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 |
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Q36418881 | Keratin K18 increases cystic fibrosis transmembrane conductance regulator (CFTR) surface expression by binding to its C-terminal hydrophobic patch |
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Q42807806 | Lateral mobility of L-type calcium channels in synaptic terminals of retinal bipolar cells |
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Q36483405 | Localization to the cortical cytoskeleton is necessary for Nf2/merlin-dependent epidermal growth factor receptor silencing |
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