scholarly article | Q13442814 |
review article | Q7318358 |
P50 | author | Stefan Pöhlmann | Q37063445 |
P2093 | author name string | Martin Spiegel | |
Teresa Plegge | |||
P2860 | cites work | Entry of bunyaviruses into mammalian cells | Q39694035 |
Polymorphism and structural maturation of bunyamwera virus in Golgi and post-Golgi compartments | Q39699159 | ||
A retention signal necessary and sufficient for Golgi localization maps to the cytoplasmic tail of a Bunyaviridae (Uukuniemi virus) membrane glycoprotein | Q39879992 | ||
The unique architecture of Bunyamwera virus factories around the Golgi complex | Q39973171 | ||
Localization to the Golgi complex of Uukuniemi virus glycoproteins G1 and G2 expressed from cloned cDNAs | Q40066470 | ||
Expression strategy of a phlebovirus: biogenesis of proteins from the Rift Valley fever virus M segment | Q40108424 | ||
TI-VAMP/VAMP7 and VAMP3/cellubrevin: two v-SNARE proteins involved in specific steps of the autophagy/multivesicular body pathways. | Q50596559 | ||
A signal for Golgi retention in the bunyavirus G1 glycoprotein | Q60032099 | ||
Morphogenesis of sandfly viruses (Bunyaviridae family) | Q60032319 | ||
Metagenomic analysis of fever, thrombocytopenia and leukopenia syndrome (FTLS) in Henan Province, China: discovery of a new bunyavirus | Q21131405 | ||
Molecular evolution of Azagny virus, a newfound hantavirus harbored by the West African pygmy shrew (Crocidura obscurior) in Côte d'Ivoire | Q21245097 | ||
IFITM proteins restrict viral membrane hemifusion | Q21558779 | ||
Phylogeny and origins of hantaviruses harbored by bats, insectivores, and rodents | Q21558780 | ||
A dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin (DC-SIGN)-related protein is highly expressed on human liver sinusoidal endothelial cells and promotes HIV-1 infection | Q24290940 | ||
Dendritic-cell-specific ICAM3-grabbing non-integrin is essential for the productive infection of human dendritic cells by mosquito-cell-derived dengue viruses | Q24536024 | ||
DC-SIGNR, a DC-SIGN homologue expressed in endothelial cells, binds to human and simian immunodeficiency viruses and activates infection in trans | Q24601035 | ||
Fever with thrombocytopenia associated with a novel bunyavirus in China | Q24615216 | ||
Shared ancestry between a newfound mole-borne hantavirus and hantaviruses harbored by cricetid rodents | Q24625338 | ||
Crystal structure of glycoprotein C from Rift Valley fever virus | Q24628170 | ||
DC-SIGN (CD209) mediates dengue virus infection of human dendritic cells | Q24673466 | ||
DC-SIGN and CLEC-2 mediate human immunodeficiency virus type 1 capture by platelets | Q24673797 | ||
Proteomics computational analyses suggest that the carboxyl terminal glycoproteins of Bunyaviruses are class II viral fusion protein (beta-penetrenes) | Q24800750 | ||
Histone deacetylase 8 is required for centrosome cohesion and influenza A virus entry | Q27348760 | ||
In vitro translation of Uukuniemi virus-specific RNAs: identification of a nonstructural protein and a precursor to the membrane glycoproteins | Q27477800 | ||
Processing and membrane topology of the spike proteins G1 and G2 of Uukuniemi virus | Q27480767 | ||
Immunocytochemical analysis of Uukuniemi virus budding compartments: role of the intermediate compartment and the Golgi stack in virus maturation | Q27480779 | ||
The Cytoplasmic Tails of Uukuniemi Virus (Bunyaviridae) GN and GC Glycoproteins Are Important for Intracellular Targeting and the Budding of Virus-Like Particles | Q27481505 | ||
Insights into bunyavirus architecture from electron cryotomography of Uukuniemi virus | Q27485488 | ||
Formation and intracellular transport of a heterodimeric viral spike protein complex | Q27485688 | ||
The NSm proteins of Rift Valley fever virus are dispensable for maturation, replication and infection | Q27485926 | ||
Uukuniemi virus glycoproteins accumulate in and cause morphological changes of the Golgi complex in the absence of virus maturation | Q27486802 | ||
Uukuniemi virus maturation: immunofluorescence microscopy with monoclonal glycoprotein-specific antibodies | Q27486903 | ||
Posttranslational processing of Uukuniemi virus glycoproteins G1 and G2 | Q27486995 | ||
Molecular phylogeny of a newfound hantavirus in the Japanese shrew mole (Urotrichus talpoides) | Q27487050 | ||
Monosaccharide sequence of protein-bound glycans of Uukuniemi virus | Q27487054 | ||
Differential Use of the C-Type Lectins L-SIGN and DC-SIGN for Phlebovirus Endocytosis. | Q40113451 | ||
Rift Valley fever virus M segment: use of recombinant vaccinia viruses to study Phlebovirus gene expression | Q40129877 | ||
The glycoprotein cytoplasmic tail of Uukuniemi virus (Bunyaviridae) interacts with ribonucleoproteins and is critical for genome packaging | Q40182219 | ||
Synthesis, proteolytic processing and complex formation of N-terminally nested precursor proteins of the Rift Valley fever virus glycoproteins | Q40233812 | ||
Development and characterization of a Rift Valley fever virus cell-cell fusion assay using alphavirus replicon vectors | Q40237419 | ||
Heparan sulfate facilitates Rift Valley fever virus entry into the cell | Q40273179 | ||
DC-SIGN as a receptor for phleboviruses | Q40318139 | ||
Role of N-linked glycans on bunyamwera virus glycoproteins in intracellular trafficking, protein folding, and virus infectivity | Q40361575 | ||
Key Golgi factors for structural and functional maturation of bunyamwera virus | Q40384617 | ||
Electron cryo-microscopy and single-particle averaging of Rift Valley fever virus: evidence for GN-GC glycoprotein heterodimers | Q40397884 | ||
Rift Valley fever virus NSs mRNA is transcribed from an incoming anti-viral-sense S RNA segment | Q40499504 | ||
Completion of molecular characterization of Toscana phlebovirus genome: nucleotide sequence, coding strategy of M genomic segment and its amino acid sequence comparison to other phleboviruses. | Q40645888 | ||
Uukuniemi virus maturation: accumulation of virus particles and viral antigens in the Golgi complex | Q40680022 | ||
Rift Valley fever virus M segment: phlebovirus expression strategy and protein glycosylation | Q40774379 | ||
Rift Valley fever virus M segment: cellular localization of M segment-encoded proteins | Q40783794 | ||
Rift Valley fever virus M segment: cell-free transcription and translation of virus-complementary RNA. | Q40785843 | ||
Complete nucleotide sequence of the M RNA segment of Uukuniemi virus encoding the membrane glycoproteins G1 and G2. | Q40794024 | ||
Complete sequences of the glycoproteins and M RNA of Punta Toro phlebovirus compared to those of Rift Valley fever virus | Q40816475 | ||
Complete nucleotide sequence of the M RNA segment of Rift Valley fever virus | Q40816483 | ||
Function of the KKXX motif in endoplasmic reticulum retrieval of a transmembrane protein depends on the length and structure of the cytoplasmic domain. | Q41066070 | ||
Hantavirus in bat, Sierra Leone | Q42573357 | ||
The Hantaan virus glycoprotein precursor is cleaved at the conserved pentapeptide WAASA. | Q43786323 | ||
The dendritic cell-specific adhesion receptor DC-SIGN internalizes antigen for presentation to T cells | Q43891685 | ||
Assembly of G1 and G2 glycoprotein oligomers in Punta Toro virus-infected cells. | Q44414344 | ||
Maturation of hantaan virus glycoproteins G1 and G2 | Q44431738 | ||
Bunyaviridae: morphologic and morphogenetic similarities of Bunyamwera serologic supergroup viruses and several other arthropod-borne viruses | Q44737053 | ||
A membrane glycoprotein that accumulates intracellularly: Cellular processing of the large glycoprotein of LaCrosse virus | Q45800188 | ||
Intracellular accumulation of Punta Toro virus glycoproteins expressed from cloned cDNA. | Q45833753 | ||
Golgi complex localization of the Punta Toro virus G2 protein requires its association with the G1 protein | Q45854318 | ||
Short cytoplasmic sequences serve as retention signals for transmembrane proteins in the endoplasmic reticulum | Q46051539 | ||
Three-Dimensional Organization of Rift Valley Fever Virus Revealed by Cryoelectron Tomography | Q27487138 | ||
Single-particle cryo-electron microscopy of Rift Valley fever virus | Q27488344 | ||
Novel Hantavirus Sequences in Shrew, Guinea | Q27489141 | ||
Structural basis for selective recognition of oligosaccharides by DC-SIGN and DC-SIGNR | Q27636713 | ||
DC-SIGN, a dendritic cell-specific HIV-1-binding protein that enhances trans-infection of T cells | Q28138968 | ||
Non-muscle myosin II takes centre stage in cell adhesion and migration | Q28262326 | ||
Mycobacteria target DC-SIGN to suppress dendritic cell function | Q28616857 | ||
Identification of a consensus motif for retention of transmembrane proteins in the endoplasmic reticulum | Q29620019 | ||
An assembly model of rift valley Fever virus | Q30419750 | ||
Sandfly-borne phleboviruses of Eurasia and Africa: epidemiology, genetic diversity, geographic range, control measures | Q30656385 | ||
Distinction between Bunyaviridae genera by surface structure and comparison with Hantaan virus using negative stain electron microscopy | Q30677567 | ||
Rift Valley fever virus incorporates the 78 kDa glycoprotein into virions matured in mosquito C6/36 cells. | Q31149260 | ||
MYH9-related platelet disorders | Q33384311 | ||
Person-to-person transmission of severe fever with thrombocytopenia syndrome virus | Q33397384 | ||
Pathogenesis of emerging severe fever with thrombocytopenia syndrome virus in C57/BL6 mouse model | Q33401592 | ||
Severe fever with thrombocytopenia virus glycoproteins are targeted by neutralizing antibodies and can use DC-SIGN as a receptor for pH-dependent entry into human and animal cell lines | Q33405724 | ||
Nonmuscle myosin heavy chain IIA is a critical factor contributing to the efficiency of early infection of severe fever with thrombocytopenia syndrome virus | Q33411102 | ||
Systematic review of severe fever with thrombocytopenia syndrome: virology, epidemiology, and clinical characteristics | Q33411913 | ||
Emerging phleboviruses | Q33652514 | ||
β2 integrin mediates hantavirus-induced release of neutrophil extracellular traps | Q33826861 | ||
Recent advances in the molecular and cellular biology of bunyaviruses | Q34002210 | ||
Genome-wide small interfering RNA screens reveal VAMP3 as a novel host factor required for Uukuniemi virus late penetration | Q34057815 | ||
Uukuniemi Phlebovirus assembly and secretion leave a functional imprint on the virion glycome | Q34059387 | ||
The Rift Valley fever accessory proteins NSm and P78/NSm-GN are distinct determinants of virus propagation in vertebrate and invertebrate hosts | Q34440401 | ||
Bunyavirus-vector interactions | Q34448192 | ||
Selective susceptibility of human skin antigen presenting cells to productive dengue virus infection | Q34634803 | ||
Thottapalayam virus: a presumptive arbovirus isolated from a shrew in India | Q34701862 | ||
Efficient cellular release of Rift Valley fever virus requires genomic RNA. | Q34704620 | ||
Oropouche virus entry into HeLa cells involves clathrin and requires endosomal acidification | Q34847784 | ||
NSm and 78-kilodalton proteins of Rift Valley fever virus are nonessential for viral replication in cell culture. | Q35024013 | ||
Bovine lactoferrin inhibits Toscana virus infection by binding to heparan sulphate | Q35159976 | ||
Bunyavirus mRNA synthesis is coupled to translation to prevent premature transcription termination | Q35752857 | ||
Thrips transmission of tospoviruses. | Q35764863 | ||
Non-muscle myosin IIA is a functional entry receptor for herpes simplex virus-1 | Q39644485 | ||
Characterization of the Golgi retention motif of Rift Valley fever virus G(N) glycoprotein | Q39686341 | ||
Arboviral encephalitides: transmission, emergence, and pathogenesis | Q35778817 | ||
RNASEK is required for internalization of diverse acid-dependent viruses | Q35795990 | ||
The tetanus neurotoxin-sensitive and insensitive routes to and from the plasma membrane: fast and slow pathways? | Q36090718 | ||
NSm protein of Rift Valley fever virus suppresses virus-induced apoptosis | Q36315241 | ||
DC-SIGN is the major Mycobacterium tuberculosis receptor on human dendritic cells | Q36370434 | ||
Rift Valley fever virus strain MP-12 enters mammalian host cells via caveola-mediated endocytosis | Q36397378 | ||
Acid-activated structural reorganization of the Rift Valley fever virus Gc fusion protein | Q36414218 | ||
A Haploid Genetic Screen Identifies Heparan Sulfate Proteoglycans Supporting Rift Valley Fever Virus Infection | Q36481559 | ||
beta3 Integrins mediate the cellular entry of hantaviruses that cause respiratory failure | Q36507782 | ||
Molecular biology and genetic diversity of Rift Valley fever virus | Q36652695 | ||
Assembly and polarized release of Punta Toro virus and effects of brefeldin A | Q36682441 | ||
Oligomerization, transport, and Golgi retention of Punta Toro virus glycoproteins | Q36820901 | ||
Organization of the M genomic segment of Toscana phlebovirus. | Q36843927 | ||
IFITM-2 and IFITM-3 but not IFITM-1 restrict Rift Valley fever virus | Q37036679 | ||
Class II enveloped viruses | Q37905942 | ||
Cytoplasmic tails of bunyavirus Gn glycoproteins-Could they act as matrix protein surrogates? | Q38077395 | ||
The physiological role of DC-SIGN: a tale of mice and men. | Q38100871 | ||
IFITMs restrict the replication of multiple pathogenic viruses | Q38146443 | ||
IFITM proteins-cellular inhibitors of viral entry. | Q38183567 | ||
Hantavirus Gn and Gc envelope glycoproteins: key structural units for virus cell entry and virus assembly | Q38206351 | ||
Virus and cell fusion mechanisms | Q38226984 | ||
Lipid interactions during virus entry and infection | Q38240675 | ||
The evolution and emergence of hantaviruses | Q38308623 | ||
LSECtin interacts with filovirus glycoproteins and the spike protein of SARS coronavirus | Q38323040 | ||
Structural basis for distinct ligand-binding and targeting properties of the receptors DC-SIGN and DC-SIGNR. | Q38340145 | ||
Understanding Rift Valley fever: contributions of animal models to disease characterization and control | Q38366135 | ||
Low pH and Anionic Lipid-dependent Fusion of Uukuniemi Phlebovirus to Liposomes | Q38799398 | ||
Role of the cytosolic tails of Rift Valley fever virus envelope glycoproteins in viral morphogenesis. | Q39046970 | ||
Generation and analysis of infectious virus-like particles of uukuniemi virus (bunyaviridae): a useful system for studying bunyaviral packaging and budding | Q39292370 | ||
Cellular entry of hantaviruses which cause hemorrhagic fever with renal syndrome is mediated by beta3 integrins. | Q39550459 | ||
Targeting of a short peptide derived from the cytoplasmic tail of the G1 membrane glycoprotein of Uukuniemi virus (Bunyaviridae) to the Golgi complex | Q39582889 | ||
Transient association of calnexin and calreticulin with newly synthesized G1 and G2 glycoproteins of uukuniemi virus (family Bunyaviridae). | Q39594960 | ||
P275 | copyright license | Creative Commons Attribution | Q6905323 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 7 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | virus | Q808 |
viral protein | Q952587 | ||
viral entry into host cell | Q4118894 | ||
virology | Q7215 | ||
viral envelope proteins | Q66008752 | ||
carbohydrate | Q11358 | ||
P304 | page(s) | 202 | |
P577 | publication date | 2016-01-01 | |
2016-07-21 | |||
P1433 | published in | Viruses | Q7935305 |
P1476 | title | The Role of Phlebovirus Glycoproteins in Viral Entry, Assembly and Release | |
P478 | volume | 8 |
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