| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Terence S. Dermody | Q87776424 |
| Pranav Danthi | Q42084766 | ||
| Bernardo A Mainou | Q42351721 | ||
| P2093 | author name string | Eva Kirchner | |
| Kristen M Guglielmi | |||
| Thilo Stehle | |||
| P2860 | cites work | Viral shedding and transmission between hosts determined by reovirus L2 gene | Q70141371 |
| Distinct pathways of viral spread in the host determined by reovirus S1 gene segment | Q70145205 | ||
| The symmetry of the reovirus outer shell | Q70376562 | ||
| Fate of parental reovirus in infected cell | Q70731978 | ||
| Reovirus: evidence for a second step in the intracellular uncoating and transcriptase activation process | Q70779231 | ||
| Absolute linkage of virulence and central nervous system cell tropism of reoviruses to viral hemagglutinin | Q72133339 | ||
| 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 | ||
| Essential role for cathepsin S in MHC class II-associated invariant chain processing and peptide loading | Q24328923 | ||
| Cytosolic adaptor protein Dab2 is an intracellular ligand of endocytic receptor gp600/megalin | Q24532029 | ||
| Lysosomal cysteine proteases: facts and opportunities | Q24535678 | ||
| Differential sensitivity of normal and transformed human cells to reovirus infection | Q24633362 | ||
| Junctional adhesion molecule, a novel member of the immunoglobulin superfamily that distributes at intercellular junctions and modulates monocyte transmigration | Q24682572 | ||
| Maturation cleavage required for infectivity of a nodavirus | Q27486191 | ||
| A triple beta-spiral in the adenovirus fibre shaft reveals a new structural motif for a fibrous protein | Q27620295 | ||
| Structure of the reovirus core at 3.6 A resolution | Q27622391 | ||
| Structure of the reovirus outer capsid and dsRNA-binding protein sigma3 at 1.8 A resolution | Q27630251 | ||
| Crystal structure of reovirus attachment protein sigma1 reveals evolutionary relationship to adenovirus fiber | Q27637218 | ||
| Structure of the reovirus membrane-penetration protein, Mu1, in a complex with is protector protein, Sigma3 | Q27637699 | ||
| RNA synthesis in a cage--structural studies of reovirus polymerase lambda3 | Q27640090 | ||
| Crystal structure of human junctional adhesion molecule 1: Implications for reovirus binding | Q27640992 | ||
| Reovirus polymerase λ3 localized by cryo-electron microscopy of virions at a resolution of 7.6 Å | Q27642516 | ||
| The reovirus sigma1 aspartic acid sandwich: a trimerization motif poised for conformational change | Q27643831 | ||
| Structure of Reovirus σ1 in Complex with Its Receptor Junctional Adhesion Molecule-A | Q27653146 | ||
| Identification and characterisation of human Junctional Adhesion Molecule (JAM) | Q28145696 | ||
| Junction adhesion molecule is a receptor for reovirus | Q28203704 | ||
| NPXY, a sequence often found in cytoplasmic tails, is required for coated pit-mediated internalization of the low density lipoprotein receptor | Q28254985 | ||
| Attachment and cell entry of mammalian orthoreovirus | Q28257821 | ||
| Internal/structures containing transcriptase-related proteins in top component particles of mammalian orthoreovirus | Q28272793 | ||
| Herpes simplex virus-1 entry into cells mediated by a novel member of the TNF/NGF receptor family | Q28295196 | ||
| Emerging roles for cysteine proteases in human biology | Q28306260 | ||
| Disabled-2 colocalizes with the LDLR in clathrin-coated pits and interacts with AP-2 | Q28511801 | ||
| Endosomal proteolysis of the Ebola virus glycoprotein is necessary for infection | Q28588877 | ||
| HIV-1 entry into CD4+ cells is mediated by the chemokine receptor CC-CKR-5 | Q29616094 | ||
| Chemokine receptors as HIV-1 coreceptors: roles in viral entry, tropism, and disease | Q29616432 | ||
| Pathways of chaperone-mediated protein folding in the cytosol | Q29618887 | ||
| Reovirus mu1 structural rearrangements that mediate membrane penetration | Q30159626 | ||
| Structure of the carboxy-terminal receptor-binding domain of avian reovirus fibre sigmaC. | Q30160104 | ||
| The structure of the bacteriophage PRD1 spike sheds light on the evolution of viral capsid architecture. | Q30160264 | ||
| Structural similarities in the cellular receptors used by adenovirus and reovirus | Q30163909 | ||
| A novel mechanism for the acquisition of virulence by a human influenza A virus | Q30431264 | ||
| Independent regulation of reovirus membrane penetration and apoptosis by the mu1 phi domain | Q33396212 | ||
| HIV-1 attachment: another look. | Q33601938 | ||
| Cleavage susceptibility of reovirus attachment protein sigma1 during proteolytic disassembly of virions is determined by a sequence polymorphism in the sigma1 neck | Q33784880 | ||
| Reovirus-induced apoptosis requires activation of transcription factor NF-kappaB. | Q33800833 | ||
| Mutant cells selected during persistent reovirus infection do not express mature cathepsin L and do not support reovirus disassembly. | Q33823560 | ||
| Adaptation of reovirus to growth in the presence of protease inhibitor E64 segregates with a mutation in the carboxy terminus of viral outer-capsid protein sigma3. | Q33838136 | ||
| Reovirus binding to cell surface sialic acid potentiates virus-induced apoptosis | Q33839080 | ||
| Identification of carbohydrate-binding domains in the attachment proteins of type 1 and type 3 reoviruses | Q33874116 | ||
| Organ-specific roles for transcription factor NF-kappaB in reovirus-induced apoptosis and disease | Q33914633 | ||
| Type 3 reovirus neuroinvasion after intramuscular inoculation: direct invasion of nerve terminals and age-dependent pathogenesis | Q33963215 | ||
| Adenovirus protein VI mediates membrane disruption following capsid disassembly. | Q33984709 | ||
| Features of reovirus outer capsid protein mu1 revealed by electron cryomicroscopy and image reconstruction of the virion at 7.0 Angstrom resolution | Q34019963 | ||
| The J.D. mutation in familial hypercholesterolemia: amino acid substitution in cytoplasmic domain impedes internalization of LDL receptors | Q34196707 | ||
| Reovirus variants selected for resistance to ammonium chloride have mutations in viral outer-capsid protein sigma3. | Q34301756 | ||
| Virion disassembly is required for apoptosis induced by reovirus | Q34330619 | ||
| A single mutation in the carboxy terminus of reovirus outer-capsid protein sigma 3 confers enhanced kinetics of sigma 3 proteolysis, resistance to inhibitors of viral disassembly, and alterations in sigma 3 structure | Q34347831 | ||
| Reovirus therapy of tumors with activated Ras pathway | Q34479740 | ||
| Genome delivery and ion channel properties are altered in VP4 mutants of poliovirus. | Q34976192 | ||
| Complete in vitro assembly of the reovirus outer capsid produces highly infectious particles suitable for genetic studies of the receptor-binding protein | Q39606223 | ||
| Sites and determinants of early cleavages in the proteolytic processing pathway of reovirus surface protein sigma3. | Q39683392 | ||
| Strategy for nonenveloped virus entry: a hydrophobic conformer of the reovirus membrane penetration protein micro 1 mediates membrane disruption | Q39684830 | ||
| Bovine papillomavirus type 1: from clathrin to caveolin | Q39766716 | ||
| Rescue of maturation-defective flock house virus infectivity with noninfectious, mature, viruslike particles | Q40035957 | ||
| Reovirus M2 gene is associated with chromium release from mouse L cells | Q40046935 | ||
| Reovirus apoptosis and virulence are regulated by host cell membrane penetration efficiency | Q40062777 | ||
| Retinoic acid-inducible gene-I and interferon-beta promoter stimulator-1 augment proapoptotic responses following mammalian reovirus infection via interferon regulatory factor-3. | Q40125620 | ||
| Reovirus guanylyltransferase is L2 gene product lambda 2. | Q40131290 | ||
| Reovirus binding determinants in junctional adhesion molecule-A. | Q40142387 | ||
| Reovirus outer capsid protein micro1 induces apoptosis and associates with lipid droplets, endoplasmic reticulum, and mitochondria | Q40243163 | ||
| A molecular dynamics study of reovirus attachment protein sigma1 reveals conformational changes in sigma1 structure | Q40284028 | ||
| Beta1 integrin mediates internalization of mammalian reovirus | Q40311619 | ||
| SARS coronavirus, but not human coronavirus NL63, utilizes cathepsin L to infect ACE2-expressing cells | Q40341738 | ||
| The delta region of outer-capsid protein micro 1 undergoes conformational change and release from reovirus particles during cell entry. | Q40344603 | ||
| Endocytosis by random initiation and stabilization of clathrin-coated pits | Q40520631 | ||
| Putative autocleavage of outer capsid protein micro1, allowing release of myristoylated peptide micro1N during particle uncoating, is critical for cell entry by reovirus. | Q40530759 | ||
| Isolation and molecular characterization of a novel type 3 reovirus from a child with meningitis | Q40561414 | ||
| Cathepsin S supports acid-independent infection by some reoviruses | Q40608252 | ||
| Electron microscopy study of reovirus reaction cores | Q40632118 | ||
| Structure-function analysis of reovirus binding to junctional adhesion molecule 1. Implications for the mechanism of reovirus attachment | Q40635854 | ||
| Cathepsin L and cathepsin B mediate reovirus disassembly in murine fibroblast cells | Q40734800 | ||
| Oncolytic reovirus against ovarian and colon cancer. | Q40742634 | ||
| Utilization of sialic acid as a coreceptor enhances reovirus attachment by multistep adhesion strengthening | Q40845786 | ||
| Two Modes of Entry of Reovirus Particles into L Cells | Q41031906 | ||
| Differential interaction of reovirus type 3 with sialylated receptor components on animal cells | Q41465134 | ||
| Influenza virus hemagglutinin with multibasic cleavage site is activated by furin, a subtilisin-like endoprotease | Q41505675 | ||
| Isolation and enzymatic characterization of protein λ2, the reovirus guanylyltransferase | Q41659753 | ||
| Peptides released from reovirus outer capsid form membrane pores that recruit virus particles. | Q41855783 | ||
| Cathepsin L is involved in proteolytic processing of the Hendra virus fusion protein | Q42042006 | ||
| A plasmid-based reverse genetics system for animal double-stranded RNA viruses. | Q42084718 | ||
| Junctional adhesion molecule-A is required for hematogenous dissemination of reovirus | Q42085912 | ||
| Complete nucleotide sequence of reovirus L2 gene and deduced amino acid sequence of viral mRNA guanylyltransferase. | Q42648183 | ||
| IkappaB kinase subunits alpha and gamma are required for activation of NF-kappaB and induction of apoptosis by mammalian reovirus | Q42957125 | ||
| JAM-A-independent, antibody-mediated uptake of reovirus into cells leads to apoptosis | Q43181943 | ||
| Reovirus protein lambda 3 is a poly(C)-dependent poly(G) polymerase | Q43576087 | ||
| Digestion pattern of reovirus outer capsid protein sigma3 determined by mass spectrometry | Q43743062 | ||
| Age dependent susceptibility to Reovirus type 3 encephalitis: role of viral and host factors | Q44434583 | ||
| Viral RNA Polymerases: Electron Microscopy of Reovirus Reaction Cores | Q45000386 | ||
| Stoichiometry of reovirus structural proteins in virus, ISVP, and core particles | Q45756975 | ||
| Genetics of reovirus: identification of the ds RNA segments encoding the polypeptides of the mu and sigma size classes | Q47316030 | ||
| Binding site for S-adenosyl-L-methionine in a central region of mammalian reovirus lambda2 protein. Evidence for activities in mRNA cap methylation. | Q52565526 | ||
| Prevalence of Reovirus‐Specific Antibodies in Young Children in Nashville, Tennessee | Q56481070 | ||
| The mechanisms of reovirus uncoating and gene activation in vivo | Q67294193 | ||
| The nature of the polypeptide encoded by each of the 10 double-stranded RNA segments of reovirus type 3 | Q67412668 | ||
| Mechanism of formation of reovirus mRNA 5'-terminal blocked and methylated sequence, m7GpppGmpC | Q67525409 | ||
| Biochemical and biophysical characterization of the reovirus cell attachment protein sigma 1: evidence that it is a homotrimer | Q67944238 | ||
| Active site localization in a viral mRNA capping enzyme | Q68457689 | ||
| Effect of neuraminidase treatment of cells and effect of soluble glycoproteins on type 3 reovirus attachment to murine L cells | Q36852462 | ||
| Intracellular digestion of reovirus particles requires a low pH and is an essential step in the viral infectious cycle. | Q36915422 | ||
| Activation and characterization of the reovirus transcriptase: genetic analysis | Q36936630 | ||
| Direct spread of reovirus from the intestinal lumen to the central nervous system through vagal autonomic nerve fibers | Q37500830 | ||
| Identification of the guanylyltransferase region and active site in reovirus mRNA capping protein lambda2. | Q38316274 | ||
| Junctional adhesion molecule a serves as a receptor for prototype and field-isolate strains of mammalian reovirus | Q38324922 | ||
| The alpha-anomeric form of sialic acid is the minimal receptor determinant recognized by reovirus | Q38343681 | ||
| Flexibility of the adenovirus fiber is required for efficient receptor interaction | Q38353615 | ||
| Identification of an NF-kappaB-dependent gene network in cells infected by mammalian reovirus. | Q38519145 | ||
| Reovirus virion-like particles obtained by recoating infectious subvirion particles with baculovirus-expressed sigma3 protein: an approach for analyzing sigma3 functions during virus entry. | Q39549886 | ||
| In vitro recoating of reovirus cores with baculovirus-expressed outer-capsid proteins mu1 and sigma3. | Q39550452 | ||
| Protease cleavage of reovirus capsid protein mu1/mu1C is blocked by alkyl sulfate detergents, yielding a new type of infectious subvirion particle. | Q39577260 | ||
| Molecular basis of reovirus virulence: Role of the S1 gene | Q35054361 | ||
| Structural evidence for common functions and ancestry of the reovirus and adenovirus attachment proteins | Q35081788 | ||
| Utilization of sialic acid as a coreceptor is required for reovirus-induced biliary disease | Q35095524 | ||
| Invasion of host cells by JC virus identifies a novel role for caveolae in endosomal sorting of noncaveolar ligands | Q35101449 | ||
| The viral sigma1 protein and glycoconjugates containing alpha2-3-linked sialic acid are involved in type 1 reovirus adherence to M cell apical surfaces | Q35104539 | ||
| Mammalian reovirus, a nonfusogenic nonenveloped virus, forms size-selective pores in a model membrane. | Q35133892 | ||
| Binding of type 3 reovirus by a domain of the sigma 1 protein important for hemagglutination leads to infection of murine erythroleukemia cells | Q35614021 | ||
| Infectious subvirion particles of reovirus type 3 Dearing exhibit a loss in infectivity and contain a cleaved sigma 1 protein | Q35845209 | ||
| Differences in the capacity of reovirus strains to induce apoptosis are determined by the viral attachment protein sigma 1 | Q35850820 | ||
| Role of the mu 1 protein in reovirus stability and capacity to cause chromium release from host cells. | Q35853771 | ||
| Linkage between reovirus-induced apoptosis and inhibition of cellular DNA synthesis: role of the S1 and M2 genes | Q35872484 | ||
| Reovirus variants selected during persistent infections of L cells contain mutations in the viral S1 and S4 genes and are altered in viral disassembly | Q35877228 | ||
| Mutations in type 3 reovirus that determine binding to sialic acid are contained in the fibrous tail domain of viral attachment protein sigma1. | Q35877813 | ||
| Thermostabilizing mutations in reovirus outer-capsid protein mu1 selected by heat inactivation of infectious subvirion particles | Q35879120 | ||
| Mutations in reovirus outer-capsid protein sigma3 selected during persistent infections of L cells confer resistance to protease inhibitor E64 | Q35887561 | ||
| Glycoconjugate glycans as viral receptors | Q36194868 | ||
| Conformational changes induced in the human immunodeficiency virus envelope glycoprotein by soluble CD4 binding | Q36230268 | ||
| Early steps in reovirus infection are associated with dramatic changes in supramolecular structure and protein conformation: analysis of virions and subviral particles by cryoelectron microscopy and image reconstruction | Q36232691 | ||
| Peyer's patch dendritic cells process viral antigen from apoptotic epithelial cells in the intestine of reovirus-infected mice | Q36399901 | ||
| NPXY motifs in the beta1 integrin cytoplasmic tail are required for functional reovirus entry | Q36498196 | ||
| Drug evaluation: Reolysin--wild-type reovirus as a cancer therapeutic. | Q36506689 | ||
| Proteolytic processing of reovirus is required for adherence to intestinal M cells | Q36638339 | ||
| Isolation and genetic characterization of ethanol-resistant reovirus mutants | Q36644956 | ||
| Ion channels induced in lipid bilayers by subvirion particles of the nonenveloped mammalian reoviruses | Q36660165 | ||
| A carboxy-terminal fragment of protein mu 1/mu 1C is present in infectious subvirion particles of mammalian reoviruses and is proposed to have a role in penetration | Q36684993 | ||
| Cells and viruses with mutations affecting viral entry are selected during persistent infections of L cells with mammalian reoviruses. | Q36686120 | ||
| A role for molecular chaperone Hsc70 in reovirus outer capsid disassembly | Q36769116 | ||
| A sigma 1 region important for hemagglutination by serotype 3 reovirus strains | Q36784412 | ||
| A positive-feedback mechanism promotes reovirus particle conversion to the intermediate associated with membrane penetration | Q36802470 | ||
| Intraluminal proteolytic activation plays an important role in replication of type 1 reovirus in the intestines of neonatal mice | Q36804334 | ||
| Structure of the reovirus cell-attachment protein: a model for the domain organization of sigma 1. | Q36808171 | ||
| Molecular structure of the cell-attachment protein of reovirus: correlation of computer-processed electron micrographs with sequence-based predictions | Q36808217 | ||
| Sigma 1 protein of mammalian reoviruses extends from the surfaces of viral particles | Q36826294 | ||
| Proteolytic digestion of reovirus in the intestinal lumens of neonatal mice | Q36831570 | ||
| P921 | main subject | Reovirus | Q69812835 |
| P304 | page(s) | 91-119 | |
| P577 | publication date | 2010-01-01 | |
| P1433 | published in | Current Topics in Microbiology and Immunology | Q15752446 |
| P1476 | title | From touchdown to transcription: the reovirus cell entry pathway | |
| P478 | volume | 343 |
| Q38228539 | Basics of virology. |
| Q36294722 | Cell Walls and the Convergent Evolution of the Viral Envelope |
| Q39406121 | Cell entry-associated conformational changes in reovirus particles are controlled by host protease activity |
| Q55387260 | Clathrin-mediated endocytosis is a candidate entry sorting mechanism for Bombyx mori cypovirus. |
| Q39329417 | Comparative proteomic analyses demonstrate enhanced interferon and STAT-1 activation in reovirus T3D-infected HeLa cells |
| Q30155993 | Determinants of strain-specific differences in efficiency of reovirus entry |
| Q33938568 | Endocytosis of viruses and bacteria |
| Q37832047 | Enter the kill zone: initiation of death signaling during virus entry. |
| Q39524228 | Grass carp reovirus-GD108 fiber protein is involved in cell attachment |
| Q92989195 | How Many Mammalian Reovirus Proteins are involved in the Control of the Interferon Response? |
| Q35826221 | Human metapneumovirus (HMPV) binding and infection are mediated by interactions between the HMPV fusion protein and heparan sulfate |
| Q39593763 | Lysosomal localization and mechanism of membrane penetration influence nonenveloped virus activation of the NLRP3 inflammasome. |
| Q36155563 | Mechanisms of reovirus bloodstream dissemination |
| Q26775033 | Potential for Improving Potency and Specificity of Reovirus Oncolysis with Next-Generation Reovirus Variants |
| Q59791688 | Real-Time Dissecting the Entry and Intracellular Dynamics of Single Reovirus Particle |
| Q38912745 | Reduction of virion-associated σ1 fibers on oncolytic reovirus variants promotes adaptation toward tumorigenic cells |
| Q36850813 | Reovirus activates a caspase-independent cell death pathway. |
| Q38743317 | Reovirus μ1 Protein Affects Infectivity by Altering Virus-Receptor Interactions. |
| Q37713871 | Rotaviruses reach late endosomes and require the cation-dependent mannose-6-phosphate receptor and the activity of cathepsin proteases to enter the cell |
| Q30538733 | Similar uptake but different trafficking and escape routes of reovirus virions and infectious subvirion particles imaged in polarized Madin-Darby canine kidney cells. |
| Q38112009 | Structure and assembly of complex viruses |
| Q59349733 | Synthesis and Translation of Viral mRNA in Reovirus-Infected Cells: Progress and Remaining Questions |
| Q34532116 | Targeting human dendritic cells via DEC-205 using PLGA nanoparticles leads to enhanced cross-presentation of a melanoma-associated antigen |
| Q39441933 | The cellular chaperone hsc70 is specifically recruited to reovirus viral factories independently of its chaperone function. |
| Q39088516 | The μ1 72-96 loop controls conformational transitions during reovirus cell entry. |
| Q39204304 | Transient high level mammalian reovirus replication in a bat epithelial cell line occurs without cytopathic effect |
| Q36718104 | Unraveling protein-protein interactions in clathrin assemblies via atomic force spectroscopy. |
| Q37909045 | Viral weapons of membrane destruction: variable modes of membrane penetration by non-enveloped viruses |
| Q37202578 | Viroporins customize host cells for efficient viral propagation |
| Q59358423 | Virus-Receptor Interactions: The Key to Cellular Invasion |
| Q36438385 | αvβ3-integrin is a major sensor and activator of innate immunity to herpes simplex virus-1. |
| Q35075118 | αvβ6- and αvβ8-integrins serve as interchangeable receptors for HSV gH/gL to promote endocytosis and activation of membrane fusion |
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