| scholarly article | Q13442814 |
| P2093 | author name string | Folma Buss | |
| John Kendrick-Jones | |||
| Gudrun Ihrke | |||
| Claudia Puri | |||
| Josephine Sui-Yan Au | |||
| P2860 | cites work | The localization of myosin VI at the golgi complex and leading edge of fibroblasts and its phosphorylation and recruitment into membrane ruffles of A431 cells after growth factor stimulation | Q22008538 |
| Mu1B, a novel adaptor medium chain expressed in polarized epithelial cells | Q22010072 | ||
| Myosin VI is an actin-based motor that moves backwards | Q22010643 | ||
| Myosin VI isoform localized to clathrin-coated vesicles with a role in clathrin-mediated endocytosis | Q24291429 | ||
| Myosin VI binds to and localises with Dab2, potentially linking receptor-mediated endocytosis and the actin cytoskeleton | Q24294845 | ||
| Optineurin links myosin VI to the Golgi complex and is involved in Golgi organization and exocytosis | Q24300284 | ||
| Myo6 facilitates the translocation of endocytic vesicles from cell peripheries | Q24307920 | ||
| Differential recognition of tyrosine-based basolateral signals by AP-1B subunit mu1B in polarized epithelial cells | Q24530204 | ||
| Distribution and function of AP-1 clathrin adaptor complexes in polarized epithelial cells | Q24670526 | ||
| Rab8, a small GTPase involved in vesicular traffic between the TGN and the basolateral plasma membrane | Q24673790 | ||
| Features of influenza HA required for apical sorting differ from those required for association with DRMs or MAL. | Q40616496 | ||
| Cdc42 controls secretory and endocytic transport to the basolateral plasma membrane of MDCK cells | Q40918582 | ||
| Tyrosine-based membrane protein sorting signals are differentially interpreted by polarized Madin-Darby canine kidney and LLC-PK1 epithelial cells. | Q41005449 | ||
| Vesicular stomatitis virus glycoprotein contains a dominant cytoplasmic basolateral sorting signal critically dependent upon a tyrosine. | Q41573489 | ||
| Differential use of two AP-3-mediated pathways by lysosomal membrane proteins | Q42823981 | ||
| Basolateral sorting of LDL receptor in MDCK cells: the cytoplasmic domain contains two tyrosine-dependent targeting determinants | Q43610720 | ||
| 2,3-Butanedione monoxime (BDM) as a myosin inhibitor | Q44358175 | ||
| Beta-COP is essential for biosynthetic membrane transport from the endoplasmic reticulum to the Golgi complex in vivo | Q45345741 | ||
| Regulated conformation of myosin V. | Q47368896 | ||
| Three-dimensional structure of the myosin V inhibited state by cryoelectron tomography | Q83177861 | ||
| Rab proteins as membrane organizers | Q27860861 | ||
| The exocyst is an effector for Sec4p, targeting secretory vesicles to sites of exocytosis | Q27934654 | ||
| FIP-2, a coiled-coil protein, links Huntingtin to Rab8 and modulates cellular morphogenesis | Q28141525 | ||
| A novel clathrin adaptor complex mediates basolateral targeting in polarized epithelial cells | Q28146062 | ||
| NPXY, a sequence often found in cytoplasmic tails, is required for coated pit-mediated internalization of the low density lipoprotein receptor | Q28254985 | ||
| Sec6/8 complex is recruited to cell-cell contacts and specifies transport vesicle delivery to the basal-lateral membrane in epithelial cells | Q28273946 | ||
| Competing sorting signals guide endolyn along a novel route to lysosomes in MDCK cells | Q28364005 | ||
| Endolyn is a mucin-like type I membrane protein targeted to lysosomes by its cytoplasmic tail | Q28573664 | ||
| Clathrin-mediated endocytosis in AP-2-depleted cells | Q29620378 | ||
| Identification of an apical sorting determinant in the cytoplasmic tail of megalin | Q30164968 | ||
| The epithelial-specific adaptor AP1B mediates post-endocytic recycling to the basolateral membrane. | Q30331083 | ||
| Differently anchored influenza hemagglutinin mutants display distinct interaction dynamics with mutual rafts | Q30441859 | ||
| GPI-anchored proteins are directly targeted to the apical surface in fully polarized MDCK cells | Q30480379 | ||
| Vectorial insertion of apical and basolateral membrane proteins in polarized epithelial cells revealed by quantitative 3D live cell imaging | Q30480381 | ||
| Actin dependence of polarized receptor recycling in Madin-Darby canine kidney cell endosomes | Q30857070 | ||
| Relationships between EGFR signaling-competent and endocytosis-competent membrane microdomains | Q33841378 | ||
| Mutant rab8 Impairs docking and fusion of rhodopsin-bearing post-Golgi membranes and causes cell death of transgenic Xenopus rods | Q33944067 | ||
| Membrane traffic in polarized epithelial cells | Q33954492 | ||
| Transport Protein Trafficking in Polarized Cells | Q35564818 | ||
| The cargo-binding domain regulates structure and activity of myosin 5 | Q35752269 | ||
| Organization of vesicular trafficking in epithelia | Q36058478 | ||
| Structural requirements and sequence motifs for polarized sorting and endocytosis of LDL and Fc receptors in MDCK cells. | Q36234444 | ||
| Apical plasma membrane proteins and endolyn-78 travel through a subapical compartment in polarized WIF-B hepatocytes. | Q36255300 | ||
| Mutations in the middle of the transmembrane domain reverse the polarity of transport of the influenza virus hemagglutinin in MDCK epithelial cells | Q36256212 | ||
| Myosin II is involved in the production of constitutive transport vesicles from the TGN. | Q36268178 | ||
| Recycling endosomes can serve as intermediates during transport from the Golgi to the plasma membrane of MDCK cells | Q36322619 | ||
| 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 | ||
| A single amino acid substitution in a hydrophobic domain causes temperature-sensitive cell-surface transport of a mutant viral glycoprotein | Q36901086 | ||
| A di-leucine motif mediates endocytosis and basolateral sorting of macrophage IgG Fc receptors in MDCK cells. | Q37633898 | ||
| Differential distribution of low-density lipoprotein-receptor-related protein (LRP) and megalin in polarized epithelial cells is determined by their cytoplasmic domains | Q38355580 | ||
| cdc42 regulates the exit of apical and basolateral proteins from the trans-Golgi network | Q39645140 | ||
| Loss of myosin VI reduces secretion and the size of the Golgi in fibroblasts from Snell's waltzer mice | Q39698975 | ||
| Involvement of ezrin/moesin in de novo actin assembly on phagosomal membranes | Q40386859 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 103-114 | |
| P577 | publication date | 2007-04-02 | |
| P1433 | published in | Journal of Cell Biology | Q1524550 |
| P1476 | title | Myosin VI is required for sorting of AP-1B-dependent cargo to the basolateral domain in polarized MDCK cells | |
| P478 | volume | 177 |
| Q38117545 | Actin acting at the Golgi. |
| Q37023376 | Analysis of AQP4 trafficking vesicle dynamics using a high-content approach. |
| Q48003997 | Apical cytoskeletons and junctional complexes as a combined system in epithelial cell sheets |
| Q37634760 | Apical trafficking in epithelial cells: signals, clusters and motors |
| Q24324187 | BREK/LMTK2 is a myosin VI-binding protein involved in endosomal membrane trafficking |
| Q36905164 | Cellular and molecular biology of optineurin |
| Q37620955 | Clathrin and AP1B: key roles in basolateral trafficking through trans-endosomal routes |
| Q37035184 | Coiled-coil-mediated dimerization is not required for myosin VI to stabilize actin during spermatid individualization in Drosophila melanogaster |
| Q35253046 | Direct interactions of adaptor protein complexes 1 and 2 with the copper transporter ATP7A mediate its anterograde and retrograde trafficking |
| Q37135682 | Diverse functions of myosin VI elucidated by an isoform-specific α-helix domain |
| Q53175756 | Dock7: a GEF for Rho-family GTPases and a novel myosin VI-binding partner in neuronal PC12 cells. |
| Q36385806 | Dynamic exchange of myosin VI on endocytic structures |
| Q55261436 | Dysfunction of Optineurin in Amyotrophic Lateral Sclerosis and Glaucoma. |
| Q37668615 | Effects of mutations and deletions in the human optineurin gene. |
| Q38119533 | Emerging role of the scaffolding protein Dlg1 in vesicle trafficking |
| Q37114569 | Exiting the Golgi complex |
| Q41962020 | Expression and localization of myosin VI in developing mouse spermatids |
| Q36665969 | Genetic characterization of the Drosophila jaguar322 mutant reveals that complete myosin VI loss of function is not lethal |
| Q36972087 | Hepatocyte polarity |
| Q24658390 | How are the cellular functions of myosin VI regulated within the cell? |
| Q35599430 | Induction of autophagy in rats upon overexpression of wild-type and mutant optineurin gene |
| Q38694139 | Interaction between optineurin and Rab1a regulates autophagosome formation in neuroblastoma cells. |
| Q35747240 | Involvement of unconventional myosin VI in myoblast function and myotube formation. |
| Q38913936 | Lentivirus-Mediated Silencing of Myosin VI Inhibits Proliferation and Cell Cycle Progression in Human Lung Cancer Cells |
| Q41531965 | Loss of cargo binding in the human myosin VI deafness mutant (R1166X) leads to increased actin filament binding |
| Q42693475 | Loss of myosin VI no insert isoform (NoI) induces a defect in clathrin-mediated endocytosis and leads to caveolar endocytosis of transferrin receptor |
| Q27336244 | Loss of optineurin in vivo results in elevated cell death and alters axonal trafficking dynamics |
| Q30486228 | Mutant huntingtin impairs post-Golgi trafficking to lysosomes by delocalizing optineurin/Rab8 complex from the Golgi apparatus |
| Q42216901 | Myosin 1 controls membrane shape by coupling F-Actin to membrane |
| Q36723224 | Myosin VI Contains a Compact Structural Motif that Binds to Ubiquitin Chains |
| Q58450109 | Myosin VI and branched actin filaments mediate membrane constriction and fission of melanosomal tubule carriers |
| Q30497821 | Myosin VI and its binding partner optineurin are involved in secretory vesicle fusion at the plasma membrane. |
| 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 |
| Q36119767 | Myosin VI and vinculin cooperate during the morphogenesis of cadherin cell cell contacts in mammalian epithelial cells |
| Q39605394 | Myosin VI in PC12 cells plays important roles in cell migration and proliferation but not in catecholamine secretion. |
| Q36850126 | Myosin VI in skeletal muscle: its localization in the sarcoplasmic reticulum, neuromuscular junction and muscle nuclei. |
| Q47224790 | Myosin VI in the nucleus of neurosecretory PC12 Cells: Stimulation-dependent nuclear translocation and interaction with nuclear proteins. |
| Q30480755 | Myosin VI is required for targeted membrane transport during cytokinesis |
| Q50502817 | Myosin VI regulates actin dynamics and melanosome biogenesis. |
| Q27329752 | Myosin VI regulates actin structure specialization through conserved cargo-binding domain sites |
| Q30534452 | Myosin VI small insert isoform maintains exocytosis by tethering secretory granules to the cortical actin |
| Q26850080 | Myosin motor proteins are involved in the final stages of the secretory pathways |
| Q30416190 | Myosin-1c regulates the dynamic stability of E-cadherin-based cell-cell contacts in polarized Madin-Darby canine kidney cells. |
| Q30513859 | Myosin-X functions in polarized epithelial cells |
| Q27004163 | Myosins in cell junctions |
| Q54977052 | Optineurin: A Coordinator of Membrane-Associated Cargo Trafficking and Autophagy. |
| Q38197884 | Organization and execution of the epithelial polarity programme |
| Q43779285 | Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell. |
| Q39783600 | Overexpression of myosin VI in prostate cancer cells enhances PSA and VEGF secretion, but has no effect on endocytosis |
| Q34270230 | Polarized sorting and trafficking in epithelial cells |
| Q27334656 | Posttranslational modifications, localization, and protein interactions of optineurin, the product of a glaucoma gene |
| Q37597342 | Potential roles of myosin VI in cell motility |
| Q35953865 | Protein kinase C δ regulates the release of collagen type I from vascular smooth muscle cells via regulation of Cdc42. |
| Q37350410 | Protein trafficking in polarized cells |
| Q33924469 | Rab8 interacts with distinct motifs in alpha2B- and beta2-adrenergic receptors and differentially modulates their transport |
| Q41990495 | Rab8-optineurin-myosin VI: analysis of interactions and functions in the secretory pathway |
| Q35631603 | Reconstitution of the ERG Gene Expression Network Reveals New Biomarkers and Therapeutic Targets in ERG Positive Prostate Tumors |
| 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. |
| Q37167379 | Role of membrane traffic in the generation of epithelial cell asymmetry. |
| Q26750773 | Role of the epithelial cell-specific clathrin adaptor complex AP-1B in cell polarity |
| Q24650918 | T6BP and NDP52 are myosin VI binding partners with potential roles in cytokine signalling and cell adhesion |
| Q37488634 | Taking the scenic route: biosynthetic traffic to the plasma membrane in polarized epithelial cells |
| Q38155160 | The cortical acto-Myosin network: from diffusion barrier to functional gateway in the transport of neurosecretory vesicles to the plasma membrane |
| Q58493545 | The role of the cytoskeleton in the structure and function of the Golgi apparatus |
| Q36567245 | Tissue organization by cadherin adhesion molecules: dynamic molecular and cellular mechanisms of morphogenetic regulation |
| Q38026746 | Toward an integrative view of Optineurin functions |
| Q92156441 | Unconventional Myosins: How Regulation Meets Function |
| Q28910487 | Use of fluorescence-activated vesicle sorting for isolation of Naked2-associated, basolaterally targeted exocytic vesicles for proteomics analysis |
| Q41590764 | Yeast genetic interaction screen of human genes associated with amyotrophic lateral sclerosis: identification of MAP2K5 kinase as a potential drug target |
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