Nuclear targeting of incoming human foamy virus Gag proteins involves a centriolar step. - Wikidata - awgldk - TriplyDB

Nuclear targeting of incoming human foamy virus Gag proteins involves a centriolar step.

Nuclear targeting of incoming human foamy virus Gag proteins involves a centriolar step.

http://www.wikidata.org/entity/Q39878092

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Establishment of a functional human immunodeficiency virus type 1 (HIV-1) reverse transcription complex involves the cytoskeleton Early steps of retrovirus replicative cycle A novel function for spumaretrovirus integrase: an early requirement for integrase-mediated cleavage of 2 LTR circles.Foamy virus budding and release Human foamy virus reverse transcription that occurs late in the viral replication cycle Differential pH-dependent cellular uptake pathways among foamy viruses elucidated using dual-colored fluorescent particles Centrosomal latency of incoming foamy viruses in resting cells.Modulation of phosphate uptake and amphotropic murine leukemia virus entry by posttranslational modifications of PIT-2 Packaging cell lines for simian foamy virus type 1 vectors.The foamy virus genome remains unintegrated in the nuclei of G1/S phase-arrested cells, and integrase is critical for preintegration complex transport into the nucleus.Identification of a conserved residue of foamy virus Gag required for intracellular capsid assembly.Human immunodeficiency virus type 1 Vif protein is packaged into the nucleoprotein complex through an interaction with viral genomic RNA.Element-specific localization of Drosophila retrotransposon Gag proteins occurs in both nucleus and cytoplasm.Transduction of human NOD/SCID-repopulating cells with both lymphoid and myeloid potential by foamy virus vectors.Investigating the intercellular spreading properties of the foamy virus Gag protein.A nuclear export signal within the structural Gag protein is required for prototype foamy virus replication Intracellular targeting of Gag proteins of the Drosophila telomeric retrotransposons HIV infection of non-dividing cells: a divisive problem.Retroviral vectors: post entry events and genomic alterations.High-titer foamy virus vector transduction and integration sites of human CD34(+) cell-derived SCID-repopulating cells.Beyond plasma membrane targeting: role of the MA domain of Gag in retroviral genome encapsidation.Intracellular trafficking of plasmids for gene therapy: mechanisms of cytoplasmic movement and nuclear import Centrosome and retroviruses: the dangerous liaisons.Retroviral proteins that interact with the host cell cytoskeleton Cell cycle requirements for transduction by foamy virus vectors compared to those of oncovirus and lentivirus vectors.Early events in foamy virus-host interaction and intracellular trafficking Prototype foamy virus gag nuclear localization: a novel pathway among retroviruses Human foamy virus capsid formation requires an interaction domain in the N terminus of Gag.Infection of nondividing cells by Rous sarcoma virus.Intra- and intercellular trafficking of the foamy virus auxiliary bet protein.Further characterization of equine foamy virus reveals unusual features among the foamy viruses Analysis of prototype foamy virus particle-host cell interaction with autofluorescent retroviral particles.Foamy virus envelope glycoprotein-mediated entry involves a pH-dependent fusion process.Biphasic DNA synthesis in spumaviruses.Carboxy-terminal cleavage of the human foamy virus Gag precursor molecule is an essential step in the viral life cycle.Correct capsid assembly mediated by a conserved YXXLGL motif in prototype foamy virus Gag is essential for infectivity and reverse transcription of the viral genome.Vaccinia virus infection disrupts microtubule organization and centrosome function.Foamy virus integration.Dynein Regulators Are Important for Ecotropic Murine Leukemia Virus Infection.Foamy virus as a gene transfer vector to the central nervous system.

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P2860

Nuclear targeting of incoming human foamy virus Gag proteins involves a centriolar step.

http://www.wikidata.org/entity/Q39878092

description

1997 nî lūn-bûn

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1997年の論文

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1997年学术文章

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1997年学术文章

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1997年学术文章

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1997年学术文章

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1997年学术文章

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1997年學術文章

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1997年學術文章

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1997年學術文章

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name

Nuclear targeting of incoming human foamy virus Gag proteins involves a centriolar step.

@en

Nuclear targeting of incoming human foamy virus Gag proteins involves a centriolar step.

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type

label

Nuclear targeting of incoming human foamy virus Gag proteins involves a centriolar step.

@en

Nuclear targeting of incoming human foamy virus Gag proteins involves a centriolar step.

@nl

prefLabel

Nuclear targeting of incoming human foamy virus Gag proteins involves a centriolar step.

@en

Nuclear targeting of incoming human foamy virus Gag proteins involves a centriolar step.

@nl

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Nuclear targeting of incoming human foamy virus Gag proteins involves a centriolar step

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Puvion-Dutilleul F

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Périès J

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Saïb A

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Schmid M

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de Thé H

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P2860

Active nuclear import of human immunodeficiency virus type 1 preintegration complexes

Cleavage of structural proteins during the assembly of the head of bacteriophage T4

A nuclear localization signal within HIV-1 matrix protein that governs infection of non-dividing cells

HIV-1 entry into quiescent primary lymphocytes: molecular analysis reveals a labile, latent viral structure

p17 and p17-containing gag precursors of input human immunodeficiency virus are transported into the nuclei of infected cells

HIV nuclear import is governed by the phosphotyrosine-mediated binding of matrix to the core domain of integrase

HIV-1 infection of nondividing cells: C-terminal tyrosine phosphorylation of the viral matrix protein is a key regulator

Selective extraction of polyoma DNA from infected mouse cell cultures

In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector

Golgi apparatus in chick skeletal muscle: changes in its distribution during end plate development and after denervation

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