Published in J Virol on December 09, 2009
Phosphatidylinositol 3-kinase-, actin-, and microtubule-dependent transport of Semliki Forest Virus replication complexes from the plasma membrane to modified lysosomes. J Virol (2010) 1.52
RNA-RNA and RNA-protein interactions in coronavirus replication and transcription. RNA Biol (2011) 1.21
The ubiquitin-proteasome system plays an important role during various stages of the coronavirus infection cycle. J Virol (2010) 1.04
Severe acute respiratory syndrome coronavirus nonstructural proteins 3, 4, and 6 induce double-membrane vesicles. MBio (2013) 1.04
Visualizing coronavirus RNA synthesis in time by using click chemistry. J Virol (2012) 0.98
Mobility and interactions of coronavirus nonstructural protein 4. J Virol (2011) 0.93
Recombination in avian gamma-coronavirus infectious bronchitis virus. Viruses (2011) 0.93
The coronavirus nucleocapsid protein is dynamically associated with the replication-transcription complexes. J Virol (2010) 0.92
An autophagy-independent role for LC3 in equine arteritis virus replication. Autophagy (2012) 0.92
Dynamic imaging of the hepatitis C virus NS5A protein during a productive infection. J Virol (2014) 0.87
Coronavirus replicase-reporter fusions provide quantitative analysis of replication and replication complex formation. J Virol (2014) 0.85
Unconventional use of LC3 by coronaviruses through the alleged subversion of the ERAD tuning pathway. Viruses (2011) 0.85
Biogenesis and dynamics of the coronavirus replicative structures. Viruses (2012) 0.84
A new cistron in the murine hepatitis virus replicase gene. J Virol (2010) 0.84
Competitive fitness in coronaviruses is not correlated with size or number of double-membrane vesicles under reduced-temperature growth conditions. MBio (2014) 0.84
Coronavirus infection induces DNA replication stress partly through interaction of its nonstructural protein 13 with the p125 subunit of DNA polymerase δ. J Biol Chem (2011) 0.82
Untangling membrane rearrangement in the nidovirales. DNA Cell Biol (2014) 0.81
Coronavirus membrane-associated papain-like proteases induce autophagy through interacting with Beclin1 to negatively regulate antiviral innate immunity. Protein Cell (2014) 0.79
Coronavirus envelope (E) protein remains at the site of assembly. Virology (2015) 0.79
Dependence of coronavirus RNA replication on an NH2-terminal partial nonstructural protein 1 in cis. J Virol (2014) 0.77
Illuminating the Sites of Enterovirus Replication in Living Cells by Using a Split-GFP-Tagged Viral Protein. mSphere (2016) 0.75
Purification, crystallization and preliminary X-ray analysis of nonstructural protein 2 (nsp2) from avian infectious bronchitis virus. Acta Crystallogr Sect F Struct Biol Cryst Commun (2012) 0.75
In Situ Tagged nsp15 Reveals Interactions with Coronavirus Replication/Transcription Complex-Associated Proteins. MBio (2017) 0.75
Mechanisms of Cellular Membrane Reorganization to Support Hepatitis C Virus Replication. Viruses (2016) 0.75
Unique and conserved features of genome and proteome of SARS-coronavirus, an early split-off from the coronavirus group 2 lineage. J Mol Biol (2003) 9.09
Studying protein dynamics in living cells. Nat Rev Mol Cell Biol (2001) 8.43
Virus entry: open sesame. Cell (2006) 6.33
Virus-encoded proteinases and proteolytic processing in the Nidovirales. J Gen Virol (2000) 4.83
Mechanisms and enzymes involved in SARS coronavirus genome expression. J Gen Virol (2003) 4.66
Modification of intracellular membrane structures for virus replication. Nat Rev Microbiol (2008) 4.04
The coronavirus spike protein is a class I virus fusion protein: structural and functional characterization of the fusion core complex. J Virol (2003) 3.71
RNA replication of mouse hepatitis virus takes place at double-membrane vesicles. J Virol (2002) 3.69
Nuclear envelope breakdown proceeds by microtubule-induced tearing of the lamina. Cell (2002) 3.64
Retargeting of coronavirus by substitution of the spike glycoprotein ectodomain: crossing the host cell species barrier. J Virol (2000) 3.46
Nidovirales: evolving the largest RNA virus genome. Virus Res (2006) 3.41
Cryosectioning and immunolabeling. Nat Protoc (2007) 3.23
Viral RNA replication in association with cellular membranes. Curr Top Microbiol Immunol (2005) 3.18
SARS-coronavirus replication is supported by a reticulovesicular network of modified endoplasmic reticulum. PLoS Biol (2008) 3.16
The group-specific murine coronavirus genes are not essential, but their deletion, by reverse genetics, is attenuating in the natural host. Virology (2002) 2.72
A superhighway to virus infection. Cell (2006) 2.58
A contemporary view of coronavirus transcription. J Virol (2006) 2.47
A mechanical explanation of RNA pseudoknot function in programmed ribosomal frameshifting. Nature (2006) 2.41
Major genetic marker of nidoviruses encodes a replicative endoribonuclease. Proc Natl Acad Sci U S A (2004) 2.41
Identification and characterization of severe acute respiratory syndrome coronavirus replicase proteins. J Virol (2004) 2.38
Severe acute respiratory syndrome coronavirus nsp1 protein suppresses host gene expression by promoting host mRNA degradation. Proc Natl Acad Sci U S A (2006) 2.31
Multiple enzymatic activities associated with severe acute respiratory syndrome coronavirus helicase. J Virol (2004) 2.29
Ultrastructure and origin of membrane vesicles associated with the severe acute respiratory syndrome coronavirus replication complex. J Virol (2006) 2.20
Discovery of an RNA virus 3'->5' exoribonuclease that is critically involved in coronavirus RNA synthesis. Proc Natl Acad Sci U S A (2006) 2.07
Wrapping things up about virus RNA replication. Traffic (2005) 2.00
Identification of severe acute respiratory syndrome coronavirus replicase products and characterization of papain-like protease activity. J Virol (2004) 1.97
Monoclonal antibodies to double-stranded RNA as probes of RNA structure in crude nucleic acid extracts. Nucleic Acids Res (1991) 1.92
Coronavirus non-structural protein 1 is a major pathogenicity factor: implications for the rational design of coronavirus vaccines. PLoS Pathog (2007) 1.78
The nsp2 replicase proteins of murine hepatitis virus and severe acute respiratory syndrome coronavirus are dispensable for viral replication. J Virol (2005) 1.71
Severe acute respiratory syndrome coronavirus nsp1 suppresses host gene expression, including that of type I interferon, in infected cells. J Virol (2008) 1.69
A second, non-canonical RNA-dependent RNA polymerase in SARS coronavirus. EMBO J (2006) 1.69
Insights into SARS-CoV transcription and replication from the structure of the nsp7-nsp8 hexadecamer. Nat Struct Mol Biol (2005) 1.68
Intracellular processing of the N-terminal ORF 1a proteins of the coronavirus MHV-A59 requires multiple proteolytic events. Virology (1992) 1.67
The severe acute respiratory syndrome coronavirus Nsp15 protein is an endoribonuclease that prefers manganese as a cofactor. J Virol (2004) 1.67
Colocalization and membrane association of murine hepatitis virus gene 1 products and De novo-synthesized viral RNA in infected cells. J Virol (1999) 1.67
A dynamic view of hepatitis C virus replication complexes. J Virol (2008) 1.66
Mouse hepatitis virus 3C-like protease cleaves a 22-kilodalton protein from the open reading frame 1a polyprotein in virus-infected cells and in vitro. J Virol (1998) 1.61
The severe acute respiratory syndrome-coronavirus replicative protein nsp9 is a single-stranded RNA-binding subunit unique in the RNA virus world. Proc Natl Acad Sci U S A (2004) 1.61
SARS-coronavirus replication/transcription complexes are membrane-protected and need a host factor for activity in vitro. PLoS Pathog (2008) 1.59
Cleavage inhibition of the murine coronavirus spike protein by a furin-like enzyme affects cell-cell but not virus-cell fusion. J Virol (2004) 1.58
The nsp9 replicase protein of SARS-coronavirus, structure and functional insights. Structure (2004) 1.55
High fidelity of murine hepatitis virus replication is decreased in nsp14 exoribonuclease mutants. J Virol (2007) 1.54
Coronavirus nonstructural protein 16 is a cap-0 binding enzyme possessing (nucleoside-2'O)-methyltransferase activity. J Virol (2008) 1.52
Functional and genetic analysis of coronavirus replicase-transcriptase proteins. PLoS Pathog (2005) 1.52
Intracellular location and translocation of silent and active poliovirus replication complexes. J Gen Virol (2005) 1.44
Analysis of intraviral protein-protein interactions of the SARS coronavirus ORFeome. PLoS One (2007) 1.42
Characterization of the expression, intracellular localization, and replication complex association of the putative mouse hepatitis virus RNA-dependent RNA polymerase. J Virol (2003) 1.41
Correlative light-electron microscopy (CLEM) combining live-cell imaging and immunolabeling of ultrathin cryosections. Nat Methods (2008) 1.40
Predicted membrane topology of the coronavirus protein E1. Biochemistry (1986) 1.38
Mouse hepatitis virus replicase proteins associate with two distinct populations of intracellular membranes. J Virol (2000) 1.38
Cytoplasmic dynein-associated structures move bidirectionally in vivo. J Cell Sci (2002) 1.37
Mouse hepatitis coronavirus RNA replication depends on GBF1-mediated ARF1 activation. PLoS Pathog (2008) 1.36
Cytoskeletal requirements for hepatitis C virus (HCV) RNA synthesis in the HCV replicon cell culture system. J Virol (2003) 1.35
Membrane assembly of the triple-spanning coronavirus M protein. Individual transmembrane domains show preferred orientation. J Biol Chem (1992) 1.35
Localization and membrane topology of coronavirus nonstructural protein 4: involvement of the early secretory pathway in replication. J Virol (2007) 1.32
Membrane topology of murine coronavirus replicase nonstructural protein 3. Virology (2007) 1.31
Genome-wide analysis of protein-protein interactions and involvement of viral proteins in SARS-CoV replication. PLoS One (2008) 1.29
Mouse hepatitis virus replicase protein complexes are translocated to sites of M protein accumulation in the ERGIC at late times of infection. Virology (2001) 1.29
Mutagenesis of the murine hepatitis virus nsp1-coding region identifies residues important for protein processing, viral RNA synthesis, and viral replication. Virology (2005) 1.26
Coronaviruses as vectors: position dependence of foreign gene expression. J Virol (2003) 1.25
Crystal structure of nonstructural protein 10 from the severe acute respiratory syndrome coronavirus reveals a novel fold with two zinc-binding motifs. J Virol (2006) 1.24
Topology and membrane anchoring of the coronavirus replication complex: not all hydrophobic domains of nsp3 and nsp6 are membrane spanning. J Virol (2008) 1.23
Processing of open reading frame 1a replicase proteins nsp7 to nsp10 in murine hepatitis virus strain A59 replication. J Virol (2007) 1.22
The SARS-Coronavirus PLnc domain of nsp3 as a replication/transcription scaffolding protein. Virus Res (2008) 1.20
Comparison of six different murine coronavirus JHM variants by monoclonal antibodies against the E2 glycoprotein. Virology (1989) 1.18
A complex zinc finger controls the enzymatic activities of nidovirus helicases. J Virol (2005) 1.13
Mutation in murine coronavirus replication protein nsp4 alters assembly of double membrane vesicles. Virology (2008) 1.13
Localization of mouse hepatitis virus open reading frame 1A derived proteins. J Neurovirol (1998) 1.03
Visualizing the dynamic behavior of poliovirus plus-strand RNA in living host cells. Nucleic Acids Res (2005) 1.03
Biochemical and genetic analyses of murine hepatitis virus Nsp15 endoribonuclease. J Virol (2007) 1.00
Coronaviruses as vectors: stability of foreign gene expression. J Virol (2005) 0.99
Vaccinia virus-induced microtubule-dependent cellular rearrangements. Traffic (2006) 0.97
Targeting non-human coronaviruses to human cancer cells using a bispecific single-chain antibody. Gene Ther (2005) 0.94
The non-structural protein Nsp10 of mouse hepatitis virus binds zinc ions and nucleic acids. FEBS Lett (2006) 0.94
Vaccinia-virus-induced cellular contractility facilitates the subcellular localization of the viral replication sites. Traffic (2006) 0.90
A novel mutation in murine hepatitis virus nsp5, the viral 3C-like proteinase, causes temperature-sensitive defects in viral growth and protein processing. J Virol (2008) 0.87
Murine coronaviruses encoding nsp2 at different genomic loci have altered replication, protein expression, and localization. J Virol (2008) 0.82
Cyclooxygenase activity is important for efficient replication of mouse hepatitis virus at an early stage of infection. Virol J (2007) 0.82
Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes. Autophagy (2007) 20.92
Guidelines for the use and interpretation of assays for monitoring autophagy. Autophagy (2012) 20.08
Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC. Nature (2013) 6.39
The coronavirus spike protein is a class I virus fusion protein: structural and functional characterization of the fusion core complex. J Virol (2003) 3.71
Atg17 regulates the magnitude of the autophagic response. Mol Biol Cell (2005) 3.71
Emerging regulation and functions of autophagy. Nat Cell Biol (2013) 3.24
SNARE proteins are required for macroautophagy. Cell (2011) 2.99
An Atg9-containing compartment that functions in the early steps of autophagosome biogenesis. J Cell Biol (2010) 2.98
Coronaviruses Hijack the LC3-I-positive EDEMosomes, ER-derived vesicles exporting short-lived ERAD regulators, for replication. Cell Host Microbe (2010) 2.75
The group-specific murine coronavirus genes are not essential, but their deletion, by reverse genetics, is attenuating in the natural host. Virology (2002) 2.72
Atg21 is a phosphoinositide binding protein required for efficient lipidation and localization of Atg8 during uptake of aminopeptidase I by selective autophagy. Mol Biol Cell (2004) 2.51
The Ras/cAMP-dependent protein kinase signaling pathway regulates an early step of the autophagy process in Saccharomyces cerevisiae. J Biol Chem (2004) 2.40
SARS coronavirus, but not human coronavirus NL63, utilizes cathepsin L to infect ACE2-expressing cells. J Biol Chem (2005) 2.36
Seeing is believing: the impact of electron microscopy on autophagy research. Autophagy (2011) 2.22
Single-cell analysis of population context advances RNAi screening at multiple levels. Mol Syst Biol (2012) 2.13
Exit from the Golgi is required for the expansion of the autophagosomal phagophore in yeast Saccharomyces cerevisiae. Mol Biol Cell (2010) 2.10
The mitochondrial contact site complex, a determinant of mitochondrial architecture. EMBO J (2011) 1.94
Severe acute respiratory syndrome coronavirus (SARS-CoV) infection inhibition using spike protein heptad repeat-derived peptides. Proc Natl Acad Sci U S A (2004) 1.89
Lipid droplets are functionally connected to the endoplasmic reticulum in Saccharomyces cerevisiae. J Cell Sci (2011) 1.86
Dissection of the influenza A virus endocytic routes reveals macropinocytosis as an alternative entry pathway. PLoS Pathog (2011) 1.66
Impaired Antibody-mediated Protection and Defective IgA B-Cell Memory in Experimental Infection of Adults with Respiratory Syncytial Virus. Am J Respir Crit Care Med (2015) 1.65
Live, attenuated coronavirus vaccines through the directed deletion of group-specific genes provide protection against feline infectious peritonitis. J Virol (2004) 1.62
Cleavage inhibition of the murine coronavirus spike protein by a furin-like enzyme affects cell-cell but not virus-cell fusion. J Virol (2004) 1.58
Recombinant soluble, multimeric HA and NA exhibit distinctive types of protection against pandemic swine-origin 2009 A(H1N1) influenza virus infection in ferrets. J Virol (2010) 1.55
Switching species tropism: an effective way to manipulate the feline coronavirus genome. J Virol (2003) 1.54
Cathepsin L functionally cleaves the severe acute respiratory syndrome coronavirus class I fusion protein upstream of rather than adjacent to the fusion peptide. J Virol (2008) 1.47
Selective types of autophagy in yeast. Biochim Biophys Acta (2009) 1.44
Qualitative and quantitative ultrastructural analysis of the membrane rearrangements induced by coronavirus. Cell Microbiol (2010) 1.43
Multiple roles of the cytoskeleton in autophagy. Biol Rev Camb Philos Soc (2009) 1.43
Atg23 is essential for the cytoplasm to vacuole targeting pathway and efficient autophagy but not pexophagy. J Biol Chem (2003) 1.39
The puzzling origin of the autophagosomal membrane. F1000 Biol Rep (2011) 1.38
Mouse hepatitis coronavirus replication induces host translational shutoff and mRNA decay, with concomitant formation of stress granules and processing bodies. Cell Microbiol (2007) 1.38
Adenosine deaminase acts as a natural antagonist for dipeptidyl peptidase 4-mediated entry of the Middle East respiratory syndrome coronavirus. J Virol (2013) 1.37
Mouse hepatitis coronavirus RNA replication depends on GBF1-mediated ARF1 activation. PLoS Pathog (2008) 1.36
A picky eater: exploring the mechanisms of selective autophagy in human pathologies. Traffic (2007) 1.36
Feline infectious peritonitis: insights into feline coronavirus pathobiogenesis and epidemiology based on genetic analysis of the viral 3c gene. J Gen Virol (2009) 1.36
A role for Atg8-PE deconjugation in autophagosome biogenesis. Autophagy (2012) 1.35
Phosphorylation of a membrane curvature-sensing motif switches function of the HOPS subunit Vps41 in membrane tethering. J Cell Biol (2010) 1.34
The influenza A virus hemagglutinin glycosylation state affects receptor-binding specificity. Virology (2010) 1.33
Only two residues are responsible for the dramatic difference in receptor binding between swine and new pandemic H1 hemagglutinin. J Biol Chem (2010) 1.32
A cryosectioning procedure for the ultrastructural analysis and the immunogold labelling of yeast Saccharomyces cerevisiae. Traffic (2008) 1.30
A single immunization with soluble recombinant trimeric hemagglutinin protects chickens against highly pathogenic avian influenza virus H5N1. PLoS One (2010) 1.28
Molecular interactions in the assembly of coronaviruses. Adv Virus Res (2005) 1.27
Coxsackievirus mutants that can bypass host factor PI4KIIIβ and the need for high levels of PI4P lipids for replication. Cell Res (2012) 1.27
Vps41 phosphorylation and the Rab Ypt7 control the targeting of the HOPS complex to endosome-vacuole fusion sites. Mol Biol Cell (2009) 1.26
Coronaviruses as vectors: position dependence of foreign gene expression. J Virol (2003) 1.25
Topology and membrane anchoring of the coronavirus replication complex: not all hydrophobic domains of nsp3 and nsp6 are membrane spanning. J Virol (2008) 1.23
The CORVET subunit Vps8 cooperates with the Rab5 homolog Vps21 to induce clustering of late endosomal compartments. Mol Biol Cell (2009) 1.23
Murine coronavirus with an extended host range uses heparan sulfate as an entry receptor. J Virol (2005) 1.18
Virulence of Newcastle disease virus: what is known so far? Vet Res (2011) 1.18
Reticulophagy and ribophagy: regulated degradation of protein production factories. Int J Cell Biol (2012) 1.16
Structural protein requirements in equine arteritis virus assembly. J Virol (2004) 1.16
Hidden behind autophagy: the unconventional roles of ATG proteins. Traffic (2013) 1.15
Coronaviruses maintain viability despite dramatic rearrangements of the strictly conserved genome organization. J Virol (2002) 1.15
Infectious bursal disease virus capsid protein VP3 interacts both with VP1, the RNA-dependent RNA polymerase, and with viral double-stranded RNA. J Virol (2002) 1.13
Gain, preservation, and loss of a group 1a coronavirus accessory glycoprotein. J Virol (2008) 1.12
Spike protein fusion peptide and feline coronavirus virulence. Emerg Infect Dis (2012) 1.09
Inhibition of the ubiquitin-proteasome system affects influenza A virus infection at a postfusion step. J Virol (2010) 1.09
Hemagglutinin receptor specificity and structural analyses of respiratory droplet-transmissible H5N1 viruses. J Virol (2013) 1.08
The 29-nucleotide deletion present in human but not in animal severe acute respiratory syndrome coronaviruses disrupts the functional expression of open reading frame 8. J Virol (2007) 1.07
Retracted Role of the SEL1L:LC3-I complex as an ERAD tuning receptor in the mammalian ER. Mol Cell (2012) 1.06
The ubiquitin-proteasome system plays an important role during various stages of the coronavirus infection cycle. J Virol (2010) 1.04
Role of endocytosis and low pH in murine hepatitis virus strain A59 cell entry. J Virol (2007) 1.04
Regulation of autophagy in yeast Saccharomyces cerevisiae. Biochim Biophys Acta (2009) 1.04
Complete genome sequence and taxonomic position of anguillid herpesvirus 1. J Gen Virol (2009) 1.04
Cryo-electron tomography of mouse hepatitis virus: Insights into the structure of the coronavirion. Proc Natl Acad Sci U S A (2009) 1.02
Central ions and lateral asparagine/glutamine zippers stabilize the post-fusion hairpin conformation of the SARS coronavirus spike glycoprotein. Virology (2005) 1.01
A dual role for K63-linked ubiquitin chains in multivesicular body biogenesis and cargo sorting. Mol Biol Cell (2012) 1.00
The glycosylation status of the murine hepatitis coronavirus M protein affects the interferogenic capacity of the virus in vitro and its ability to replicate in the liver but not the brain. Virology (2003) 1.00
Functional separation of endosomal fusion factors and the class C core vacuole/endosome tethering (CORVET) complex in endosome biogenesis. J Biol Chem (2012) 1.00
Sequence analysis of feline coronaviruses and the circulating virulent/avirulent theory. Emerg Infect Dis (2011) 0.99
Coronaviruses as vectors: stability of foreign gene expression. J Virol (2005) 0.99
Influenza A virus entry into cells lacking sialylated N-glycans. Proc Natl Acad Sci U S A (2012) 0.98
Atg18 function in autophagy is regulated by specific sites within its β-propeller. J Cell Sci (2012) 0.98
Visualizing coronavirus RNA synthesis in time by using click chemistry. J Virol (2012) 0.98