| scholarly article | Q13442814 |
| P2093 | author name string | B Baxt | |
| S Neff | |||
| P2860 | cites work | ICAP-1, a novel beta1 integrin cytoplasmic domain-associated protein, binds to a conserved and functionally important NPXY sequence motif of beta1 integrin | Q24308783 |
| A structural basis for integrin activation by the cytoplasmic tail of the alpha IIb-subunit | Q27621430 | ||
| Integrins: versatility, modulation, and signaling in cell adhesion | Q27860844 | ||
| NPXY, a sequence often found in cytoplasmic tails, is required for coated pit-mediated internalization of the low density lipoprotein receptor | Q28254985 | ||
| The role of conserved amino acid motifs within the integrin beta3 cytoplasmic domain in triggering focal adhesion kinase phosphorylation | Q28305581 | ||
| Integrins alpha v beta 3 and alpha v beta 5 promote adenovirus internalization but not virus attachment | Q29615852 | ||
| Inducible tyrosine phosphorylation of the beta3 integrin requires the alphaV integrin cytoplasmic tail | Q71825691 | ||
| Development of a structural model for the cytoplasmic domain of an integrin | Q74445738 | ||
| Distinct involvement of beta3 integrin cytoplasmic domain tyrosine residues 747 and 759 in integrin-mediated cytoskeletal assembly and phosphotyrosine signaling | Q74516914 | ||
| Tyrosine phosphorylation of the beta3 cytoplasmic domain mediates integrin-cytoskeletal interactions | Q74567473 | ||
| The vitronectin receptor associates with clathrin-coated membrane domains via the cytoplasmic domain of its beta5 subunit | Q77153450 | ||
| Phosphorylation sites in the integrin beta3 cytoplasmic domain in intact platelets | Q77800942 | ||
| RGD and other recognition sequences for integrins | Q29616331 | ||
| Foot-and-mouth disease virus virulent for cattle utilizes the integrin alpha(v)beta3 as its receptor. | Q33782587 | ||
| Adenovirus internalization and infection require dynamin | Q33783549 | ||
| Cell adhesion molecules: selectins and integrins. | Q33824566 | ||
| The Talin head domain binds to integrin beta subunit cytoplasmic tails and regulates integrin activation | Q33874977 | ||
| Acid-dependent ligand dissociation and recycling of LDL receptor mediated by growth factor homology region | Q34180927 | ||
| Functional domains of the poliovirus receptor | Q34592708 | ||
| Antibodies to the vitronectin receptor (integrin alpha V beta 3) inhibit binding and infection of foot-and-mouth disease virus to cultured cells | Q35838328 | ||
| Weak bases and ionophores rapidly and reversibly raise the pH of endocytic vesicles in cultured mouse fibroblasts | Q36209351 | ||
| Integrin cytoplasmic domains mediate inside-out signal transduction | Q36233869 | ||
| Integrin beta 3 cytoplasmic tail is necessary and sufficient for regulation of alpha 5 beta 1 phagocytosis by alpha v beta 3 and integrin-associated protein | Q36235842 | ||
| Requirement of the NPXY motif in the integrin beta 3 subunit cytoplasmic tail for melanoma cell migration in vitro and in vivo. | Q36382612 | ||
| Identification of a functionally important sequence in the cytoplasmic tail of integrin beta 3 by using cell-permeable peptide analogs | Q37270758 | ||
| The membrane-cytoplasm interface of integrin alpha subunits is critical for receptor latency | Q37382664 | ||
| A beta turn in the cytoplasmic tail of the integrin alpha v subunit influences conformation and ligand binding of alpha v beta 3. | Q38311241 | ||
| Amino acid motifs required for isolated beta cytoplasmic domains to regulate 'in trans' beta1 integrin conformation and function in cell attachment. | Q38330359 | ||
| Mutations in the cytoplasmic domain of the integrin beta1 chain indicate a role for endocytosis factors in bacterial internalization | Q38360033 | ||
| Coxsackievirus and adenovirus receptor cytoplasmic and transmembrane domains are not essential for coxsackievirus and adenovirus infection. | Q39552063 | ||
| Adenovirus endocytosis via alpha(v) integrins requires phosphoinositide-3-OH kinase | Q39577792 | ||
| Adenovirus endocytosis requires actin cytoskeleton reorganization mediated by Rho family GTPases. | Q39581979 | ||
| The epithelial integrin alphavbeta6 is a receptor for foot-and-mouth disease virus | Q39584959 | ||
| Regulation of adenovirus membrane penetration by the cytoplasmic tail of integrin beta5. | Q39589868 | ||
| 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 | ||
| Tissue culture adaptation of foot-and-mouth disease virus selects viruses that bind to heparin and are attenuated in cattle. | Q39880172 | ||
| Biological applications of ionophores | Q40596967 | ||
| Ligation of integrin alpha5beta1 is required for internalization of vitronectin by integrin alphavbeta3. | Q41132432 | ||
| Internalization of a major group human rhinovirus does not require cytoplasmic or transmembrane domains of ICAM-1 | Q41624412 | ||
| Integrin cytoplasmic tyrosine motif is required for outside-in alphaIIbbeta3 signalling and platelet function | Q41700251 | ||
| Effect of lysosomotropic compounds on early events in foot-and-mouth disease virus replication | Q41913787 | ||
| Transmembrane-truncated alphavbeta3 integrin retains high affinity for ligand binding: evidence for an 'inside-out' suppressor? | Q42060863 | ||
| The clathrin endocytic pathway in viral infection | Q42651304 | ||
| Requirement of integrin beta3 tyrosine 747 for beta3 tyrosine phosphorylation and regulation of alphavbeta3 avidity | Q42666465 | ||
| Early interactions of foot-and-mouth disease virus with cultured cells | Q45803463 | ||
| The conserved membrane-proximal region of an integrin cytoplasmic domain specifies ligand binding affinity. | Q45938073 | ||
| Integrin beta cytoplasmic domains differentially bind to cytoskeletal proteins. | Q46376510 | ||
| Regulation of conformation and ligand binding function of integrin alpha5beta1 by the beta1 cytoplasmic domain | Q46599137 | ||
| A conserved sequence motif in the integrin beta3 cytoplasmic domain is required for its specific interaction with beta3-endonexin | Q46741501 | ||
| Conserved functions of the cytoplasmic domains of integrin beta subunits | Q47731039 | ||
| Regulation of the extracellular ligand binding activity of integrins. | Q47935070 | ||
| Determination of the Border between the Transmembrane and Cytoplasmic Domains of Human Integrin Subunits | Q57083866 | ||
| Divalent Cations Differentially Regulate Integrin αIIbCytoplasmic Tail Binding to β3and to Calcium- and Integrin-binding Protein | Q57998264 | ||
| Migration of human polymorphonuclear leukocytes through a synovial fibroblast barrier is mediated by both beta 2 (CD11/CD18) integrins and the beta 1 (CD29) integrins VLA-5 and VLA-6 | Q71700722 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | foot-and-mouth disease | Q152401 |
| foot-and-mouth disease virus | Q1911079 | ||
| P1104 | number of pages | 6 | |
| P304 | page(s) | 527-532 | |
| P577 | publication date | 2001-01-01 | |
| P1433 | published in | Journal of Virology | Q1251128 |
| P1476 | title | The ability of integrin alpha(v)beta(3) To function as a receptor for foot-and-mouth disease virus is not dependent on the presence of complete subunit cytoplasmic domains | |
| P478 | volume | 75 |
| 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 |
| Q45370424 | Analysis of SAT1 type foot-and-mouth disease virus capsid proteins: influence of receptor usage on the properties of virus particles. |
| Q40409606 | Analysis of foot-and-mouth disease virus internalization events in cultured cells |
| Q45351505 | Comparative analysis of cloned cDNAs encoding Chinese yellow cattle and Gansu black swine integrin receptors for foot-and-mouth disease virus |
| Q40782833 | De novo formation of focal complex-like structures in host cells by invading Streptococci. |
| Q36105475 | Establishment and evaluation of a murine ανβ3-integrin-expressing cell line with increased susceptibility to Foot-and-mouth disease virus |
| Q34547126 | Foot-and-mouth disease |
| Q39700273 | Foot-and-mouth disease virus receptors: comparison of bovine alpha(V) integrin utilization by type A and O viruses |
| Q35066053 | How foot-and-mouth disease virus receptor mediates foot-and-mouth disease virus infection |
| Q40567879 | Integrin alphavbeta8 functions as a receptor for foot-and-mouth disease virus: role of the beta-chain cytodomain in integrin-mediated infection. |
| Q34395684 | Integrin β3 is required in infection and proliferation of classical swine fever virus |
| Q91568149 | Integrin β3, a RACK1 interacting protein, is critical for porcine reproductive and respiratory syndrome virus infection and NF-κB activation in Marc-145 cells |
| Q37492311 | Interactions of foot-and-mouth disease virus with soluble bovine alphaVbeta3 and alphaVbeta6 integrins |
| Q45731502 | Macrophage phagocytosis of foot-and-mouth disease virus may create infectious carriers |
| Q34749464 | Mechanisms of foot-and-mouth disease virus tropism inferred from differential tissue gene expression |
| Q30364489 | Myocarditis associated with foot-and-mouth disease virus type O in lambs. |
| Q39602424 | Role of the cytoplasmic domain of the beta-subunit of integrin alpha(v)beta6 in infection by foot-and-mouth disease virus |
| Q27471608 | Selection of peptide entry motifs by bacterial surface display |
| Q35291117 | Structural basis of nonenveloped virus cell entry |
| Q35044853 | Structure and receptor binding. |
| 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. |
| Q41889160 | Use of confocal immunofluorescence microscopy to localize viral nonstructural proteins and potential sites of replication in pigs experimentally infected with foot-and-mouth disease virus |
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