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Antagonism of PP2A is an independent and conserved function of HIV-1 Vif and causes cell cycle arrest.

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Title: Antagonism of PP2A is an independent and conserved function of HIV-1 Vif and causes cell cycle arrest.
Authors: Marelli S; Department of Medicine, University of Cambridge, Cambridge, United Kingdom.; Cambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), University of Cambridge, Cambridge, United Kingdom., Williamson JC; Department of Medicine, University of Cambridge, Cambridge, United Kingdom.; Cambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), University of Cambridge, Cambridge, United Kingdom., Protasio AV; Department of Medicine, University of Cambridge, Cambridge, United Kingdom.; Cambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), University of Cambridge, Cambridge, United Kingdom., Naamati A; Department of Medicine, University of Cambridge, Cambridge, United Kingdom.; Cambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), University of Cambridge, Cambridge, United Kingdom., Greenwood EJ; Department of Medicine, University of Cambridge, Cambridge, United Kingdom.; Cambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), University of Cambridge, Cambridge, United Kingdom., Deane JE; Department of Clinical Neuroscience, University of Cambridge, Cambridge, United Kingdom.; Cambridge Institute for Medical Research (CIMR), University of Cambridge, Cambridge, United Kingdom., Lehner PJ; Department of Medicine, University of Cambridge, Cambridge, United Kingdom.; Cambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), University of Cambridge, Cambridge, United Kingdom., Matheson NJ; Department of Medicine, University of Cambridge, Cambridge, United Kingdom.; Cambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), University of Cambridge, Cambridge, United Kingdom.
Source: ELife [Elife] 2020 Apr 15; Vol. 9. Date of Electronic Publication: 2020 Apr 15.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: eLife Sciences Publications, Ltd Country of Publication: England NLM ID: 101579614 Publication Model: Electronic Cited Medium: Internet ISSN: 2050-084X (Electronic) Linking ISSN: 2050084X NLM ISO Abbreviation: Elife Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Antagonism of PP2A is an independent and conserved function of HIV-1 Vif and causes cell cycle arrest.
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  Data: <searchLink fieldCode="AU" term="%22Marelli+S%22">Marelli S</searchLink>; Department of Medicine, University of Cambridge, Cambridge, United Kingdom.; Cambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), University of Cambridge, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Williamson+JC%22">Williamson JC</searchLink>; Department of Medicine, University of Cambridge, Cambridge, United Kingdom.; Cambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), University of Cambridge, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Protasio+AV%22">Protasio AV</searchLink>; Department of Medicine, University of Cambridge, Cambridge, United Kingdom.; Cambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), University of Cambridge, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Naamati+A%22">Naamati A</searchLink>; Department of Medicine, University of Cambridge, Cambridge, United Kingdom.; Cambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), University of Cambridge, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Greenwood+EJ%22">Greenwood EJ</searchLink>; Department of Medicine, University of Cambridge, Cambridge, United Kingdom.; Cambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), University of Cambridge, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Deane+JE%22">Deane JE</searchLink>; Department of Clinical Neuroscience, University of Cambridge, Cambridge, United Kingdom.; Cambridge Institute for Medical Research (CIMR), University of Cambridge, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Lehner+PJ%22">Lehner PJ</searchLink>; Department of Medicine, University of Cambridge, Cambridge, United Kingdom.; Cambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), University of Cambridge, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Matheson+NJ%22">Matheson NJ</searchLink>; Department of Medicine, University of Cambridge, Cambridge, United Kingdom.; Cambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), University of Cambridge, Cambridge, United Kingdom.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22eLife+Sciences+Publications%2C+Ltd%22">eLife Sciences Publications, Ltd </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101579614 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2050-084X (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%222050084X%22">2050084X </searchLink><i>NLM ISO Abbreviation: </i>Elife <i>Subsets: </i>MEDLINE
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        Value: 10.7554/eLife.53036
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