Temporal fate mapping reveals age-linked heterogeneity in naive T lymphocytes in mice.
about
Establishment and Maintenance of the Human Naïve CD4+ T-Cell CompartmentMemory CD4 T cell subsets are kinetically heterogeneous and replenished from naive T cells at high levels.A physiologically based kinetic model for elucidating the in vivo distribution of administered mesenchymal stem cells.Dynamics of Recent Thymic Emigrants in Young Adult Mice.On being the right size: antibody repertoire formation in the mouse and human.Visualization and Modeling of the In Vivo Distribution of Mesenchymal Stem Cells.Age is not just a number: Naive T cells increase their ability to persist in the circulation over time.T Cell Receptor-Major Histocompatibility Complex Interaction Strength Defines Trafficking and CD103+ Memory Status of CD8 T Cells in the Brain.The Confluence of Sex Hormones and Aging on Immunity.
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P2860
Temporal fate mapping reveals age-linked heterogeneity in naive T lymphocytes in mice.
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2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年學術文章
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2015年學術文章
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name
Temporal fate mapping reveals age-linked heterogeneity in naive T lymphocytes in mice.
@ast
Temporal fate mapping reveals age-linked heterogeneity in naive T lymphocytes in mice.
@en
type
label
Temporal fate mapping reveals age-linked heterogeneity in naive T lymphocytes in mice.
@ast
Temporal fate mapping reveals age-linked heterogeneity in naive T lymphocytes in mice.
@en
prefLabel
Temporal fate mapping reveals age-linked heterogeneity in naive T lymphocytes in mice.
@ast
Temporal fate mapping reveals age-linked heterogeneity in naive T lymphocytes in mice.
@en
P2860
P356
P1476
Temporal fate mapping reveals age-linked heterogeneity in naive T lymphocytes in mice
@en
P2093
Andrew J Yates
Graeme Gossel
P2860
P304
P356
10.1073/PNAS.1517246112
P407
P577
2015-11-25T00:00:00Z