scholarly article | Q13442814 |
P50 | author | Cathy L. Miller | Q38319404 |
P2093 | author name string | John S L Parker | |
Max L Nibert | |||
Teresa J Broering | |||
Jonghwa Kim | |||
Jason B Dinoso | |||
Caroline D S Piggott | |||
P2860 | cites work | Structure of the reovirus core at 3.6 A resolution | Q27622391 |
RNA synthesis in a cage--structural studies of reovirus polymerase lambda3 | Q27640090 | ||
Internal/structures containing transcriptase-related proteins in top component particles of mammalian orthoreovirus | Q28272793 | ||
Aggresomes: a cellular response to misfolded proteins | Q28292275 | ||
The M1 gene is associated with differences in the temperature optimum of the transcriptase activity in reovirus core particles | Q28775716 | ||
Aggresomes, inclusion bodies and protein aggregation | Q29615253 | ||
RNA polymerase activity in purified reoviruses | Q30532564 | ||
Reovirus mu2 protein determines strain-specific differences in the rate of viral inclusion formation in L929 cells | Q31774257 | ||
Reovirus sigmaNS protein is required for nucleation of viral assembly complexes and formation of viral inclusions. | Q33836647 | ||
Reovirus core protein mu2 determines the filamentous morphology of viral inclusion bodies by interacting with and stabilizing microtubules. | Q34122036 | ||
RNA interference: antiviral defense and genetic tool | Q34711481 | ||
Reovirus σNS and μNS Proteins Form Cytoplasmic Inclusion Structures in the Absence of Viral Infection | Q34976721 | ||
Small reovirus particle composed solely of sigma NS with specificity for binding different nucleic acids. | Q35239662 | ||
The penetration of reovirus RNA and initiation of its genetic function in L-strain fibroblasts | Q36189245 | ||
Immunofluorescent localization of double-stranded RNA in reovirus-infected cells | Q69909642 | ||
The interaction of mammalian reoviruses with the cytoskeleton of monkey kidney CV-1 cells | Q70679241 | ||
Characterization of anti-reovirus immunoglobulins secreted by cloned hybridoma cell lines | Q70891866 | ||
Studies on the intracellular synthesis of reovirus-specified proteins | Q71554391 | ||
Reovirus: RNA polymerase activity in purified virions | Q72299931 | ||
Characterization and structural localization of the reovirus lambda 3 protein | Q72484237 | ||
Mammalian reovirus L2 gene and lambda2 core spike protein sequences and whole-genome comparisons of reoviruses type 1 Lang, type 2 Jones, and type 3 Dearing | Q74449255 | ||
Structure of mammalian orthoreovirus particles | Q74585498 | ||
Sigma 1 protein of mammalian reoviruses extends from the surfaces of viral particles | Q36826294 | ||
Monoclonal antibodies to reovirus reveal structure/function relationships between capsid proteins and genetics of susceptibility to antibody action | Q36828429 | ||
Activation and characterization of the reovirus transcriptase: genetic analysis | Q36936630 | ||
Reovirus protein sigmaNS binds in multiple copies to single-stranded RNA and shares properties with single-stranded DNA binding proteins | Q38311437 | ||
Studies on the structure of reovirus cores: Selective removal of polypeptide λ2 | Q39085390 | ||
In vitro recoating of reovirus cores with baculovirus-expressed outer-capsid proteins mu1 and sigma3. | Q39550452 | ||
Reovirus nonstructural protein muNS binds to core particles but does not inhibit their transcription and capping activities | Q39591375 | ||
The hydrophilic amino-terminal arm of reovirus core shell protein lambda1 is dispensable for particle assembly | Q39686182 | ||
Reovirus sigma NS protein localizes to inclusions through an association requiring the mu NS amino terminus | Q39741994 | ||
Mammalian reovirus nonstructural protein microNS forms large inclusions and colocalizes with reovirus microtubule-associated protein micro2 in transfected cells | Q39753074 | ||
Reovirus guanylyltransferase is L2 gene product lambda 2. | Q40131290 | ||
The structure and function of the reovirus genome | Q40304672 | ||
The delta region of outer-capsid protein micro 1 undergoes conformational change and release from reovirus particles during cell entry. | Q40344603 | ||
Aggresomes resemble sites specialized for virus assembly | Q40603651 | ||
Transcription In Vitro by Reovirus-Associated Ribonucleic Acid-Dependent Polymerase | Q40709706 | ||
Reoviruses and the interferon system. | Q41040736 | ||
Amino terminus of reovirus nonstructural protein sigma NS is important for ssRNA binding and nucleoprotein complex formation | Q41068675 | ||
Generation of reovirus core-like particles in cells infected with hybrid vaccinia viruses that express genome segments L1, L2, L3, and S2. | Q41511090 | ||
Reovirus genome segment assortment into progeny genomes studied by the use of monoclonal antibodies directed against reovirus proteins | Q41631747 | ||
Assembly of the reovirus outer capsid requires mu 1/sigma 3 interactions which are prevented by misfolded sigma 3 protein in temperature-sensitive mutant tsG453. | Q41633883 | ||
Mammalian reovirus M3 gene sequences and conservation of coiled-coil motifs near the carboxyl terminus of the microNS protein | Q42612836 | ||
Cytochemical, fluorescent-antibody and electron microscopic studies on the growth of reovirus (ECHO 10) in tissue culture | Q43500409 | ||
Reovirus morphogenesis. Corelike particles in cells infected at 39 degrees with wild-type reovirus and temperature-sensitive mutants of groups B and G. | Q43533239 | ||
Reovirus protein lambda 3 is a poly(C)-dependent poly(G) polymerase | Q43576087 | ||
Mutational analysis of a mammalian reovirus mRNA capping enzyme | Q43897367 | ||
A positive-strand RNA virus replication complex parallels form and function of retrovirus capsids | Q45733045 | ||
The sequences of reovirus serotype 3 genome segments M1 and M3 encoding the minor protein mu 2 and the major nonstructural protein mu NS, respectively | Q48300735 | ||
Binding site for S-adenosyl-L-methionine in a central region of mammalian reovirus lambda2 protein. Evidence for activities in mRNA cap methylation. | Q52565526 | ||
Multiple forms of SS → DS RNA polymerase activity in reovirus-infected cells | Q53847255 | ||
Characterization of transcriptase and replicase particles isolated from reovirus-infected cells | Q67345969 | ||
Reovirus-coded polypeptides in infected cells: Isolation of two native monomeric polypeptides with affinity for single-stranded and double-stranded RNA, respectively | Q67446847 | ||
Polypeptide components of virions, top component and cores of reovirus type 3 | Q68603064 | ||
The induction of interferon by temperature-sensitive mutants of reovirus, UV-irradiated reovirus, and subviral reovirus particles | Q68654795 | ||
Temperature-sensitive mutants of reovirus. I. Patterns of gene expression by mutants of groups C, D, and E | Q69452858 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Reovirus | Q69812835 |
P304 | page(s) | 1882-1892 | |
P577 | publication date | 2004-02-01 | |
P1433 | published in | Journal of Virology | Q1251128 |
P1476 | title | Reovirus nonstructural protein mu NS recruits viral core surface proteins and entering core particles to factory-like inclusions | |
P478 | volume | 78 |
Q34006244 | A guide to viral inclusions, membrane rearrangements, factories, and viroplasm produced during virus replication |
Q39046931 | Amino acids 78 and 79 of Mammalian Orthoreovirus protein µNS are necessary for stress granule localization, core protein λ2 interaction, and de novo virus replication. |
Q61447732 | Antiviral Responses and Biological Concequences of Infection in Salmonid Erythrocytes |
Q35621405 | Aquareovirus NS80 Initiates Efficient Viral Replication by Retaining Core Proteins within Replication-Associated Viral Inclusion Bodies |
Q34592621 | Aquareovirus NS80 recruits viral proteins to its inclusions, and its C-terminal domain is the primary driving force for viral inclusion formation |
Q36863582 | Aquareovirus protein VP6 colocalizes with NS80 protein in infected and transfected cells |
Q40338701 | Avian reovirus microNS protein forms homo-oligomeric inclusions in a microtubule-independent fashion, which involves specific regions of its C-terminal domain |
Q40162412 | Avian reovirus temperature-sensitive mutant tsA12 has a lesion in major core protein sigmaA and is defective in assembly |
Q40429759 | Carboxyl-proximal regions of reovirus nonstructural protein muNS necessary and sufficient for forming factory-like inclusions |
Q40055051 | Characterization of a replicating mammalian orthoreovirus with tetracysteine tagged μNS for live cell visualization of viral factories |
Q36077953 | Characterization of grass carp reovirus minor core protein VP4. |
Q39678562 | Characterization of the nonstructural protein NS80 of grass carp reovirus |
Q58618419 | DNA vaccine expressing the non-structural proteins of Piscine orthoreovirus delay the kinetics of PRV infection and induces moderate protection against heart -and skeletal muscle inflammation in Atlantic salmon (Salmo salar) |
Q37713862 | Development of continuous cell culture of brown planthopper to trace the early infection process of oryzaviruses in insect vector cells |
Q39997322 | Formation of the factory matrix is an important, though not a sufficient function of nonstructural protein mu NS during reovirus infection |
Q64068315 | Function, Architecture, and Biogenesis of Reovirus Replication Neoorganelles |
Q35003905 | Functional investigation of grass carp reovirus nonstructural protein NS80. |
Q30356543 | Gene-specific inhibition of reovirus replication by RNA interference. |
Q35857383 | Guanidine hydrochloride inhibits mammalian orthoreovirus growth by reversibly blocking the synthesis of double-stranded RNA. |
Q92989195 | How Many Mammalian Reovirus Proteins are involved in the Control of the Interferon Response? |
Q38765667 | Identification and characterization of two cleavage fragments from the Aquareovirus nonstructural protein NS80. |
Q37127878 | Identification of functional domains in reovirus replication proteins muNS and mu2. |
Q39991940 | Increased ubiquitination and other covariant phenotypes attributed to a strain- and temperature-dependent defect of reovirus core protein mu2. |
Q40381336 | Interaction of Mal de Río Cuarto virus (Fijivirus genus) proteins and identification of putative factors determining viroplasm formation and decay. |
Q40194299 | Interaction of rice dwarf virus outer capsid P8 protein with rice glycolate oxidase mediates relocalization of P8. |
Q33558325 | Localization of mammalian orthoreovirus proteins to cytoplasmic factory-like structures via nonoverlapping regions of microNS |
Q40088765 | Mammalian Orthoreovirus Factories Modulate Stress Granule Protein Localization by Interaction with G3BP1. |
Q98509945 | Mammalian orthoreovirus core protein μ2 reorganizes host microtubule-organizing center components |
Q41844888 | Mammalian orthoreovirus particles induce and are recruited into stress granules at early times postinfection |
Q39642017 | Molecular characterization of nonstructural protein NS38 of grass carp reovirus |
Q47555849 | Non-structural protein σ1s is required for optimal reovirus protein expression |
Q34721254 | Nonstructural protein NS80 is crucial in recruiting viral components to form aquareoviral factories |
Q41095710 | Nonstructural protein Pns12 of rice dwarf virus is a principal regulator for viral replication and infection in its insect vector |
Q27314173 | Protein expression redirects vesicular stomatitis virus RNA synthesis to cytoplasmic inclusions |
Q40530759 | Putative autocleavage of outer capsid protein micro1, allowing release of myristoylated peptide micro1N during particle uncoating, is critical for cell entry by reovirus. |
Q38918571 | Recovery of infectious bluetongue virus from RNA. |
Q30536173 | Recruitment of cellular clathrin to viral factories and disruption of clathrin-dependent trafficking |
Q54209646 | Reovirus Nonstructural Protein σNS Acts as an RNA-Stability Factor Promoting Viral Genome Replication. |
Q37621639 | Reovirus forms neo-organelles for progeny particle assembly within reorganized cell membranes. |
Q40052207 | Reovirus inhibits interferon production by sequestering IRF3 into viral factories. |
Q39307482 | Reovirus replication protein μ2 influences cell tropism by promoting particle assembly within viral inclusions |
Q36397535 | Reovirus uses multiple endocytic pathways for cell entry. |
Q56395824 | Reovirus σNS and μNS Proteins Remodel the Endoplasmic Reticulum to Build Replication Neo-Organelles |
Q37945206 | Role of lipids on entry and exit of bluetongue virus, a complex non-enveloped virus |
Q34228672 | Rotavirus glycoprotein NSP4 is a modulator of viral transcription in the infected cell. |
Q34905720 | Sequence analysis of the genome of piscine orthoreovirus (PRV) associated with heart and skeletal muscle inflammation (HSMI) in Atlantic salmon (Salmo salar). |
Q37441928 | Sequences of avian reovirus M1, M2 and M3 genes and predicted structure/function of the encoded mu proteins |
Q40142474 | Silencing and complementation of reovirus core protein mu2: functional correlations with mu2-microtubule association and differences between virus- and plasmid-derived mu2. |
Q35922315 | The N-Terminal of Aquareovirus NS80 Is Required for Interacting with Viral Proteins and Viral Replication |
Q39441933 | The cellular chaperone hsc70 is specifically recruited to reovirus viral factories independently of its chaperone function. |
Q49894263 | The dynamics of both filamentous and globular mammalian reovirus viral factories rely on the microtubule network |
Q38805732 | The non-structural protein μNS of piscine orthoreovirus (PRV) forms viral factory-like structures |
Q39318008 | Viral hijacking of host caspases: an emerging category of pathogen-host interactions. |
Q45406516 | Virus-derived platforms for visualizing protein associations inside cells |
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