scholarly article | Q13442814 |
P2093 | author name string | Y Li | |
T Shioda | |||
M Takeda | |||
Y Sakai | |||
Y Nagai | |||
H Sakata | |||
A Kato | |||
M Asakawa | |||
F Kobune | |||
P2860 | cites work | The human CD46 molecule is a receptor for measles virus (Edmonston strain) | Q24317745 |
The paramyxovirus, Sendai virus, V protein encodes a luxury function required for viral pathogenesis | Q24532096 | ||
Physical association of moesin and CD46 as a receptor complex for measles virus | Q24675691 | ||
Eukaryotic transient-expression system based on recombinant vaccinia virus that synthesizes bacteriophage T7 RNA polymerase | Q27860943 | ||
Molecular characterization of fusion regulatory protein-1 (FRP-1) that induces multinucleated giant cell formation of monocytes and HIV gp160-mediated cell fusion. FRP-1 and 4F2/CD98 are identical molecules | Q28289671 | ||
Measles viruses with altered envelope protein cytoplasmic tails gain cell fusion competence. | Q34069549 | ||
Propagation in tissue cultures of cytopathogenic agents from patients with measles | Q34235751 | ||
Moesin: a cell membrane protein linked with susceptibility to measles virus infection | Q34346265 | ||
Epstein-Barr virus: transformation, cytopathic changes, and viral antigens in squirrel monkey and marmoset leukocytes | Q34688308 | ||
Measles virus. Historical review, isolation, and behavior in various systems. | Q35354060 | ||
RNA polymerase of vesicular stomatitis virus specifically associates with translation elongation factor-1 alphabetagamma for its activity | Q35864304 | ||
Marmoset lymphoblastoid cells as a sensitive host for isolation of measles virus | Q36800851 | ||
Importance of the cysteine-rich carboxyl-terminal half of V protein for Sendai virus pathogenesis | Q39881303 | ||
Antigenomes in Sendai virions and Sendai virus-infected cells | Q39935115 | ||
Human membrane cofactor protein (CD46) acts as a cellular receptor for measles virus. | Q40047494 | ||
Sendai virus C proteins are categorically nonessential gene products but silencing their expression severely impairs viral replication and pathogenesis | Q41038886 | ||
Nonhuman primate models of measles | Q41194027 | ||
Measles virus haemagglutinin induces down-regulation of gp57/67, a molecule involved in virus binding. | Q41548414 | ||
Measles virus: both the haemagglutinin and fusion glycoproteins are required for fusion | Q41696651 | ||
Host cell proteins required for measles virus reproduction | Q41738157 | ||
Measles virus: a summary of experiments concerned with isolation, properties, and behavior | Q45719939 | ||
Protein interactions entered into by the measles virus P, V, and C proteins | Q45771826 | ||
Protein Factors Required for In Vitro Transcription of Sendai Virus Genome1 | Q45787777 | ||
Transcriptive complex of Newcastle disease virus. I. Both L and P proteins are required to constitute an active complex | Q45794815 | ||
Localization and characterization of Sendai virus nonstructural C and C' proteins by antibodies against synthetic peptides | Q45835522 | ||
Measles battle loses potent weapon | Q54442144 | ||
Preliminary tests of a highly attenuated measles vaccine | Q79414099 | ||
P433 | issue | 11 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | measles | Q79793 |
P304 | page(s) | 8690-8696 | |
P577 | publication date | 1998-11-01 | |
P1433 | published in | Journal of Virology | Q1251128 |
P1476 | title | Measles virus attenuation associated with transcriptional impediment and a few amino acid changes in the polymerase and accessory proteins | |
P478 | volume | 72 |
Q39804400 | A highly attenuated measles virus vaccine strain encodes a fully functional C protein |
Q36314971 | A human lung carcinoma cell line supports efficient measles virus growth and syncytium formation via a SLAM- and CD46-independent mechanism. |
Q36541009 | A molecularly cloned Schwarz strain of measles virus vaccine induces strong immune responses in macaques and transgenic mice |
Q33817891 | A recombinant measles vaccine virus expressing wild-type glycoproteins: consequences for viral spread and cell tropism |
Q34342086 | Activity of polymerase proteins of vaccine and wild-type measles virus strains in a minigenome replication assay |
Q39796666 | Adaptation of Puumala hantavirus to cell culture is associated with point mutations in the coding region of the L segment and in the noncoding regions of the S segment |
Q39682212 | Adaptation of wild-type measles virus to tissue culture |
Q42013767 | Altered interaction of the matrix protein with the cytoplasmic tail of hemagglutinin modulates measles virus growth by affecting virus assembly and cell-cell fusion. |
Q33821235 | Altered virulence of vaccine strains of measles virus after prolonged replication in human tissue. |
Q39601579 | Analysis of the noncoding regions of measles virus strains in the Edmonston vaccine lineage |
Q48193127 | Changes in the receptorbinding haemagglutinin protein of wild-type morbilliviruses are not required for adaptation to Vero cells |
Q33803102 | Clinical isolates of measles virus use CD46 as a cellular receptor |
Q40860398 | Comparative nucleotide sequence analyses of the entire genomes of B95a cell-isolated and vero cell-isolated measles viruses from the same patient |
Q33835693 | Comparison of predicted amino acid sequences of measles virus strains in the Edmonston vaccine lineage |
Q26750558 | Constraints on the Genetic and Antigenic Variability of Measles Virus |
Q40347995 | Contributions of matrix and large protein genes of the measles virus edmonston strain to growth in cultured cells as revealed by recombinant viruses |
Q39684407 | Efficiency of measles virus entry and dissemination through different receptors |
Q33809740 | Evasion of host defenses by measles virus: wild-type measles virus infection interferes with induction of Alpha/Beta interferon production |
Q92881586 | Humanized Mice for Live-Attenuated Vaccine Research: From Unmet Potential to New Promises |
Q34353249 | Identification of a second major site for CD46 binding in the hemagglutinin protein from a laboratory strain of measles virus (MV): potential consequences for wild-type MV infection |
Q39594360 | Infection of chicken embryonic fibroblasts by measles virus: adaptation at the virus entry level. |
Q35363337 | Junin virus infects mouse cells and induces innate immune responses. |
Q46300761 | Measles Vaccine |
Q37388577 | Measles virus for cancer therapy |
Q42265147 | Measles viruses possessing the polymerase protein genes of the Edmonston vaccine strain exhibit attenuated gene expression and growth in cultured cells and SLAM knock-in mice |
Q40191590 | Multiple amino acid substitutions in hemagglutinin are necessary for wild-type measles virus to acquire the ability to use receptor CD46 efficiently. |
Q42546324 | Previously unrecognized amino acid substitutions in the hemagglutinin and fusion proteins of measles virus modulate cell-cell fusion, hemadsorption, virus growth, and penetration rate |
Q34338440 | Recombinant wild-type and edmonston strain measles viruses bearing heterologous H proteins: role of H protein in cell fusion and host cell specificity |
Q33808180 | Recovery of pathogenic measles virus from cloned cDNA |
Q39683763 | Restriction of measles virus RNA synthesis by a mouse host cell line: trans-complementation by polymerase components or a human cellular factor(s) |
Q40612116 | Role of fusion protein cleavage site in the virulence of Newcastle disease virus |
Q37336531 | The L gene of J paramyxovirus plays a critical role in viral pathogenesis. |
Q35531354 | The SI strain of measles virus derived from a patient with subacute sclerosing panencephalitis possesses typical genome alterations and unique amino acid changes that modulate receptor specificity and reduce membrane fusion activity. |
Q36845605 | The large polymerase protein is associated with the virulence of Newcastle disease virus |
Q39675666 | The viral replication complex is associated with the virulence of Newcastle disease virus |
Q33805855 | Versatility of the accessory C proteins of Sendai virus: contribution to virus assembly as an additional role |
Q37971051 | Virulence of Newcastle disease virus: what is known so far? |
Q33803482 | Virus entry is a major determinant of cell tropism of Edmonston and wild-type strains of measles virus as revealed by vesicular stomatitis virus pseudotypes bearing their envelope proteins |
Q36509497 | Wild type measles virus attenuation independent of type I IFN. |
Q35747417 | Wild-Type Measles Virus is Intrinsically Dual-Tropic. |
Q35153050 | Wild-type measles viruses with non-standard genome lengths |
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