review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Ludger Johannes | Q33116275 |
Christophe Lamaze | Q56561595 | ||
P2093 | author name string | Christophe Lamaze | |
Ludger Johannes | |||
P2860 | cites work | Extraction of cholesterol with methyl-beta-cyclodextrin perturbs formation of clathrin-coated endocytic vesicles | Q24657869 |
Early/recycling endosomes-to-TGN transport involves two SNARE complexes and a Rab6 isoform | Q24671033 | ||
AP-2/Eps15 interaction is required for receptor-mediated endocytosis | Q24683348 | ||
Functional rafts in cell membranes | Q27860768 | ||
Endocytosis is required for the growth of vacuolar H(+)-ATPase-defective yeast: identification of six new END genes | Q27934841 | ||
Dynamic association of human insulin receptor with lipid rafts in cells lacking caveolae | Q28343941 | ||
Lipid rafts reconstituted in model membranes | Q28353906 | ||
Functionally different GPI proteins are organized in different domains on the neuronal surface | Q28580230 | ||
Sorting of GPI-anchored proteins to glycolipid-enriched membrane subdomains during transport to the apical cell surface | Q29547857 | ||
Loss of caveolae, vascular dysfunction, and pulmonary defects in caveolin-1 gene-disrupted mice | Q29615180 | ||
Endocytosis and molecular sorting | Q29616706 | ||
Caveolin, a protein component of caveolae membrane coats | Q29619795 | ||
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 | ||
Caveolar endocytosis of simian virus 40 reveals a new two-step vesicular-transport pathway to the ER | Q29620552 | ||
Caveolae are highly immobile plasma membrane microdomains, which are not involved in constitutive endocytic trafficking | Q30857066 | ||
Intracellular targeting of the endoplasmic reticulum/nuclear envelope by retrograde transport may determine cell hypersensitivity to verotoxin via globotriaosyl ceramide fatty acid isoform traffic | Q48254988 | ||
Rac is required for constitutive macropinocytosis by dendritic cells but does not control its downregulation. | Q52166799 | ||
Caveolar internalization of growth hormone. | Q52533318 | ||
Involvement of cellular caveolae in bacterial entry into mast cells. | Q52540262 | ||
Endocytosis | Q57374715 | ||
Endothelial caveolae have the molecular transport machinery for vesicle budding, docking, and fusion including VAMP, NSF, SNAP, annexins, and GTPases | Q72315760 | ||
Organized endothelial cell surface signal transduction in caveolae distinct from glycosylphosphatidylinositol-anchored protein microdomains | Q73119457 | ||
pH-independent retrograde targeting of glycolipids to the Golgi complex | Q74254690 | ||
Membrane microdomains and caveolae | Q33712427 | ||
Constitutive macropinocytosis in oncogene-transformed fibroblasts depends on sequential permanent activation of phosphoinositide 3-kinase and phospholipase C. | Q33845148 | ||
Membrane rafts and signaling by the multichain immune recognition receptors | Q33898940 | ||
Auditory feedback in learning and maintenance of vocal behaviour. | Q33938389 | ||
Targeting of Shiga toxin B-subunit to retrograde transport route in association with detergent-resistant membranes | Q33944092 | ||
Distinction between signaling mechanisms in lipid rafts vs. caveolae | Q33950363 | ||
Function of Rho family proteins in actin dynamics during phagocytosis and engulfment | Q34056991 | ||
Selective inhibition of adaptor complex-mediated vesiculation | Q34156651 | ||
The endocytic pathway: a mosaic of domains | Q34389525 | ||
The recycling endosome of Madin-Darby canine kidney cells is a mildly acidic compartment rich in raft components | Q34745959 | ||
SNARE proteins are highly enriched in lipid rafts in PC12 cells: implications for the spatial control of exocytosis. | Q35888471 | ||
YOLK PROTEIN UPTAKE IN THE OOCYTE OF THE MOSQUITO AEDES AEGYPTI. L | Q36186016 | ||
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 | ||
Filipin-dependent inhibition of cholera toxin: evidence for toxin internalization and activation through caveolae-like domains | Q36255404 | ||
An endocytosed TGN38 chimeric protein is delivered to the TGN after trafficking through the endocytic recycling compartment in CHO cells. | Q36255652 | ||
Direct pathway from early/recycling endosomes to the Golgi apparatus revealed through the study of shiga toxin B-fragment transport | Q36255884 | ||
Involvement of the ubiquitin/proteasome system in sorting of the interleukin 2 receptor beta chain to late endocytic compartments | Q36280110 | ||
Endocytic sorting of lipid analogues differing solely in the chemistry of their hydrophobic tails. | Q36293356 | ||
Rapid cycling of lipid raft markers between the cell surface and Golgi complex | Q36360365 | ||
Legionella pneumophila is internalized by a macropinocytotic uptake pathway controlled by the Dot/Icm system and the mouse Lgn1 locus | Q36369590 | ||
Phosphatidylinositol 4,5-bisphosphate and Arf6-regulated membrane traffic. | Q36376901 | ||
Acute cholesterol depletion inhibits clathrin-coated pit budding | Q36380759 | ||
Raft association of SNAP receptors acting in apical trafficking in Madin-Darby canine kidney cells | Q36450084 | ||
Sorting of sphingolipids in epithelial (Madin-Darby canine kidney) cells | Q36472379 | ||
Endocytosis without clathrin (a minireview). | Q37324831 | ||
Human immunodeficiency virus type 1 entry into macrophages mediated by macropinocytosis | Q39605166 | ||
TGN38/41 recycles between the cell surface and the TGN: brefeldin A affects its rate of return to the TGN. | Q40365311 | ||
Rapid stimulation of pinocytosis in human carcinoma cells A-431 by epidermal growth factor | Q40729001 | ||
Immunoelectron microscopic localization of cholesterol using biotinylated and non-cytolytic perfringolysin O. | Q40762561 | ||
Interleukin 2 receptors and detergent-resistant membrane domains define a clathrin-independent endocytic pathway | Q40791242 | ||
Surfing on a retrograde wave: how does Shiga toxin reach the endoplasmic reticulum? | Q40847412 | ||
Retention of prominin in microvilli reveals distinct cholesterol-based lipid micro-domains in the apical plasma membrane. | Q40855892 | ||
Induction of caveolae in the apical plasma membrane of Madin-Darby canine kidney cells | Q40898884 | ||
Activation of Src family kinase yes induced by Shiga toxin binding to globotriaosyl ceramide (Gb3/CD77) in low density, detergent-insoluble microdomains | Q40915784 | ||
Regulated migration of epidermal growth factor receptor from caveolae | Q40923075 | ||
Role of lipid modifications in targeting proteins to detergent-resistant membrane rafts. Many raft proteins are acylated, while few are prenylated. | Q40977491 | ||
Endocytosis, intracellular transport, and cytotoxic action of Shiga toxin and ricin | Q41169583 | ||
Regulated internalization of caveolae | Q41418184 | ||
Capture and processing of exogenous antigens for presentation on MHC molecules. | Q41464375 | ||
Endocytosis from coated pits of Shiga toxin: a glycolipid-binding protein from Shigella dysenteriae 1. | Q41575546 | ||
Distinct endocytotic pathways in epidermal growth factor-stimulated human carcinoma A431 cells | Q41592405 | ||
Toxin entry: retrograde transport through the secretory pathway | Q41705146 | ||
EFA6, a sec7 domain-containing exchange factor for ARF6, coordinates membrane recycling and actin cytoskeleton organization | Q41819398 | ||
Clathrin-dependent and -independent internalization of plasma membrane sphingolipids initiates two Golgi targeting pathways | Q41981023 | ||
Caveolin-1 is a negative regulator of caveolae-mediated endocytosis to the endoplasmic reticulum | Q42823399 | ||
P433 | issue | 7 | |
P304 | page(s) | 443-451 | |
P577 | publication date | 2002-07-01 | |
P1433 | published in | Traffic | Q1572846 |
P1476 | title | Clathrin-dependent or not: is it still the question? | |
P478 | volume | 3 |
Q40325555 | 9-O-acetylation of exogenously added ganglioside GD3. The GD3 molecule induces its own O-acetylation machinery |
Q37838443 | A comparison of peptide and folate receptor targeting of cancer cells: from single agent to nanoparticle |
Q28253785 | A heparan sulfate-facilitated and raft-dependent macropinocytosis of eosinophil cationic protein |
Q57184168 | A novel luminescent bifunctional POSS as a molecular platform for biomedical applications |
Q36582968 | Adaptor protein complex 2-mediated, clathrin-dependent endocytosis, and related gene activities, are a prominent feature during maturation stage amelogenesis |
Q40481969 | Agonist-induced endocytosis of CC chemokine receptor 5 is clathrin dependent. |
Q36899294 | Alternate routes for drug delivery to the cell interior: pathways to the Golgi apparatus and endoplasmic reticulum |
Q38997400 | Antimicrobial chitosan nanodroplets: new insights for ultrasound-mediated adjuvant treatment of skin infection. |
Q38315978 | Assays for functional properties of Rab34 in macropinosome formation |
Q57374304 | Association of Yeast Transporters with Detergent-Resistant Membranes Correlates with Their Cell-Surface Location |
Q36624085 | Bacterial protein toxins and lipids: role in toxin targeting and activity |
Q39008986 | Bluetongue virus entry into cells |
Q79263707 | Bradykinin shifts endothelial fluid passage from para- to transcellular routes |
Q35138171 | Caveolae/raft-dependent endocytosis |
Q35057320 | Caveolae: anchored, multifunctional platforms in the lipid ocean |
Q37747047 | Cellular endocytosis and gene delivery |
Q36032645 | Cellular stress failure in ventilator-injured lungs |
Q37031515 | Characterization of a nonclathrin endocytic pathway: membrane cargo and lipid requirements |
Q36510436 | Cholesterol is required for endocytosis and endosomal escape of adenovirus type 2. |
Q34311540 | Clathrin adaptor epsinR is required for retrograde sorting on early endosomal membranes |
Q36321346 | Clathrin- and caveolin-1-independent endocytosis: entry of simian virus 40 into cells devoid of caveolae |
Q37014909 | Clathrin-independent internalization and recycling |
Q35127933 | Control of vesicular trafficking by Rho GTPases |
Q33730191 | DNA-encapsulated magnesium phosphate nanoparticles elicit both humoral and cellular immune responses in mice |
Q35001873 | Distinct mechanisms of clathrin-independent endocytosis have unique sphingolipid requirements |
Q33782857 | Early steps of clathrin-mediated endocytosis involved in phagosomal escape of Fcgamma receptor-targeted adenovirus |
Q34178947 | Effects of cholesterol on CCK-1 receptors and caveolin-3 proteins recycling in human gallbladder muscle |
Q40058864 | Electropermeabilization of endocytotic vesicles in B16 F1 mouse melanoma cells |
Q35153223 | Endocytic trafficking of glycosphingolipids in sphingolipid storage diseases |
Q35032078 | Endocytosis and sorting of glycosphingolipids in sphingolipid storage disease |
Q38099153 | Endocytosis of gene delivery vectors: from clathrin-dependent to lipid raft-mediated endocytosis |
Q34708980 | Endocytosis of titanium dioxide nanoparticles in prostate cancer PC-3M cells. |
Q46958375 | Evidence for a clathrin-mediated recycling of albumin in human term placenta |
Q37207271 | Exploiting lipid raft transport with membrane targeted nanoparticles: a strategy for cytosolic drug delivery |
Q34325683 | Extracellular signal-regulated kinase regulates clathrin-independent endosomal trafficking |
Q40088007 | Formyl peptide-receptor like-1 requires lipid raft and extracellular signal-regulated protein kinase to activate inhibitor-kappa B kinase in human U87 astrocytoma cells |
Q36810273 | Gene delivery to vascular endothelium using chemical vectors: implications for cardiovascular gene therapy |
Q24564896 | HIV-1 Tat enters T cells using coated pits before translocating from acidified endosomes and eliciting biological responses |
Q30164778 | Human Rhinovirus Type 2 Is Internalized by Clathrin-Mediated Endocytosis |
Q24647570 | Identification of a developmentally regulated pathway of membrane retrieval in neuronal growth cones |
Q35406238 | Imaging the intracellular degradation of biodegradable polymer nanoparticles |
Q33483363 | In vitro intracellular trafficking of virulence antigen during infection by Yersinia pestis. |
Q34348512 | Influenza virus can enter and infect cells in the absence of clathrin-mediated endocytosis |
Q36118043 | Inhibition of caveolar uptake, SV40 infection, and beta1-integrin signaling by a nonnatural glycosphingolipid stereoisomer |
Q35189406 | Insider information: what viruses tell us about endocytosis |
Q43415353 | Interferon-inducible transmembrane proteins of the innate immune response act as membrane organizers by influencing clathrin and v-ATPase localization and function |
Q28479259 | Interleukin-4 alters early phagosome phenotype by modulating class I PI3K dependent lipid remodeling and protein recruitment |
Q37174499 | Internalization of the opioid growth factor, [Met5]-enkephalin, is dependent on clathrin-mediated endocytosis for downregulation of cell proliferation |
Q33721938 | Investigation of endocytosis and cytotoxicity of poly-d, l-lactide-poly(ethylene glycol) micro/nano-particles in osteoblast cells |
Q37869242 | Lipid rafts, caveolae, caveolin-1, and entry by Chlamydiae into host cells |
Q35189398 | Lipids in endocytic membrane transport and sorting |
Q39570673 | Macropinocytosis inhibitors and Arf6 regulate ErbB3 nuclear localization in prostate cancer cells |
Q28088286 | Macropinocytosis: a pathway to protozoan infection |
Q36924383 | Macropinocytosis: searching for an endocytic identity and role in the uptake of cell penetrating peptides |
Q34370155 | Mechanism of uptake and incorporation of the non-human sialic acid N-glycolylneuraminic acid into human cells |
Q36447793 | Membrane microdomains, caveolae, and caveolar endocytosis of sphingolipids |
Q45038661 | Membrane retrieval in neutrophils during phagocytosis: inhibition by M protein-expressing S. pyogenes bacteria |
Q24338142 | Metabolism of vertebrate amino sugars with N-glycolyl groups: elucidating the intracellular fate of the non-human sialic acid N-glycolylneuraminic acid |
Q34717590 | Mycoplasma pneumoniae CARDS toxin is internalized via clathrin-mediated endocytosis |
Q37058812 | Nanovehicular intracellular delivery systems |
Q81249836 | Non-genomic steroid effects: merging membrane fluidity and receptor-mediated responses |
Q30381073 | Non-viral gene delivery using nanoparticles. |
Q34150166 | Parvovirus infection of cells by using variants of the feline transferrin receptor altering clathrin-mediated endocytosis, membrane domain localization, and capsid-binding domains |
Q36602254 | Pathogen recognition and development of particulate vaccines: does size matter? |
Q37115553 | Peptide-functionalized poly(ethylene glycol) star polymers: DNA delivery vehicles with multivalent molecular architecture |
Q40217887 | Poly-L-lysine-coated nanoparticles: a potent delivery system to enhance DNA vaccine efficacy |
Q36132002 | Protein toxins: intracellular trafficking for targeted therapy. |
Q37350410 | Protein trafficking in polarized cells |
Q47795586 | Proteomic analysis of clathrin interactions in trypanosomes reveals dynamic evolution of endocytosis. |
Q36095722 | RAB-10 regulates glutamate receptor recycling in a cholesterol-dependent endocytosis pathway |
Q30481387 | RNA interference in J774 macrophages reveals a role for coronin 1 in mycobacterial trafficking but not in actin-dependent processes |
Q24561595 | Rab22a regulates the recycling of membrane proteins internalized independently of clathrin |
Q24316875 | Rabenosyn-5 and EHD1 interact and sequentially regulate protein recycling to the plasma membrane |
Q28477472 | Rapid internalization of the oncogenic K+ channel K(V)10.1 |
Q42858237 | Regulation of sodium pump endocytosis by cardiotonic steroids: Molecular mechanisms and physiological implications |
Q33841378 | Relationships between EGFR signaling-competent and endocytosis-competent membrane microdomains |
Q40413356 | Role of clathrin-mediated endocytosis during vesicular stomatitis virus entry into host cells |
Q24561585 | SGEF, a RhoG guanine nucleotide exchange factor that stimulates macropinocytosis |
Q33693031 | Secreted luciferase for in vivo evaluation of systemic protein delivery in mice |
Q36803842 | Separate endocytic pathways regulate IL-5 receptor internalization and signaling |
Q34719609 | Shiga toxin induces tubular membrane invaginations for its uptake into cells |
Q35118772 | Sliding doors: clathrin-coated pits or caveolae? |
Q41668344 | Stat-mediated signaling induced by type I and type II interferons (IFNs) is differentially controlled through lipid microdomain association and clathrin-dependent endocytosis of IFN receptors |
Q28119105 | Syntaxin 1B suppresses macropinocytosis and semaphorin 3A-induced growth cone collapse |
Q45286133 | TGFalpha expression impairs Trastuzumab-induced HER2 downregulation |
Q40184296 | Temperature-, concentration- and cholesterol-dependent translocation of L- and D-octa-arginine across the plasma and nuclear membrane of CD34+ leukaemia cells. |
Q24652273 | The GTPase-activating protein GRAF1 regulates the CLIC/GEEC endocytic pathway |
Q41532049 | The effects of collagen-rich extracellular matrix on the intracellular delivery of glycol chitosan nanoparticles in human lung fibroblasts |
Q34535813 | The kidney in vitamin B12 and folate homeostasis: characterization of receptors for tubular uptake of vitamins and carrier proteins |
Q35746736 | The uroepithelium: not just a passive barrier |
Q97885914 | Toxoplasma gondii Mechanisms of Entry Into Host Cells |
Q39428872 | Transferrin adsorption onto PLGA nanoparticles governs their interaction with biological systems from blood circulation to brain cancer cells |
Q37386413 | Tumour microenvironment-responsive lipoic acid nanoparticles for targeted delivery of docetaxel to lung cancer |
Q40326559 | Venezuelan equine encephalitis virus entry mechanism requires late endosome formation and resists cell membrane cholesterol depletion |
Q37359629 | Vesicle formation and endocytosis: function, machinery, mechanisms, and modeling |
Q37422827 | Why does endocytosis in single cells care which side up? |
Q54918559 | ‘Caveolae’ Review Series. |
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