| P50 | author | Jean-Louis Palgen | Q63707736 |
| | Matteo Porotto | Q101403329 |
| | Anne Moscona | Q113032251 |
| P2093 | author name string | Laura M Palermo | |
| | Eric M Jurgens | |
| P2860 | cites work | Cedar virus: a novel Henipavirus isolated from Australian bats | Q21090488 |
| | Adherens junction protein nectin-4 is the epithelial receptor for measles virus | Q24295305 |
| | The human CD46 molecule is a receptor for measles virus (Edmonston strain) | Q24317745 |
| | Ephrin-B2 ligand is a functional receptor for Hendra virus and Nipah virus | Q24532042 |
| | Second sialic acid binding site in Newcastle disease virus hemagglutinin-neuraminidase: implications for fusion | Q24600140 |
| | Modes of paramyxovirus fusion: a Henipavirus perspective | Q24604089 |
| | Crystal structure of measles virus hemagglutinin provides insight into effective vaccines | Q24669991 |
| | Henipavirus mediated membrane fusion, virus entry and targeted therapeutics | Q27002511 |
| | Membrane fusion tropism and heterotypic functional activities of the Nipah virus and Hendra virus envelope glycoproteins | Q27472931 |
| | Viral membrane fusion | Q27486639 |
| | Crystal structure of the multifunctional paramyxovirus hemagglutinin-neuraminidase | Q27627919 |
| | The structure of the fusion glycoprotein of Newcastle disease virus suggests a novel paradigm for the molecular mechanism of membrane fusion | Q27631011 |
| | Structure of the haemagglutinin-neuraminidase from human parainfluenza virus type III | Q27642969 |
| | Structural basis of Nipah and Hendra virus attachment to their cell-surface receptor ephrin-B2 | Q27650639 |
| | Host cell recognition by the henipaviruses: Crystal structures of the Nipah G attachment glycoprotein and its complex with ephrin-B3 | Q27651214 |
| | Structure of the measles virus hemagglutinin bound to the CD46 receptor | Q27658662 |
| | Dimeric Architecture of the Hendra Virus Attachment Glycoprotein: Evidence for a Conserved Mode of Assembly | Q27660451 |
| | Structure of the Newcastle disease virus F protein in the post-fusion conformation | Q27661271 |
| | Effects of multiple amino acids of the parainfluenza virus 5 fusion protein on its haemagglutinin-neuraminidase-independent fusion activity | Q45387370 |
| | Structure of the measles virus hemagglutinin | Q45399149 |
| | Newcastle disease virus may enter cells by caveolae-mediated endocytosis | Q45407925 |
| | A mature and fusogenic form of the Nipah virus fusion protein requires proteolytic processing by cathepsin L. | Q45420084 |
| | Structure of the parainfluenza virus 5 F protein in its metastable, prefusion conformation | Q45421033 |
| | The nipah virus fusion protein is cleaved within the endosomal compartment | Q45447131 |
| | Anti-G protein antibody responses to respiratory syncytial virus infection or vaccination are associated with inhibition of G protein CX3C-CX3CR1 binding and leukocyte chemotaxis | Q45553949 |
| | Neuraminidase treatment of respiratory syncytial virus-infected cells or virions, but not target cells, enhances cell-cell fusion and infection | Q45722004 |
| | The mumps virus SH protein is a membrane protein and not essential for virus growth | Q45766382 |
| | Molecular characterisation of Atlantic salmon paramyxovirus (ASPV): A novel paramyxovirus associated with proliferative gill inflammation | Q56768908 |
| | Measles virus fusion machinery activated by sialic acid binding globular domain | Q39083962 |
| | A stabilized headless measles virus attachment protein stalk efficiently triggers membrane fusion | Q39106872 |
| | Regulation of paramyxovirus fusion activation: the hemagglutinin-neuraminidase protein stabilizes the fusion protein in a pretriggered state. | Q39275444 |
| | Characterization of human metapneumovirus F protein-promoted membrane fusion: critical roles for proteolytic processing and low pH. | Q39304996 |
| | The second receptor binding site of the globular head of the Newcastle disease virus hemagglutinin-neuraminidase activates the stalk of multiple paramyxovirus receptor binding proteins to trigger fusion | Q39375677 |
| | Activation of the Nipah virus fusion protein in MDCK cells is mediated by cathepsin B within the endosome-recycling compartment. | Q39406187 |
| | Spring-loaded model revisited: paramyxovirus fusion requires engagement of a receptor binding protein beyond initial triggering of the fusion protein | Q39462591 |
| | The fusion glycoprotein of human respiratory syncytial virus facilitates virus attachment and infectivity via an interaction with cellular heparan sulfate | Q39592019 |
| | Identification of a linear heparin binding domain for human respiratory syncytial virus attachment glycoprotein G. | Q39595322 |
| | Functional analysis of recombinant respiratory syncytial virus deletion mutants lacking the small hydrophobic and/or attachment glycoprotein gene | Q39603697 |
| | Strength of envelope protein interaction modulates cytopathicity of measles virus | Q39683453 |
| | Glycoprotein interactions in paramyxovirus fusion | Q39900113 |
| | Role of endocytosis and cathepsin-mediated activation in Nipah virus entry | Q40002207 |
| | Relative affinity of the human parainfluenza virus type 3 hemagglutinin-neuraminidase for sialic acid correlates with virus-induced fusion activity. | Q40047823 |
| | N-glycans on Nipah virus fusion protein protect against neutralization but reduce membrane fusion and viral entry | Q40287207 |
| | Parainfluenza virus infection of young children: estimates of the population-based burden of hospitalization | Q40399153 |
| | Nipah virus conforms to the rule of six in a minigenome replication assay | Q40583497 |
| | Recombinant respiratory syncytial viruses with deletions in the NS1, NS2, SH, and M2-2 genes are attenuated in vitro and in vivo | Q40868890 |
| | Recombinant vesicular stomatitis virus expressing respiratory syncytial virus (RSV) glycoproteins: RSV fusion protein can mediate infection and cell fusion | Q40976386 |
| | The paramyxovirus SV5 small hydrophobic (SH) protein is not essential for virus growth in tissue culture cells | Q41003033 |
| | Cell tropism and pathogenesis of measles virus in monkeys | Q41023141 |
| | Heparin-dependent attachment of respiratory syncytial virus (RSV) to host cells | Q41138783 |
| | The heads of the measles virus attachment protein move to transmit the fusion-triggering signal | Q41836179 |
| | Respiratory syncytial virus G protein CX3C motif impairs human airway epithelial and immune cell responses | Q41838015 |
| | Paramyxovirus RNA editing and the requirement for hexamer genome length. | Q41865769 |
| | Entry of Newcastle Disease Virus into the host cell: role of acidic pH and endocytosis | Q41924449 |
| | Cathepsin L is involved in proteolytic processing of the Hendra virus fusion protein | Q42042006 |
| | Low-pH-induced membrane fusion mediated by human metapneumovirus F protein is a rare, strain-dependent phenomenon | Q42148034 |
| | Human metapneumovirus infection in children hospitalized for wheezing | Q42412739 |
| | Genetic analysis of J-virus and Beilong virus using minireplicons | Q43791199 |
| | Trimeric transmembrane domain interactions in paramyxovirus fusion proteins: roles in protein folding, stability, and function | Q37388782 |
| | Amino acid substitutions in the F-specific domain in the stalk of the newcastle disease virus HN protein modulate fusion and interfere with its interaction with the F protein | Q37596488 |
| | Biological significance of the second receptor binding site of Newcastle disease virus hemagglutinin-neuraminidase protein | Q37596521 |
| | Fusion activation through attachment protein stalk domains indicates a conserved core mechanism of paramyxovirus entry into cells | Q37713834 |
| | Roles of the putative integrin-binding motif of the human metapneumovirus fusion (f) protein in cell-cell fusion, viral infectivity, and pathogenesis | Q37713859 |
| | Henipaviruses: an updated review focusing on the pteropid reservoir and features of transmission. | Q38019635 |
| | Paramyxovirus entry | Q38123989 |
| | The changing face of the henipaviruses. | Q38133043 |
| | Paramyxovirus evasion of innate immunity: Diverse strategies for common targets | Q38156883 |
| | Newcastle disease virus: current status and our understanding | Q38192846 |
| | Heparin-like structures on respiratory syncytial virus are involved in its infectivity in vitro. | Q38334591 |
| | Structure of the measles virus hemagglutinin bound to its cellular receptor SLAM | Q27666483 |
| | Structure of Respiratory Syncytial Virus Fusion Glycoprotein in the Postfusion Conformation Reveals Preservation of Neutralizing Epitopes | Q27668015 |
| | Structure of the Newcastle disease virus hemagglutinin-neuraminidase (HN) ectodomain reveals a four-helix bundle stalk | Q27672276 |
| | Structure of the cleavage-activated prefusion form of the parainfluenza virus 5 fusion protein | Q27673665 |
| | Structure and Mutagenesis of the Parainfluenza Virus 5 Hemagglutinin-Neuraminidase Stalk Domain Reveals a Four-Helix Bundle and the Role of the Stalk in Fusion Promotion | Q27674994 |
| | Structure of the parainfluenza virus 5 (PIV5) hemagglutinin-neuraminidase (HN) ectodomain | Q27679696 |
| | Interaction between the Hemagglutinin-Neuraminidase and Fusion Glycoproteins of Human Parainfluenza Virus Type III Regulates Viral Growth In Vivo | Q27680424 |
| | SLAM (CDw150) is a cellular receptor for measles virus | Q28145297 |
| | Identification of nucleolin as a cellular receptor for human respiratory syncytial virus | Q28245563 |
| | Membrane fusion machines of paramyxoviruses: capture of intermediates of fusion | Q28345073 |
| | A general strategy to endow natural fusion-protein-derived peptides with potent antiviral activity | Q28729918 |
| | Global burden of acute lower respiratory infections due to respiratory syncytial virus in young children: a systematic review and meta-analysis | Q29619821 |
| | Role of sequence and structure of the Hendra fusion protein fusion peptide in membrane fusion | Q30417577 |
| | Transmembrane orientation and possible role of the fusogenic peptide from parainfluenza virus 5 (PIV5) in promoting fusion | Q30498517 |
| | Fatal measles virus infection prevented by brain-penetrant fusion inhibitors | Q30557599 |
| | Complete genome sequence of Fer-de-Lance virus reveals a novel gene in reptilian paramyxoviruses | Q30891208 |
| | CD150 (SLAM) is a receptor for measles virus but is not involved in viral contact-mediated proliferation inhibition | Q30987804 |
| | Small interfering RNA profiling reveals key role of clathrin-mediated endocytosis and early endosome formation for infection by respiratory syncytial virus | Q33284309 |
| | Entry and fusion of emerging paramyxoviruses | Q33619233 |
| | Respiratory syncytial virus (RSV) SH and G proteins are not essential for viral replication in vitro: clinical evaluation and molecular characterization of a cold-passaged, attenuated RSV subgroup B mutant | Q33738521 |
| | Inhibition of Nipah virus infection in vivo: targeting an early stage of paramyxovirus fusion activation during viral entry | Q33741962 |
| | Influence of the human parainfluenza virus 3 attachment protein's neuraminidase activity on its capacity to activate the fusion protein | Q33782736 |
| | Membrane fusion promoted by increasing surface densities of the paramyxovirus F and HN proteins: comparison of fusion reactions mediated by simian virus 5 F, human parainfluenza virus type 3 F, and influenza virus HA. | Q33784602 |
| | A single amino acid change in the Newcastle disease virus fusion protein alters the requirement for HN protein in fusion | Q33787073 |
| | Structure of the uncleaved ectodomain of the paramyxovirus (hPIV3) fusion protein | Q33855371 |
| | The measles virus hemagglutinin stalk: structures and functions of the central fusion activation and membrane-proximal segments | Q33887869 |
| | Cleavage of the human respiratory syncytial virus fusion protein at two distinct sites is required for activation of membrane fusion | Q33934074 |
| | Infection of nonhuman primates with recombinant human metapneumovirus lacking the SH, G, or M2-2 protein categorizes each as a nonessential accessory protein and identifies vaccine candidates | Q33984333 |
| | Tumor cell marker PVRL4 (nectin 4) is an epithelial cell receptor for measles virus | Q34013640 |
| | The NS1 protein of human respiratory syncytial virus is a potent inhibitor of minigenome transcription and RNA replication | Q34069934 |
| | Novel paramyxoviruses in free-ranging European bats. | Q34318362 |
| | Hemagglutinin-neuraminidase of human parainfluenza 3: role of the neuraminidase in the viral life cycle | Q34367580 |
| | Mutations in the cytoplasmic domain of a paramyxovirus fusion glycoprotein rescue syncytium formation and eliminate the hemagglutinin-neuraminidase protein requirement for membrane fusion | Q34462207 |
| | Triggering of human parainfluenza virus 3 fusion protein (F) by the hemagglutinin-neuraminidase (HN) protein: an HN mutation diminishes the rate of F activation and fusion | Q34745220 |
| | Role of cellular glycosaminoglycans and charged regions of viral G protein in human metapneumovirus infection | Q34825946 |
| | Triggering of the newcastle disease virus fusion protein by a chimeric attachment protein that binds to Nipah virus receptors | Q34978997 |
| | Mutation at residue 523 creates a second receptor binding site on human parainfluenza virus type 1 hemagglutinin-neuraminidase protein | Q35024321 |
| | Unraveling a three-step spatiotemporal mechanism of triggering of receptor-induced Nipah virus fusion and cell entry. | Q35053036 |
| | Nipah virus uses leukocytes for efficient dissemination within a host | Q35140337 |
| | Premature activation of the paramyxovirus fusion protein before target cell attachment with corruption of the viral fusion machinery | Q35515383 |
| | Capture and imaging of a prehairpin fusion intermediate of the paramyxovirus PIV5 | Q35641392 |
| | Mechanism of fusion triggering by human parainfluenza virus type III: communication between viral glycoproteins during entry | Q35643883 |
| | Receptor-binding specificity of the human parainfluenza virus type 1 hemagglutinin-neuraminidase glycoprotein | Q35664943 |
| | A second receptor binding site on human parainfluenza virus type 3 hemagglutinin-neuraminidase contributes to activation of the fusion mechanism | Q35785169 |
| | The paramyxovirus fusion protein C-terminal region: mutagenesis indicates an indivisible protein unit | Q35826179 |
| | Beyond anchoring: the expanding role of the hendra virus fusion protein transmembrane domain in protein folding, stability, and function. | Q35826196 |
| | Human metapneumovirus (HMPV) binding and infection are mediated by interactions between the HMPV fusion protein and heparan sulfate | Q35826221 |
| | Paramyxovirus fusion and entry: multiple paths to a common end | Q35943669 |
| | Structural rearrangements of the central region of the morbillivirus attachment protein stalk domain trigger F protein refolding for membrane fusion | Q35956606 |
| | Adaptation of human parainfluenza virus to airway epithelium reveals fusion properties required for growth in host tissue | Q36029211 |
| | Mutations in the stalk of the measles virus hemagglutinin protein decrease fusion but do not interfere with virus-specific interaction with the homologous fusion protein | Q36098830 |
| | Fusion activation by a headless parainfluenza virus 5 hemagglutinin-neuraminidase stalk suggests a modular mechanism for triggering | Q36300779 |
| | Reversible inhibition of fusion activity of a paramyxovirus fusion protein by an engineered disulfide bond in the membrane-proximal external region | Q36363793 |
| | N-Glycans on the Nipah virus attachment glycoprotein modulate fusion and viral entry as they protect against antibody neutralization | Q36363882 |
| | Membrane fusion triggering: three modules with different structure and function in the upper half of the measles virus attachment protein stalk | Q36385788 |
| | Triggering the measles virus membrane fusion machinery | Q36397970 |
| | Mechanism for active membrane fusion triggering by morbillivirus attachment protein | Q36506813 |
| | Complementation between avirulent Newcastle disease virus and a fusion protein gene expressed from a retrovirus vector: requirements for membrane fusion | Q36680205 |
| | Fusion properties of cells persistently infected with human parainfluenza virus type 3: participation of hemagglutinin-neuraminidase in membrane fusion | Q36692466 |
| | Measles virus blind to its epithelial cell receptor remains virulent in rhesus monkeys but cannot cross the airway epithelium and is not shed | Q36726124 |
| | Engineered intermonomeric disulfide bonds in the globular domain of Newcastle disease virus hemagglutinin-neuraminidase protein: implications for the mechanism of fusion promotion | Q36949597 |
| | Residues in the stalk domain of the hendra virus g glycoprotein modulate conformational changes associated with receptor binding | Q36949836 |
| | Envelope protein dynamics in paramyxovirus entry | Q36994390 |
| | Paramyxoviruses: different receptors - different mechanisms of fusion | Q37019201 |
| | Low-pH triggering of human metapneumovirus fusion: essential residues and importance in entry | Q37051640 |
| | Human parainfluenza virus infection of the airway epithelium: viral hemagglutinin-neuraminidase regulates fusion protein activation and modulates infectivity. | Q37232820 |
| | Identification of a region in the stalk domain of the nipah virus receptor binding protein that is critical for fusion activation | Q37252586 |
| | Mutations in the parainfluenza virus 5 fusion protein reveal domains important for fusion triggering and metastability | Q37336715 |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | virology | Q7215 |
| P304 | page(s) | 1-32 | |
| P577 | publication date | 2015-01-01 | |
| P1433 | published in | Progress in Molecular Biology and Translational Science | Q15753415 |
| P1476 | title | Unity in diversity: shared mechanism of entry among paramyxoviruses | |
| P478 | volume | 129 | |