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Digoxin reveals a functional connection between HIV-1 integration preference and T-cell activation
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Digoxin reveals a functional connection between HIV-1 integration preference and T-cell activation

PLoS pathogens, 2017-07, Vol.13 (7), p.e1006460 [Peer Reviewed Journal]

COPYRIGHT 2017 Public Library of Science ;COPYRIGHT 2017 Public Library of Science ;2017 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Zhyvoloup A, Melamed A, Anderson I, Planas D, Lee C-H, Kriston-Vizi J, et al. (2017) Digoxin reveals a functional connection between HIV-1 integration preference and T-cell activation. PLoS Pathog 13(7): e1006460. https://doi.org/10.1371/journal.ppat.1006460 ;Distributed under a Creative Commons Attribution 4.0 International License ;2017 Zhyvoloup et al 2017 Zhyvoloup et al ;2017 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Zhyvoloup A, Melamed A, Anderson I, Planas D, Lee C-H, Kriston-Vizi J, et al. (2017) Digoxin reveals a functional connection between HIV-1 integration preference and T-cell activation. PLoS Pathog 13(7): e1006460. https://doi.org/10.1371/journal.ppat.1006460 ;ISSN: 1553-7374 ;ISSN: 1553-7366 ;EISSN: 1553-7374 ;DOI: 10.1371/journal.ppat.1006460 ;PMID: 28727807

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2
HIV-1 selectively targets gut-homing CCR6+CD4+ T cells via mTOR-dependent mechanisms
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HIV-1 selectively targets gut-homing CCR6+CD4+ T cells via mTOR-dependent mechanisms

JCI insight, 2017-08, Vol.2 (15) [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;Copyright © 2017, American Society for Clinical Investigation 2017 American Society for Clinical Investigation ;ISSN: 2379-3708 ;EISSN: 2379-3708 ;DOI: 10.1172/jci.insight.93230 ;PMID: 28768913

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