scholarly article | Q13442814 |
P50 | author | Dieter Blaas | Q90775034 |
P2093 | author name string | Hannes Zwickl | |
Luc Snyers | |||
P2860 | cites work | Cancer Research | Q326097 |
Localization of low molecular weight GTP binding proteins to exocytic and endocytic compartments | Q24316079 | ||
Canine and feline parvoviruses can use human or feline transferrin receptors to bind, enter, and infect cells | Q24529509 | ||
Direct binding of occupied urokinase receptor (uPAR) to LDL receptor-related protein is required for endocytosis of uPAR and regulation of cell surface urokinase activity | Q24633333 | ||
Amphiphysin heterodimers: potential role in clathrin-mediated endocytosis | Q24653769 | ||
Extraction of cholesterol with methyl-beta-cyclodextrin perturbs formation of clathrin-coated endocytic vesicles | Q24657869 | ||
Simultaneous binding of PtdIns(4,5)P2 and clathrin by AP180 in the nucleation of clathrin lattices on membranes | Q27629289 | ||
Structure of the LDL receptor extracellular domain at endosomal pH | Q27640067 | ||
Differential functions of members of the low density lipoprotein receptor family suggested by their distinct endocytosis rates | Q28209002 | ||
Internalization of echovirus 1 in caveolae. | Q39682421 | ||
A novel cell entry pathway for a DAF-using human enterovirus is dependent on lipid rafts | Q39684666 | ||
Conformational Changes, Plasma Membrane Penetration, and Infection by Human Rhinovirus Type 2: Role of Receptors and Low pH | Q39748620 | ||
Uncoating of human rhinovirus serotype 2 from late endosomes | Q40040947 | ||
A distinct class of endosome mediates clathrin-independent endocytosis to the Golgi complex | Q40738477 | ||
Internalization of cholera toxin by different endocytic mechanisms | Q40768765 | ||
Interleukin 2 receptors and detergent-resistant membrane domains define a clathrin-independent endocytic pathway | Q40791242 | ||
Induction of caveolae in the apical plasma membrane of Madin-Darby canine kidney cells | Q40898884 | ||
Early stages of influenza virus entry into Mv-1 lung cells: involvement of dynamin | Q40903864 | ||
Tightly regulated and inducible expression of dominant interfering dynamin mutant in stably transformed HeLa cells | Q41386363 | ||
Vacuolar ATPase activity is required for endosomal carrier vesicle formation | Q41495121 | ||
Infectious entry pathway for canine parvovirus | Q41640746 | ||
The clathrin endocytic pathway in viral infection | Q42651304 | ||
Genetic deficiency in low density lipoprotein receptor-related protein confers cellular resistance to Pseudomonas exotoxin A. Evidence that this protein is required for uptake and degradation of multiple ligands | Q42807171 | ||
Entry pathway of vesicular stomatitis virus into different host cells | Q42992016 | ||
A neutralizing epitope on human rhinovirus type 2 includes amino acid residues between 153 and 164 of virus capsid protein VP2. | Q43838716 | ||
Lipoplex-mediated transfection of mammalian cells occurs through the cholesterol-dependent clathrin-mediated pathway of endocytosis | Q43903254 | ||
Mechanism of entry of human rhinovirus 2 into HeLa cells | Q44926821 | ||
Hantaan virus enters cells by clathrin-dependent receptor-mediated endocytosis | Q45733381 | ||
Involvement of caveolae in the uptake of respiratory syncytial virus antigen by dendritic cells | Q45748328 | ||
A novel role for Rab5-GDI in ligand sequestration into clathrin-coated pits | Q50337405 | ||
LDL receptor-related protein internalizes and degrades uPA-PAI-1 complexes and is essential for embryo implantation | Q52478181 | ||
GPI-anchored proteins are delivered to recycling endosomes via a distinct cdc42-regulated, clathrin-independent pinocytic pathway. | Q53973070 | ||
Inhibition of endocytosis by anti-clathrin antibodies | Q58164318 | ||
Effect of reduced endocytosis induced by hypotonic shock and potassium depletion on the infection of Hep 2 cells by picornaviruses | Q70175500 | ||
Inhibition of clathrin-dependent endocytosis has multiple effects on human rhinovirus serotype 2 cell entry | Q73178513 | ||
The YXXL motif, but not the two NPXY motifs, serves as the dominant endocytosis signal for low density lipoprotein receptor-related protein | Q73626284 | ||
Elevated endosomal pH in HeLa cells overexpressing mutant dynamin can affect infection by pH-sensitive viruses | Q74567141 | ||
Hypercholesterolemia in low density lipoprotein receptor knockout mice and its reversal by adenovirus-mediated gene delivery | Q29615235 | ||
Inhibition of rab5 GTPase activity stimulates membrane fusion in endocytosis | Q29618143 | ||
Induction of mutant dynamin specifically blocks endocytic coated vesicle formation | Q29620182 | ||
Lipid domain structure of the plasma membrane revealed by patching of membrane components | Q29620204 | ||
SH3-domain-containing proteins function at distinct steps in clathrin-coated vesicle formation | Q30175316 | ||
Crystal structure of the amphiphysin-2 SH3 domain and its role in the prevention of dynamin ring formation | Q30176060 | ||
JC virus enters human glial cells by clathrin-dependent receptor-mediated endocytosis. | Q30326112 | ||
Adenovirus internalization and infection require dynamin | Q33783549 | ||
Cellular uptake and infection by canine parvovirus involves rapid dynamin-regulated clathrin-mediated endocytosis, followed by slower intracellular trafficking | Q33797871 | ||
Adaptors for clathrin-mediated traffic | Q33804351 | ||
Dynamin is required for recombinant adeno-associated virus type 2 infection | Q33825510 | ||
Dynamin GTPase domain mutants block endocytic vesicle formation at morphologically distinct stages | Q33946654 | ||
Endocytosis without clathrin coats | Q34092223 | ||
Biogenesis of the sorting endosome: the role of Rab5. | Q34156726 | ||
Depletion of intracellular potassium arrests coated pit formation and receptor-mediated endocytosis in fibroblasts | Q34248300 | ||
Clathrin-binding proteins: got a motif? Join the network! | Q34328624 | ||
Association of the caveola vesicular system with cellular entry by filoviruses | Q34338277 | ||
Clathrin-mediated endocytosis: membrane factors pull the trigger | Q34341954 | ||
Influenza virus can enter and infect cells in the absence of clathrin-mediated endocytosis | Q34348512 | ||
eps15 and eps15R are essential components of the endocytic pathway. | Q34450339 | ||
Clathrin-dependent or not: is it still the question? | Q34669446 | ||
Dissecting virus entry via endocytosis | Q34697258 | ||
Members of the low density lipoprotein receptor family mediate cell entry of a minor-group common cold virus | Q35077224 | ||
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 | ||
The LDL receptor clustering motif interacts with the clathrin terminal domain in a reverse turn conformation | Q36256170 | ||
Dynamin:GTP controls the formation of constricted coated pits, the rate limiting step in clathrin-mediated endocytosis | Q36328657 | ||
Clathrin exchange during clathrin-mediated endocytosis | Q36380009 | ||
Acute cholesterol depletion inhibits clathrin-coated pit budding | Q36380759 | ||
Bound simian virus 40 translocates to caveolin-enriched membrane domains, and its entry is inhibited by drugs that selectively disrupt caveolae | Q37383445 | ||
Very-low-density lipoprotein receptor fragment shed from HeLa cells inhibits human rhinovirus infection | Q38331452 | ||
Effect of bafilomycin A1 and nocodazole on endocytic transport in HeLa cells: implications for viral uncoating and infection | Q39582929 | ||
Role of the cytoplasmic domain of the beta-subunit of integrin alpha(v)beta6 in infection by foot-and-mouth disease virus | Q39602424 | ||
Entry of human parechovirus 1. | Q39607190 | ||
Major and minor receptor group human rhinoviruses penetrate from endosomes by different mechanisms. | Q39642336 | ||
P433 | issue | 9 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | microbiology | Q7193 |
immunology | Q101929 | ||
endocytosis | Q189814 | ||
P1104 | number of pages | 10 | |
P304 | page(s) | 5360-5369 | |
P577 | publication date | 2003-05-01 | |
P1433 | published in | Journal of Virology | Q1251128 |
P1476 | title | Human rhinovirus type 2 is internalized by clathrin-mediated endocytosis | |
Human Rhinovirus Type 2 Is Internalized by Clathrin-Mediated Endocytosis | |||
P478 | volume | 77 |
Q38017490 | Acid-dependent viral entry. |
Q42003294 | Alzheimer's disease gene signature says: beware of brain viral infections |
Q47683169 | Catching the common cold |
Q47444412 | Characterization of rhinovirus subviral A particles via capillary electrophoresis, electron microscopy and gas-phase electrophoretic mobility molecular analysis: Part I. |
Q36510436 | Cholesterol is required for endocytosis and endosomal escape of adenovirus type 2. |
Q47269211 | Cryo-EM Structure of Seneca Valley Virus Procapsid |
Q34120236 | Different rotavirus strains enter MA104 cells through different endocytic pathways: the role of clathrin-mediated endocytosis. |
Q42069725 | Early events in integrin alphavbeta6-mediated cell entry of foot-and-mouth disease virus |
Q30835561 | Echovirus 1 endocytosis into caveosomes requires lipid rafts, dynamin II, and signaling events. |
Q40120364 | Echovirus 6 strains derived from a clinical isolate show differences in haemagglutination ability and cell entry pathway |
Q39720210 | Endocytosis of hepatitis C virus non-enveloped capsid-like particles induces MAPK-ERK1/2 signaling events. |
Q39603603 | Entry of a heparan sulphate-binding HRV8 variant strictly depends on dynamin but not on clathrin, caveolin, and flotillin |
Q42252543 | Entry of human rhinovirus 89 via ICAM-1 into HeLa epithelial cells is inhibited by actin skeleton disruption and by bafilomycin |
Q35077445 | Entry of tiger frog virus (an Iridovirus) into HepG2 cells via a pH-dependent, atypical, caveola-mediated endocytosis pathway |
Q39744139 | Human rhinovirus 14 enters rhabdomyosarcoma cells expressing icam-1 by a clathrin-, caveolin-, and flotillin-independent pathway |
Q43153233 | Human rhinovirus type 2 uncoating at the plasma membrane is not affected by a pH gradient but is affected by the membrane potential |
Q40624785 | Human rhinovirus type 2-antibody complexes enter and infect cells via Fc-gamma receptor IIB1. |
Q36943799 | Human rhinovirus-induced inflammatory responses are inhibited by phosphatidylserine containing liposomes |
Q40686820 | ICAM-1 Binding Rhinoviruses A89 and B14 Uncoat in Different Endosomal Compartments |
Q40262541 | ICAM-1 Binding Rhinoviruses Enter HeLa Cells via Multiple Pathways and Travel to Distinct Intracellular Compartments for Uncoating |
Q40546017 | Identification of the human rhinovirus serotype 1A binding site on the murine low-density lipoprotein receptor by using human-mouse receptor chimeras |
Q46246174 | Impairing the function of MLCK, myosin Va or myosin Vb disrupts Rhinovirus B14 replication. |
Q38838830 | Inhibition of endocytic pathways impacts cytomegalovirus maturation. |
Q36242115 | Interactions between virus proteins and host cell membranes during the viral life cycle |
Q30478844 | Internalization of novel non-viral vector TAT-streptavidin into human cells |
Q39882487 | Internalization of swine vesicular disease virus into cultured cells: a comparative study with foot-and-mouth disease virus. |
Q42850509 | Liposomal nanocontainers as models for viral infection: monitoring viral genomic RNA transfer through lipid membranes. |
Q41863567 | Low pH-triggered beta-propeller switch of the low-density lipoprotein receptor assists rhinovirus infection |
Q35041004 | Mechanisms of single-stranded phosphorothioate modified antisense oligonucleotide accumulation in hepatocytes |
Q36976819 | Multiple receptors involved in human rhinovirus attachment to live cells |
Q41497346 | N- and 6-O-sulfated heparan sulfates mediate internalization of coxsackievirus B3 variant PD into CHO-K1 cells |
Q107111822 | NPC1-regulated dynamic of clathrin-coated pits is essential for viral entry |
Q28255965 | Neutralization of a common cold virus by concatemers of the third ligand binding module of the VLDL-receptor strongly depends on the number of modules |
Q40334830 | Nonneutralizing human rhinovirus serotype 2-specific monoclonal antibody 2G2 attaches to the region that undergoes the most dramatic changes upon release of the viral RNA. |
Q34847784 | Oropouche virus entry into HeLa cells involves clathrin and requires endosomal acidification |
Q41619024 | Picornaviruses |
Q28074854 | Principles of Virus Uncoating: Cues and the Snooker Ball |
Q40090477 | Productive entry of type C foot-and-mouth disease virus into susceptible cultured cells requires clathrin and is dependent on the presence of plasma membrane cholesterol |
Q42090065 | Productive entry pathways of human rhinoviruses |
Q34474526 | Proteomic analysis of host brain components that bind to infectious particles in Creutzfeldt-Jakob disease |
Q43112390 | Recombinant VP4 of human rhinovirus induces permeability in model membranes |
Q38172661 | Rhinoviral infection and asthma: the detection and management of rhinoviruses by airway epithelial cells. |
Q38166378 | Rhinovirus-Induced Exacerbations of Asthma and COPD. |
Q38767263 | Rhinoviruses and Their Receptors: Implications for Allergic Disease |
Q40413356 | Role of clathrin-mediated endocytosis during vesicular stomatitis virus entry into host cells |
Q39043135 | Role of endocytic uptake in transfection efficiency of solid lipid nanoparticles-based nonviral vectors |
Q39190363 | The Unresolved Role of Interferon-λ in Asthma Bronchiale |
Q37962258 | The cell biology of receptor-mediated virus entry |
Q33842994 | The minor receptor group of human rhinovirus (HRV) includes HRV23 and HRV25, but the presence of a lysine in the VP1 HI loop is not sufficient for receptor binding |
Q36686322 | Therapeutic and prophylactic activity of itraconazole against human rhinovirus infection in a murine model |
Q47344196 | Twelve receptor molecules attach per viral particle of human rhinovirus serotype 2 via multiple modules |
Q26750146 | Viral entry pathways: the example of common cold viruses |
Q31115290 | Viral uncoating is directional: exit of the genomic RNA in a common cold virus starts with the poly-(A) tail at the 3'-end |