Implications of a quasispecies genome structure: effect of frequent, naturally occurring amino acid substitutions on the antigenicity of foot-and-mouth disease virus
about
Hepatitis C virus (HCV) circulates as a population of different but closely related genomes: quasispecies nature of HCV genome distributionReal time forecasting of near-future evolutionNew vaccine design based on defective genomes that combines features of attenuated and inactivated vaccinesHuman Memory B Cells Producing Potent Cross-Neutralizing Antibodies against Human Parechovirus: Implications for Prevalence, Treatment, and Diagnosis.Evolution subverting essentiality: dispensability of the cell attachment Arg-Gly-Asp motif in multiply passaged foot-and-mouth disease virus.Greater numbers of nucleotide substitutions are introduced into the genomic RNA of bovine viral diarrhea virus during acute infections of pregnant cattle than of non-pregnant cattleA review of the possible mechanisms for the persistence of foot-and-mouth disease virus.Vaccines prepared from chimeras of foot-and-mouth disease virus (FMDV) induce neutralizing antibodies and protective immunity to multiple serotypes of FMDV.Split decomposition: a technique to analyze viral evolution.Converging antigenic structure of a recombinant viral peptide displayed on different frameworks of carrier proteins.A similar pattern of interaction for different antibodies with a major antigenic site of foot-and-mouth disease virus: implications for intratypic antigenic variation.Cell recognition by foot-and-mouth disease virus that lacks the RGD integrin-binding motif: flexibility in aphthovirus receptor usage.Memory in viral quasispecies.Effects of macromolecular crowding on the inhibition of virus assembly and virus-cell receptor recognition.A single amino acid substitution in nonstructural protein 3A can mediate adaptation of foot-and-mouth disease virus to the guinea pig.Biological effect of Muller's Ratchet: distant capsid site can affect picornavirus protein processing.A large-scale evaluation of peptide vaccines against foot-and-mouth disease: lack of solid protection in cattle and isolation of escape mutants.Tissue culture adaptation of foot-and-mouth disease virus selects viruses that bind to heparin and are attenuated in cattle.Cell culture adaptation of Puumala hantavirus changes the infectivity for its natural reservoir, Clethrionomys glareolus, and leads to accumulation of mutants with altered genomic RNA S segment.Efficient neutralization of foot-and-mouth disease virus by monovalent antibody bindingUnprocessed foot-and-mouth disease virus capsid precursor displays discontinuous epitopes involved in viral neutralization.Animal-derived antigenic variants of foot-and-mouth disease virus type A12 have low affinity for cells in culture.Antigenic heterogeneity of a foot-and-mouth disease virus serotype in the field is mediated by very limited sequence variation at several antigenic sites.Genetically engineered foot-and-mouth disease viruses with poly(C) tracts of two nucleotides are virulent in mice.Distinct repertoire of antigenic variants of foot-and-mouth disease virus in the presence or absence of immune selection.Identification of neutralizing antigenic sites on VP1 and VP2 of type A5 foot-and-mouth disease virus, defined by neutralization-resistant variants.Evolution of the capsid protein genes of foot-and-mouth disease virus: antigenic variation without accumulation of amino acid substitutions over six decades.Antigenic stability of foot-and-mouth disease virus variants on serial passage in cell culture.Fitness alteration of foot-and-mouth disease virus mutants: measurement of adaptability of viral quasispecies.Unique amino acid substitutions in the capsid proteins of foot-and-mouth disease virus from a persistent infection in cell culture.Structure of the major antigenic loop of foot-and-mouth disease virus complexed with a neutralizing antibody: direct involvement of the Arg-Gly-Asp motif in the interactionSystematic replacement of amino acid residues within an Arg-Gly-Asp-containing loop of foot-and-mouth disease virus and effect on cell recognition.Genetic heterogeneity of the envelope 2 gene and eradication of hepatitis C virus after a second course of interferon-alpha.Use of substituted and tandem-repeated peptides to probe the relevance of the highly conserved RGD tripeptide in the immune response against foot-and-mouth disease virus.Cyclic disulfide model of the major antigenic site of serotype-C foot-and-mouth disease virus. Synthetic, conformational and immunochemical studies.Distinct mechanisms of antibody-mediated enzymatic reactivation in beta-galactosidase molecular sensors.Engineering of Escherichia coli beta-galactosidase for solvent display of a functional scFv antibody fragment.Generation and characterisation of recombinant FMDV antibodies: Applications for advancing diagnostic and laboratory assaysSuccessful mimicry of a complex viral antigen by multiple peptide insertions in a carrier protein
P2860
Q27486234-ACF11E49-53CE-4288-8F7A-1A7AE3A78B96Q28728760-FB16EFC5-CB70-4CA6-BBD0-63A78C17115CQ33573531-8466A54D-E46E-4A73-A00B-D1767EDB0050Q35861163-88AE984A-B803-4EC9-A72D-5E348F350A37Q36240271-2FC56993-CDD9-41B0-9C7B-2EEB28476006Q36367570-2BCF4A07-4992-4EBE-B00E-2CFF91EC7C08Q36503699-1A41C5A4-1A7E-4106-9BF7-0709D88F05E2Q36636915-C4267687-5AAA-42D2-8CF0-F6D4E53D9C94Q36646892-74CB796A-97BF-45A7-A593-FDA0FCF7128BQ36836779-22964F40-27AC-42D9-A443-DD57C58F26D0Q39577442-2770A1E3-9731-42E0-A9E0-BF8F4A7DB428Q39589175-3C296EB4-D081-4BF7-BBEE-13D10C01E847Q39590428-8ED45187-49E9-4BA9-8FC8-038AC06D0C1DQ39600262-D2F4872D-4218-46B5-9577-BE24AB92E49EQ39606030-D8B3C90B-0FF1-4CDF-867F-CBB314C4FFD2Q39858755-F53F6402-1395-4E30-939C-874D2D2841F2Q39878888-0C0EE4BD-F1EC-4102-81F7-360C04CE8ECAQ39880172-A2B62810-BDD0-4C21-A03E-F5743ECCB84AQ40015470-52C1483E-0E4F-4230-8266-D040FC7D27DBQ40015576-B6B96FB4-B8A7-4156-8BAF-8CA81B7E1BB8Q40038261-207E701B-2B32-4421-A17E-642403819409Q40038672-DFCFEFAD-5BF8-416D-BBB5-002C2DE296CBQ40039364-9ACB7EE5-77DC-4E96-BBF1-C4C72BA317D8Q40046794-860CF36C-0C19-4706-8F32-AB98D0E40066Q40047520-9BB6002C-AE9E-4E99-9DF5-E08FF3D90779Q40063046-3DFA43CC-55FC-40D6-BD36-78E8B1B6C934Q40065855-8599ED00-63EE-4487-AAAF-C188252D827FQ40067382-5FD1F9BE-0FC8-429F-9E9D-0B5FE51D60E3Q40067391-7E87B7FE-4A08-412C-A427-D7D6EA5E3C85Q40104899-52220975-8770-4A7E-8BCC-8566BBD0D3ACQ40806410-7FF48A31-5E3E-4CCF-A560-F3AF4DACC959Q41197317-B5FB3605-7038-400D-8FAF-AF4EBBD48B9BQ43039761-0AF60D6D-C038-499D-B444-D2E6E7C4852FQ45786718-78ADED9B-2E23-4EC2-A194-B2CCDA588467Q45786825-7B1FCE5D-B804-4483-9C1A-50ACCEECC358Q46506117-216392EB-08A3-4B9A-A5E9-9A8A9754C3CCQ54532880-E744FAB9-A072-40CC-87D0-27FE9032B8B3Q58775200-00D45122-CBD8-4FEF-A6C0-D4457EBFF2E1Q59201855-000AA392-384E-4E09-8252-6F9ADDE3494D
P2860
Implications of a quasispecies genome structure: effect of frequent, naturally occurring amino acid substitutions on the antigenicity of foot-and-mouth disease virus
description
1989 nî lūn-bûn
@nan
1989 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
Implications of a quasispecies ...... f foot-and-mouth disease virus
@ast
Implications of a quasispecies ...... f foot-and-mouth disease virus
@en
Implications of a quasispecies ...... f foot-and-mouth disease virus
@nl
type
label
Implications of a quasispecies ...... f foot-and-mouth disease virus
@ast
Implications of a quasispecies ...... f foot-and-mouth disease virus
@en
Implications of a quasispecies ...... f foot-and-mouth disease virus
@nl
prefLabel
Implications of a quasispecies ...... f foot-and-mouth disease virus
@ast
Implications of a quasispecies ...... f foot-and-mouth disease virus
@en
Implications of a quasispecies ...... f foot-and-mouth disease virus
@nl
P2093
P2860
P356
P1476
Implications of a quasispecies ...... f foot-and-mouth disease virus
@en
P2093
Martínez MA
P2860
P304
P356
10.1073/PNAS.86.15.5883
P407
P577
1989-08-01T00:00:00Z