Abstract
In this issue of Immunity, Chopp et. al. use single-cell transcriptomics and epigenomics in mice and human samples to delineate developmental trajectories of αβ T cell subsets and refine the kinetic selection model of CD4+ and CD8+ T cell lineage commitment.
Copyright © 2020 Elsevier Inc. All rights reserved.
Publication types
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Research Support, N.I.H., Extramural
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Comment
MeSH terms
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Animals
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Cell Differentiation
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Epigenomics
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Humans
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Mice
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Receptors, Antigen, T-Cell, alpha-beta* / genetics
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Receptors, Antigen, T-Cell, gamma-delta* / genetics
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T-Lymphocyte Subsets
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Transcriptome
Substances
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Receptors, Antigen, T-Cell, alpha-beta
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Receptors, Antigen, T-Cell, gamma-delta