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Benoit Barbeau

Researcher at Université du Québec à Montréal

Publications -  105
Citations -  8777

Benoit Barbeau is an academic researcher from Université du Québec à Montréal. The author has contributed to research in topics: Jurkat cells & Long terminal repeat. The author has an hindex of 35, co-authored 101 publications receiving 7911 citations. Previous affiliations of Benoit Barbeau include Laval University & Université du Québec.

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Upregulation of Human T-Cell Leukemia Virus Type 1 Antisense Transcription by the Viral Tax Protein

TL;DR: It is shown that the viral Tax protein upregulates antisense transcription through its action on the TRE sequences located in the 3′ long terminal repeat in the HTLV-1 genome.
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Detection of the HIV-1 Minus-Strand-Encoded Antisense Protein and Its Association with Autophagy

TL;DR: This study provides the first detection of antisense protein (ASP) in mammalian cells by Western blotting and suggests ASP-induced autophagy might explain the inherent difficulty in detecting this viral protein and might justify its presumed low abundance in infected cells.
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Induction of galectin-1 expression by HTLV-I Tax and its impact on HTLV-I infectivity

TL;DR: It is demonstrated that galectin-1 expression and release are higher in HTLV-I-infected T cells in comparison to uninfecting T cells, and that this modulation could play an important role in HT LV-I infection by stabilizing both cell-to-cell and virus-cell interactions.
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Regulation of nuclear factor of activated T cells by phosphotyrosyl-specific phosphatase activity: a positive effect on HIV-1 long terminal repeat-driven transcription and a possible implication of SHP-1.

TL;DR: Exposure of leukemic T cells and human peripheral blood mononuclear cells to bis-peroxovanadium PTP inhibitors markedly induce activation and nuclear translocation of NFAT and it is proposed that this activation is participating in HIV-1 LTR stimulation by PTP inhibition.
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Analysis of proviruses integrated in Fli-1 and Evi-1 regions in Cas-Br-E MuLV-induced non-T-, non-B-cell leukemias.

TL;DR: Among the Cas-Br-E-induced non-T-, non-B-cell leukemias, viral integrations were found in the Fli-1 and Evi- 1 region in 71% (36 out of 51) and 22% (16 out of 72) of the tumors analyzed, respectively, suggesting that the formation of these MCF recombinants is not essential for activation of Fli, and that ecotropic Cas- Br-E already possesses the required sequences