Characterization of the transcriptional repressive element of the human cytomegalovirus immediate-early US3 gene.

Item

http://www.wikidata.org/entity/Q39581391

description

1998 nî lūn-bûn

@nan

1998年の論文

@ja

1998年論文

@yue

1998年論文

@zh-hant

1998年論文

@zh-hk

1998年論文

@zh-mo

1998年論文

@zh-tw

1998年论文

@wuu

1998年论文

@zh

1998年论文

@zh-cn

name

Characterization of the transc ...... irus immediate-early US3 gene.

@en

Characterization of the transc ...... irus immediate-early US3 gene.

@nl

type

Item

label

Characterization of the transc ...... irus immediate-early US3 gene.

@en

Characterization of the transc ...... irus immediate-early US3 gene.

@nl

prefLabel

Characterization of the transc ...... irus immediate-early US3 gene.

@en

Characterization of the transc ...... irus immediate-early US3 gene.

@nl

P1476

Characterization of the transc ...... virus immediate-early US3 gene

@en

P2093

B J Biegalke

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P2860

Human cytomegalovirus US3 impairs transport and maturation of major histocompatibility complex class I heavy chains.

In vivo footprinting of a muscle specific enhancer by ligation mediated PCR.

The human cytomegalovirus US3 immediate-early protein lacking the putative transmembrane domain regulates gene expression.

Repression of the herpes simplex virus 1 alpha 4 gene by its gene product (ICP4) within the context of the viral genome is conditioned by the distance and stereoaxial alignment of the ICP4 DNA binding site relative to the TATA box

Cellular or viral protein binding to a cytomegalovirus promoter transcription initiation site: effects on transcription.

Two distinct upstream regulatory domains containing multicopy cellular transcription factor binding sites provide basal repression and inducible enhancer characteristics to the immediate-early IES (US3) promoter from human cytomegalovirus

Evidence that the UL84 gene product of human cytomegalovirus is essential for promoting oriLyt-dependent DNA replication and formation of replication compartments in cotransfection assays

An in vitro system for human cytomegalovirus immediate early 2 protein (IE2)-mediated site-dependent repression of transcription and direct binding of IE2 to the major immediate early promoter.

Repression of the herpes simplex virus 1 alpha 4 gene by its gene product occurs within the context of the viral genome and is associated with all three identified cognate sites

The product of ORF O located within the domain of herpes simplex virus 1 genome transcribed during latent infection binds to and inhibits in vitro binding of infected cell protein 4 to its cognate DNA site.

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5457-5463

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scholarly article

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English

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P478

http://www.w3.org/2001/XMLSchema#string

P577

1998-07-01T00:00:00Z

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P698

9621001

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P921

Cytomegalovirus

P932

110182

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