Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Artem I. Mikelov"'
Autor:
Elena I. Kovalenko, Ivan V. Zvyagin, Maria A. Streltsova, Artem I. Mikelov, Sofya A. Erokhina, William G. Telford, Alexander M. Sapozhnikov, Yury B. Lebedev
Publikováno v:
Frontiers in Immunology, Vol 11 (2021)
T cells that express CD56 in peripheral blood of healthy humans represent a heterogeneous and poorly studied subset. In this work, we analyzed this subset for NKG2C expression. In both CD56+ and CD56− subsets most of the NKG2C+ T cells had a phenot
Externí odkaz:
https://doaj.org/article/acce40ba91d940298fca962bf001f776
Autor:
Mikhail V. Pogorelyy, Alla D. Fedorova, James E. McLaren, Kristin Ladell, Dmitri V. Bagaev, Alexey V. Eliseev, Artem I. Mikelov, Anna E. Koneva, Ivan V. Zvyagin, David A. Price, Dmitry M. Chudakov, Mikhail Shugay
Publikováno v:
Genome Medicine, Vol 10, Iss 1, Pp 1-14 (2018)
Abstract Background Adaptive immune responses to newly encountered pathogens depend on the mobilization of antigen-specific clonotypes from a vastly diverse pool of naive T cells. Using recent advances in immune repertoire sequencing technologies, mo
Externí odkaz:
https://doaj.org/article/845a169f8e4440afa7d30ed71f7b4f65
Autor:
Artem I. Mikelov, Evgeniia I. Alekseeva, Ekaterina A. Komech, Dmitriy B. Staroverov, Maria A. Turchaninova, Mikhail Shugay, Dmitriy M. Chudakov, Georgii A. Bazykin, Ivan V. Zvyagin
Publikováno v:
eLife. 11
The stability and plasticity of B cell-mediated immune memory ensures the ability to respond to the repeated challenges. We have analyzed the longitudinal dynamics of immunoglobulin heavy chain repertoires from memory B cells, plasmablasts, and plasm
Autor:
David Price, Anna E. Koneva, James E. McLaren, Ivan V. Zvyagin, Kristin Ladell, Dmitri V. Bagaev, Mikhail Shugay, Alla D. Fedorova, Alexey V. Eliseev, Dmitry M. Chudakov, Mikhail V. Pogorelyy, Artem I. Mikelov
Publikováno v:
Genome Medicine
Genome Medicine, Vol 10, Iss 1, Pp 1-14 (2018)
Genome Medicine, Vol 10, Iss 1, Pp 1-14 (2018)
Background Adaptive immune responses to newly encountered pathogens depend on the mobilization of antigen-specific clonotypes from a vastly diverse pool of naive T cells. Using recent advances in immune repertoire sequencing technologies, models of t