(Q28287194)

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Sharon Delgado

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Maria Vanegas

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Eric M Poeschla

Journal of Biological Chemistry

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language of work or name

English

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publication date

31 December 2004

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published in

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volume

279

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issue

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page(s)

55570-7

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cites work

Isolation of cDNAs encoding novel transcription coactivators p52 and p75 reveals an alternate regulatory mechanism of transcriptional activation

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Purification, cloning, and characterization of a human coactivator, PC4, that mediates transcriptional activation of class II genes

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Activation of LEDGF gene by thermal-and oxidative-stresses

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LEDGF, a survival factor, activates stress-related genes.

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LEDGF/p75: a novel nuclear autoantigen at the crossroads of cell survival and apoptosis

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A novel transcriptional coactivator, p52, functionally interacts with the essential splicing factor ASF/SF2

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LEDGF/p75 determines cellular trafficking of diverse lentiviral but not murine oncoretroviral integrase proteins and is a component of functional lentiviral preintegration complexes

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Spatial and temporal dynamics of two alternatively spliced regulatory factors, lens epithelium-derived growth factor (ledgf/p75) and p52, in the nucleus

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HIV-1 infection of nondividing cells through the recognition of integrase by the importin/karyopherin pathway

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Nuclear localization of human immunodeficiency virus type 1 integrase expressed as a fusion protein with green fluorescent protein.

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Cellular Distribution and Karyophilic Properties of Matrix, Integrase, and Vpr Proteins from the Human and Simian Immunodeficiency Viruses

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The karyophilic properties of human immunodeficiency virus type 1 integrase are not required for nuclear import of proviral DNA.

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Subcellular localization of feline immunodeficiency virus integrase and mapping of its karyophilic determinant

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HIV-1 integrase forms stable tetramers and associates with LEDGF/p75 protein in human cells

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LEDGF/p75 is essential for nuclear and chromosomal targeting of HIV-1 integrase in human cells

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The 26S proteasome: a molecular machine designed for controlled proteolysis

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How the ubiquitin-proteasome system controls transcription

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Subcellular localization of proteasomes and their regulatory complexes in mammalian cells.

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Subpopulations of proteasomes in rat liver nuclei, microsomes and cytosol

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Electron microscopic localization of the multicatalytic proteinase complex in rat liver and in cultured cells

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Subcellular localization, stoichiometry, and protein levels of 26 S proteasome subunits in yeast

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The ubiquitin-proteasome pathway: on protein death and cell life

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Ornithine decarboxylase is degraded by the 26S proteasome without ubiquitination

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Determinants of proteasome recognition of ornithine decarboxylase, a ubiquitin-independent substrate

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Proteasomal turnover of p21Cip1 does not require p21Cip1 ubiquitination

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A proteasome howdunit: the case of the missing signal

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Ubiquitin-independent proteolytic functions of the proteasome

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Proteasome inhibition interferes with gag polyprotein processing, release, and maturation of HIV-1 and HIV-2

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A role for ubiquitin ligase recruitment in retrovirus release

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Intracellular transport of human immunodeficiency virus type 1 integrase

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Degradation of HIV-1 integrase by the N-end rule pathway

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The antiretroviral enzyme APOBEC3G is degraded by the proteasome in response to HIV-1 Vif

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HIV-1 Vif protein binds the editing enzyme APOBEC3G and induces its degradation

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HIV-1 Vif Blocks the Antiviral Activity of APOBEC3G by Impairing Both Its Translation and Intracellular Stability

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Induction of APOBEC3G Ubiquitination and Degradation by an HIV-1 Vif-Cul5-SCF Complex

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Resting CD4+ T cells from human immunodeficiency virus type 1 (HIV-1)-infected individuals carry integrated HIV-1 genomes within actively transcribed host genes

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Reduced ubiquitin-dependent degradation of c-Jun after phosphorylation by MAP kinases

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Codon optimization of the HIV-1 vpu and vif genes stabilizes their mRNA and allows for highly efficient Rev-independent expression

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c-Myc proteolysis by the ubiquitin-proteasome pathway: stabilization of c-Myc in Burkitt's lymphoma cells

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Dimerization with PEBP2beta protects RUNX1/AML1 from ubiquitin-proteasome-mediated degradation

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Human hRad1 but not hRad9 protects hHus1 from ubiquitin-proteasomal degradation

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Activation of the cyclin-dependent kinase CTDK-I requires the heterodimerization of two unstable subunits

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HIV-1 integration in the human genome favors active genes and local hotspots

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Transcription start regions in the human genome are favored targets for MLV integration

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Identifiers

DOI

10.1074/JBC.M408508200

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

15475359

1 reference

Consolidated OpenCitations Corpus – April 2017