scholarly article | Q13442814 |
P2093 | author name string | Hua Zhang | |
Haolong Cong | |||
Po Tien | |||
Lei Song | |||
Ning Du | |||
Wenliang Zhang | |||
Hongchao Tian | |||
P2860 | cites work | Identification of the myelin oligodendrocyte glycoprotein as a cellular receptor for rubella virus | Q24635006 |
The function of intermediate filaments in cell shape and cytoskeletal integrity | Q24671696 | ||
Crystal structure of human enterovirus 71 3C protease | Q27666945 | ||
Atomic structure of the vimentin central -helical domain and its implications for intermediate filament assembly | Q27671298 | ||
Crystal Structure of the Japanese Encephalitis Virus Envelope Protein | Q27676100 | ||
Structure of human enterovirus 71 in complex with a capsid-binding inhibitor | Q27676881 | ||
At the acidic edge: emerging functions for lysosomal membrane proteins | Q28182104 | ||
Scavenger receptor B2 is a cellular receptor for enterovirus 71 | Q28249350 | ||
Lysosomal integral membrane protein II binds thrombospondin-1. Structure-function homology with the cell adhesion molecule CD36 defines a conserved recognition motif | Q28262922 | ||
Endothelial targeting of cowpea mosaic virus (CPMV) via surface vimentin | Q28475414 | ||
Human SCARB2-mediated entry and endocytosis of EV71 | Q28478931 | ||
The intermediate filament protein vimentin is a new target for epigallocatechin gallate | Q33211958 | ||
The essential role of clathrin-mediated endocytosis in the infectious entry of human enterovirus 71. | Q33721725 | ||
Tyrosine Sulfation of the Amino Terminus of PSGL-1 Is Critical for Enterovirus 71 Infection | Q33747574 | ||
Interaction of Theiler's virus with intermediate filaments of infected cells | Q33785960 | ||
An epidemic of enterovirus 71 infection in Taiwan. Taiwan Enterovirus Epidemic Working Group. | Q33875086 | ||
Neurologic complications in children with enterovirus 71 infection | Q33875092 | ||
Purification and characterization of enterovirus 71 viral particles produced from vero cells grown in a serum-free microcarrier bioreactor system. | Q33908518 | ||
Cellular receptors for viruses: links to tropism and pathogenesis | Q33919202 | ||
Japanese encephalitis virus interacts with vimentin to facilitate its entry into porcine kidney cell line | Q33974547 | ||
Clinical features, diagnosis, and management of enterovirus 71. | Q34144978 | ||
Brief overview on cellular virus receptors | Q34556322 | ||
Enterovirus 71 protease 2Apro targets MAVS to inhibit anti-viral type I interferon responses | Q34649632 | ||
Adaptive mutations in the genomes of enterovirus 71 strains following infection of mouse cells expressing human P-selectin glycoprotein ligand-1. | Q34837231 | ||
Annexin II binds to capsid protein VP1 of enterovirus 71 and enhances viral infectivity. | Q35531212 | ||
A mouse-adapted enterovirus 71 strain causes neurological disease in mice after oral infection | Q35702513 | ||
A non-mouse-adapted enterovirus 71 (EV71) strain exhibits neurotropism, causing neurological manifestations in a novel mouse model of EV71 infection | Q35826494 | ||
Molecular determinants of enterovirus 71 viral entry: cleft around GLN-172 on VP1 protein interacts with variable region on scavenge receptor B 2. | Q35838900 | ||
Human SCARB2-dependent infection by coxsackievirus A7, A14, and A16 and enterovirus 71 | Q35943455 | ||
Cooperative effect of the attenuation determinants derived from poliovirus sabin 1 strain is essential for attenuation of enterovirus 71 in the NOD/SCID mouse infection model | Q36483299 | ||
An outbreak of hand, foot, and mouth disease in Singapore | Q36874541 | ||
Lymphocyte and antibody responses reduce enterovirus 71 lethality in mice by decreasing tissue viral loads | Q37232853 | ||
Sialylated glycans as receptor and inhibitor of enterovirus 71 infection to DLD-1 intestinal cells | Q37362417 | ||
Virology, epidemiology, pathogenesis, and control of enterovirus 71. | Q37801742 | ||
Functional comparison of SCARB2 and PSGL1 as receptors for enterovirus 71. | Q39213405 | ||
A novel minicircle vector based system for inhibting the replication and gene expression of enterovirus 71 and coxsackievirus A16. | Q39291516 | ||
Mouse adaptation of a sub-genogroup B5 strain of human enterovirus 71 is associated with a novel lysine to glutamic acid substitution at position 244 in protein VP1. | Q39350594 | ||
Enterovirus 71 disrupts interferon signaling by reducing the level of interferon receptor 1 | Q39410081 | ||
Identification of a human SCARB2 region that is important for enterovirus 71 binding and infection. | Q39578725 | ||
Adaptation of Sindbis virus to BHK cells selects for use of heparan sulfate as an attachment receptor. | Q39580237 | ||
The largest outbreak of hand; foot and mouth disease in Singapore in 2008: the role of enterovirus 71 and coxsackievirus A strains. | Q39827005 | ||
Human P-selectin glycoprotein ligand-1 is a functional receptor for enterovirus 71. | Q39835244 | ||
Herpes simplex virus type 1 and pseudorabies virus bind to a common saturable receptor on Vero cells that is not heparan sulfate. | Q40046756 | ||
Epidemic of Hand, Foot and Mouth Disease Associated with Enterovirus 71 Infection | Q40123768 | ||
Vimentin function in lymphocyte adhesion and transcellular migration | Q40326248 | ||
Defining the cellular target(s) of porcine reproductive and respiratory syndrome virus blocking monoclonal antibody 7G10. | Q40336014 | ||
Deaths of children during an outbreak of hand, foot, and mouth disease in sarawak, malaysia: clinical and pathological characteristics of the disease. For the Outbreak Study Group | Q40614108 | ||
Structure and assembly properties of the intermediate filament protein vimentin: the role of its head, rod and tail domains | Q41144453 | ||
Targeting of lysosomal integral membrane protein LIMP II. The tyrosine-lacking carboxyl cytoplasmic tail of LIMP II is sufficient for direct targeting to lysosomes | Q41665769 | ||
Filamin A is required for vimentin-mediated cell adhesion and spreading | Q41874654 | ||
The molecular basis of mouse adaptation by human enterovirus 71. | Q42659419 | ||
A large-scale epidemic of hand, foot and mouth disease associated with enterovirus 71 infection in Japan in 1978 | Q44546376 | ||
Passive protection against lethal enterovirus 71 infection in newborn mice by neutralizing antibodies elicited by a synthetic peptide. | Q44566080 | ||
P-selectin binding to P-selectin glycoprotein ligand-1 induces an intermediate state of alphaMbeta2 activation and acts cooperatively with extracellular stimuli to support maximal adhesion of human neutrophils | Q44951891 | ||
An investigation of epidemic enterovirus 71 infection in Taiwan, 2008: clinical, virologic, and serologic features | Q45096500 | ||
Mutations in VP2 and VP1 capsid proteins increase infectivity and mouse lethality of enterovirus 71 by virus binding and RNA accumulation enhancement | Q45361800 | ||
Neurogenic pulmonary oedema and enterovirus 71 encephalomyelitis | Q48359714 | ||
Neurodevelopment and Cognition in Children after Enterovirus 71 Infection | Q56787299 | ||
Salt-stable interaction of the amino-terminal head region of vimentin with the alpha-helical rod domain of cytoplasmic intermediate filament proteins and its relevance to protofilament structure and filament formation and stability | Q68204407 | ||
Activation of human leukocytes reduces surface P-selectin glycoprotein ligand-1 (PSGL-1, CD162) and adhesion to P-selectin in vitro | Q74183213 | ||
Important contributions of P-selectin glycoprotein ligand-1-mediated secondary capture to human monocyte adhesion to P-selectin, E-selectin, and TNF-alpha-activated endothelium under flow in vitro | Q77186293 | ||
Enterovirus 71 infection: a new threat to global public health? | Q82263969 | ||
P433 | issue | 10 | |
P1104 | number of pages | 18 | |
P304 | page(s) | 5816-5833 | |
P577 | publication date | 2014-03-12 | |
P1433 | published in | Journal of Virology | Q1251128 |
P1476 | title | Cell surface vimentin is an attachment receptor for enterovirus 71. | |
P478 | volume | 88 |
Q58801223 | A VP1 mutation acquired during an enterovirus 71 disseminated infection confers heparan sulfate binding ability and modulates ex vivo tropism |
Q41933373 | A selective bottleneck shapes the evolutionary mutant spectra of enterovirus A71 during viral dissemination in humans |
Q42823044 | A versatile approach towards multivalent saccharide displays on magnetic nanoparticles and phospholipid vesicles |
Q35543248 | APOBEC3A cytidine deaminase induces RNA editing in monocytes and macrophages |
Q59360170 | Amino acid variation at VP1-145 of enterovirus 71 determines attachment receptor usage and neurovirulence in human scavenger receptor B2 transgenic mice |
Q37243489 | Amphotericin B Inhibits Enterovirus 71 Replication by Impeding Viral Entry. |
Q38405180 | Analysis of EV71 infection progression using triple-SILAC-based proteomics approach |
Q57174474 | Annexin A2 binds to vimentin and contributes to porcine reproductive and respiratory syndrome virus multiplication |
Q51545645 | Anti-vimentin Antibodies Present at the Time of Transplantation May Predict Early Development of Interstitial Fibrosis/Tubular Atrophy. |
Q51334188 | Cell Entry of C3 Exoenzyme from Clostridium botulinum. |
Q35641079 | Cell surface nucleolin facilitates enterovirus 71 binding and infection |
Q92559736 | Cellular receptors for enterovirus A71 |
Q37064293 | Cooperative effect of the VP1 amino acids 98E, 145A and 169F in the productive infection of mouse cell lines by enterovirus 71 (BS strain). |
Q37347350 | Enterovirus 71 2B Induces Cell Apoptosis by Directly Inducing the Conformational Activation of the Proapoptotic Protein Bax |
Q37416863 | Enterovirus 71 infection of motor neuron-like NSC-34 cells undergoes a non-lytic exit pathway |
Q35112613 | Enterovirus 71 virion-associated galectin-1 facilitates viral replication and stability |
Q27468727 | Enterovirus A71 DNA-Launched Infectious Clone as a Robust Reverse Genetic Tool |
Q64948345 | Enterovirus A71 VP1 Variation A289T Decreases the Central Nervous System Infectivity via Attenuation of Interactions between VP1 and Vimentin In Vitro and In Vivo. |
Q90071181 | Enterovirus A71 capsid protein VP1 increases blood-brain barrier permeability and virus receptor vimentin on the brain endothelial cells |
Q110733552 | Extracellular vimentin is an attachment factor that facilitates SARS-CoV-2 entry into human endothelial cells |
Q99591465 | Functional Characterization of Pepper Vein Banding Virus-Encoded Proteins and Their Interactions: Implications in Potyvirus Infection |
Q94585875 | HSC70 is required for infectious bursal disease virus (IBDV) infection in DF-1 cells |
Q66679475 | Heparan Sulfate Proteoglycans and Viral Attachment: True Receptors or Adaptation Bias? |
Q90427339 | Heparan sulfate attachment receptor is a major selection factor for attenuated enterovirus 71 mutants during cell culture adaptation |
Q36434217 | Identification of Positively Charged Residues in Enterovirus 71 Capsid Protein VP1 Essential for Production of Infectious Particles. |
Q91790386 | Improved Isolation of Mesenchymal Stem Cells Based on Interactions between N-Acetylglucosamine-Bearing Polymers and Cell-Surface Vimentin |
Q54284559 | In wound repair vimentin mediates the transition of mesenchymal leader cells to a myofibroblast phenotype. |
Q52682461 | Invasion of the Brain by Listeria monocytogenes Is Mediated by InlF and Host Cell Vimentin. |
Q91915011 | Involvement of VCP/UFD1/Nucleolin in the viral entry of Enterovirus A species |
Q40803672 | Laminin receptor is an interacting partner for viral outer capsid protein VP5 in grass carp reovirus infection. |
Q53826871 | Matrix stiffness modulates infection of endothelial cells by Listeria monocytogenes via expression of cell surface vimentin. |
Q39038694 | Mechanisms leading from systemic autoimmunity to joint-specific disease in rheumatoid arthritis |
Q47885797 | Migration-based selections of antibodies that convert bone marrow into trafficking microglia-like cells that reduce brain amyloid β. |
Q93197806 | Molecular Pathogenicity of Enteroviruses Causing Neurological Disease |
Q91725853 | Neutrophil extracellular traps induced by VP1 contribute to pulmonary edema during EV71 infection |
Q35188294 | Proteomic analysis of human brain microvascular endothelial cells reveals differential protein expression in response to enterovirus 71 infection |
Q90533096 | Recent Progress on Functional Genomics Research of Enterovirus 71 |
Q38966855 | Recent advances from studies on the role of structural proteins in enterovirus infection |
Q66679579 | Recent advances on the role of host factors during non-poliovirus enteroviral infections |
Q26772127 | Rhinoviruses and Respiratory Enteroviruses: Not as Simple as ABC |
Q94957058 | Role of cell surface vimentin in Chandipura virus replication in Neuro-2a cells |
Q63561174 | Saikosaponin D suppresses enterovirus A71 infection by inhibiting autophagy |
Q28388816 | Suppression of Vimentin Phosphorylation by the Avian Reovirus p17 through Inhibition of CDK1 and Plk1 Impacting the G2/M Phase of the Cell Cycle |
Q37652678 | Suramin interacts with the positively charged region surrounding the 5-fold axis of the EV-A71 capsid and inhibits multiple enterovirus A. |
Q64910082 | The Group B Streptococcal surface antigen I/II protein, BspC, interacts with host vimentin to promote adherence to brain endothelium and inflammation during the pathogenesis of meningitis. |
Q35693536 | The Role of VP1 Amino Acid Residue 145 of Enterovirus 71 in Viral Fitness and Pathogenesis in a Cynomolgus Monkey Model |
Q28550039 | The Suramin Derivative NF449 Interacts with the 5-fold Vertex of the Enterovirus A71 Capsid to Prevent Virus Attachment to PSGL-1 and Heparan Sulfate |
Q34289956 | The approved pediatric drug suramin identified as a clinical candidate for the treatment of EV71 infection-suramin inhibits EV71 infection in vitro and in vivo |
Q39093658 | The enterovirus 71 procapsid binds neutralizing antibodies and rescues virus infection in vitro |
Q59360173 | VP1 amino acid residue 145 of enterovirus 71 is a key residue for its receptor attachment and resistance to neutralizing antibody during cynomolgus monkey infection |
Q39162997 | VP1 residues around the five-fold axis of enterovirus A71 mediate heparan sulfate interaction |
Q38701705 | Vimentin Modulates Infectious Internalization of Human Papillomavirus 16 Pseudovirions. |
Q35692691 | Vimentin filament organization and stress sensing depend on its single cysteine residue and zinc binding. |
Q26751516 | Vimentin in Bacterial Infections |
Q92436429 | Vimentin modulates apoptosis and inflammatory cytokine release by a human monocytic cell line (THP-1) in response to lipopolysaccharides in vitro |
Q47593142 | Vimentin modulates infectious porcine circovirus type 2 in PK-15 cells. |
Q91883970 | Viral engagement with host receptors blocked by a novel class of tryptophan dendrimers that targets the 5-fold-axis of the enterovirus-A71 capsid |
Q89573859 | [Effect of vimentin on activation of NLRP3 inflammasome in the brain of mice with EV71 infection] |
Search more.