Recovery of human metapneumovirus genetic lineages a and B from cloned cDNA.
about
Human metapneumovirus M2-2 protein inhibits innate cellular signaling by targeting MAVSHuman Metapneumovirus: lessons learned over the first decadePhylogenetic and phylodynamic analyses of human metapneumovirus in Buenos Aires (Argentina) for a three-year period (2009-2011)Cell Type-Specific Recognition of Human Metapneumoviruses (HMPVs) by Retinoic Acid-Inducible Gene I (RIG-I) and TLR7 and Viral Interference of RIG-I Ligand Recognition by HMPV-B1 PhosphoproteinDeletion of M2 gene open reading frames 1 and 2 of human metapneumovirus: effects on RNA synthesis, attenuation, and immunogenicityRational design of human metapneumovirus live attenuated vaccine candidates by inhibiting viral mRNA cap methyltransferaseSmall hydrophobic protein of human metapneumovirus does not affect virus replication and host gene expression in vitroCytotoxic T-lymphocyte epitope vaccination protects against human metapneumovirus infection and disease in mice.Small Animal Models for Human Metapneumovirus: Cotton Rat is More Permissive than Hamster and Mouse.Effect of in vitro syncytium formation on the severity of human metapneumovirus disease in a murine modelZinc binding activity of human metapneumovirus M2-1 protein is indispensable for viral replication and pathogenesis in vivo.Frequent frameshift and point mutations in the SH gene of human metapneumovirus passaged in vitro.Genomic analysis of four human metapneumovirus prototypesThe role of reverse genetics in the development of vaccines against respiratory viruses.Intracellular processing, glycosylation, and cell surface expression of human metapneumovirus attachment glycoprotein.The human metapneumovirus fusion protein mediates entry via an interaction with RGD-binding integrins.Epidemiology of human metapneumovirus.Live vaccines for human metapneumovirus designed by reverse genetics.Antiviral Activity of Favipiravir (T-705) against a Broad Range of Paramyxoviruses In Vitro and against Human Metapneumovirus in Hamsters.Phosphorylation of Human Metapneumovirus M2-1 Protein Upregulates Viral Replication and Pathogenesis.Roles of the putative integrin-binding motif of the human metapneumovirus fusion (f) protein in cell-cell fusion, viral infectivity, and pathogenesis.Human metapneumovirus antagonism of innate immune responses.Recombinant Immunomodulating Lentogenic or Mesogenic Oncolytic Newcastle Disease Virus for Treatment of Pancreatic Adenocarcinoma.Modulation of Host Immunity by the Human Metapneumovirus.Intravenously injected Newcastle disease virus in non-human primates is safe to use for oncolytic virotherapy.Residues of the human metapneumovirus fusion (F) protein critical for its strain-related fusion phenotype: implications for the virus replication cycle.Rescue of recombinant Newcastle disease virus: current cloning strategies and RNA polymerase provision systems.Deletion of human metapneumovirus M2-2 increases mutation frequency and attenuates growth in hamsters.Development and optimization of a direct plaque assay for human and avian metapneumovirusesThe conserved YAGL motif in human metapneumovirus is required for higher-order cellular assemblies of the matrix protein and for virion production.Human metapneumovirus nucleoprotein and phosphoprotein interact and provide the minimal requirements for inclusion body formation.Recovery of a Paramyxovirus, the Human Metapneumovirus, from Cloned cDNA.NK-cell receptors NKp46 and NCR1 control human metapneumovirus infection.Suppression of human metapneumovirus (HMPV) infection by the innate sensing gene CEACAM1.Excessive production and extreme editing of human metapneumovirus defective interfering RNA is associated with type I IFN induction.Construction of an eGFP Expression Plasmid under Control of T7 Promoter and IRES Sequence for Assay of T7 RNA Polymerase Activity in Mammalian Cell Lines.Genetic diversity and evolution of human metapneumovirus fusion protein over twenty yearsAn S101P substitution in the putative cleavage motif of the human metapneumovirus fusion protein is a major determinant for trypsin-independent growth in vero cells and does not alter tissue tropism in hamsters.
P2860
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P2860
Recovery of human metapneumovirus genetic lineages a and B from cloned cDNA.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Recovery of human metapneumovirus genetic lineages a and B from cloned cDNA.
@ast
Recovery of human metapneumovirus genetic lineages a and B from cloned cDNA.
@en
type
label
Recovery of human metapneumovirus genetic lineages a and B from cloned cDNA.
@ast
Recovery of human metapneumovirus genetic lineages a and B from cloned cDNA.
@en
prefLabel
Recovery of human metapneumovirus genetic lineages a and B from cloned cDNA.
@ast
Recovery of human metapneumovirus genetic lineages a and B from cloned cDNA.
@en
P2093
P2860
P1433
P1476
Recovery of human metapneumovirus genetic lineages a and B from cloned cDNA.
@en
P2093
Aurelia A Haller
Bernadette G van den Hoogen
Chin-Fen Yang
Jasmine Kaur
Jeanne H Schickli
Miranda de Graaf
Richard R Spaete
Roderick S Tang
Sander Herfst
P2860
P304
P356
10.1128/JVI.78.15.8264-8270.2004
P407
P577
2004-08-01T00:00:00Z