| P50 | author | Till Rümenapf | Q30512616 |
| P2093 | author name string | Thomas Krey | |
| | Heinz-Jürgen Thiel | |
| P2860 | cites work | Enzymatic reduction of disulfide bonds in lysosomes: characterization of a gamma-interferon-inducible lysosomal thiol reductase (GILT) | Q22011094 |
| | Tight control of gene expression in mammalian cells by tetracycline-responsive promoters | Q24564850 |
| | Extraction of cholesterol with methyl-beta-cyclodextrin perturbs formation of clathrin-coated endocytic vesicles | Q24657869 |
| | The central proline of an internal viral fusion peptide serves two important roles | Q27469628 |
| | Formation and characterization of the trimeric form of the fusion protein of Semliki Forest Virus | Q27469686 |
| | Passage of classical swine fever virus in cultured swine kidney cells selects virus variants that bind to heparan sulfate due to a single amino acid change in envelope protein E(rns) | Q27469695 |
| | Study of the mechanism of antiviral action of iminosugar derivatives against bovine viral diarrhea virus | Q27469853 |
| | A Cellular J-Domain Protein Modulates Polyprotein Processing and Cytopathogenicity of a Pestivirus | Q27469858 |
| | Role of metastability and acidic pH in membrane fusion by tick-borne encephalitis virus. | Q27469927 |
| | Membrane interactions of the tick-borne encephalitis virus fusion protein E at low pH. | Q27472865 |
| | Oligomeric rearrangement of tick-borne encephalitis virus envelope proteins induced by an acidic pH | Q27478446 |
| | On the entry of Semliki forest virus into BHK-21 cells | Q27482326 |
| | Cell fusion by Semliki Forest, influenza, and vesicular stomatitis viruses | Q27482329 |
| | Hepatitis C virus and other flaviviridae viruses enter cells via low density lipoprotein receptor | Q27485871 |
| | Membrane and protein interactions of a soluble form of the Semliki Forest virus fusion protein | Q27485999 |
| | Hog cholera virus: molecular composition of virions from a pestivirus | Q27486544 |
| | Fusion function of the Semliki Forest virus spike is activated by proteolytic cleavage of the envelope glycoprotein precursor p62 | Q27486570 |
| | Pestivirus glycoprotein which induces neutralizing antibodies forms part of a disulfide-linked heterodimer | Q27486595 |
| | Structure of the dengue virus envelope protein after membrane fusion | Q27643009 |
| | Conformational change and protein-protein interactions of the fusion protein of Semliki Forest virus | Q27643010 |
| | Structure of influenza haemagglutinin at the pH of membrane fusion | Q27730888 |
| | Inhibition of human immunodeficiency virus infection by agents that interfere with thiol-disulfide interchange upon virus-receptor interaction | Q28369689 |
| | Endocytosis and molecular sorting | Q29616706 |
| | Induction of mutant dynamin specifically blocks endocytic coated vesicle formation | Q29620182 |
| | Caveolar endocytosis of simian virus 40 reveals a new two-step vesicular-transport pathway to the ER | Q29620552 |
| | JC virus enters human glial cells by clathrin-dependent receptor-mediated endocytosis. | Q30326112 |
| | Isomerization of the intersubunit disulphide-bond in Env controls retrovirus fusion | Q30448089 |
| | The protein disulphide-isomerase family: unravelling a string of folds | Q33543247 |
| | Endocytosis: How dynamin sets vesicles PHree! | Q33606865 |
| | Structural basis for membrane fusion by enveloped viruses | Q33637921 |
| | Cellular uptake and infection by canine parvovirus involves rapid dynamin-regulated clathrin-mediated endocytosis, followed by slower intracellular trafficking | Q33797871 |
| | Reversibility in fusion protein conformational changes. The intriguing case of rhabdovirus-induced membrane fusion. | Q33917120 |
| | Sulfhydryl involvement in fusion mechanisms | Q33917135 |
| | Role of the N-terminal peptides of viral envelope proteins in membrane fusion. | Q33933461 |
| | Membrane fusion of Semliki Forest virus in a model system: correlation between fusion kinetics and structural changes in the envelope glycoprotein | Q34043702 |
| | Structures and mechanisms in flavivirus fusion | Q34070126 |
| | The machinery for flavivirus fusion with host cell membranes | Q34331567 |
| | Association of the caveola vesicular system with cellular entry by filoviruses | Q34338277 |
| | Murine coronavirus membrane fusion is blocked by modification of thiols buried within the spike protein | Q35864708 |
| | Fusion of Semliki forest virus with the plasma membrane can be induced by low pH. | Q36201795 |
| | Mis-assembly of clathrin lattices on endosomes reveals a regulatory switch for coated pit formation | Q36233556 |
| | Rabies virus-induced membrane fusion pathway | Q36328481 |
| | Influenza hemagglutinin is spring-loaded by a metastable native conformation | Q36809584 |
| | Effects of lysosomotropic weak bases on infection of BHK-21 cells by Sindbis virus. | Q36896646 |
| | CD46 is a cellular receptor for bovine viral diarrhea virus | Q36960740 |
| | Mechanisms of enveloped virus entry into cells | Q37914723 |
| | Virus entry into animal cells | Q38226881 |
| | Interactions of bovine viral diarrhoea virus glycoprotein E(rns) with cell surface glycosaminoglycans | Q38316245 |
| | Role of the cytoplasmic domain of the beta-subunit of integrin alpha(v)beta6 in infection by foot-and-mouth disease virus | Q39602424 |
| | Heparan sulfate proteoglycans initiate dengue virus infection of hepatocytes | Q40612983 |
| | The pestivirus E(rns) glycoprotein interacts with E2 in both infected cells and mature virions | Q40626980 |
| | Swine and ruminant pestiviruses require the same cellular factor to enter bovine cells. | Q40668065 |
| | Thermal and pH stability of pestiviruses | Q40730223 |
| | Flaviviruses can mediate fusion from without in Aedes albopictus mosquito cell cultures | Q40776708 |
| | Analyses of disulfides present in the rubella virus E1 glycoprotein | Q41116151 |
| | Involvement of the vacuolar H(+)-ATPase in animal virus entry | Q41438119 |
| | pH-independent HIV entry into CD4-positive T cells via virus envelope fusion to the plasma membrane | Q41764642 |
| | The clathrin endocytic pathway in viral infection | Q42651304 |
| | Clathrin and HA2 adaptors: effects of potassium depletion, hypertonic medium, and cytosol acidification | Q42770097 |
| | The Murray Valley encephalitis virus prM protein confers acid resistance to virus particles and alters the expression of epitopes within the R2 domain of E glycoprotein | Q42980684 |
| | Entry pathway of vesicular stomatitis virus into different host cells | Q42992016 |
| | Coiled coils in both intracellular vesicle and viral membrane fusion | Q44268531 |
| | Hantaan virus enters cells by clathrin-dependent receptor-mediated endocytosis | Q45733381 |
| | Temperature dependence of fusion by sendai virus | Q45742427 |
| | The mode of entry of herpes simplex virus type 1 into Vero cells | Q45834625 |
| | Membrane Cofactor Protein (CD46) Is a Basolateral Protein That Is Not Endocytosed | Q57197594 |
| | Localization of protein disulfide isomerase to the external surface of the platelet plasma membrane | Q72030923 |
| | Characterization of protein disulphide isomerase released from activated platelets | Q72343698 |
| | Inhibition of clathrin-dependent endocytosis has multiple effects on human rhinovirus serotype 2 cell entry | Q73178513 |
| P433 | issue | 7 | |
| P921 | main subject | virology | Q7215 |
| P304 | page(s) | 4191-4200 | |
| P577 | publication date | 2005-04-01 | |
| P1433 | published in | Journal of Virology | Q1251128 |
| P1476 | title | Acid-resistant bovine pestivirus requires activation for pH-triggered fusion during entry | |
| P478 | volume | 79 | |