scholarly article | Q13442814 |
P356 | DOI | 10.1083/JCB.109.6.2817 |
P8608 | Fatcat ID | release_livouw2htfgotp6bf2bobpv3yi |
P932 | PMC publication ID | 2115929 |
P698 | PubMed publication ID | 2592406 |
P5875 | ResearchGate publication ID | 277534955 |
P50 | author | Kai Simons | Q880181 |
Robert Bacallao | Q58811297 | ||
P2093 | author name string | E Karsenti | |
E H Stelzer | |||
C Dotti | |||
C Antony | |||
P2860 | cites work | Identification of a novel force-generating protein, kinesin, involved in microtubule-based motility | Q24601419 |
On the mechanism of unidirectional killing in mixtures of two cytotoxic T lymphocytes. Unidirectional polarization of cytoplasmic organelles and the membrane-associated cytoskeleton in the effector cell | Q24682926 | ||
The role of the cell adhesion molecule uvomorulin in the formation and maintenance of the epithelial junctional complex | Q28289033 | ||
Identification of ZO-1: a high molecular weight polypeptide associated with the tight junction (zonula occludens) in a variety of epithelia | Q28299935 | ||
Microtubules and actin filaments are not critically involved in the biogenesis of epithelial cell surface polarity | Q30442334 | ||
The trans Golgi network: sorting at the exit site of the Golgi complex. | Q34562583 | ||
Role of laminin A chain in the development of epithelial cell polarity. | Q52249864 | ||
Expression and distribution of cell adhesion molecule uvomorulin in mouse preimplantation embryos | Q58808025 | ||
Visualization of the structural polarity of microtubules | Q59056670 | ||
Structural and chemical characterization of isolated centrosomes | Q69466305 | ||
Microtubules and microfilaments in newt neurulation | Q70597684 | ||
Importance of fixation in immunohistochemistry: use of formaldehyde solutions at variable pH for the localization of tyrosine hydroxylase | Q72641619 | ||
Microtubule polarities indicate that nucleation and capture of microtubules occurs at cell surfaces in Drosophila | Q34683658 | ||
Cytoplasmic microtubules in tissue culture cells appear to grow from an organizing structure towards the plasma membrane | Q35988091 | ||
Release of putative exocytic transport vesicles from perforated MDCK cells | Q36000218 | ||
The Golgi apparatus in chick corneal epithelium: changes in intracellular position during development | Q36191719 | ||
Assembly of enveloped viruses in Madin-Darby canine kidney cells: polarized budding from single attached cells and from clusters of cells in suspension | Q36207208 | ||
Studies on the development and maintenance of epithelial cell surface polarity with monoclonal antibodies | Q36210403 | ||
Effect of microtubule assembly status on the intracellular processing and surface expression of an integral protein of the plasma membrane | Q36211315 | ||
Associations of elements of the Golgi apparatus with microtubules | Q36211367 | ||
Intracellular translocation of fluorescent sphingolipids in cultured fibroblasts: endogenously synthesized sphingomyelin and glucocerebroside analogues pass through the Golgi apparatus en route to the plasma membrane | Q36211654 | ||
Fate of microtubule-organizing centers during myogenesis in vitro | Q36211715 | ||
The Golgi apparatus remains associated with microtubule organizing centers during myogenesis | Q36212550 | ||
Microtubule-acting drugs lead to the nonpolarized delivery of the influenza hemagglutinin to the cell surface of polarized Madin-Darby canine kidney cells | Q36215887 | ||
Formation of the apical pole of epithelial (Madin-Darby canine kidney) cells: polarity of an apical protein is independent of tight junctions while segregation of a basolateral marker requires cell-cell interactions | Q36216030 | ||
Redistribution of microtubules and pericentriolar material during the development of polarity in mouse blastomeres | Q36216159 | ||
MAP 1C is a microtubule-activated ATPase which translocates microtubules in vitro and has dynein-like properties | Q36217545 | ||
Control of microtubule nucleation and stability in Madin-Darby canine kidney cells: the occurrence of noncentrosomal, stable detyrosinated microtubules | Q36217674 | ||
Nocodazole, a microtubule-active drug, interferes with apical protein delivery in cultured intestinal epithelial cells (Caco-2). | Q36219864 | ||
Role of microtubules in polarized delivery of apical membrane proteins to the brush border of the intestinal epithelium | Q36220274 | ||
Development of tight junctions de novo in the mouse early embryo: control of assembly of the tight junction-specific protein, ZO-1 | Q36220478 | ||
Localization of the tight junction protein, ZO-1, is modulated by extracellular calcium and cell-cell contact in Madin-Darby canine kidney epithelial cells | Q36221082 | ||
Tridimensional structure of the Golgi apparatus of nonciliated epithelial cells of the ductuli efferentes in rat: an electron microscope stereoscopic study | Q36297188 | ||
Sorting of sphingolipids in epithelial (Madin-Darby canine kidney) cells | Q36472379 | ||
Microtubule distribution in cultured cells and intact tissues: improved immunolabeling resolution through the use of reversible embedment cytochemistry | Q37535850 | ||
Development and alteration of polarity | Q38624094 | ||
Three-dimensional architecture of the Golgi apparatus in Sertoli cells of the rat | Q39541824 | ||
From egg to epithelium | Q39544473 | ||
The directed migration of eukaryotic cells | Q39760603 | ||
Microtubules and the organization of the Golgi complex | Q39827448 | ||
Cell shape and membrane changes in the eight-cell mouse embryo: Prerequisites for morphogenesis of the blastocyst | Q39967911 | ||
Three-dimensional structure of the Golgi apparatus. | Q40324365 | ||
Monensin and FCCP inhibit the intracellular transport of alphavirus membrane glycoproteins | Q41280453 | ||
Transcytosis of the G protein of vesicular stomatitis virus after implantation into the apical plasma membrane of Madin-Darby canine kidney cells. I. Involvement of endosomes and lysosomes | Q41465036 | ||
Transcytosis of the G protein of vesicular stomatitis virus after implantation into the apical membrane of Madin-Darby canine kidney cells. II. Involvement of the Golgi complex | Q41466620 | ||
Cell-adhesion molecule uvomorulin is localized in the intermediate junctions of adult intestinal epithelial cells | Q41468891 | ||
A functional assay for proteins involved in establishing an epithelial occluding barrier: identification of a uvomorulin-like polypeptide | Q41498808 | ||
A microtubule-binding protein associated with membranes of the Golgi apparatus | Q41523540 | ||
Development of cell surface polarity in the epithelial Madin-Darby canine kidney (MDCK) cell line. | Q41584376 | ||
Synthesis of membrane glycoproteins in rat small-intestinal villus cells. Effect of colchicine on the redistribution of l-[1,5,6-3H]fucose-labelled membrane glycoproteins among Golgi, lateral basal and microvillus membranes | Q41834954 | ||
Flexible-substratum technique for viewing cells from the side: some in vivo properties of primary (9+0) cilia in cultured kidney epithelia | Q42122002 | ||
A dissection of the mechanisms generating and stabilizing polarity in mouse 8- and 16-cell blastomeres: the role of cytoskeletal elements | Q42503513 | ||
Reclustering of scattered Golgi elements occurs along microtubules | Q45826013 | ||
The microtubule-organizing complex and the Golgi apparatus are co-localized around the entire nuclear envelope of interphase cardiac myocytes | Q46930529 | ||
P433 | issue | 6 Pt 1 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 2817-2832 | |
P577 | publication date | 1989-12-01 | |
P1433 | published in | Journal of Cell Biology | Q1524550 |
P1476 | title | The subcellular organization of Madin-Darby canine kidney cells during the formation of a polarized epithelium | |
P478 | volume | 109 |
Q42536120 | 7-nitrobenz-2-oxa-1,3-diazole-4-yl-labeled phospholipids in lipid membranes: differences in fluorescence behavior. |
Q93190121 | A New Look at the Functional Organization of the Golgi Ribbon |
Q28000060 | A conserved signal and GTPase complex are required for the ciliary transport of polycystin-1. |
Q47792211 | A formiminotransferase cyclodeaminase isoform is localized to the Golgi complex and can mediate interaction of trans-Golgi network-derived vesicles with microtubules |
Q34272989 | A functional link between localized Oskar, dynamic microtubules, and endocytosis |
Q41815933 | A membrane-bound form of glutamate dehydrogenase possesses an ATP-dependent high-affinity microtubule-binding activity |
Q30480519 | A molecular mechanism directly linking E-cadherin adhesion to initiation of epithelial cell surface polarity |
Q40682959 | A novel sorting motif in the glutamate transporter excitatory amino acid transporter 3 directs its targeting in Madin-Darby canine kidney cells and hippocampal neurons. |
Q34198556 | A role for the centrosome and PAR-3 in the hand-off of MTOC function during epithelial polarization |
Q39683968 | A tyrosine-based motif in the cytoplasmic tail of pseudorabies virus glycoprotein B is important for both antibody-induced internalization of viral glycoproteins and efficient cell-to-cell spread |
Q41089066 | AMF-R tubules concentrate in a pericentriolar microtubule domain after MSV transformation of epithelial MDCK cells |
Q36531380 | Accumulation of a microtubule-binding protein, pp170, at desmosomal plaques |
Q41589126 | Activation of an inducible c-FosER fusion protein causes loss of epithelial polarity and triggers epithelial-fibroblastoid cell conversion |
Q37945232 | Alphaherpesviruses and the cytoskeleton in neuronal infections. |
Q36981654 | An integrin-ILK-microtubule network orients cell polarity and lumen formation in glandular epithelium |
Q36849271 | An intercellular polyamine transfer via gap junctions regulates proliferation and response to stress in epithelial cells |
Q40051383 | Analysis of detergent-resistant membranes of Helicobacter pylori infected gastric adenocarcinoma cells reveals a role for MARK2/Par1b in CagA-mediated disruption of cellular polarity |
Q24319256 | Anchorage of microtubule minus ends to adherens junctions regulates epithelial cell-cell contacts |
Q34501400 | Anchoring junctions as drug targets: role in contraceptive development |
Q48003997 | Apical cytoskeletons and junctional complexes as a combined system in epithelial cell sheets |
Q36255300 | Apical plasma membrane proteins and endolyn-78 travel through a subapical compartment in polarized WIF-B hepatocytes. |
Q37634760 | Apical trafficking in epithelial cells: signals, clusters and motors |
Q36863316 | Apiconuclear organization of microtubules does not specify protein delivery from the trans-Golgi network to different membrane domains in polarized epithelial cells |
Q39320358 | Assembly and Egress of an Alphaherpesvirus Clockwork. |
Q24674773 | Assembly of centrosomal proteins and microtubule organization depends on PCM-1 |
Q24307694 | Asymmetric CLASP-dependent nucleation of noncentrosomal microtubules at the trans-Golgi network |
Q77366116 | Atypical microtubule organization in undifferentiated human colon cancer cells |
Q36483157 | CAMSAP3 orients the apical-to-basal polarity of microtubule arrays in epithelial cells. |
Q36236091 | CDC42 and Rac1 control different actin-dependent processes in the Drosophila wing disc epithelium. |
Q30560513 | CLASP2 interacts with p120-catenin and governs microtubule dynamics at adherens junctions |
Q57974921 | Cadherin-mediated regulation of microtubule dynamics |
Q37749618 | Cell polarity in motion: redefining mammary tissue organization through EMT and cell polarity transitions. |
Q34858133 | Cell-cell adhesion and signalling |
Q24680892 | Centriolar satellites: molecular characterization, ATP-dependent movement toward centrioles and possible involvement in ciliogenesis |
Q73149478 | Centrosomal deployment of gamma-tubulin and pericentrin: evidence for a microtubule-nucleating domain and a minus-end docking domain in certain mouse epithelial cells |
Q36233614 | Centrosome assembly in vitro: role of gamma-tubulin recruitment in Xenopus sperm aster formation |
Q36321279 | Centrosome fragments and microtubules are transported asymmetrically away from division plane in anaphase |
Q38587415 | Centrosome function and assembly in animal cells. |
Q40922496 | Changes of G-actin localisation in the mitotic spindle region or nucleus during mitosis and after heat shock: a histochemical study of G-actin in various cell lines with fluorescent labelled vitamin D-binding protein. |
Q41694861 | Characterization and cellular localization of the epithelial Na+ channel. Studies using an anti-Na+ channel antibody raised by an antiidiotypic route |
Q44062292 | Claudin localization in cilia of the retinal pigment epithelium |
Q36015653 | Coordinated protein sorting, targeting and distribution in polarized cells |
Q24309611 | Copper-dependent interaction of dynactin subunit p62 with the N terminus of ATP7B but not ATP7A |
Q24291366 | Cytoplasmic dynein regulation by subunit heterogeneity and its role in apical transport |
Q36534832 | Cytoplasmic dynein-dependent vesicular transport from early to late endosomes |
Q41050998 | Cytoplasmic regulation of the movement of E-cadherin on the free cell surface as studied by optical tweezers and single particle tracking: corralling and tethering by the membrane skeleton. |
Q41739446 | Cytoskeletal control of centrioles movement during the establishment of polarity in Madin-Darby canine kidney cells |
Q41651809 | Desmosome assembly in MDCK epithelial cells does not require the presence of functional microtubules |
Q36236738 | Different biosynthetic transport routes to the plasma membrane in BHK and CHO cells |
Q33922521 | Differential microtubule requirements for transcytosis in MDCK cells |
Q42172254 | Differentiation of RPE cells from integration-free iPS cells and their cell biological characterization. |
Q37598856 | Distinct pathways for basolateral targeting of membrane and secretory proteins in polarized epithelial cells |
Q48313484 | Distribution of calcium/calmodulin-dependent protein kinase II in rat ileal enterocytes |
Q52591547 | Drosophila APC2 and Armadillo participate in tethering mitotic spindles to cortical actin. |
Q24670543 | Dynactin is required for microtubule anchoring at centrosomes |
Q30670894 | Dynamic spectrin/ankyrin-G microdomains promote lateral membrane assembly by opposing endocytosis. |
Q34692063 | Dynamics of the endoplasmic reticulum and golgi apparatus during early sea urchin development |
Q35953923 | EB1-recruited microtubule +TIP complexes coordinate protrusion dynamics during 3D epithelial remodeling. |
Q36940792 | Ectoplasmic ("Junctional") Specializations in Mammalian Sertoli Cells: Influence on Spermatogenic Cells |
Q28640132 | Effect of a dynein inhibitor on vasopressin action in toad urinary bladder |
Q34445900 | Effect of disruption of actin filaments by Clostridium botulinum C2 toxin on insulin secretion in HIT-T15 cells and pancreatic islets |
Q41658148 | Effect of monensin on ricin and fluid phase transport in polarized MDCK cells |
Q36224231 | Effect of nocodazole on vesicular traffic to the apical and basolateral surfaces of polarized MDCK cells |
Q33834938 | Efficient electroporation of DNA and protein into confluent and differentiated epithelial cells in culture |
Q34190679 | Endocytic traffic in polarized epithelial cells: role of the actin and microtubule cytoskeleton |
Q34240633 | Endoplasmic reticulum of animal cells and its organization into structural and functional domains |
Q24317263 | Epiblast integrity requires CLASP and Dystroglycan-mediated microtubule anchoring to the basal cortex |
Q35795702 | Epithelial Cell Polarity Alters Rho-GTPase Responses toPseudomonas aeruginosa |
Q41033983 | Epithelial and fibroblastoid cells contain numerous cell-type specific putative microtubule-regulating proteins, among which are ezrin and fodrin |
Q35875268 | Epithelial cell polarization is a determinant in the infectious outcome of immunoglobulin A-mediated entry by Epstein-Barr virus. |
Q47645711 | Exogenous Gene Transmission of Isocitrate Dehydrogenase 2 Mimics Ischemic Preconditioning Protection. |
Q46162589 | Expression of kinesin heavy chain isoforms in retinal pigment epithelial cells |
Q34583202 | FAPP2, cilium formation, and compartmentalization of the apical membrane in polarized Madin-Darby canine kidney (MDCK) cells. |
Q30477543 | Feedback interactions between cell-cell adherens junctions and cytoskeletal dynamics in newt lung epithelial cells |
Q41850145 | Feedback-tracking microrheology in living cells |
Q33274498 | Four-dimensional imaging of filter-grown polarized epithelial cells |
Q57374359 | From Cytoskeleton to Polarity and Chemoreception in the Gut Epithelium |
Q24685695 | GCP6 binds to intermediate filaments: a novel function of keratins in the organization of microtubules in epithelial cells |
Q42816674 | GPI-anchored human placental alkaline phosphatase has a nonpolarized distribution on the cell surface of mouse cerebellar granule neurons in vitro |
Q34200154 | Galectin-9 trafficking regulates apical-basal polarity in Madin-Darby canine kidney epithelial cells |
Q88614622 | Genetically induced microtubule disruption in the mouse intestine impairs intracellular organization and transport |
Q57356472 | Golgi apparatus and epithelial cell polarity |
Q36076559 | Golgi positioning: are we looking at the right MAP? |
Q24678887 | Gp135/podocalyxin and NHERF-2 participate in the formation of a preapical domain during polarization of MDCK cells |
Q24318662 | Identification and molecular characterization of E-MAP-115, a novel microtubule-associated protein predominantly expressed in epithelial cells |
Q47245796 | Immuno-fluorescent Labeling of Microtubules and Centrosomal Proteins in Ex Vivo Intestinal Tissue and 3D In Vitro Intestinal Organoids |
Q36911226 | In vitro reconstitution of microtubule plus end-directed, GTPgammaS-sensitive motility of Golgi membranes |
Q37272347 | In vitro studies of endocytic membrane traffic |
Q34437696 | Increased LAMP-2 polylactosamine glycosylation is associated with its slower Golgi transit during establishment of a polarized MDCK epithelial monolayer |
Q24633520 | Inhibition of cell migration and cell division correlates with distinct effects of microtubule inhibiting drugs |
Q24685845 | Insoluble gamma-tubulin-containing structures are anchored to the apical network of intermediate filaments in polarized CACO-2 epithelial cells |
Q37479445 | Intermediate filaments in Caenorhabditis elegans. |
Q36787622 | Intermediate filaments: a role in epithelial polarity |
Q41189092 | Internalization of Pseudomonas aeruginosa Strain PAO1 into Epithelial Cells Is Promoted by Interaction of a T6SS Effector with the Microtubule Network |
Q41408663 | Involvement of microtubule motors in basolateral and apical transport in kidney cells. |
Q34069997 | KIF17 stabilizes microtubules and contributes to epithelial morphogenesis by acting at MT plus ends with EB1 and APC. |
Q43937710 | KIF5C, a kinesin motor involved in apical trafficking of MDCK cells |
Q24685497 | KIFC3, a microtubule minus end-directed motor for the apical transport of annexin XIIIb-associated Triton-insoluble membranes |
Q24602789 | Laminin-based cell adhesion anchors microtubule plus ends to the epithelial cell basal cortex through LL5alpha/beta |
Q24680571 | Listeria monocytogenes exploits normal host cell processes to spread from cell to cell |
Q24316079 | Localization of low molecular weight GTP binding proteins to exocytic and endocytic compartments |
Q41651446 | Low intracellular pH induces redistribution of fodrin and instabilization of lateral walls in MDCK cells |
Q41589122 | Lysosome recruitment and fusion are early events required for trypanosome invasion of mammalian cells |
Q32046981 | MDCK cell cultures as an epithelial in vitro model: cytoskeleton and tight junctions as indicators for the definition of age-related stages by confocal microscopy. |
Q36322073 | Mammalian PAR-1 determines epithelial lumen polarity by organizing the microtubule cytoskeleton |
Q36222258 | Meeting of the apical and basolateral endocytic pathways of the Madin-Darby canine kidney cell in late endosomes. |
Q35200853 | Membrane dynamics and the regulation of epithelial cell polarity |
Q34549906 | Membrane lipidome of an epithelial cell line |
Q44412834 | Membrane repolarization is delayed in proximal tubules after ischemia-reperfusion: possible role of microtubule-organizing centers |
Q37783445 | Membrane trafficking in protozoa SNARE proteins, H+-ATPase, actin, and other key players in ciliates |
Q33244760 | Microtubular organization and its involvement in the biogenetic pathways of plasma membrane proteins in Caco-2 intestinal epithelial cells |
Q39164302 | Microtubule Motors in Establishment of Epithelial Cell Polarity |
Q43185676 | Microtubule assembly in cultured myoblasts and myotubes following nocodazole induced microtubule depolymerisation |
Q74234608 | Microtubule configurations and post-translational alpha-tubulin modifications during mammalian spermatogenesis |
Q41245385 | Microtubule dynamic turnover is suppressed during polarization and stimulated in hepatocyte growth factor scattered Madin-Darby canine kidney epithelial cells |
Q36535006 | Microtubule dynamics in fish melanophores |
Q27310679 | Microtubule motors transport phagosomes in the RPE, and lack of KLC1 leads to AMD-like pathogenesis |
Q36772906 | Microtubule perturbation inhibits intracellular transport of an apical membrane glycoprotein in a substrate-dependent manner in polarized Madin-Darby canine kidney epithelial cells |
Q33922061 | Microtubule perturbation retards both the direct and the indirect apical pathway but does not affect sorting of plasma membrane proteins in intestinal epithelial cells (Caco-2). |
Q42454520 | Microtubule plus-end and minus-end capture at adherens junctions is involved in the assembly of apico-basal arrays in polarised epithelial cells |
Q36765288 | Microtubule release from the centrosome |
Q46438354 | Microtubule-dependent vesicle transport: modulation of channel and transporter activity in liver and kidney |
Q27334393 | Microtubules and Lis-1/NudE/dynein regulate invasive cell-on-cell migration in Drosophila |
Q30585855 | Microtubules are required for efficient epithelial tight junction homeostasis and restoration |
Q34303771 | Microtubules are stabilized in confluent epithelial cells but not in fibroblasts |
Q92947057 | Microtubules promote intercellular contractile force transmission during tissue folding |
Q30809823 | Microtubules regulate disassembly of epithelial apical junctions |
Q73511577 | Microvillus inclusion disease: a genetic defect affecting apical membrane protein traffic in intestinal epithelium |
Q36070596 | Migrating transformed MDCK cells are able to structurally polarize a voltage-activated K+ channel |
Q33744940 | Mobility and cytoskeletal interactions of cell adhesion receptors |
Q41527017 | Modulation of transcytotic and direct targeting pathways in a polarized thyroid cell line |
Q37533644 | Molecular and cellular mechanisms involved in transepithelial transport |
Q35623188 | Molecular aspects of membrane trafficking in paramecium |
Q42070997 | Molecular motors and a spectrin matrix associate with Golgi membranes in vitro |
Q30442241 | Molecular motors are differentially distributed on Golgi membranes from polarized epithelial cells |
Q37682753 | Movers and shakers or anchored: Caenorhabditis elegans nuclei achieve it with KASH/SUN. |
Q36529343 | Multilayering and loss of apical polarity in MDCK cells transformed with viral K-ras |
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Q24320152 | Nesprin 4 is an outer nuclear membrane protein that can induce kinesin-mediated cell polarization |
Q35558424 | Neuronal Polarity and Trafficking |
Q37783808 | New insights into the dynamics of cell adhesions |
Q24304250 | Nezha/CAMSAP3 and CAMSAP2 cooperate in epithelial-specific organization of noncentrosomal microtubules |
Q37708556 | Ninein is essential for apico-basal microtubule formation and CLIP-170 facilitates its redeployment to non-centrosomal microtubule organizing centres |
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Q46529799 | Nucleation and capture of large cell surface-associated microtubule arrays that are not located near centrosomes in certain cochlear epithelial cells |
Q38197884 | Organization and execution of the epithelial polarity programme |
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Q36058478 | Organization of vesicular trafficking in epithelia |
Q36534977 | Orientation of spindle axis and distribution of plasma membrane proteins during cell division in polarized MDCKII cells |
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Q40725999 | Over-expression of PAR-3 suppresses contact-mediated inhibition of cell migration in MDCK cells. |
Q77538001 | Over-expression of betaI tubulin in MDCK cells and incorporation of exogenous betaI tubulin into microtubules interferes with adhesion and spreading |
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Q38595378 | PH-domain-dependent selective transport of p75 by kinesin-3 family motors in non-polarized MDCK cells |
Q24608070 | Paclitaxel-Dependent Cell Lines Reveal a Novel Drug Activity |
Q41368290 | Pancreatic tau related maps: Biochemical and immunofluorescence analysis in a tumoral cell line |
Q24564641 | Par-1 promotes a hepatic mode of apical protein trafficking in MDCK cells |
Q37092368 | Patronin/Shot Cortical Foci Assemble the Noncentrosomal Microtubule Array that Specifies the Drosophila Anterior-Posterior Axis. |
Q41456379 | Permeabilization of MDCK cells with cholesterol binding agents: dependence on substratum and confluency |
Q36233782 | Phorbol myristate acetate-mediated stimulation of transcytosis and apical recycling in MDCK cells |
Q28506566 | Phosphorylation of Kif26b promotes its polyubiquitination and subsequent proteasomal degradation during kidney development |
Q41678560 | Planar polarization of Drosophila and vertebrate epithelia |
Q71018409 | Polarity and nucleation of microtubules in polarized epithelial cells |
Q48106910 | Polarity of processes with Golgi apparatus in a subpopulation of type I astrocytes |
Q37016287 | Polarization-dependent selective transport to the apical membrane by KIF5B in MDCK cells |
Q34544069 | Polycystic kidney disease: cell division without a c(l)ue? |
Q36653270 | Possible involvement of microtubule disruption in bipolar budding of a Sendai virus mutant, F1-R, in epithelial MDCK cells. |
Q37350410 | Protein trafficking in polarized cells |
Q24673790 | Rab8, a small GTPase involved in vesicular traffic between the TGN and the basolateral plasma membrane |
Q28579885 | Rapid downregulation of rat renal Na/P(i) cotransporter in response to parathyroid hormone involves microtubule rearrangement |
Q36234135 | Receptor-mediated transcytosis of IgA in MDCK cells is via apical recycling endosomes |
Q40785479 | Regulation of cell surface polarity in renal epithelia |
Q36529642 | Regulation of desmosome assembly in MDCK epithelial cells: coordination of membrane core and cytoplasmic plaque domain assembly at the plasma membrane |
Q36224185 | Regulation of microtubule dynamics and nucleation during polarization in MDCK II cells. |
Q37342290 | Remodeling epithelial cell organization: transitions between front-rear and apical-basal polarity |
Q41640637 | Remodeling the cell surface distribution of membrane proteins during the development of epithelial cell polarity |
Q35735308 | Role of the microtubular system in morphological organization of normal and oncogene-transfected epithelial cells |
Q30442177 | Roles for Rac1 and Cdc42 in planar polarization and hair outgrowth in the wing of Drosophila |
Q35672131 | SMRT analysis of MTOC and nuclear positioning reveals the role of EB1 and LIC1 in single-cell polarization. |
Q34672405 | Selective alterations in biosynthetic and endocytic protein traffic in Madin-Darby canine kidney epithelial cells expressing mutants of the small GTPase Rac1. |
Q58349613 | Self-organisation processes in living matter |
Q36320526 | Self-organization of an acentrosomal microtubule network at the basal cortex of polarized epithelial cells |
Q35130198 | Septin GTPases spatially guide microtubule organization and plus end dynamics in polarizing epithelia |
Q24299890 | Signals regulating trafficking of Menkes (MNK; ATP7A) copper-translocating P-type ATPase in polarized MDCK cells |
Q74558339 | Simulated microgravity conditions enhance differentiation of cultured PC12 cells towards the neuroendocrine phenotype |
Q36922007 | Sorting of plasma membrane proteins in epithelial cells |
Q40828152 | Spatiotemporal expression of catenins, ZO-1, and occludin during early polarization of hepatic WIF-B9 cells |
Q37847591 | Sphingolipid trafficking and purification in Chlamydia trachomatis-infected cells |
Q42695660 | Sphingomyelin metabolism is involved in the differentiation of MDCK cells induced by environmental hypertonicity |
Q64067351 | Sphingosine kinase and sphingosine-1-phosphate regulate epithelial cell architecture by the modulation of de novo sphingolipid synthesis |
Q34326611 | Spindle pole body-anchored Kar3 drives the nucleus along microtubules from another nucleus in preparation for nuclear fusion during yeast karyogamy |
Q47148963 | Study of Ethanol-Induced Golgi Disorganization Reveals the Potential Mechanism of Alcohol-Impaired N-Glycosylation. |
Q36274033 | Substrate recognition by osteoclast precursors induces C-src/microtubule association. |
Q40986907 | TGN38 cycles via the basolateral membrane of polarized Caco-2 cells |
Q28288175 | Targeting and trafficking of the human thiamine transporter-2 in epithelial cells |
Q42826937 | Targeting of CFTR protein is linked to the polarization of human pancreatic duct cells in culture |
Q28260778 | Targeting of SNAP-23 and SNAP-25 in polarized epithelial cells |
Q92763215 | The Golgi Apparatus in Polarized Neuroepithelial Stem Cells and Their Progeny: Canonical and Noncanonical Features |
Q35534441 | The Golgi apparatus in the endomembrane-rich gastric parietal cells exist as functional stable mini-stacks dispersed throughout the cytoplasm |
Q30458666 | The LINC complex is essential for hearing |
Q36273826 | The apical submembrane cytoskeleton participates in the organization of the apical pole in epithelial cells |
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Q41141157 | The centrosome in animal cells and its functional homologs in plant and yeast cells. |
Q34180608 | The chlamydial inclusion preferentially intercepts basolaterally directed sphingomyelin-containing exocytic vacuoles. |
Q36290578 | The cytoplasmic tail of rhodopsin acts as a novel apical sorting signal in polarized MDCK cells |
Q33796503 | The cytoskeleton of digestive epithelia in health and disease |
Q37333603 | The epithelial polarity program: machineries involved and their hijacking by cancer. |
Q34137950 | The fodrin-ankyrin cytoskeleton of choroid plexus preferentially colocalizes with apical Na+K(+)-ATPase rather than with basolateral anion exchanger AE2 |
Q89763104 | The multifarious regulation of the apical junctional complex |
Q37982369 | The plasma membrane potential and the organization of the actin cytoskeleton of epithelial cells |
Q34749194 | The posttranslational modification of tubulin undergoes a switch from detyrosination to acetylation as epithelial cells become polarized |
Q39144944 | The role of apical cell-cell junctions and associated cytoskeleton in mechanotransduction |
Q45986717 | The role of kinesin, dynein and microtubules in pancreatic secretion. |
Q40845657 | The role of microtubule-based motor proteins in maintaining the structure and function of the Golgi complex |
Q58612503 | The role of microtubules in the regulation of epithelial junctions |
Q40675232 | Three-dimensional analysis of post-Golgi carrier exocytosis in epithelial cells |
Q58798740 | Tissue-specific degradation of essential centrosome components reveals distinct microtubule populations at microtubule organizing centers |
Q39485999 | Tools for micropatterning epithelial cells into microcolonies on transwell filter substrates |
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