| scholarly article | Q13442814 |
| P50 | author | Gergely L Lukacs | Q38322272 |
| P2093 | author name string | A S Verkman | |
| Peter M Haggie | |||
| Jung Kyung Kim | |||
| P2860 | cites work | A Golgi-associated PDZ domain protein modulates cystic fibrosis transmembrane regulator plasma membrane expression | Q24291900 |
| A kinase-regulated mechanism controls CFTR channel gating by disrupting bivalent PDZ domain interactions | Q24311225 | ||
| A C-terminal motif found in the beta2-adrenergic receptor, P2Y1 receptor and cystic fibrosis transmembrane conductance regulator determines binding to the Na+/H+ exchanger regulatory factor family of PDZ proteins | Q24316901 | ||
| Quantum dots for live cells, in vivo imaging, and diagnostics | Q24532049 | ||
| Rapid hop diffusion of a G-protein-coupled receptor in the plasma membrane as revealed by single-molecule techniques | Q24538587 | ||
| Inhibition of cystic fibrosis transmembrane conductance regulator by novel interaction with the metabolic sensor AMP-activated protein kinase | Q24617464 | ||
| Characterization of a protein cofactor that mediates protein kinase A regulation of the renal brush border membrane Na(+)-H+ exchanger | Q24629554 | ||
| Misfolding diverts CFTR from recycling to degradation: quality control at early endosomes | Q24676764 | ||
| Protein kinase A associates with cystic fibrosis transmembrane conductance regulator via an interaction with ezrin | Q28118810 | ||
| The PDZ-interacting domain of cystic fibrosis transmembrane conductance regulator is required for functional expression in the apical plasma membrane | Q28138284 | ||
| Accessory protein facilitated CFTR-CFTR interaction, a molecular mechanism to potentiate the chloride channel activity | Q28142263 | ||
| A kinase-regulated PDZ-domain interaction controls endocytic sorting of the beta2-adrenergic receptor | Q28145098 | ||
| Assembly and Trafficking of a Multiprotein ROMK (Kir 1.1) Channel Complex by PDZ Interactions | Q28182435 | ||
| Protein kinase C epsilon-dependent regulation of cystic fibrosis transmembrane regulator involves binding to a receptor for activated C kinase (RACK1) and RACK1 binding to Na+/H+ exchange regulatory factor | Q28214893 | ||
| Regulation of CFTR chloride channels by syntaxin and Munc18 isoforms | Q28255553 | ||
| Peptide binding consensus of the NHE-RF-PDZ1 domain matches the C-terminal sequence of cystic fibrosis transmembrane conductance regulator (CFTR) | Q28272686 | ||
| An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton | Q28277503 | ||
| Paradigm Shift of the Plasma Membrane Concept from the Two-Dimensional Continuum Fluid to the Partitioned Fluid: High-Speed Single-Molecule Tracking of Membrane Molecules | Q29011044 | ||
| ERM proteins and merlin: integrators at the cell cortex | Q29619893 | ||
| Membrane lateral diffusion and capture of CFTR within transient confinement zones. | Q30477935 | ||
| Increased diffusional mobility of CFTR at the plasma membrane after deletion of its C-terminal PDZ binding motif | Q33195731 | ||
| A PDZ-interacting domain in CFTR is an apical membrane polarization signal | Q33902133 | ||
| E3KARP mediates the association of ezrin and protein kinase A with the cystic fibrosis transmembrane conductance regulator in airway cells | Q33909378 | ||
| Single-particle tracking: the distribution of diffusion coefficients | Q33915302 | ||
| Small-molecule correctors of defective DeltaF508-CFTR cellular processing identified by high-throughput screening. | Q33925348 | ||
| Diffusion dynamics of glycine receptors revealed by single-quantum dot tracking | Q34270675 | ||
| Discovery of glycine hydrazide pore-occluding CFTR inhibitors: mechanism, structure-activity analysis, and in vivo efficacy | Q34336290 | ||
| A macromolecular complex of beta 2 adrenergic receptor, CFTR, and ezrin/radixin/moesin-binding phosphoprotein 50 is regulated by PKA | Q34468233 | ||
| Regulation of cystic fibrosis transmembrane conductance regulator single-channel gating by bivalent PDZ-domain-mediated interaction | Q34662162 | ||
| Effects of C-terminal deletions on cystic fibrosis transmembrane conductance regulator function in cystic fibrosis airway epithelia | Q34762614 | ||
| The role of receptor diffusion in the organization of the postsynaptic membrane | Q35097310 | ||
| The role of regulated CFTR trafficking in epithelial secretion | Q35141221 | ||
| Macromolecular complexes of cystic fibrosis transmembrane conductance regulator and its interacting partners | Q36151796 | ||
| COOH-terminal truncations promote proteasome-dependent degradation of mature cystic fibrosis transmembrane conductance regulator from post-Golgi compartments | Q36326371 | ||
| The cystic fibrosis transmembrane conductance regulator is regulated by a direct interaction with the protein phosphatase 2A. | Q40359721 | ||
| Polar expression of ErbB-2/HER2 in epithelia. Bimodal regulation by Lin-7. | Q40635663 | ||
| The role of the C terminus and Na+/H+ exchanger regulatory factor in the functional expression of cystic fibrosis transmembrane conductance regulator in nonpolarized cells and epithelia | Q40662051 | ||
| PDZ domain interaction controls the endocytic recycling of the cystic fibrosis transmembrane conductance regulator | Q40712140 | ||
| Phospholipids undergo hop diffusion in compartmentalized cell membrane | Q40726143 | ||
| Receptor activation and homer differentially control the lateral mobility of metabotropic glutamate receptor 5 in the neuronal membrane. | Q40730633 | ||
| PKA holoenzyme is functionally coupled to CFTR by AKAPs | Q40901386 | ||
| Butyrate increases apical membrane CFTR but reduces chloride secretion in MDCK cells | Q40935945 | ||
| C-terminal truncations destabilize the cystic fibrosis transmembrane conductance regulator without impairing its biogenesis. A novel class of mutation | Q40939810 | ||
| Rapid and persistent modulation of actin dynamics regulates postsynaptic reorganization underlying bidirectional plasticity. | Q42825535 | ||
| Differential activity-dependent regulation of the lateral mobilities of AMPA and NMDA receptors. | Q44945678 | ||
| Effects of growth surface on differentiation of cultures of human tracheal epithelium | Q46118016 | ||
| New insights into cystic fibrosis: molecular switches that regulate CFTR | Q56680230 | ||
| Association of cystic fibrosis transmembrane conductance regulator and protein phosphatase 2C | Q73041185 | ||
| Efficient endocytosis of the cystic fibrosis transmembrane conductance regulator requires a tyrosine-based signal | Q77912061 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 12 | |
| P921 | main subject | quantum dot | Q1133068 |
| quantum biology | Q1429339 | ||
| P1104 | number of pages | 9 | |
| P304 | page(s) | 4937-4945 | |
| P577 | publication date | 2006-09-20 | |
| P1433 | published in | Molecular Biology of the Cell | Q2338259 |
| P1476 | title | Tracking of quantum dot-labeled CFTR shows near immobilization by C-terminal PDZ interactions | |
| P478 | volume | 17 |
| Q24319113 | A CD317/tetherin-RICH2 complex plays a critical role in the organization of the subapical actin cytoskeleton in polarized epithelial cells |
| Q42243496 | A hierarchy of signals regulates entry of membrane proteins into the ciliary membrane domain in epithelial cells |
| Q38873028 | A molecular switch in the scaffold NHERF1 enables misfolded CFTR to evade the peripheral quality control checkpoint |
| Q91710428 | Agonists that stimulate secretion promote the recruitment of CFTR into membrane lipid microdomains |
| Q42106954 | Analysis of Microscopic Parameters of Single-Particle Trajectories in Neurons |
| Q34181530 | Apical Scaffolding Protein NHERF2 Modulates the Localization of Alternatively Spliced Plasma Membrane Ca2+ Pump 2B Variants in Polarized Epithelial Cells |
| Q30482870 | Aquaporin-4 dynamics in orthogonal arrays in live cells visualized by quantum dot single particle tracking |
| Q40027003 | Beta-oestradiol rescues DeltaF508CFTR functional expression in human cystic fibrosis airway CFBE41o- cells through the up-regulation of NHERF1. |
| Q33907394 | CFTR in a lipid raft-TNFR1 complex modulates gap junctional intercellular communication and IL-8 secretion. |
| Q41118731 | Cholesterol modulates CFTR confinement in the plasma membrane of primary epithelial cells |
| Q30503440 | Confinement of β(1)- and β(2)-adrenergic receptors in the plasma membrane of cardiomyocyte-like H9c2 cells is mediated by selective interactions with PDZ domain and A-kinase anchoring proteins but not caveolae |
| Q37359391 | Contact-mode high-resolution high-speed atomic force microscopy movies of the purple membrane. |
| Q26824750 | Control of cystic fibrosis transmembrane conductance regulator membrane trafficking: not just from the endoplasmic reticulum to the Golgi |
| Q38078917 | Cystic fibrosis transmembrane conductance regulator (ABCC7) structure |
| Q30601949 | Cytoskeletal confinement of CX3CL1 limits its susceptibility to proteolytic cleavage by ADAM10 |
| Q35169502 | Defective adenosine-stimulated cAMP production in cystic fibrosis airway epithelia: a novel role for CFTR in cell signaling |
| Q30488992 | Determinants of aquaporin-4 assembly in orthogonal arrays revealed by live-cell single-molecule fluorescence imaging |
| Q30491186 | Dynamic partitioning of a glycosyl-phosphatidylinositol-anchored protein in glycosphingolipid-rich microdomains imaged by single-quantum dot tracking |
| Q39564417 | Dynamic redistribution of calcium sensitive potassium channels (hK(Ca)3.1) in migrating cells |
| Q40011043 | Dynamics of single potassium channel proteins in the plasma membrane of migrating cells |
| Q28914742 | Engineered protein connectivity to actin mimics PDZ-dependent recycling of G protein-coupled receptors but not its regulation by Hrs |
| Q41989850 | Enhanced cell-surface stability of rescued DeltaF508 cystic fibrosis transmembrane conductance regulator (CFTR) by pharmacological chaperones |
| Q61798802 | Friend or Foe: The Role of the Cytoskeleton in Influenza A Virus Assembly |
| Q38971505 | From the endoplasmic reticulum to the plasma membrane: mechanisms of CFTR folding and trafficking |
| Q38748484 | Human airway epithelial cells investigated by atomic force microscopy: A hint to cystic fibrosis epithelial pathology. |
| Q34532754 | Hypertension-linked mutation of α-adducin increases CFTR surface expression and activity in HEK and cultured rat distal convoluted tubule cells |
| Q36704481 | Investigating membrane protein dynamics in living cells |
| Q36418881 | Keratin K18 increases cystic fibrosis transmembrane conductance regulator (CFTR) surface expression by binding to its C-terminal hydrophobic patch |
| Q34276506 | Kinetics of G-protein-coupled receptor endosomal trafficking pathways revealed by single quantum dots |
| Q42807806 | Lateral mobility of L-type calcium channels in synaptic terminals of retinal bipolar cells |
| Q24680871 | Lipid rafts and B cell signaling |
| Q36783966 | Local modulation of cystic fibrosis conductance regulator: cytoskeleton and compartmentalized cAMP signalling |
| Q36483405 | Localization to the cortical cytoskeleton is necessary for Nf2/merlin-dependent epidermal growth factor receptor silencing |
| Q24294850 | Long-range nonanomalous diffusion of quantum dot-labeled aquaporin-1 water channels in the cell plasma membrane |
| Q30483292 | Monomeric CFTR in plasma membranes in live cells revealed by single molecule fluorescence imaging |
| Q37621669 | Motor and tail homology 1 (Th1) domains antagonistically control myosin-1 dynamics |
| Q28569226 | NHERF-1 binds to Mrp2 and regulates hepatic Mrp2 expression and function |
| Q33571668 | Na+/H+ exchanger regulatory factor 1 overexpression-dependent increase of cytoskeleton organization is fundamental in the rescue of F508del cystic fibrosis transmembrane conductance regulator in human airway CFBE41o- cells |
| Q26827112 | New light on ion channel imaging by total internal reflection fluorescence (TIRF) microscopy |
| Q34107567 | Probing cellular events, one quantum dot at a time |
| Q39467422 | Protein trafficking rates assessed by quantum dot quenching with bromocresol green |
| Q41822425 | QUANTUM DOT SINGLE MOLECULE TRACKING REVEALS A WIDE RANGE OF DIFFUSIVE MOTIONS OF MEMBRANE TRANSPORT PROTEINS. |
| Q39030974 | Quantitative analysis of ezrin turnover dynamics in the actin cortex. |
| Q38332140 | Quantum dots for quantitative imaging: from single molecules to tissue |
| Q36295153 | Quantum dots: synthesis, bioapplications, and toxicity |
| Q37050934 | RACK1 interacts with filamin-A to regulate plasma membrane levels of the cystic fibrosis transmembrane conductance regulator. |
| Q36481817 | Reduced PDZ interactions of rescued ΔF508CFTR increases its cell surface mobility. |
| Q38037204 | Regulation from within: the cytoskeleton in transmembrane signaling |
| Q35170848 | Regulation of ABCC6 trafficking and stability by a conserved C-terminal PDZ-like sequence |
| Q92637479 | Regulation of CFTR Biogenesis by the Proteostatic Network and Pharmacological Modulators |
| Q30483607 | Regulation of caveolin-1 membrane trafficking by the Na/K-ATPase. |
| Q38594795 | Repairing the basic defect in cystic fibrosis - one approach is not enough. |
| Q38009859 | Resolving the kinetics of lipid, protein and peptide diffusion in membranes |
| Q37443850 | Reversible, temperature-dependent supramolecular assembly of aquaporin-4 orthogonal arrays in live cell membranes |
| Q45845463 | Segmentation of 3D Trajectories Acquired by TSUNAMI Microscope: An Application to EGFR Trafficking |
| Q33761328 | Serum- and glucocorticoid-induced protein kinase 1 (SGK1) increases the cystic fibrosis transmembrane conductance regulator (CFTR) in airway epithelial cells by phosphorylating Shank2E protein |
| Q30479722 | Single-particle tracking of membrane protein diffusion in a potential: simulation, detection, and application to confined diffusion of CFTR Cl- channels |
| Q40070826 | Spatial structure and diffusive dynamics from single-particle trajectories using spline analysis. |
| Q33843016 | Stabilizing rescued surface-localized δf508 CFTR by potentiation of its interaction with Na(+)/H(+) exchanger regulatory factor 1. |
| Q42650380 | Strategies for the etiological therapy of cystic fibrosis |
| Q36975737 | Tether and trap: regulation of membrane-raft dynamics by actin-binding proteins. |
| Q36985840 | The Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Uses its C-Terminus to Regulate the A2B Adenosine Receptor |
| Q92093768 | The bidirectional relationship between CFTR and lipids |
| Q37827577 | The cystic fibrosis transmembrane conductance regulator's expanding SNARE interactome |
| Q42567672 | The formation of acetylcholine receptor clusters visualized with quantum dots |
| Q34322410 | The membrane skeleton controls diffusion dynamics and signaling through the B cell receptor |
| Q30491433 | The transmembrane protein CBP plays a role in transiently anchoring small clusters of Thy-1, a GPI-anchored protein, to the cytoskeleton |
| Q37431815 | Tracking bio-molecules in live cells using quantum dots |
| Q48507720 | Transmembrane Pickets Connect Cyto- and Pericellular Skeletons Forming Barriers to Receptor Engagement |
| Q37154378 | Visualizing ion channel dynamics at the plasma membrane |
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