review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1007/82_2017_25 |
P8608 | Fatcat ID | release_lwswogi7bfaetethffne2a2np4 |
P932 | PMC publication ID | 7119980 |
P698 | PubMed publication ID | 28643204 |
P50 | author | Marjolein Kikkert | Q89544440 |
Martijn J van Hemert | Q37368755 | ||
P2093 | author name string | Eric J Snijder | |
Adriaan H de Wilde | |||
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The nucleocapsid protein of severe acute respiratory syndrome-coronavirus inhibits the activity of cyclin-cyclin-dependent kinase complex and blocks S phase progression in mammalian cells | Q40326049 | ||
SARS coronavirus, but not human coronavirus NL63, utilizes cathepsin L to infect ACE2-expressing cells | Q40341738 | ||
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Coronavirus replication complex formation utilizes components of cellular autophagy | Q40603146 | ||
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Side effects of alpha interferon in chronic hepatitis C. | Q40646343 | ||
Polypyrimidine-tract-binding protein affects transcription but not translation of mouse hepatitis virus RNA. | Q40683467 | ||
Middle East respiratory syndrome coronavirus M protein suppresses type I interferon expression through the inhibition of TBK1-dependent phosphorylation of IRF3. | Q40707626 | ||
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MERS coronavirus neutralizing antibodies in camels, Eastern Africa, 1983-1997. | Q34641572 | ||
MERS-coronavirus replication induces severe in vitro cytopathology and is strongly inhibited by cyclosporin A or interferon-α treatment | Q34650943 | ||
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Crystal structure of the Middle East respiratory syndrome coronavirus (MERS-CoV) papain-like protease bound to ubiquitin facilitates targeted disruption of deubiquitinating activity to demonstrate its role in innate immune suppression | Q34683256 | ||
Human coronaviruses: what do they cause? | Q34703054 | ||
The SARS coronavirus papain like protease can inhibit IRF3 at a post activation step that requires deubiquitination activity | Q34746496 | ||
Modulation of the unfolded protein response by the severe acute respiratory syndrome coronavirus spike protein | Q35024223 | ||
Severe acute respiratory syndrome coronavirus nsp1 protein suppresses host gene expression by promoting host mRNA degradation | Q35036515 | ||
p53 degradation by a coronavirus papain-like protease suppresses type I interferon signaling | Q35048996 | ||
Evidence that TMPRSS2 activates the severe acute respiratory syndrome coronavirus spike protein for membrane fusion and reduces viral control by the humoral immune response | Q35076795 | ||
Ribose 2'-O-methylation provides a molecular signature for the distinction of self and non-self mRNA dependent on the RNA sensor Mda5. | Q35239001 | ||
A SARS-like cluster of circulating bat coronaviruses shows potential for human emergence | Q36702376 | ||
Middle East Respiratory Syndrome Coronavirus NS4b Protein Inhibits Host RNase L Activation. | Q36755302 | ||
Signal transduction in SARS-CoV-infected cells | Q36807258 | ||
The structural and accessory proteins M, ORF 4a, ORF 4b, and ORF 5 of Middle East respiratory syndrome coronavirus (MERS-CoV) are potent interferon antagonists | Q36922964 | ||
SARS Coronavirus Papain-Like Protease Inhibits the TLR7 Signaling Pathway through Removing Lys63-Linked Polyubiquitination of TRAF3 and TRAF6. | Q36939205 | ||
Coronavirus receptor switch explained from the stereochemistry of protein-carbohydrate interactions and a single mutation | Q36978142 | ||
Are nidoviruses hijacking the autophagy machinery? | Q37011226 | ||
Severe acute respiratory syndrome coronavirus nonstructural proteins 3, 4, and 6 induce double-membrane vesicles | Q37105681 | ||
The cellular interactome of the coronavirus infectious bronchitis virus nucleocapsid protein and functional implications for virus biology | Q37123444 | ||
SARS coronavirus spike protein-induced innate immune response occurs via activation of the NF-kappaB pathway in human monocyte macrophages in vitro | Q37234254 | ||
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Antiviral activity of chloroquine against human coronavirus OC43 infection in newborn mice | Q37274730 | ||
Toll-like receptor 4 deficiency increases disease and mortality after mouse hepatitis virus type 1 infection of susceptible C3H mice | Q37333738 | ||
Middle East respiratory syndrome coronavirus infection mediated by the transmembrane serine protease TMPRSS2. | Q37336487 | ||
Antagonism of RNase L Is Required for Murine Coronavirus Replication in Kupffer Cells and Liver Sinusoidal Endothelial Cells but Not in Hepatocytes. | Q37347335 | ||
Proteolytic processing of Middle East respiratory syndrome coronavirus spikes expands virus tropism | Q37379647 | ||
A two-pronged strategy to suppress host protein synthesis by SARS coronavirus Nsp1 protein | Q37442279 | ||
Murine coronavirus nonstructural protein p28 arrests cell cycle in G0/G1 phase. | Q37511558 | ||
EGFR and EphA2 are host factors for hepatitis C virus entry and possible targets for antiviral therapy | Q37609988 | ||
Recognizing and avoiding siRNA off-target effects for target identification and therapeutic application | Q37665303 | ||
Recognition of viruses by cytoplasmic sensors | Q37671348 | ||
Attenuation and restoration of severe acute respiratory syndrome coronavirus mutant lacking 2'-o-methyltransferase activity | Q37713866 | ||
Middle east respiratory syndrome coronavirus 4a protein is a double-stranded RNA-binding protein that suppresses PACT-induced activation of RIG-I and MDA5 in the innate antiviral response. | Q37713995 | ||
Viral subversion of the host protein synthesis machinery | Q37946208 | ||
SARS coronavirus pathogenesis: host innate immune responses and viral antagonism of interferon | Q38008817 | ||
Cyclophilin involvement in the replication of hepatitis C virus and other viruses. | Q38040256 | ||
Biogenesis and dynamics of the coronavirus replicative structures | Q38064286 | ||
Involvement of autophagy in coronavirus replication | Q38064294 | ||
Unfolded protein response in hepatitis C virus infection | Q38218108 | ||
Cell cycle regulation during viral infection | Q38218288 | ||
Human coronavirus NL63 replication is cyclophilin A-dependent and inhibited by non-immunosuppressive cyclosporine A-derivatives including Alisporivir | Q30317509 | ||
The economic impact of SARS: how does the reality match the predictions? | Q30369051 | ||
PLP2 of mouse hepatitis virus A59 (MHV-A59) targets TBK1 to negatively regulate cellular type I interferon signaling pathway | Q31001219 | ||
SYNCRIP, a member of the heterogeneous nuclear ribonucleoprotein family, is involved in mouse hepatitis virus RNA synthesis | Q31127282 | ||
The interaction of the SARS coronavirus non-structural protein 10 with the cellular oxido-reductase system causes an extensive cytopathic effect | Q33223190 | ||
Identification of human kinases involved in hepatitis C virus replication by small interference RNA library screening. | Q33303326 | ||
Coronavirus spike protein inhibits host cell translation by interaction with eIF3f | Q33317266 | ||
SARS-coronavirus replication/transcription complexes are membrane-protected and need a host factor for activity in vitro | Q33331393 | ||
Polypyrimidine tract-binding protein binds to the leader RNA of mouse hepatitis virus and serves as a regulator of viral transcription | Q33639841 | ||
Organelle-like membrane compartmentalization of positive-strand RNA virus replication factories | Q33687656 | ||
Coronaviruses post-SARS: update on replication and pathogenesis | Q33694361 | ||
Viral induction of central nervous system innate immune responses | Q33707371 | ||
Structure, Function, and Evolution of Coronavirus Spike Proteins | Q33760875 | ||
Host protein interactions with the 3' end of bovine coronavirus RNA and the requirement of the poly(A) tail for coronavirus defective genome replication | Q33787055 | ||
Polypyrimidine tract-binding protein binds to the complementary strand of the mouse hepatitis virus 3' untranslated region, thereby altering RNA conformation. | Q33822722 | ||
Deubiquitinating and interferon antagonism activities of coronavirus papain-like proteases. | Q33826676 | ||
Mitochondrial aconitase binds to the 3' untranslated region of the mouse hepatitis virus genome | Q33838446 | ||
Heterogeneous nuclear ribonucleoprotein a1 binds to the 3'-untranslated region and mediates potential 5'-3'-end cross talks of mouse hepatitis virus RNA. | Q33851638 | ||
Inhibitors of cathepsin L prevent severe acute respiratory syndrome coronavirus entry | Q33920306 | ||
Murine coronavirus induces type I interferon in oligodendrocytes through recognition by RIG-I and MDA5. | Q33990644 | ||
The spike protein of SARS-CoV--a target for vaccine and therapeutic development | Q34015988 | ||
Annexin A2 binds RNA and reduces the frameshifting efficiency of infectious bronchitis virus | Q34019804 | ||
The PDZ-binding motif of severe acute respiratory syndrome coronavirus envelope protein is a determinant of viral pathogenesis. | Q34047499 | ||
Screening of an FDA-approved compound library identifies four small-molecule inhibitors of Middle East respiratory syndrome coronavirus replication in cell culture | Q34058365 | ||
The SARS-coronavirus-host interactome: identification of cyclophilins as target for pan-coronavirus inhibitors | Q34064211 | ||
Receptor usage and cell entry of bat coronavirus HKU4 provide insight into bat-to-human transmission of MERS coronavirus | Q34120263 | ||
Quantitative proteomics using stable isotope labeling with amino acids in cell culture reveals changes in the cytoplasmic, nuclear, and nucleolar proteomes in Vero cells infected with the coronavirus infectious bronchitis virus | Q34122188 | ||
Murine coronavirus replication induces cell cycle arrest in G0/G1 phase. | Q34151707 | ||
Binding of the 5'-untranslated region of coronavirus RNA to zinc finger CCHC-type and RNA-binding motif 1 enhances viral replication and transcription | Q34169554 | ||
Cyclin-dependent protein kinases: key regulators of the eukaryotic cell cycle | Q34296821 | ||
RNA replication of mouse hepatitis virus takes place at double-membrane vesicles | Q34336367 | ||
Evaluation of the role of heterogeneous nuclear ribonucleoprotein A1 as a host factor in murine coronavirus discontinuous transcription and genome replication | Q34487799 | ||
Heterogeneous nuclear ribonucleoprotein A1 regulates RNA synthesis of a cytoplasmic virus | Q34488873 | ||
To sense or not to sense viral RNA--essentials of coronavirus innate immune evasion. | Q38218501 | ||
Antiviral RNA recognition and assembly by RLR family innate immune sensors | Q38235759 | ||
The role of immunophilins in viral infection | Q38274889 | ||
Hepatitis C virus RNA replication and assembly: living on the fat of the land | Q38294573 | ||
The Membrane Protein of Severe Acute Respiratory Syndrome Coronavirus Functions as a Novel Cytosolic Pathogen-Associated Molecular Pattern To Promote Beta Interferon Induction via a Toll-Like-Receptor-Related TRAF3-Independent Mechanism | Q38404223 | ||
Genetic deficiency and polymorphisms of cyclophilin A reveal its essential role for Human Coronavirus 229E replication | Q38576023 | ||
The ORF4b-encoded accessory proteins of Middle East respiratory syndrome coronavirus and two related bat coronaviruses localize to the nucleus and inhibit innate immune signalling | Q38595331 | ||
Middle East respiratory syndrome and severe acute respiratory syndrome | Q38725989 | ||
Feline coronavirus replication is affected by both cyclophilin A and cyclophilin B. | Q38728281 | ||
Continuous and Discontinuous RNA Synthesis in Coronaviruses | Q38766707 | ||
Fat(al) attraction: Picornaviruses Usurp Lipid Transfer at Membrane Contact Sites to Create Replication Organelles | Q38791454 | ||
MDA5 Is Critical to Host Defense during Infection with Murine Coronavirus. | Q38831191 | ||
Nucleocapsid phosphorylation and RNA helicase DDX1 recruitment enables coronavirus transition from discontinuous to continuous transcription | Q38949481 | ||
Evidence for an Ancestral Association of Human Coronavirus 229E with Bats | Q38953340 | ||
The Nonstructural Proteins Directing Coronavirus RNA Synthesis and Processing. | Q38973838 | ||
Membrane rearrangements mediated by coronavirus nonstructural proteins 3 and 4. | Q38984988 | ||
TGEV nucleocapsid protein induces cell cycle arrest and apoptosis through activation of p53 signaling | Q39022978 | ||
Infectious bronchitis virus generates spherules from zippered endoplasmic reticulum membranes | Q39073500 | ||
Transmissible gastroenteritis virus infection induces cell cycle arrest at S and G2/M phases via p53-dependent pathway | Q39085922 | ||
Effect of chloroquine on feline infectious peritonitis virus infection in vitro and in vivo | Q39155625 | ||
TMPRSS2 activates the human coronavirus 229E for cathepsin-independent host cell entry and is expressed in viral target cells in the respiratory epithelium | Q39174513 | ||
Alisporivir inhibits MERS- and SARS-coronavirus replication in cell culture, but not SARS-coronavirus infection in a mouse model | Q39191241 | ||
An autophagy-independent role for LC3 in equine arteritis virus replication | Q39238402 | ||
Cyclophilin inhibitors block arterivirus replication by interfering with viral RNA synthesis | Q39244702 | ||
Suppression of feline coronavirus replication in vitro by cyclosporin A. | Q39356376 | ||
The coronavirus endoribonuclease Nsp15 interacts with retinoblastoma tumor suppressor protein | Q39402493 | ||
Bat severe acute respiratory syndrome-like coronavirus ORF3b homologues display different interferon antagonist activities | Q39455786 | ||
Regulation of the p38 mitogen-activated protein kinase and dual-specificity phosphatase 1 feedback loop modulates the induction of interleukin 6 and 8 in cells infected with coronavirus infectious bronchitis virus. | Q39465762 | ||
Coronavirus nsp6 proteins generate autophagosomes from the endoplasmic reticulum via an omegasome intermediate | Q39498858 | ||
SARS-CoV nucleocapsid protein antagonizes IFN-β response by targeting initial step of IFN-β induction pathway, and its C-terminal region is critical for the antagonism. | Q39639817 | ||
Attachment of mouse hepatitis virus to O-acetylated sialic acid is mediated by hemagglutinin-esterase and not by the spike protein | Q39694566 | ||
Coronavirus infection induces DNA replication stress partly through interaction of its nonstructural protein 13 with the p125 subunit of DNA polymerase δ. | Q39707460 | ||
Qualitative and quantitative ultrastructural analysis of the membrane rearrangements induced by coronavirus | Q39749967 | ||
P577 | publication date | 2017-06-23 | |
P1433 | published in | Current Topics in Microbiology and Immunology | Q15752446 |
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