A cluster of dispensable genes within the human cytomegalovirus genome short component: IRS1, US1 through US5, and the US6 family.
about
A novel human cytomegalovirus glycoprotein, gpUS9, which promotes cell-to-cell spread in polarized epithelial cells, colocalizes with the cytoskeletal proteins E-cadherin and F-actin.Evasion of cellular antiviral responses by human cytomegalovirus TRS1 and IRS1Activation of transcription of the human cytomegalovirus early UL4 promoter by the Ets transcription factor binding element.Transcriptional regulation of the human cytomegalovirus US11 early gene.Human cytomegalovirus infection of placental cytotrophoblasts in vitro and in utero: implications for transmission and pathogenesis.Human cytomegalovirus US3 impairs transport and maturation of major histocompatibility complex class I heavy chains.Role of regulatory elements and the MAPK/ERK or p38 MAPK pathways for activation of human cytomegalovirus gene expression.A recombinant rhesus cytomegalovirus expressing enhanced green fluorescent protein retains the wild-type phenotype and pathogenicity in fetal macaques.Murine cytomegalovirus m02 gene family protects against natural killer cell-mediated immune surveillance.Mutant human cytomegalovirus lacking the immediate-early TRS1 coding region exhibits a late defectHuman cytomegalovirus US7, US8, US9, and US10 are cytoplasmic glycoproteins, not found at cell surfaces, and US9 does not mediate cell-to-cell spread.The human cytomegalovirus US3 immediate-early protein lacking the putative transmembrane domain regulates gene expression.Multiple regulatory events influence human cytomegalovirus DNA polymerase (UL54) expression during viral infectionMurine cytomegalovirus with a deletion of genes spanning HindIII-J and -I displays altered cell and tissue tropismTwo 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 cytomegalovirusCharacterization of the human cytomegalovirus irs1 and trs1 genes: a second immediate-early transcription unit within irs1 whose product antagonizes transcriptional activation.The role of ATF in regulating the human cytomegalovirus DNA polymerase (UL54) promoter during viral infection.Human cytomegalovirus US2 destabilizes major histocompatibility complex class I heavy chains.Essential role of protein kinase R antagonism by TRS1 in human cytomegalovirus replication.Genes in the HindIII J fragment of the murine cytomegalovirus genome are dispensable for growth in cultured cells: insertion mutagenesis with a lacZ/gpt cassette.Use of recombinant virus to assess human cytomegalovirus early and late promoters in the context of the viral genome.Expression and analysis of the human cytomegalovirus UL80-encoded protease: identification of autoproteolytic sitesTegument proteins of human cytomegalovirusNovel method based on "en passant" mutagenesis coupled with a gaussia luciferase reporter assay for studying the combined effects of human cytomegalovirus mutations.The tiers and dimensions of evasion of the type I interferon response by human cytomegalovirus.Congenital cytomegalovirus infection: molecular mechanisms mediating viral pathogenesis.Human cytomegalovirus TRS1 protein is required for efficient assembly of DNA-containing capsids.Activation of the Antiviral Kinase PKR and Viral Countermeasures.Separate DNA elements containing ATF/CREB and IE86 binding sites differentially regulate the human cytomegalovirus UL112-113 promoter at early and late times in the infectionDouble-stranded RNA binding by a heterodimeric complex of murine cytomegalovirus m142 and m143 proteins.Binding and nuclear relocalization of protein kinase R by human cytomegalovirus TRS1.Characterization of the transcriptional repressive element of the human cytomegalovirus immediate-early US3 gene.Cloning of the human cytomegalovirus (HCMV) genome as an infectious bacterial artificial chromosome in Escherichia coli: a new approach for construction of HCMV mutants.Human cytomegalovirus with IE-2 (UL122) deleted fails to express early lytic genes.The HCMV membrane glycoprotein US10 selectively targets HLA-G for degradation.A human cytomegalovirus deleted of internal repeats replicates with near wild type efficiency but fails to undergo genome isomerizationMultiple independent loci within the human cytomegalovirus unique short region down-regulate expression of major histocompatibility complex class I heavy chains.Regulation of human cytomegalovirus US3 gene transcription by a cis-repressive sequence.The dominant phosphoprotein pp65 (UL83) of human cytomegalovirus is dispensable for growth in cell culture.Identification of the mouse cytomegalovirus genomic region affecting major histocompatibility complex class I molecule transport.
P2860
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P2860
A cluster of dispensable genes within the human cytomegalovirus genome short component: IRS1, US1 through US5, and the US6 family.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
A cluster of dispensable genes ...... rough US5, and the US6 family.
@en
type
label
A cluster of dispensable genes ...... rough US5, and the US6 family.
@en
prefLabel
A cluster of dispensable genes ...... rough US5, and the US6 family.
@en
P2860
P1433
P1476
A cluster of dispensable genes ...... rough US5, and the US6 family.
@en
P2093
Muzithras VP
P2860
P304
P407
P577
1992-04-01T00:00:00Z