Pages that link to "Q41776935"
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The following pages link to Regulation of plasma membrane recycling by CFTR. (Q41776935):
Displayed 50 items.
- Homozygous disruption of the murine mdr2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease (Q24322810) (← links)
- Defective regulation of gap junctional coupling in cystic fibrosis pancreatic duct cells (Q24563188) (← links)
- Identification of a nonneuronal isoform of synaptotagmin (Q24563413) (← links)
- Recycling of E-cadherin: a potential mechanism for regulating cadherin dynamics (Q24651967) (← links)
- ClC-5, the chloride channel mutated in Dent's disease, colocalizes with the proton pump in endocytotically active kidney cells (Q24672098) (← links)
- Mechanisms of lipid malabsorption in Cystic Fibrosis: the impact of essential fatty acids deficiency (Q24806288) (← links)
- Golgi localization and functionally important domains in the NH2 and COOH terminus of the yeast CLC putative chloride channel Gef1p (Q27935848) (← links)
- The ABC of channel regulation (Q28297235) (← links)
- A membrane lipid imbalance plays a role in the phenotypic expression of cystic fibrosis in cftr(-/-) mice (Q28505262) (← links)
- Subcellular localization of CFTR to endosomes in a ductal epithelium (Q28573599) (← links)
- Efficient gene transfer into human normal and cystic fibrosis tracheal gland serous cells with synthetic vectors (Q31484629) (← links)
- Syntaxin 1A inhibits CFTR chloride channels by means of domain-specific protein-protein interactions (Q33567267) (← links)
- Role of organelle pH in tumor cell biology and drug resistance (Q33611090) (← links)
- The regulation of epithelial cell cAMP- and calcium-dependent chloride channels (Q33637654) (← links)
- Expression of cystic fibrosis transmembrane conductance regulator in paracervical ganglia. (Q33638309) (← links)
- Terminal glycosylation in cystic fibrosis (Q33778431) (← links)
- Liver involvement in cystic fibrosis. (Q33784011) (← links)
- Influence of phosphorylation by protein kinase A on CFTR at the cell surface and endoplasmic reticulum (Q33784420) (← links)
- Cystic fibrosis transmembrane conductance regulator activation by roflumilast contributes to therapeutic benefit in chronic bronchitis (Q33799668) (← links)
- Yet another role for the cystic fibrosis transmembrane conductance regulator (Q33806101) (← links)
- DeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis (Q33854446) (← links)
- Impaired cell volume regulation in intestinal crypt epithelia of cystic fibrosis mice (Q33881778) (← links)
- Cystic fibrosis transmembrane conductance regulator dysfunction in VIP knockout mice (Q33913037) (← links)
- Mechanisms underlying regulated CFTR trafficking (Q33953477) (← links)
- Shiga toxin-producing Escherichia coli can impair T84 cell structure and function without inducing attaching/effacing lesions. (Q34002495) (← links)
- Linkage of azurophil granule secretion in neutrophils to chloride ion transport and endosomal transcytosis (Q34119970) (← links)
- Localization of cystic fibrosis transmembrane conductance regulator mRNA in the human gastrointestinal tract by in situ hybridization (Q34120803) (← links)
- Cysteine string protein interacts with and modulates the maturation of the cystic fibrosis transmembrane conductance regulator (Q34131032) (← links)
- Regulated Cl transport, K and Cl permeability, and exocytosis in T84 cells (Q34142830) (← links)
- CFTR-mediated Cl(-) transport in the acinar and duct cells of rabbit lacrimal gland (Q34266487) (← links)
- Terminal glycosylation and disease: influence on cancer and cystic fibrosis (Q34290906) (← links)
- The cystic fibrosis transmembrane conductance regulator: an intriguing protein with pleiotropic functions (Q34355404) (← links)
- Endocytic trafficking routes of wild type and DeltaF508 cystic fibrosis transmembrane conductance regulator (Q34359205) (← links)
- The epithelial sodium channel (ENaC) establishes a trafficking vesicle pool responsible for its regulation (Q34431427) (← links)
- Electrolyte transport in the mammalian colon: mechanisms and implications for disease (Q34482550) (← links)
- Insulin-like growth factor 1 (IGF-1) enhances the protein expression of CFTR. (Q34652853) (← links)
- The diagnostic applications of saliva--a review (Q34720733) (← links)
- Chloride channels in the kidney: lessons learned from knockout animals (Q34993939) (← links)
- Defective adenosine-stimulated cAMP production in cystic fibrosis airway epithelia: a novel role for CFTR in cell signaling (Q35169502) (← links)
- CFTR! (Q35334619) (← links)
- Rapid endocytosis of the cystic fibrosis transmembrane conductance regulator chloride channel (Q35399378) (← links)
- Update on pathogenesis of cystic fibrosis lung disease (Q35554386) (← links)
- Resveratrol ameliorates abnormalities of fluid and electrolyte secretion in a hypoxia-Induced model of acquired CFTR deficiency (Q35623246) (← links)
- Expression and localization of the cystic fibrosis transmembrane conductance regulator mRNA and its protein in rat brain (Q35751613) (← links)
- Selective up-regulation of chemokine IL-8 expression in cystic fibrosis bronchial gland cells in vivo and in vitro (Q35753331) (← links)
- CFTR and chaperones: processing and degradation. (Q35764311) (← links)
- Genotypic analysis of respiratory mucous sulfation defects in cystic fibrosis. (Q35769195) (← links)
- Defective regulatory volume decrease in human cystic fibrosis tracheal cells because of altered regulation of intermediate conductance Ca2+-dependent potassium channels (Q35874293) (← links)
- Macromolecular interactions and ion transport in cystic fibrosis (Q35901540) (← links)
- Role of Interaction and Nucleoside Diphosphate Kinase B in Regulation of the Cystic Fibrosis Transmembrane Conductance Regulator Function by cAMP-Dependent Protein Kinase A. (Q35947847) (← links)