Quantitative proteomic analysis of HIV-1 infected CD4+ T cells reveals an early host response in important biological pathways: protein synthesis, cell proliferation, and T-cell activation. (Q35980749)

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English	Quantitative proteomic analysis of HIV-1 infected CD4+ T cells reveals an early host response in important biological pathways: protein synthesis, cell proliferation, and T-cell activation.	scientific article

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30 January 2020

Quantitative proteomic analysis of HIV-1 infected CD4+ T cells reveals an early host response in important biological pathways: protein synthesis, cell proliferation, and T-cell activation (English)

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Alejandro Wolf-Yadlin

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Michael G Katze

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Arti T Navare

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Pavel Sova

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David E Purdy

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Jeffrey M Weiss

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Marcus J Korth

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Stewart T Chang

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Sean C Proll

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Tahmina A Jahan

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Alexei L Krasnoselsky

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Robert E Palermo

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26 April 2012

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30 January 2020

Global landscape of HIV-human protein complexes

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2 October 2017

Next-generation sequencing reveals HIV-1-mediated suppression of T cell activation and RNA processing and regulation of noncoding RNA expression in a CD4+ T cell line

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CD43 interaction with ezrin-radixin-moesin (ERM) proteins regulates T-cell trafficking and CD43 phosphorylation

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Identification of Tat-SF1 cellular targets by exon array analysis reveals dual roles in transcription and splicing

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Proteomic analysis of HIV-infected macrophages

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Dynamic host energetics and cytoskeletal proteomes in human immunodeficiency virus type 1-infected human primary CD4 cells: analysis by multiplexed label-free mass spectrometry

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Quantitative analysis of human immunodeficiency virus type 1-infected CD4+ cell proteome: dysregulated cell cycle progression and nuclear transport coincide with robust virus production

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