Inhibition of in vivo and in vitro transcription by monoclonal antibodies prepared against wheat germ RNA polymerase II that react with the heptapeptide repeat of eukaryotic RNA polymerase II.
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Assembly of the Nuclear Transcription and Processing Machinery: Cajal Bodies (Coiled Bodies) and TranscriptosomesThe HRPT2 tumor suppressor gene product parafibromin associates with human PAF1 and RNA polymerase IIThe cellular factor TRP-185 regulates RNA polymerase II binding to HIV-1 TAR RNAA cofactor, TIP30, specifically enhances HIV-1 Tat-activated transcriptionFunctional studies of the carboxy-terminal repeat domain of Drosophila RNA polymerase II in vivoStudies of nematode TFIIE function reveal a link between Ser-5 phosphorylation of RNA polymerase II and the transition from transcription initiation to elongationSpecific binding of RNA polymerase II to the human immunodeficiency virus trans-activating region RNA is regulated by cellular cofactors and TatMutations in the three largest subunits of yeast RNA polymerase II that affect enzyme assemblymRNA capping enzyme is recruited to the transcription complex by phosphorylation of the RNA polymerase II carboxy-terminal domainTrans-activation by human immunodeficiency virus Tat protein requires the C-terminal domain of RNA polymerase IIThe HIV transactivator TAT binds to the CDK-activating kinase and activates the phosphorylation of the carboxy-terminal domain of RNA polymerase IIA functional interaction between the survival motor neuron complex and RNA polymerase IIDual roles for Spt5 in pre-mRNA processing and transcription elongation revealed by identification of Spt5-associated proteins.Mutations in the second largest subunit of RNA polymerase II cause 6-azauracil sensitivity in yeast and increased transcriptional arrest in vitroRtr1 is the Saccharomyces cerevisiae homolog of a novel family of RNA polymerase II-binding proteins.The Paf1 complex physically and functionally associates with transcription elongation factors in vivo.Diverse roles of RNA polymerase II-associated factor 1 complex in different subpathways of nucleotide excision repair.CTD kinase large subunit is encoded by CTK1, a gene required for normal growth of Saccharomyces cerevisiae.Rpb7 can interact with RNA polymerase II and support transcription during some stresses independently of Rpb4Regulation of rRNA synthesis by TATA-binding protein-associated factor Mot1.Evidence that Spt4, Spt5, and Spt6 control transcription elongation by RNA polymerase II in Saccharomyces cerevisiaeMot1-mediated control of transcription complex assembly and activity.Modulation of Rad26- and Rpb9-mediated DNA repair by different promoter elements.Tat modifies the activity of CDK9 to phosphorylate serine 5 of the RNA polymerase II carboxyl-terminal domain during human immunodeficiency virus type 1 transcriptionCREB-binding protein (CBP)/p300 and RNA polymerase II colocalize in transcriptionally active domains in the nucleusDifferent phosphorylated forms of RNA polymerase II and associated mRNA processing factors during transcriptionControl of developmental regulators by Polycomb in human embryonic stem cellsInability to enter S phase and defective RNA polymerase II CTD phosphorylation in mice lacking Mat1A nuclear matrix protein interacts with the phosphorylated C-terminal domain of RNA polymerase II.The C-terminal domain of the largest subunit of RNA polymerase II interacts with a novel set of serine/arginine-rich proteinsUp-regulation of P-TEFb by the MEK1-extracellular signal-regulated kinase signaling pathway contributes to stimulated transcription elongation of immediate early genes in neuroendocrine cellsDirect isolation and identification of promoters in the human genomeRNA synthesis precision is regulated by preinitiation complex turnover.Sequential entry of components of the gene expression machinery into daughter nucleiRNA polymerase II carboxy-terminal domain kinases: emerging clues to their function.T-loop phosphorylated Cdk9 localizes to nuclear speckle domains which may serve as sites of active P-TEFb function and exchange between the Brd4 and 7SK/HEXIM1 regulatory complexes.Mouse models of human phenylketonuria.Essential functional interactions of SAGA, a Saccharomyces cerevisiae complex of Spt, Ada, and Gcn5 proteins, with the Snf/Swi and Srb/mediator complexesTrichinella spiralis-infected muscle cells: abundant RNA polymerase II in nuclear speckle domains colocalizes with nuclear antigenscdk-7 Is required for mRNA transcription and cell cycle progression in Caenorhabditis elegans embryos.
P2860
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P2860
Inhibition of in vivo and in vitro transcription by monoclonal antibodies prepared against wheat germ RNA polymerase II that react with the heptapeptide repeat of eukaryotic RNA polymerase II.
description
1989 nî lūn-bûn
@nan
1989年の論文
@ja
1989年学术文章
@wuu
1989年学术文章
@zh-cn
1989年学术文章
@zh-hans
1989年学术文章
@zh-my
1989年学术文章
@zh-sg
1989年學術文章
@yue
1989年學術文章
@zh
1989年學術文章
@zh-hant
name
Inhibition of in vivo and in v ...... eukaryotic RNA polymerase II.
@en
Inhibition of in vivo and in v ...... eukaryotic RNA polymerase II.
@nl
type
label
Inhibition of in vivo and in v ...... eukaryotic RNA polymerase II.
@en
Inhibition of in vivo and in v ...... eukaryotic RNA polymerase II.
@nl
prefLabel
Inhibition of in vivo and in v ...... eukaryotic RNA polymerase II.
@en
Inhibition of in vivo and in v ...... eukaryotic RNA polymerase II.
@nl
P2093
P1476
Inhibition of in vivo and in v ...... eukaryotic RNA polymerase II.
@en
P2093
Aronson DB
Burgess RR
Steinberg TH
Thompson NE
P304
11511-11520
P407
P577
1989-07-01T00:00:00Z