D
Daniel Henaff
Researcher at Centre national de la recherche scientifique
Publications - 21
Citations - 816
Daniel Henaff is an academic researcher from Centre national de la recherche scientifique. The author has contributed to research in topics: Internalization & Endosome. The author has an hindex of 13, co-authored 19 publications receiving 739 citations. Previous affiliations of Daniel Henaff include Université de Montréal & University of Montpellier.
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Journal ArticleDOI
The cell adhesion molecule "CAR" and sialic acid on human erythrocytes influence adenovirus in vivo biodistribution.
Elena Seiradake,Daniel Henaff,Harald Wodrich,Olivier Billet,Matthieu Perreau,Claire Hippert,Franck J. D. Mennechet,Guy Schoehn,Hugues Lortat-Jacob,Hanna Dreja,Sandy Ibanes,Vasiliki Kalatzis,Jennifer P. Wang,Robert W. Finberg,Stephen Cusack,Eric J. Kremer +15 more
TL;DR: It is shown that the presence of CAR on erythrocytes leads to prolonged in vivo blood half-life and significantly reduced liver infection when a CAR-tropic Ad is injected intravenously.
Journal ArticleDOI
A Capsid-Encoded PPxY-Motif Facilitates Adenovirus Entry
Harald Wodrich,Daniel Henaff,Baptist Jammart,Carolina Segura-Morales,Sigrid Seelmeir,Olivier Coux,Zsolt Ruzsics,Christopher M. Wiethoff,Eric J. Kremer +8 more
TL;DR: This study found that a PPxY motif within protein VI recruits Nedd4 E3 ubiquitin ligases to bind and ubiquitylate protein VI, providing the first evidence that virus-encoded PPxy motifs are required during virus entry, which may be of significance for several other pathogens.
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CAR-associated vesicular transport of an adenovirus in motor neuron axons.
Sara Salinas,Lynsey G. Bilsland,Daniel Henaff,Anne Weston,Anne Keriel,Giampietro Schiavo,Eric J. Kremer +6 more
TL;DR: It is proposed that CAV-2 transport is dictated by an innate trafficking of CAR, suggesting an unsuspected function for this adhesion protein during neuronal homeostasis and suggest that a single axonal transport carrier is capable of transporting functionally distinct cargoes that target different membrane compartments in the soma.
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The HBZ-SP1 isoform of human T-cell leukemia virus type I represses JunB activity by sequestration into nuclear bodies
Patrick Hivin,Jihane Basbous,Frédéric Raymond,Daniel Henaff,Charlotte Arpin-André,Véronique Robert-Hebmann,Benoit Barbeau,Jean-Michel Mesnard +7 more
TL;DR: HBZ-mediated sequestration of JunB to the HBZ-NBs may be causing the repression of Jun B activity in vivo, and it is suggested that HBZ needs cellular partners, including bZIP factors, to form HBZ -NBs.
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Herpesviruses Exploit Several Host Compartments for Envelopment
TL;DR: This review focuses on recent advances in the characterization of cellular compartment(s) potentially contributing to herpes virion final envelopment and examines the common points between seemingly distinct envelopment pathways and highlights the dynamic nature of intracellular compartments in the context of herpesvirus infections.