| scholarly article | Q13442814 |
| P356 | DOI | 10.1128/JVI.77.5.3269-3280.2003 |
| P8608 | Fatcat ID | release_2arw67f4cjcf7l6bnwruqrcx7u |
| P932 | PMC publication ID | 149744 |
| P698 | PubMed publication ID | 12584350 |
| P5875 | ResearchGate publication ID | 10903199 |
| P50 | author | Juan Pacheco | Q38800514 |
| P2093 | author name string | Peter W Mason | |
| Qizu Zhao | |||
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| Foot-and-mouth disease virus virulent for cattle utilizes the integrin alpha(v)beta3 as its receptor. | Q33782587 | ||
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| Identification and characterization of a cis-acting replication element (cre) adjacent to the internal ribosome entry site of foot-and-mouth disease virus | Q34346867 | ||
| GRP78, a coreceptor for coxsackievirus A9, interacts with major histocompatibility complex class I molecules which mediate virus internalization | Q34357149 | ||
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| Evolution subverting essentiality: dispensability of the cell attachment Arg-Gly-Asp motif in multiply passaged foot-and-mouth disease virus. | Q36240271 | ||
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| Cell recognition by foot-and-mouth disease virus that lacks the RGD integrin-binding motif: flexibility in aphthovirus receptor usage | Q39589175 | ||
| High-efficiency utilization of the bovine integrin alpha(v)beta(3) as a receptor for foot-and-mouth disease virus is dependent on the bovine beta(3) subunit | Q39592588 | ||
| Integrin alphavbeta1 is a receptor for foot-and-mouth disease virus | Q39682189 | ||
| Efficient infection of cells in culture by type O foot-and-mouth disease virus requires binding to cell surface heparan sulfate. | Q39875541 | ||
| Point mutations within the betaG-betaH loop of foot-and-mouth disease virus O1K affect virus attachment to target cells | Q39878039 | ||
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| Epitopes on foot-and-mouth disease virus outer capsid protein VP1 involved in neutralization and cell attachment | Q40133798 | ||
| High affinity interactions of Coxsackievirus A9 with integrin alphavbeta3 (CD51/61) require the CYDMKTTC sequence of beta3, but do not require the RGD sequence of the CAV-9 VP1 protein. | Q40885324 | ||
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| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | foot-and-mouth disease | Q152401 |
| foot-and-mouth disease virus | Q1911079 | ||
| P304 | page(s) | 3269-3280 | |
| P577 | publication date | 2003-03-01 | |
| P1433 | published in | Journal of Virology | Q1251128 |
| P1476 | title | Evaluation of genetically engineered derivatives of a Chinese strain of foot-and-mouth disease virus reveals a novel cell-binding site which functions in cell culture and in animals | |
| P478 | volume | 77 |
| Q41972670 | A complex extracellular sphingomyelinase of Pseudomonas aeruginosa inhibits angiogenesis by selective cytotoxicity to endothelial cells |
| Q40197802 | A second RGD motif in the 1D capsid protein of a SAT1 type foot-and-mouth disease virus field isolate is not essential for attachment to target cells |
| Q39755293 | A single amino acid substitution in the capsid of foot-and-mouth disease virus can increase acid lability and confer resistance to acid-dependent uncoating inhibition |
| Q45370424 | Analysis of SAT1 type foot-and-mouth disease virus capsid proteins: influence of receptor usage on the properties of virus particles. |
| Q40368026 | Analysis of a foot-and-mouth disease virus type A24 isolate containing an SGD receptor recognition site in vitro and its pathogenesis in cattle |
| Q40118967 | Antigenic variability of foot-and-mouth disease virus serotype O during serial cytolytic passage |
| Q97524669 | Challenges and prospects for the control of foot-and-mouth disease: an African perspective |
| Q38699140 | Differential replication of Foot-and-mouth disease viruses in mice determine lethality |
| Q33986070 | Effects of two amino acid substitutions in the capsid proteins on the interaction of two cell-adapted PanAsia-1 strains of foot-and-mouth disease virus serotype O with heparan sulfate receptor |
| Q64066280 | Engineering Responses to Amino Acid Substitutions in the VP0- and VP3-Coding Regions of PanAsia-1 Strains of Foot-and-Mouth Disease Virus Serotype O |
| Q34271606 | Evaluation of a genetically modified foot-and-mouth disease virus vaccine candidate generated by reverse genetics |
| Q59269904 | Evolution and molecular epidemiology of foot-and-mouth disease virus in China |
| Q35627059 | Evolution of cell recognition by viruses: a source of biological novelty with medical implications |
| Q36541684 | Examination of soluble integrin resistant mutants of foot-and-mouth disease virus |
| Q34547126 | Foot-and-mouth disease |
| Q39228592 | Foot-and-mouth disease virus (FMDV) with a stable FLAG epitope in the VP1 G-H loop as a new tool for studying FMDV pathogenesis |
| Q39700273 | Foot-and-mouth disease virus receptors: comparison of bovine alpha(V) integrin utilization by type A and O viruses |
| Q40128599 | Guinea pig-adapted foot-and-mouth disease virus with altered receptor recognition can productively infect a natural host |
| Q40530698 | Heparan sulfate-independent infection attenuates high-neurovirulence GDVII virus-induced encephalitis |
| Q35066053 | How foot-and-mouth disease virus receptor mediates foot-and-mouth disease virus infection |
| Q41927626 | Human rhinovirus type 89 variants use heparan sulfate proteoglycan for cell attachment |
| Q30202838 | Identification of a novel cell culture adaptation site on the capsid of foot-and-mouth disease virus |
| Q33944915 | In-vitro and in-vivo phenotype of type Asia 1 foot-and-mouth disease viruses utilizing two non-RGD receptor recognition sites. |
| Q54254626 | Influence of cell type and cell culture media on the propagation of foot-and-mouth disease virus with regard to vaccine quality. |
| Q38736899 | Insights into Jumonji C-domain containing protein 6 (JMJD6): a multifactorial role in foot-and-mouth disease virus replication in cells |
| Q40567879 | Integrin alphavbeta8 functions as a receptor for foot-and-mouth disease virus: role of the beta-chain cytodomain in integrin-mediated infection. |
| Q36821865 | Interaction between respiratory syncytial virus and glycosaminoglycans, including heparan sulfate |
| Q37492311 | Interactions of foot-and-mouth disease virus with soluble bovine alphaVbeta3 and alphaVbeta6 integrins |
| Q39679224 | Mapping of amino acid residues responsible for adhesion of cell culture-adapted foot-and-mouth disease SAT type viruses |
| Q38791120 | Pathogenesis and micro-anatomic characterization of a cell-adapted mutant foot-and-mouth disease virus in cattle: Impact of the Jumonji C-domain containing protein 6 (JMJD6) and route of inoculation |
| Q91783264 | Pathogenesis, biophysical stability and phenotypic variance of SAT2 foot-and-mouth disease virus |
| Q42183812 | Positively charged residues at the five-fold symmetry axis of cell culture-adapted foot-and-mouth disease virus permit novel receptor interactions |
| Q37252816 | Processing of the VP1/2A junction is not necessary for production of foot-and-mouth disease virus empty capsids and infectious viruses: characterization of "self-tagged" particles |
| Q36499331 | Productive Entry of Foot-and-Mouth Disease Virus via Macropinocytosis Independent of Phosphatidylinositol 3-Kinase |
| Q39997584 | Recovery of infectious foot-and-mouth disease virus from suckling mice after direct inoculation with in vitro-transcribed RNA. |
| Q39982447 | Role of Jumonji C-domain containing protein 6 (JMJD6) in infectivity of foot-and-mouth disease virus |
| Q34825946 | Role of cellular glycosaminoglycans and charged regions of viral G protein in human metapneumovirus infection |
| Q37889405 | The pathogenesis of foot-and-mouth disease II: viral pathways in swine, small ruminants, and wildlife; myotropism, chronic syndromes, and molecular virus-host interactions. |
| Q41741560 | Virus-host interactions in persistently FMDV-infected cells derived from bovine pharynx |
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