M
Mikhail Skoblov
Researcher at Far Eastern Federal University
Publications - 71
Citations - 1112
Mikhail Skoblov is an academic researcher from Far Eastern Federal University. The author has contributed to research in topics: Gene & Biology. The author has an hindex of 12, co-authored 53 publications receiving 848 citations. Previous affiliations of Mikhail Skoblov include George Mason University & Russian Academy of Sciences.
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The mammalian pannexin family is homologous to the invertebrate innexin gap junction proteins.
Ancha Baranova,Dmitry Ivanov,Nadezda Petrash,Anya Pestova,Mikhail Skoblov,Ilya V. Kelmanson,Dmitry A. Shagin,Svetlana Nazarenko,Elena Geraymovych,Oxana Litvin,Anya Tiunova,Timothy L. Born,Natalia Usman,Dmitry B. Staroverov,Sergey Lukyanov,Yury Panchin +15 more
TL;DR: Cloned genes PANX1, PANX2 and PANX3, encoding putative gap junction proteins homologous to invertebrate innexins, which constitute a new family of mammalian proteins called pannexins are revealed, pointing to their important function.
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Comprehensive Analysis of Human microRNA-mRNA Interactome.
TL;DR: This study provides initial insight into the complexity of human microRNA–mRNA interactions and reveals a group of microRNAs that are expressed at a very high level, while interacting with only a few mRNAs, which, indeed, serve as their specific expression regulators.
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Protein partners of KCTD proteins provide insights about their functional roles in cell differentiation and vertebrate development
Mikhail Skoblov,Andrey V. Marakhonov,Ekaterina S. Marakasova,A. A. Gus’kova,Vikas Chandhoke,Aybike Birerdinc,Ancha Baranova +6 more
TL;DR: A comprehensive analysis of protein-protein interactions (PPIs) allowed as mentioned in this paper to put forth a number of testable hypotheses concerning the biological functions for individual KCTD proteins, including the role of BTBD10 in post-replication DNA repair through PCNA ubiquitination.
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The role of long non-coding RNAs in the pathogenesis of hereditary diseases.
TL;DR: Fundamental research in the field of molecular genetics of lncRNA is necessary for a more complete understanding of their significance and this review is focused on hereditary diseases in the pathogenesis of which long non-coding RNAs play an important role.
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Distinct organization of the candidate tumor suppressor gene RFP2 in human and mouse: multiple mRNA isoforms in both species- and human-specific antisense transcript RFP2OS.
Ancha Baranova,Marianne Hammarsund,Dmitry Ivanov,Dmitry Ivanov,Mikhail Skoblov,Olle Sangfelt,Martin Corcoran,Tatiana Borodina,N. V. Makeeva,Anna Pestova,T. V. Tyazhelova,Svetlana Nazarenko,Francesco Gorreta,Tariq Alsheddi,Karen Schlauch,Nikitin Ea,Kapanadze Bi,Dmitry A. Shagin,A. B. Poltaraus,Andrey Ivanovich Vorobiev,Eugene R. Zabarovsky,Sergey Lukianov,Vikas Chandhoke,Rachel E. Ibbotson,David Oscier,Stefan Einhorn,Dan Grandér,N. K. Yankovsky +27 more
TL;DR: The predicted human and mouse RFP2 proteins are shown to contain a tripartite Ringing finger-B-box-coiled-coil domain (RBCC), also known as a TRIM domain, and therefore belong to a subgroup of RING finger proteins that are often involved in developmental and tumorigenic processes.