scholarly article | Q13442814 |
P2093 | author name string | MURPHY JS | |
KILBOURNE ED | |||
P2860 | cites work | Two kinds of particles with contrasting properties in influenza A virus strains from the 1957 pandemic. | Q30334503 |
Observations with the electron microscope on cells of the chick chorio-allantoic membrane infected with influenza virus | Q31045595 | ||
Evidence for genetic interaction between non-infectious and infectious influenza A viruses | Q36262882 | ||
NEUTRALIZATION OF EPIDEMIC INFLUENZA VIRUS : THE LINEAR RELATIONSHIP BETWEEN THE QUANTITY OF SERUM AND THE QUANTITY OF VIRUS NEUTRALIZED. | Q42181078 | ||
The experimental production of combination forms of virus. I. Occurrence of combination forms after simultaneous inoculation of the allantoic sac with two distinct strains of influenza virus | Q42806361 | ||
Properties of the nucleic acid of the Ryan strain of filamentous influenza virus | Q43737577 | ||
Reactivation of heat inactivated influenza virus by recombination | Q44520258 | ||
Comparative study of recombinants of different types of influenza A virus with the strain WSE. | Q44790463 | ||
Filamentous forms associated with newly isolated influenza virus | Q45398318 | ||
A genetic approach to variation in influenza viruses; recombination of characters in influenza virus strains used in mixed infections | Q45689340 | ||
Features of the MEL x NWS recombination systems in influenza A virus. IV. Increments of virulence during successive cycles of double infection with two strains of influenza A virus | Q45717508 | ||
The experimental production of combination forms of virus. VI. Reactivation of influenza viruses after inactivation by ultraviolet light | Q45720361 | ||
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 387-406 | |
P577 | publication date | 1960-03-01 | |
P1433 | published in | Journal of Experimental Medicine | Q3186912 |
P1476 | title | Genetic studies of influenza viruses. I. Viral morphology and growth capacity as exchangeable genetic traits. Rapid in ovo adaptation of early passage Asian strain isolates by combination with PR8. | |
P478 | volume | 111 |
Q45741249 | A comprehensive systematic approach to identification of influenza A virus genotype using RT-PCR and RFLP. |
Q45794432 | An immunofluorescence study of influenza virus filament formation |
Q37129134 | Antiviral Activity of Antiserum Specific for an Influenza Virus Neuraminidase |
Q40629188 | Attenuation of pathogenicity of fowl plague virus by recombination with other influenza A viruses nonpathogenic for fowl: nonexculsive dependence of pathogenicity on hemagglutinin and neuraminidase of the virus |
Q39838203 | Budding of filamentous and non-filamentous influenza A virus occurs via a VPS4 and VPS28-independent pathway |
Q36265233 | Changing viral susceptibility of a human cell line in continuous cultivation. I. Production of infective virus in a variant of the Chang conjunctival cell following infection with swine or N-WS influenza viruses |
Q41713534 | Correlation of pathogenicity and gene constellation of influenza A viruses II. Highly neurovirulent recombinants derived from non-neurovirulent or weakly neurovirulent parent virus strains |
Q30408108 | Developing vaccines to combat pandemic influenza |
Q39291818 | Direct observation of the budding and fusion of an enveloped virus by video microscopy of viable cells |
Q35706440 | Error-prone pcr-based mutagenesis strategy for rapidly generating high-yield influenza vaccine candidates. |
Q36017724 | Evaluation of influenza virus A/H3N2 and B vaccines on the basis of cross-reactivity of postvaccination human serum antibodies against influenza viruses A/H3N2 and B isolated in MDCK cells and embryonated hen eggs |
Q34482985 | Filament-producing mutants of influenza A/Puerto Rico/8/1934 (H1N1) virus have higher neuraminidase activities than the spherical wild-type |
Q40273614 | Filamentous Influenza Viruses. |
Q36276270 | Filamentous influenza virus enters cells via macropinocytosis |
Q38882756 | Filamentous influenza viruses. |
Q61798802 | Friend or Foe: The Role of the Cytoskeleton in Influenza A Virus Assembly |
Q36575180 | Functional Significance of Sialidase During Influenza Virus Multiplication: an Electron Microscope Study |
Q36551515 | Future influenza vaccines and the use of genetic recombinants |
Q33939416 | Gene constellation of influenza A virus reassortants with high growth phenotype prepared as seed candidates for vaccine production |
Q35201205 | Genetic and phenotypic analysis of reassortants of high growth and low growth strains of influenza B virus |
Q37597467 | Genetic dimorphism in influenza viruses: Characterization of stably associated hemagglutinin mutants differing in antigenicity and biological properties |
Q72614835 | Genetic interaction between influenza A viruses of human and animal origin |
Q104504774 | HA1 (Hemagglutinin) quantitation for influenza A H1N1 and H3N2 high yield reassortant vaccine candidate seed viruses by RP-UPLC |
Q28397046 | Host adaptation and transmission of influenza A viruses in mammals |
Q36097986 | Host cell dependence of viral morphology |
Q41527395 | Identification of morphological differences between avian influenza A viruses grown in chicken and duck cells. |
Q30403265 | Improvement of H5N1 influenza vaccine viruses: influence of internal gene segments of avian and human origin on production and hemagglutinin content |
Q39996684 | Influenza 1970:Unquestioned Answer and Unanswered Questions |
Q56981340 | Influenza A Virus Cell Entry, Replication, Virion Assembly and Movement |
Q37743549 | Influenza a viruses with mutations in the m1 helix six domain display a wide variety of morphological phenotypes |
Q30362983 | Influenza virus PB1 and neuraminidase gene segments can cosegregate during vaccine reassortment driven by interactions in the PB1 coding region. |
Q34913111 | Influenza virus assembly and budding |
Q45345423 | Influenza virus assembly and budding at the viral budozone. |
Q33886239 | Influenza virus hemagglutinin and neuraminidase cytoplasmic tails control particle shape |
Q33826913 | Influenza virus m2 ion channel protein is necessary for filamentous virion formation |
Q40349761 | M Gene Reassortment in H9N2 Influenza Virus Promotes Early Infection and Replication: Contribution to Rising Virus Prevalence in Chickens in China |
Q35091674 | Morphology of influenza B/Lee/40 determined by cryo-electron microscopy |
Q37424406 | Multiplicity reactivation of Newcastle disease virus |
Q40110896 | Native morphology of influenza virions |
Q30407716 | Novel vaccines against influenza viruses. |
Q36099007 | Overlapping roles of the Rous sarcoma virus Gag p10 domain in nuclear export and virion core morphology. |
Q35876587 | Presentation of Academy Medal to Edwin D. Kilbourne, M.D |
Q77349756 | Rapid confirmation by RFLP of transfer to vaccine candidate reassortment viruses of the principal 'high yield' gene of influenza A viruses |
Q36258055 | Recombinants of influenza virus type B as potential live vaccine candidates: RNA characterization and evaluation in man. |
Q27490194 | Reduction in plaque size and reduction in plaque number as differing indices of influenza virus-antibody reactions |
Q34141955 | Repository of Eurasian influenza A virus hemagglutinin and neuraminidase reverse genetics vectors and recombinant viruses |
Q33522372 | Reverse genetic platform for inactivated and live-attenuated influenza vaccine |
Q30382035 | STUDIES OF TWO KINDS OF VIRUS PARTICLES WHICH COMPRISE INFLUENZA A2 VIRUS STRAINS : I. CHARACTERIZATION OF STABLE HOMOGENEOUS SUBSTRAINS IN REACTIONS WITH SPECIFIC ANTIBODY, MUCOPROTEIN INHIBITORS, AND ERYTHROCYTES |
Q90276298 | Single-particle measurements of filamentous influenza virions reveal damage induced by freezing |
Q28391423 | Specific residues in the 2009 H1N1 swine-origin influenza matrix protein influence virion morphology and efficiency of viral spread in vitro |
Q28391618 | Spherical influenza viruses have a fitness advantage in embryonated eggs, while filament-producing strains are selected in vivo |
Q30495070 | Structural organization of a filamentous influenza A virus |
Q33189983 | Studies of two kinds of virus particles which comprise influenza A2 virus strains. III. Morphological characteristics: independence to morphological and functional traits |
Q64096033 | Super-resolution microscopy reveals significant impact of M2e-specific monoclonal antibodies on influenza A virus filament formation at the host cell surface |
Q70483036 | Testing of the strain identity of influenza vaccines by haemagglutination inhibition |
Q28278360 | The Rab11 pathway is required for influenza A virus budding and filament formation |
Q37123163 | The amphipathic helix of influenza A virus M2 protein is required for filamentous bud formation and scission of filamentous and spherical particles |
Q45853825 | The effect of virus particle size on chemiluminescence induction by influenza and Sendai viruses in mouse spleen cells |
Q79620837 | The role of viruses in neoplasia, with emphasis on human leukemia |
Q36827336 | The source of the PB1 gene in influenza vaccine reassortants selectively alters the hemagglutinin content of the resulting seed virus. |
Q37136609 | Towards multiscale modeling of influenza infection |
Q37271683 | Transport of the influenza virus genome from nucleus to nucleus |
Q45325107 | Unique directional motility of influenza C virus controlled by its filamentous morphology and short-range motions. |
Q36809532 | Use of recombination in the production of influenza vaccine strains |
Q34409178 | Vaccines: past, present and future |
Q34992609 | Variations in pH sensitivity, acid stability, and fusogenicity of three influenza virus H3 subtypes |
Search more.