Mouse hepatitis virus utilizes two carcinoembryonic antigens as alternative receptors
about
Human biliary glycoprotein gene: characterization of a family of novel alternatively spliced RNAs and their expressed proteinsFeline aminopeptidase N serves as a receptor for feline, canine, porcine, and human coronaviruses in serogroup IPersistent infection promotes cross-species transmissibility of mouse hepatitis virusCoronavirus induction of class I major histocompatibility complex expression in murine astrocytes is virus strain specificA pregnancy-specific glycoprotein is expressed in the brain and serves as a receptor for mouse hepatitis virusMouse susceptibility to mouse hepatitis virus infection is linked to viral receptor genotypeBgp2, a new member of the carcinoembryonic antigen-related gene family, encodes an alternative receptor for mouse hepatitis virusesImmunoglobulin superfamily virus receptors and the evolution of adaptive immunity.Mutational analysis of the virus and monoclonal antibody binding sites in MHVR, the cellular receptor of the murine coronavirus mouse hepatitis virus strain A59Intracellular complexes of viral spike and cellular receptor accumulate during cytopathic murine coronavirus infections.Involvement of aminopeptidase N (CD13) in infection of human neural cells by human coronavirus 229E.Purified, soluble recombinant mouse hepatitis virus receptor, Bgp1(b), and Bgp2 murine coronavirus receptors differ in mouse hepatitis virus binding and neutralizing activitiesRole of mouse hepatitis virus (MHV) receptor murine CEACAM1 in the resistance of mice to MHV infection: studies of mice with chimeric mCEACAM1a and mCEACAM1bAntigenic modules in the N-terminal S1 region of the transmissible gastroenteritis virus spike proteinExpression of the mouse hepatitis virus receptor by central nervous system microgliaPersistent infection of cultured cells with mouse hepatitis virus (MHV) results from the epigenetic expression of the MHV receptor.Thymus involution induced by mouse hepatitis virus A59 in BALB/c miceThe S2 subunit of the murine coronavirus spike protein is not involved in receptor binding.Analysis of the receptor-binding site of murine coronavirus spike proteinMolecular anatomy of mouse hepatitis virus persistence: coevolution of increased host cell resistance and virus virulence.Expression of the recombinant anchorless N-terminal domain of mouse hepatitis virus (MHV) receptor makes hamster of human cells susceptible to MHV infectionHuman carcinoembryonic antigen and biliary glycoprotein can serve as mouse hepatitis virus receptors.Amino acid substitutions in the S2 subunit of mouse hepatitis virus variant V51 encode determinants of host range expansionThe spike glycoprotein of murine coronavirus MHV-JHM mediates receptor-independent infection and spread in the central nervous systems of Ceacam1a-/- MiceMultiple type A/B heterogeneous nuclear ribonucleoproteins (hnRNPs) can replace hnRNP A1 in mouse hepatitis virus RNA synthesis.Localization of neutralizing epitopes and the receptor-binding site within the amino-terminal 330 amino acids of the murine coronavirus spike proteinMajor receptor-binding and neutralization determinants are located within the same domain of the transmissible gastroenteritis virus (coronavirus) spike proteinThe receptor for mouse hepatitis virus in the resistant mouse strain SJL is functional: implications for the requirement of a second factor for viral infection.Induction of caspase-dependent apoptosis in cultured rat oligodendrocytes by murine coronavirus is mediated during cell entry and does not require virus replication.Expression of cellular oncogene Bcl-xL prevents coronavirus-induced cell death and converts acute infection to persistent infection in progenitor rat oligodendrocytesPersistent infection of human oligodendrocytic and neuroglial cell lines by human coronavirus 229E.Acute and persistent infection of human neural cell lines by human coronavirus OC43.The coronavirus transmissible gastroenteritis virus causes infection after receptor-mediated endocytosis and acid-dependent fusion with an intracellular compartment.Conformational changes in the spike glycoprotein of murine coronavirus are induced at 37 degrees C either by soluble murine CEACAM1 receptors or by pH 8.The N-terminal region of the murine coronavirus spike glycoprotein is associated with the extended host range of viruses from persistently infected murine cells.Mouse hepatitis virus receptor activities of an MHVR/mph chimera and MHVR mutants lacking N-linked glycosylation of the N-terminal domainA role for naturally occurring variation of the murine coronavirus spike protein in stabilizing association with the cellular receptor.The murine coronavirus mouse hepatitis virus strain A59 from persistently infected murine cells exhibits an extended host range.Three different cellular proteins bind to complementary sites on the 5'-end-positive and 3'-end-negative strands of mouse hepatitis virus RNA.Redirecting coronavirus to a nonnative receptor through a virus-encoded targeting adapter.
P2860
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P2860
Mouse hepatitis virus utilizes two carcinoembryonic antigens as alternative receptors
description
1992 nî lūn-bûn
@nan
1992 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
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
name
Mouse hepatitis virus utilizes two carcinoembryonic antigens as alternative receptors
@ast
Mouse hepatitis virus utilizes two carcinoembryonic antigens as alternative receptors
@en
type
label
Mouse hepatitis virus utilizes two carcinoembryonic antigens as alternative receptors
@ast
Mouse hepatitis virus utilizes two carcinoembryonic antigens as alternative receptors
@en
prefLabel
Mouse hepatitis virus utilizes two carcinoembryonic antigens as alternative receptors
@ast
Mouse hepatitis virus utilizes two carcinoembryonic antigens as alternative receptors
@en
P2860
P1433
P1476
Mouse hepatitis virus utilizes two carcinoembryonic antigens as alternative receptors
@en
P2093
P2860
P304
P577
1992-10-01T00:00:00Z