 8; Pages: 1401
The regulation of oncogenes by microRNA is a focus of medical research. hsa-miR-203, hsa-mir-129, hsa-miR-34a, hsa-miR-34b and hsa-miR-34c are oncosuppressive microRNAs that mediate the antitumor activity of p53. We seek to evaluate the frequencies,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1395834099543e0a4dfa0a64a41591fe
Autor:
Anna A Gurageva, Yuriy L. Orlov, Mikhail I. Voevoda, Olga B. Seregina, Maria I Churkina, Vladimir N. Maksimov, T. I. Pospelova, E. N. Voropaeva
Publikováno v:
PeerJ, Vol 8, p e10335 (2020)
PeerJ
PeerJ
Background Rare single nucleotide polymorphisms (SNPs) are likely to be a crucial genetic factor for human diseases, including cancer. rs78378222 is rare SNP in 3′-untranslated region (UTR) of TP53 gene leading to disturbance of 3′-end mRNA proce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c577acf5d02b45f991110f098251218
https://peerj.com/articles/10335/
https://peerj.com/articles/10335/
Autor:
Vladimir Maximov, Viktoria Karpova, Tatyana I. Pospelova, Anastasia A. Ivanova, Anna A Gurageva, Maria I Churkina, Olga V. Beresina, E. S. Mel’nikova, E. N. Voropaeva
Publikováno v:
2020 Cognitive Sciences, Genomics and Bioinformatics (CSGB).
In this study, based on the information presented in the specialized resource CBioPortal for Cancer Genomics database, the data on the diffuse large B-cell lymphoma (DLBCL) mutation profile detected by next generation sequencing (NGS) methods have be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b1d0ed3deaed62435422afa4ad380df
https://doi.org/10.1109/csgb51356.2020.9214638
https://doi.org/10.1109/csgb51356.2020.9214638