scholarly article | Q13442814 |
P50 | author | Tomohiko Taguchi | Q57429156 |
Stephen S. Francis | Q57948781 | ||
P2093 | author name string | Heike Fölsch | |
Ira Mellman | |||
Marc Pypaert | |||
Graham Warren | |||
Agnes Lee Ang | |||
Lindsay J Murrells | |||
P2860 | cites work | Mu1B, a novel adaptor medium chain expressed in polarized epithelial cells | Q22010072 |
Differential recognition of tyrosine-based basolateral signals by AP-1B subunit mu1B in polarized epithelial cells | Q24530204 | ||
Rab11 Is Required for Trans-Golgi Network–to–Plasma Membrane Transport and a Preferential Target for GDP Dissociation Inhibitor | Q24657725 | ||
Distribution and function of AP-1 clathrin adaptor complexes in polarized epithelial cells | Q24670526 | ||
Rab11 regulates the compartmentalization of early endosomes required for efficient transport from early endosomes to the trans-golgi network | Q24681074 | ||
Rab11 regulates recycling through the pericentriolar recycling endosome | Q24681897 | ||
A novel clathrin adaptor complex mediates basolateral targeting in polarized epithelial cells | Q28146062 | ||
Sorting of mannose 6-phosphate receptors mediated by the GGAs | Q28198872 | ||
Binding of GGA2 to the lysosomal enzyme sorting motif of the mannose 6-phosphate receptor | Q28198896 | ||
Sec6/8 complex is recruited to cell-cell contacts and specifies transport vesicle delivery to the basal-lateral membrane in epithelial cells | Q28273946 | ||
Association of Rab25 and Rab11a with the apical recycling system of polarized Madin-Darby canine kidney cells | Q28293127 | ||
Signals for sorting of transmembrane proteins to endosomes and lysosomes | Q29547469 | ||
Distinct membrane domains on endosomes in the recycling pathway visualized by multicolor imaging of Rab4, Rab5, and Rab11 | Q29615018 | ||
Origins of cell polarity | Q29616587 | ||
The biogenesis of lysosomes | Q29617860 | ||
The epithelial-specific adaptor AP1B mediates post-endocytic recycling to the basolateral membrane. | Q30331083 | ||
Biosynthetic transport of the asialoglycoprotein receptor H1 to the cell surface occurs via endosomes | Q33818978 | ||
Interactions between the exocytic and endocytic pathways in polarized Madin-Darby canine kidney cells | Q33901782 | ||
Membrane traffic in polarized epithelial cells | Q33954492 | ||
The trans Golgi network: sorting at the exit site of the Golgi complex. | Q34562583 | ||
Polarized delivery of viral glycoproteins to the apical and basolateral plasma membranes of Madin-Darby canine kidney cells infected with temperature-sensitive viruses | Q36211738 | ||
Biogenesis of the rat hepatocyte plasma membrane in vivo: comparison of the pathways taken by apical and basolateral proteins using subcellular fractionation | Q36217504 | ||
Distinct transport vesicles mediate the delivery of plasma membrane proteins to the apical and basolateral domains of MDCK cells | Q36223778 | ||
Apical and basolateral endosomes of MDCK cells are interconnected and contain a polarized sorting mechanism | Q36237485 | ||
In polarized MDCK cells basolateral vesicles arise from clathrin-gamma-adaptin-coated domains on endosomal tubules | Q36255343 | ||
Kinetic analysis of secretory protein traffic and characterization of golgi to plasma membrane transport intermediates in living cells | Q36256009 | ||
The Rab8 GTPase selectively regulates AP-1B-dependent basolateral transport in polarized Madin-Darby canine kidney cells | Q36324557 | ||
The AP-1A and AP-1B clathrin adaptor complexes define biochemically and functionally distinct membrane domains | Q36324568 | ||
Sec6/8 complexes on trans-Golgi network and plasma membrane regulate late stages of exocytosis in mammalian cells | Q36380060 | ||
A subset of yeast vacuolar protein sorting mutants is blocked in one branch of the exocytic pathway | Q36381155 | ||
Delivery of raft-associated, GPI-anchored proteins to the apical surface of polarized MDCK cells by a transcytotic pathway | Q40572614 | ||
Multicolour imaging of post-Golgi sorting and trafficking in live cells | Q40827648 | ||
The receptor recycling pathway contains two distinct populations of early endosomes with different sorting functions | Q40962892 | ||
How MHC class II molecules acquire peptide cargo: biosynthesis and trafficking through the endocytic pathway | Q41020969 | ||
Inhibition of Endosome Function in CHO Cells Bearing a Temperature-sensitive Defect in the Coatomer (COPI) Component ε-COP | Q41067848 | ||
Characterization of transport of newly assembled, T cell-stimulatory MHC class II-peptide complexes from MHC class II compartments to the cell surface | Q41099576 | ||
Pinocytosis in fibroblasts. Quantitative studies in vitro | Q41189675 | ||
Newly synthesized transferrin receptors can be detected in the endosome before they appear on the cell surface. | Q41346894 | ||
Exit of newly synthesized membrane proteins from the trans cisterna of the Golgi complex to the plasma membrane | Q41480685 | ||
Common signals control low density lipoprotein receptor sorting in endosomes and the Golgi complex of MDCK cells | Q41526657 | ||
The pathways of endocytosed transferrin and secretory protein are connected in the trans-Golgi reticulum | Q41553200 | ||
Quo vadis: polarized membrane recycling in motility and phagocytosis | Q42919592 | ||
Basolateral sorting of LDL receptor in MDCK cells: the cytoplasmic domain contains two tyrosine-dependent targeting determinants | Q43610720 | ||
Comparison of the intracellular pathways of transferrin recycling and vesicular stomatitis virus membrane glycoprotein exocytosis by ultrastructural double-label cytochemistry | Q45835591 | ||
Dendritic cell maturation triggers retrograde MHC class II transport from lysosomes to the plasma membrane | Q50335826 | ||
Brefeldin A rapidly disrupts plasma membrane polarity by blocking polar sorting in common endosomes of MDCK cells | Q52544265 | ||
Biochemical sub-fractionation of the mammalian Golgi apparatus | Q73314717 | ||
AP-1B: polarized sorting at the endosome | Q79333326 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 531-543 | |
P577 | publication date | 2004-11-01 | |
P1433 | published in | Journal of Cell Biology | Q1524550 |
P1476 | title | Recycling endosomes can serve as intermediates during transport from the Golgi to the plasma membrane of MDCK cells | |
P478 | volume | 167 |
Q37512358 | A Novel Type III Endosome Transmembrane Protein, TEMP. |
Q39495520 | A PDMS-based biochip with integrated sub-micrometre position control for TIRF microscopy of the apical cell membrane |
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Q35616362 | AP1B sorts basolateral proteins in recycling and biosynthetic routes of MDCK cells |
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Q36308953 | Adaptor protein 1 complexes regulate intracellular trafficking of the kidney anion exchanger 1 in epithelial cells |
Q34396154 | Adaptor proteins involved in polarized sorting |
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Q36173957 | Antibody to AP1B adaptor blocks biosynthetic and recycling routes of basolateral proteins at recycling endosomes |
Q37634760 | Apical trafficking in epithelial cells: signals, clusters and motors |
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Q30427801 | Arf6 regulates AP-1B-dependent sorting in polarized epithelial cells |
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Q41851578 | Basolateral EGF receptor sorting regulated by functionally distinct mechanisms in renal epithelial cells |
Q47094833 | Basolateral delivery of the type I transforming growth factor beta receptor is mediated by a dominant-acting cytoplasmic motif. |
Q50116932 | Budding Yeast Has a Minimal Endomembrane System. |
Q38207963 | C. elegans as a model for membrane traffic |
Q89599347 | CDKI-73 is a Novel Pharmacological Inhibitor of Rab11 Cargo Delivery and Innate Immune Secretion |
Q27333071 | CED-10/Rac1 regulates endocytic recycling through the RAB-5 GAP TBC-2 |
Q43871029 | Caenorhabditis elegans screen reveals role of PAR-5 in RAB-11-recycling endosome positioning and apicobasal cell polarity |
Q36734480 | Cdc42 and Cellular Polarity: Emerging Roles at the Golgi |
Q35780286 | Cdc42 and Rab8a are critical for intestinal stem cell division, survival, and differentiation in mice |
Q37144188 | Cell models for studying renal physiology |
Q61067846 | Chapter 14 Mechanisms of Polarized Sorting of GPI-anchored Proteins in Epithelial Cells |
Q53514288 | Chondroitin Sulfate Accelerates Trans-Golgi-to-Surface Transport of Proteoglycan Amyloid Precursor Protein |
Q39809153 | Class I Rab11-family interacting proteins are binding targets for the Rab14 GTPase |
Q37083539 | Clathrin adaptor AP-1 complex excludes multiple postsynaptic receptors from axons in C. elegans |
Q37620955 | Clathrin and AP1B: key roles in basolateral trafficking through trans-endosomal routes |
Q41730148 | Clathrin-dependent and independent endocytic pathways in tobacco protoplasts revealed by labelling with charged nanogold |
Q30491705 | Clustering and lateral concentration of raft lipids by the MAL protein |
Q41979051 | Cofilin recruits F-actin to SPCA1 and promotes Ca2+-mediated secretory cargo sorting |
Q30447603 | Compartmentalizing the neuronal plasma membrane from axon initial segments to synapses |
Q24311880 | Consortin, a trans-Golgi network cargo receptor for the plasma membrane targeting and recycling of connexins |
Q36015653 | Coordinated protein sorting, targeting and distribution in polarized cells |
Q27967674 | Coordination of Rab8 and Rab11 in primary ciliogenesis |
Q30010252 | Cortactin controls cell motility and lamellipodial dynamics by regulating ECM secretion |
Q36515646 | Crag regulates epithelial architecture and polarized deposition of basement membrane proteins in Drosophila |
Q37874392 | Cytokine release from innate immune cells: association with diverse membrane trafficking pathways |
Q41918926 | Differential Regulation of Lipoprotein and Hepatitis C Virus Secretion by Rab1b |
Q35950439 | Differential involvement of endocytic compartments in the biosynthetic traffic of apical proteins |
Q39599824 | Differential sorting and Golgi export requirements for raft-associated and raft-independent apical proteins along the biosynthetic pathway |
Q34233404 | Direct interaction with Rab11a targets the epithelial Ca2+ channels TRPV5 and TRPV6 to the plasma membrane |
Q92127713 | Direct trafficking pathways from the Golgi apparatus to the plasma membrane |
Q35694035 | Disruption of Kv1.3 Channel Forward Vesicular Trafficking by Hypoxia in Human T Lymphocytes |
Q34370963 | Diverse autophagosome membrane sources coalesce in recycling endosomes. |
Q37036266 | Drosophila Pkaap regulates Rab4/Rab11-dependent traffic and Rab11 exocytosis of innate immune cargo |
Q36337026 | Dual pulse-chase microscopy reveals early divergence in the biosynthetic trafficking of the Na,K-ATPase and E-cadherin |
Q24294520 | Dynamin-like protein 1 at the Golgi complex: A novel component of the sorting/targeting machinery en route to the plasma membrane |
Q98469298 | EH domain binding protein 1-like 1 (EHBP1L1), a protein with calponin homology domain, is expressed in the rat testis |
Q34063804 | EHBP-1 functions with RAB-10 during endocytic recycling in Caenorhabditis elegans |
Q40034519 | EHBP1L1 coordinates Rab8 and Bin1 to regulate apical-directed transport in polarized epithelial cells |
Q89696762 | ER-to-Golgi Trafficking and Its Implication in Neurological Diseases |
Q42002722 | Effects of colchicine on localization of alkaline phosphatase in McA-RH 7777 rat hepatoma cells |
Q38119533 | Emerging Role of the Scaffolding Protein Dlg1 in Vesicle Trafficking |
Q37626900 | Emerging new roles of the pre-Golgi intermediate compartment in biosynthetic-secretory trafficking |
Q38102669 | Emerging roles of recycling endosomes |
Q24324156 | Endosomal SNARE proteins regulate CFTR activity and trafficking in epithelial cells |
Q37410089 | Epithelial cell surface polarity: the early steps. |
Q30441348 | Epithelial polarity requires septin coupling of vesicle transport to polyglutamylated microtubules. |
Q36321307 | Essential function of Drosophila Sec6 in apical exocytosis of epithelial photoreceptor cells |
Q35055724 | Essential roles of snap-29 in C. elegans |
Q39620387 | Exit of intracellular Porphyromonas gingivalis from gingival epithelial cells is mediated by endocytic recycling pathway |
Q37114569 | Exiting the Golgi complex |
Q36016985 | Exocyst requirement for endocytic traffic directed toward the apical and basolateral poles of polarized MDCK cells |
Q27938814 | Exomer: A coat complex for transport of select membrane proteins from the trans-Golgi network to the plasma membrane in yeast |
Q33949717 | Expression of Gpr177, a Wnt trafficking regulator, in mouse embryogenesis |
Q34443468 | FAPP2 is involved in the transport of apical cargo in polarized MDCK cells |
Q30574585 | Four-dimensional live imaging of apical biosynthetic trafficking reveals a post-Golgi sorting role of apical endosomal intermediates |
Q24321757 | Functional dissection of Rab GTPases involved in primary cilium formation |
Q35723855 | Functional symmetry of endomembranes |
Q30480379 | GPI-anchored proteins are directly targeted to the apical surface in fully polarized MDCK cells |
Q94447900 | GRAF2, WDR44, and MICAL1 mediate Rab8/10/11-dependent export of E-cadherin, MMP14, and CFTR ΔF508 |
Q34339120 | Galectin-4-mediated transcytosis of transferrin receptor. |
Q64054287 | Gene replacement therapy in a model of Charcot-Marie-Tooth 4C neuropathy |
Q34509747 | Global ablation of the mouse Rab11a gene impairs early embryogenesis and matrix metalloproteinase secretion |
Q57356472 | Golgi apparatus and epithelial cell polarity |
Q42286457 | Golgi-independent secretory trafficking through recycling endosomes in neuronal dendrites and spines |
Q46633545 | H-Ras dynamically interacts with recycling endosomes in CHO-K1 cells: involvement of Rab5 and Rab11 in the trafficking of H-Ras to this pericentriolar endocytic compartment. |
Q30419350 | Harnessing the power of the endosome to regulate neural development |
Q36753332 | Helping Wingless take flight: how WNT proteins are secreted |
Q36972087 | Hepatocyte Polarity |
Q24658390 | How are the cellular functions of myosin VI regulated within the cell? |
Q37035334 | How many ways through the Golgi maze? |
Q79615611 | Inefficient targeting to the endoplasmic reticulum by the signal recognition particle elicits selective defects in post-ER membrane trafficking |
Q38981236 | Influenza A virus hemagglutinin and neuraminidase mutually accelerate their apical targeting through clustering of lipid rafts |
Q42202859 | Innate immunity and exocytosis of antimicrobial peptides |
Q41826218 | Interactions between Rab and Arf GTPases regulate endosomal phosphatidylinositol-4,5-bisphosphate during endocytic recycling |
Q27673759 | Intracellular phosphatidylserine is essential for retrograde membrane traffic through endosomes |
Q37095269 | Iterative sorting of apical and basolateral cargo in Madin-Darby canine kidney cells |
Q58170925 | Itinerary of vesicles to primary cilia |
Q30540083 | Live-cell imaging of exocyst links its spatiotemporal dynamics to various stages of vesicle fusion |
Q30479122 | MT1-MMP proinvasive activity is regulated by a novel Rab8-dependent exocytic pathway. |
Q91750061 | Maturation of Lipophagic Organelles in Hepatocytes Is Dependent Upon a Rab10/Dynamin-2 Complex |
Q30423730 | Mechanisms of polarized membrane trafficking in neurons — Focusing in on endosomes |
Q30437266 | Membrane proteins follow multiple pathways to the basolateral cell surface in polarized epithelial cells |
Q37540106 | Membrane traffic within the Golgi apparatus |
Q30480986 | Mint3/X11gamma is an ADP-ribosylation factor-dependent adaptor that regulates the traffic of the Alzheimer's Precursor protein from the trans-Golgi network |
Q37379761 | Mitotic Golgi disassembly is required for bipolar spindle formation and mitotic progression |
Q39654878 | Mobile ER-to-Golgi but not post-Golgi membrane transport carriers disappear during the terminal myogenic differentiation |
Q37235102 | Monomeric IgG is neuroprotective via enhancing microglial recycling endocytosis and TNF-alpha |
Q37063364 | Morphogenesis of post-Golgi transport carriers |
Q92763162 | Multiple Roles of Rab GTPases at the Golgi |
Q39437186 | Multiple biosynthetic trafficking routes for apically secreted proteins in MDCK cells |
Q24301155 | Myosin VI and its interacting protein LMTK2 regulate tubule formation and transport to the endocytic recycling compartment. |
Q34575273 | Myosin VI and optineurin are required for polarized EGFR delivery and directed migration |
Q39735805 | Myosin VI is required for sorting of AP-1B-dependent cargo to the basolateral domain in polarized MDCK cells |
Q39454359 | N-Glycosylation instead of cholesterol mediates oligomerization and apical sorting of GPI-APs in FRT cells |
Q52591664 | New approaches for solving old problems in neuronal protein trafficking. |
Q50325662 | Newly synthesized and recycling pools of the apical protein gp135 do not occupy the same compartments |
Q40182006 | Oligomerization is a specific requirement for apical sorting of glycosyl-phosphatidylinositol-anchored proteins but not for non-raft-associated apical proteins |
Q24300284 | Optineurin links myosin VI to the Golgi complex and is involved in Golgi organization and exocytosis |
Q38197884 | Organization and execution of the epithelial polarity programme |
Q36058478 | Organization of vesicular trafficking in epithelia |
Q37086717 | Out, in and back again: PtdIns(4,5)P(2) regulates cadherin trafficking in epithelial morphogenesis. |
Q39783600 | Overexpression of myosin VI in prostate cancer cells enhances PSA and VEGF secretion, but has no effect on endocytosis |
Q34191596 | Palmitoylated Ras proteins traffic through recycling endosomes to the plasma membrane during exocytosis. |
Q42111091 | Palmitoylation pilots ras to recycling endosomes |
Q30441567 | Par3 functions in the biogenesis of the primary cilium in polarized epithelial cells |
Q24625970 | Pathways and mechanisms of endocytic recycling |
Q30436751 | Phosphatidylinositol 3,4,5-trisphosphate localization in recycling endosomes is necessary for AP-1B-dependent sorting in polarized epithelial cells |
Q36095751 | Phosphatidylinositol 4,5-bisphosphate mediates the targeting of the exocyst to the plasma membrane for exocytosis in mammalian cells |
Q40294809 | Phosphatidylinositol 5-kinase stimulates apical biosynthetic delivery via an Arp2/3-dependent mechanism |
Q27025523 | Phosphoinositides in the mammalian endo-lysosomal network |
Q54210021 | Plasma membrane insertion of KCa2.3 (SK3) is dependent upon the SNARE proteins, syntaxin-4 and SNAP23. |
Q38242786 | Plasma membrane protein polarity and trafficking in RPE cells: past, present and future |
Q33605918 | Polarity proteins and cell-cell interactions in the testis |
Q36513659 | Polarized biosynthetic traffic in renal epithelial cells: sorting, sorting, everywhere |
Q37554102 | Polarized endocytic transport: the roles of Rab11 and Rab11-FIPs in regulating cell polarity |
Q34270230 | Polarized sorting and trafficking in epithelial cells |
Q37035085 | Polarized traffic of LRP1 involves AP1B and SNX17 operating on Y-dependent sorting motifs in different pathways |
Q37631623 | Polarized traffic towards the cell surface: how to find the route |
Q40167366 | Polarized transport of Alzheimer amyloid precursor protein is mediated by adaptor protein complex AP1-1B. |
Q51009753 | Profiling and semiquantitative analysis of the cell surface proteome in human mesenchymal stem cells |
Q37350410 | Protein trafficking in polarized cells |
Q34480219 | Proteomic analysis of adaptor protein 1A coats selectively assembled on liposomes |
Q53289207 | Proteomic analysis of endosomes from genetically modified p14/MP1 mouse embryonic fibroblasts. |
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Q48218636 | Rab11 is required for tubulogenesis of Malpighian tubules in Drosophila melanogaster. |
Q51456168 | Rab11, a vesicular trafficking protein, affects endoreplication through Ras-mediated pathway in Drosophila melanogaster |
Q41665284 | Rab11a is required for apical protein localisation in the intestine. |
Q24311520 | Rab13 regulates membrane trafficking between TGN and recycling endosomes in polarized epithelial cells. |
Q39294010 | Rab5 is necessary for the biogenesis of the endolysosomal system in vivo |
Q40088439 | Rab6-interacting protein 1 links Rab6 and Rab11 function |
Q40011006 | Rab8 regulates basolateral secretory, but not recycling, traffic at the recycling endosome |
Q24676084 | Rab8-dependent recycling promotes endosomal cholesterol removal in normal and sphingolipidosis cells |
Q24303674 | Rabankyrin‐5 Interacts with EHD1 and Vps26 to Regulate Endocytic Trafficking and Retromer Function |
Q37052744 | Rabin8 regulates neurite outgrowth in both GEF activity-dependent and -independent manners |
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Q24323092 | Rap2 function requires palmitoylation and recycling endosome localization |
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Q37787522 | Recycling endosomes in apical plasma membrane domain formation and epithelial cell polarity |
Q47932235 | Recycling endosomes in human cytotoxic T lymphocytes constitute an auxiliary intracellular trafficking pathway for newly synthesized perforin |
Q52926065 | Recycling endosomes in neuronal membrane traffic |
Q30444423 | Recycling endosomes of polarized epithelial cells actively sort apical and basolateral cargos into separate subdomains |
Q30493294 | Regulation of endocytic trafficking of transferrin receptor by optineurin and its impairment by a glaucoma-associated mutant |
Q37087769 | Regulation of membrane trafficking in polarized epithelial cells. |
Q37453900 | Regulation of α2B-Adrenergic Receptor Cell Surface Transport by GGA1 and GGA2 |
Q39357458 | Retromer Guides STxB and CD8‐M6PR from Early to Recycling Endosomes, EHD1 Guides STxB from Recycling Endosome to Golgi |
Q37003924 | Retromer maintains basolateral distribution of the type II TGF-β receptor via the recycling endosome |
Q29616548 | Role of Rab GTPases in membrane traffic and cell physiology |
Q24297337 | Role of dynamin and clathrin in the cellular trafficking of flotillins |
Q37167379 | Role of membrane traffic in the generation of epithelial cell asymmetry. |
Q33938408 | Role of the endocytic machinery in the sorting of lysosome-associated membrane proteins |
Q26750773 | Role of the epithelial cell-specific clathrin adaptor complex AP-1B in cell polarity |
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