| scholarly article | Q13442814 |
| P50 | author | Samuel K Campos | Q56991195 |
| Michelle A Ozbun | Q59453176 | ||
| P2093 | author name string | Jessica L Smith | |
| P2860 | cites work | How Viruses Enter Animal Cells | Q22299358 |
| Human papillomaviruses bind a basal extracellular matrix component secreted by keratinocytes which is distinct from a membrane-associated receptor | Q40336384 | ||
| Human papillomavirus type 31b infection of human keratinocytes does not require heparan sulfate | Q40423280 | ||
| Kinetics of in vitro adsorption and entry of papillomavirus virions | Q40589262 | ||
| Infectious human papillomavirus type 31b: purification and infection of an immortalized human keratinocyte cell line | Q40695908 | ||
| Generation of papillomavirus-immortalized cell lines from normal human ectocervical, endocervical, and vaginal epithelium that maintain expression of tissue-specific differentiation proteins | Q41088834 | ||
| Surface conformational and linear epitopes on HPV-16 and HPV-18 L1 virus-like particles as defined by monoclonal antibodies | Q41172103 | ||
| Postattachment neutralization of papillomaviruses by monoclonal and polyclonal antibodies | Q41368605 | ||
| Effects of cholesterol depletion by cyclodextrin on the sphingolipid microdomains of the plasma membrane | Q42991901 | ||
| Inhibition of clathrin-coated pit assembly by an Eps15 mutant. | Q53731909 | ||
| Detergent extraction of cholera toxin and gangliosides from cultured cells and isolated membranes. | Q55489882 | ||
| Human papillomavirus infection requires cell surface heparan sulfate | Q24529079 | ||
| Identification of the alpha6 integrin as a candidate receptor for papillomaviruses | Q24678291 | ||
| Functional rafts in cell membranes | Q27860768 | ||
| Case-control study of human papillomavirus and oropharyngeal cancer | Q28301695 | ||
| Normal keratinization in a spontaneously immortalized aneuploid human keratinocyte cell line | Q29547520 | ||
| Virus entry: open sesame | Q29619349 | ||
| Tubular membrane invaginations coated by dynamin rings are induced by GTP-gamma S in nerve terminals | Q29620183 | ||
| Lipid domain structure of the plasma membrane revealed by patching of membrane components | Q29620204 | ||
| Caveolar endocytosis of simian virus 40 reveals a new two-step vesicular-transport pathway to the ER | Q29620552 | ||
| JC virus enters human glial cells by clathrin-dependent receptor-mediated endocytosis. | Q30326112 | ||
| A functional link between dynamin and the actin cytoskeleton at podosomes | Q30442034 | ||
| Evidence for a causal association between human papillomavirus and a subset of head and neck cancers | Q33180284 | ||
| Membrane microdomains and caveolae | Q33712427 | ||
| Human papillomavirus type 6b virus-like particles are able to activate the Ras-MAP kinase pathway and induce cell proliferation | Q33839349 | ||
| Production of infectious human papillomavirus independently of viral replication and epithelial cell differentiation | Q33879132 | ||
| Papillomaviruses infect cells via a clathrin-dependent pathway | Q34187267 | ||
| Biosynthesis of human papillomavirus from a continuous cell line upon epithelial differentiation | Q34236875 | ||
| Prevalence of human papillomavirus in cervical cancer: a worldwide perspective. International biological study on cervical cancer (IBSCC) Study Group | Q34313864 | ||
| Keratinocyte-secreted laminin 5 can function as a transient receptor for human papillomaviruses by binding virions and transferring them to adjacent cells | Q35024219 | ||
| Invasion of host cells by JC virus identifies a novel role for caveolae in endosomal sorting of noncaveolar ligands | Q35101449 | ||
| Neutralization of human papillomavirus with monoclonal antibodies reveals different mechanisms of inhibition | Q35947703 | ||
| Viral entry. | Q35989082 | ||
| Mis-assembly of clathrin lattices on endosomes reveals a regulatory switch for coated pit formation | Q36233556 | ||
| Dynamin at the neck of caveolae mediates their budding to form transport vesicles by GTP-driven fission from the plasma membrane of endothelium | Q36255255 | ||
| Dynamin-mediated internalization of caveolae. | Q36255260 | ||
| Clathrin- and caveolin-1-independent endocytosis: entry of simian virus 40 into cells devoid of caveolae | Q36321346 | ||
| Neutralization of animal virus infectivity by antibody | Q36827854 | ||
| Laboratory production in vivo of infectious human papillomavirus type 11 | Q36884907 | ||
| Bound simian virus 40 translocates to caveolin-enriched membrane domains, and its entry is inhibited by drugs that selectively disrupt caveolae | Q37383445 | ||
| Infection of vero cells by BK virus is dependent on caveolae | Q37583540 | ||
| Acidification of macrophage and fibroblast endocytic vesicles in vitro | Q37613595 | ||
| Papillomavirus particles assembled in 293TT cells are infectious in vivo | Q39304696 | ||
| Human papillomavirus type 31b infection of human keratinocytes and the onset of early transcription. | Q39685873 | ||
| Human papillomavirus types 16, 31, and 58 use different endocytosis pathways to enter cells | Q39732506 | ||
| Mechanisms regulating expression of the HPV 31 L1 and L2 capsid proteins and pseudovirion entry | Q40166422 | ||
| Papillomavirus virus-like particles activate the PI3-kinase pathway via alpha-6 beta-4 integrin upon binding. | Q40266285 | ||
| P433 | issue | 18 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | keratinocyte | Q1473931 |
| P304 | page(s) | 9922-9931 | |
| P577 | publication date | 2007-07-11 | |
| P1433 | published in | Journal of Virology | Q1251128 |
| P1476 | title | Human papillomavirus type 31 uses a caveolin 1- and dynamin 2-mediated entry pathway for infection of human keratinocytes | |
| P478 | volume | 81 |
| Q36978897 | Annexin A2 and S100A10 regulate human papillomavirus type 16 entry and intracellular trafficking in human keratinocytes |
| Q34641651 | Binding and neutralization characteristics of a panel of monoclonal antibodies to human papillomavirus 58. |
| Q39766716 | Bovine papillomavirus type 1: from clathrin to caveolin |
| Q34667267 | Caveolin-1 mediated uptake via langerin restricts HIV-1 infection in human Langerhans cells |
| Q36898793 | Caveolin-1-dependent infectious entry of human papillomavirus type 31 in human keratinocytes proceeds to the endosomal pathway for pH-dependent uncoating |
| Q33647192 | Cellular receptor binding and entry of human papillomavirus |
| Q33374009 | Clathrin- and caveolin-independent entry of human papillomavirus type 16--involvement of tetraspanin-enriched microdomains (TEMs) |
| Q38233232 | Coat as a dagger: the use of capsid proteins to perforate membranes during non-enveloped DNA viruses trafficking. |
| Q27026900 | Concepts of papillomavirus entry into host cells |
| Q24616134 | Current understanding of the mechanism of HPV infection |
| Q28534531 | Differential dependence on host cell glycosaminoglycans for infection of epithelial cells by high-risk HPV types |
| Q28479209 | Differentiation-dependent interpentameric disulfide bond stabilizes native human papillomavirus type 16 |
| Q64887908 | Diverse Papillomavirus Types Induce Endosomal Tubulation. |
| Q37410850 | Dynamin- and lipid raft-dependent entry of decay-accelerating factor (DAF)-binding and non-DAF-binding coxsackieviruses into nonpolarized cells |
| Q37300372 | Entry of Classical Swine Fever Virus into PK-15 Cells via a pH-, Dynamin-, and Cholesterol-Dependent, Clathrin-Mediated Endocytic Pathway That Requires Rab5 and Rab7. |
| Q27346336 | Entry of human papillomavirus type 16 by actin-dependent, clathrin- and lipid raft-independent endocytosis |
| Q34162277 | Essential roles for soluble virion-associated heparan sulfonated proteoglycans and growth factors in human papillomavirus infections. |
| Q35654397 | Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis |
| Q52625020 | Extracellular conformational changes in the capsid of human papillomaviruses contribute to asynchronous uptake into host cells. |
| Q41013083 | Fluorescently Labeled Human Papillomavirus Pseudovirions for Use in Virus Entry Experiments |
| Q38022050 | From endocytosis to membrane fusion: emerging roles of dynamin in virus entry |
| Q39724559 | Function of membrane rafts in viral lifecycles and host cellular response |
| Q43787108 | Genetic profiling to predict recurrence of early cervical cancer |
| Q39320596 | HPV entry into cells |
| Q40693093 | HPV16 Sublineage Associations With Histology-Specific Cancer Risk Using HPV Whole-Genome Sequences in 3200 Women |
| Q36844065 | HPV16 and BPV1 infection can be blocked by the dynamin inhibitor dynasore |
| Q37436158 | Heterogeneous pathways of maternal-fetal transmission of human viruses (review). |
| Q39013547 | Host cell restriction factors that limit transcription and replication of human papillomavirus. |
| Q38042837 | Host-cell factors involved in papillomavirus entry |
| Q35748557 | Human papillomavirus L2 facilitates viral escape from late endosomes via sorting nexin 17. |
| Q42206744 | Human papillomavirus infection requires the TSG101 component of the ESCRT machinery |
| Q27318457 | Human papillomavirus type 16 entry: retrograde cell surface transport along actin-rich protrusions |
| Q39843190 | Human papillomavirus type 16 infection of human keratinocytes requires clathrin and caveolin-1 and is brefeldin a sensitive |
| Q36978918 | Human papillomavirus types 16, 18, and 31 share similar endocytic requirements for entry |
| Q36481634 | Human papillomavirus: gene expression, regulation and prospects for novel diagnostic methods and antiviral therapies |
| Q33469751 | Identification of neutralizing conformational epitopes on the human papillomavirus type 31 major capsid protein and functional implications |
| Q52333281 | Imaging, Tracking and Computational Analyses of Virus Entry and Egress with the Cytoskeleton. |
| Q90826228 | Infectious bronchitis virus entry mainly depends on clathrin mediated endocytosis and requires classical endosomal/lysosomal system |
| Q39805799 | Infectious entry of equine herpesvirus-1 into host cells through different endocytic pathways. |
| Q35826126 | Infectious spleen and kidney necrosis virus (a fish iridovirus) enters Mandarin fish fry cells via caveola-dependent endocytosis |
| Q36099326 | Inhibition of transfer to secondary receptors by heparan sulfate-binding drug or antibody induces noninfectious uptake of human papillomavirus |
| Q37279580 | Inoculation of young horses with bovine papillomavirus type 1 virions leads to early infection of PBMCs prior to pseudo-sarcoid formation |
| Q33663169 | Mechanisms of cell entry by human papillomaviruses: an overview |
| Q58993983 | Molecular Signaling and Cellular Pathways for Virus Entry |
| Q28070323 | Molecular mechanisms of HPV mediated neoplastic progression |
| Q90670412 | New glimpses of caveolin-1 functions in embryonic development and human diseases |
| Q34111736 | Novel antivirals inhibit early steps in HPV infection |
| Q35868083 | Opposing effects of bacitracin on human papillomavirus type 16 infection: enhancement of binding and entry and inhibition of endosomal penetration |
| Q39803010 | Overlapping and independent structural roles for human papillomavirus type 16 L2 conserved cysteines |
| Q26801497 | Papillomavirus Infectious Pathways: A Comparison of Systems |
| Q38135529 | Papillomavirus associated diseases of the horse |
| Q34178325 | Papillomavirus infection requires gamma secretase |
| Q58764248 | Papillomaviruses and Endocytic Trafficking |
| Q38045782 | Principles of polyoma- and papillomavirus uncoating |
| Q35824681 | Real-time Imaging of Rabies Virus Entry into Living Vero cells |
| Q36586691 | Recent developments in the interactions between caveolin and pathogens |
| Q35866498 | Replication and assembly of human papillomaviruses |
| Q35150925 | Replication and partitioning of papillomavirus genomes |
| Q36397378 | Rift Valley fever virus strain MP-12 enters mammalian host cells via caveola-mediated endocytosis |
| Q37373696 | Structure, attachment and entry of polyoma- and papillomaviruses |
| Q50043357 | Superinfection Exclusion between Two High-Risk Human Papillomavirus (HPV) Types During a Co-Infection |
| Q28475787 | Target cell cyclophilins facilitate human papillomavirus type 16 infection |
| Q93048605 | The Known and Potential Intersections of Rab-GTPases in Human Papillomavirus Infections |
| Q42828087 | The L1 major capsid protein of HPV16 differentially modulates APC trafficking according to the vaccination or natural infection context |
| Q26861667 | The cytoskeleton in papillomavirus infection |
| Q35645395 | The high risk HPV16 L2 minor capsid protein has multiple transport signals that mediate its nucleocytoplasmic traffic |
| Q33970900 | The nuclear retention signal of HPV16 L2 protein is essential for incoming viral genome to transverse the trans-Golgi network |
| Q37284008 | The role of NH4Cl and cysteine proteases in Human Papillomavirus type 16 infection |
| Q24646183 | Tissue-spanning redox gradient-dependent assembly of native human papillomavirus type 16 virions |
| Q21143868 | Two highly conserved cysteine residues in HPV16 L2 form an intramolecular disulfide bond and are critical for infectivity in human keratinocytes |
| Q33905761 | Usage of heparan sulfate, integrins, and FAK in HPV16 infection |
| Q37480444 | Viral entry mechanisms: human papillomavirus and a long journey from extracellular matrix to the nucleus |
| Q35659629 | Virus activated filopodia promote human papillomavirus type 31 uptake from the extracellular matrix |
| Q40511596 | White spot syndrome virus enters crayfish hematopoietic tissue cells via clathrin-mediated endocytosis |
| Q82260773 | [HPV-associated carcinomas of the female genital tract. Molecular mechanisms of development] |
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