scholarly article | Q13442814 |
P50 | author | Hans-Dieter Klenk | Q1576857 |
Markus Moll | Q39684306 | ||
Andrea Maisner | Q46153513 | ||
P2860 | cites work | The human CD46 molecule is a receptor for measles virus (Edmonston strain) | Q24317745 |
Chimeric measles viruses with a foreign envelope | Q27469529 | ||
A matrix-less measles virus is infectious and elicits extensive cell fusion: consequences for propagation in the brain. | Q27470119 | ||
A 45,000-M(r) glycoprotein in the Sendai virus envelope triggers virus-cell fusion | Q27480846 | ||
SLAM (CDw150) is a cellular receptor for measles virus | Q28145297 | ||
Membrane fusion machines of paramyxoviruses: capture of intermediates of fusion | Q28345073 | ||
CD150 (SLAM) is a receptor for measles virus but is not involved in viral contact-mediated proliferation inhibition | Q30987804 | ||
Recombinant measles viruses efficiently entering cells through targeted receptors | Q33603475 | ||
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 recombinant measles vaccine virus expressing wild-type glycoproteins: consequences for viral spread and cell tropism | Q33817891 | ||
Measles viruses with altered envelope protein cytoplasmic tails gain cell fusion competence. | Q34069549 | ||
Receptor usage and differential downregulation of CD46 by measles virus wild-type and vaccine strains | Q34395745 | ||
The hemagglutinin of canine distemper virus determines tropism and cytopathogenicity. | Q34515872 | ||
Measles virus matrix protein specifies apical virus release and glycoprotein sorting in epithelial cells | Q35116287 | ||
Localization of monoclonal antibody epitopes and functional domains in the hemagglutinin protein of measles virus. | Q35835519 | ||
Identification of two amino acids in the hemagglutinin glycoprotein of measles virus (MV) that govern hemadsorption, HeLa cell fusion, and CD46 downregulation: phenotypic markers that differentiate vaccine and wild-type MV strains | Q35863109 | ||
Association of the parainfluenza virus fusion and hemagglutinin-neuraminidase glycoproteins on cell surfaces | Q35875690 | ||
Truncation of the COOH-terminal region of the paramyxovirus SV5 fusion protein leads to hemifusion but not complete fusion | Q36237467 | ||
Measles virus fusion: role of the cysteine-rich region of the fusion glycoprotein. | Q36637339 | ||
The rule of six, a basic feature for efficient replication of Sendai virus defective interfering RNA. | Q36651219 | ||
Alterations to influenza virus hemagglutinin cytoplasmic tail modulate virus infectivity | Q36690453 | ||
Cytoplasmic domain truncation enhances fusion activity by the exterior glycoprotein complex of human immunodeficiency virus type 2 in selected cell types | Q36698589 | ||
Aberrant membrane insertion of a cytoplasmic tail deletion mutant of the hemagglutinin-neuraminidase glycoprotein of Newcastle disease virus | Q36716138 | ||
Defective assembly and intracellular transport of mutant paramyxovirus hemagglutinin-neuraminidase proteins containing altered cytoplasmic domains. | Q36811807 | ||
Isolation of a biologically active soluble form of the hemagglutinin-neuraminidase protein of Sendai virus | Q36873984 | ||
Participation of spectrin in Sendai virus-induced fusion of human erythrocyte ghosts | Q37583290 | ||
Membrane cofactor protein with different types of N-glycans can serve as measles virus receptor | Q38293491 | ||
Binding of measles virus to membrane cofactor protein (CD46): importance of disulfide bonds and N-glycans for the receptor function | Q38303590 | ||
Recombinant measles virus requiring an exogenous protease for activation of infectivity | Q38316250 | ||
A single amino acid change in the hemagglutinin protein of measles virus determines its ability to bind CD46 and reveals another receptor on marmoset B cells | Q39579051 | ||
Polarized budding of measles virus is not determined by viral surface glycoproteins. | Q39581062 | ||
Proteolytic cleavage of the fusion protein but not membrane fusion is required for measles virus-induced immunosuppression in vitro | Q39589361 | ||
Characterization of a region of the measles virus hemagglutinin sufficient for its dimerization | Q39592048 | ||
Measles virus-induced immunosuppression in vitro is independent of complex glycosylation of viral glycoproteins and of hemifusion | Q39592719 | ||
A recombinant measles virus expressing hepatitis B virus surface antigen induces humoral immune responses in genetically modified mice. | Q39594077 | ||
Single-chain antibody displayed on a recombinant measles virus confers entry through the tumor-associated carcinoembryonic antigen | Q39605575 | ||
Human membrane cofactor protein (CD46) acts as a cellular receptor for measles virus. | Q40047494 | ||
Paramyxovirus fusion: a hypothesis for changes | Q40767649 | ||
Rescue of measles viruses from cloned DNA. | Q40790034 | ||
A single amino acid change in the cytoplasmic domains of measles virus glycoproteins H and F alters targeting, endocytosis, and cell fusion in polarized Madin-Darby canine kidney cells | Q40804996 | ||
Preferential initiation at the second AUG of the measles virus F mRNA: a role for the long untranslated region | Q41258376 | ||
Mutations in the cytoplasmic domain of the fusion glycoprotein of Newcastle disease virus depress syncytia formation | Q41326301 | ||
The attachment function of the Newcastle disease virus hemagglutinin-neuraminidase protein can be separated from fusion promotion by mutation | Q41563689 | ||
Measles virus: both the haemagglutinin and fusion glycoproteins are required for fusion | Q41696651 | ||
Host cell-dependent lateral mobility of viral glycoproteins | Q41713479 | ||
Lateral mobility of both envelope proteins (F and HN) of Sendai virus in the cell membrane is essential for cell-cell fusion | Q43876298 | ||
Measles virus glycoproteins: studies on the structure and interaction of the haemagglutinin and fusion proteins | Q43916941 | ||
Folding and oligomerization properties of a soluble and secreted form of the paramyxovirus hemagglutinin-neuraminidase glycoprotein | Q44118877 | ||
Paramyxovirus-induced syncytium cell formation is suppressed by a dominant negative fusion regulatory protein-1 (FRP-1)/CD98 mutated construct: an important role of FRP-1 in virus-induced cell fusion | Q44179527 | ||
Lipid-anchored influenza hemagglutinin promotes hemifusion, not complete fusion | Q44633908 | ||
Biased hypermutation and other genetic changes in defective measles viruses in human brain infections | Q45060135 | ||
Mapping of the primary binding site of measles virus to its receptor CD46. | Q45760982 | ||
Human parainfluenza virus type 3: Analysis of the cytoplasmic tail and transmembrane anchor of the hemagglutinin-neuraminidase protein in promoting cell fusion | Q45787436 | ||
Altered cytoplasmic domains affect intracellular transport of the vesicular stomatitis virus glycoprotein | Q45796086 | ||
A leucine zipper structure present in the measles virus fusion protein is not required for its tetramerization but is essential for fusion | Q45865094 | ||
Paramyxovirus F1 protein has two fusion peptides: implications for the mechanism of membrane fusion | Q73501709 | ||
Recombinant measles viruses expressing heterologous antigens of mumps and simian immunodeficiency viruses | Q73636588 | ||
P433 | issue | 14 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | measles | Q79793 |
P304 | page(s) | 7174-7186 | |
P577 | publication date | 2002-07-01 | |
P1433 | published in | Journal of Virology | Q1251128 |
P1476 | title | Importance of the cytoplasmic tails of the measles virus glycoproteins for fusogenic activity and the generation of recombinant measles viruses | |
P478 | volume | 76 |
Q38917869 | A scalable method to concentrate lentiviral vectors pseudotyped with measles virus glycoproteins |
Q39115436 | Actin filaments disruption and stabilization affect measles virus maturation by different mechanisms |
Q39406187 | Activation of the Nipah virus fusion protein in MDCK cells is mediated by cathepsin B within the endosome-recycling compartment. |
Q40219326 | Adaptation of canine distemper virus to canine footpad keratinocytes modifies polymerase activity and fusogenicity through amino acid substitutions in the P/V/C and H proteins |
Q42013767 | Altered interaction of the matrix protein with the cytoplasmic tail of hemagglutinin modulates measles virus growth by affecting virus assembly and cell-cell fusion. |
Q92315931 | BST2/Tetherin Overexpression Modulates Morbillivirus Glycoprotein Production to Inhibit Cell-Cell Fusion |
Q41039054 | Canine distemper virus and measles virus fusion glycoprotein trimers: partial membrane-proximal ectodomain cleavage enhances function |
Q37839350 | Cell entry of enveloped viruses. |
Q34757199 | DARPins: an efficient targeting domain for lentiviral vectors |
Q45252148 | Effect of the alterations in the fusion protein of measles virus isolated from brains of patients with subacute sclerosing panencephalitis on syncytium formation |
Q39013691 | Efficient reovirus- and measles virus-mediated pore expansion during syncytium formation is dependent on annexin A1 and intracellular calcium |
Q41979690 | Ephrin-B2 expression critically influences Nipah virus infection independent of its cytoplasmic tail |
Q39230391 | F-actin modulates measles virus cell-cell fusion and assembly by altering the interaction between the matrix protein and the cytoplasmic tail of hemagglutinin |
Q57022323 | Genetic characterization of measles virus genotype D6 subacute sclerosing panencephalitis case, Alberta, Canada |
Q40545869 | Influence of N-glycans on processing and biological activity of the nipah virus fusion protein |
Q26750552 | Measles Virus Fusion Protein: Structure, Function and Inhibition |
Q45408364 | Measles virus nucleocapsid transport to the plasma membrane requires stable expression and surface accumulation of the viral matrix protein |
Q40630442 | Mechanisms for lymphocytic choriomeningitis virus glycoprotein cleavage, transport, and incorporation into virions |
Q40949336 | Morbillivirus and henipavirus attachment protein cytoplasmic domains differently affect protein expression, fusion support and particle assembly |
Q37247965 | Mumps virus matrix, fusion, and nucleocapsid proteins cooperate for efficient production of virus-like particles |
Q36736762 | Nipah Virus Matrix Protein Influences Fusogenicity and Is Essential for Particle Infectivity and Stability |
Q38865601 | Nipah virus fusion protein: Importance of the cytoplasmic tail for endosomal trafficking and bioactivity |
Q45382182 | Nipah virus fusion protein: influence of cleavage site mutations on the cleavability by cathepsin L, trypsin and furin |
Q34020498 | Paramyxovirus assembly and budding: building particles that transmit infections |
Q35943669 | Paramyxovirus fusion and entry: multiple paths to a common end |
Q34102261 | Paramyxovirus glycoprotein incorporation, assembly and budding: a three way dance for infectious particle production. |
Q33820705 | Peste des petits ruminants virus infection of small ruminants: a comprehensive review |
Q42638118 | Role of the cytoplasmic tail domains of Bunyamwera orthobunyavirus glycoproteins Gn and Gc in virus assembly and morphogenesis |
Q37358531 | Specific targeting of human interleukin (IL)-13 receptor α2-positive cells with lentiviral vectors displaying IL-13. |
Q35182230 | Structure and function of a paramyxovirus fusion protein |
Q37589994 | Targeted cell entry of lentiviral vectors |
Q39551825 | The conserved YAGL motif in human metapneumovirus is required for higher-order cellular assemblies of the matrix protein and for virion production. |
Q45465666 | The fusion protein of wild-type canine distemper virus is a major determinant of persistent infection |
Q45447131 | The nipah virus fusion protein is cleaved within the endosomal compartment |
Q36827199 | The receptor attachment function of measles virus hemagglutinin can be replaced with an autonomous protein that binds Her2/neu while maintaining its fusion-helper function |
Q39960058 | Ubiquitous activation of the Nipah virus fusion protein does not require a basic amino acid at the cleavage site |
Q90444691 | Vectofusin-1 Improves Transduction of Primary Human Cells with Diverse Retroviral and Lentiviral Pseudotypes, Enabling Robust, Automated Closed-System Manufacturing |
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