Pages that link to "Q24307520"
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The following pages link to CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP (Q24307520):
Displaying 50 items.
- Genomic cloning, molecular characterization, and functional analysis of human CLCA1, the first human member of the family of Ca2+-activated Cl- channel proteins (Q22008050) (← links)
- Molecular cloning and transmembrane structure of hCLCA2 from human lung, trachea, and mammary gland (Q22009963) (← links)
- 17beta-Estradiol inhibits Ca2+-dependent homeostasis of airway surface liquid volume in human cystic fibrosis airway epithelia (Q22306299) (← links)
- Anoctamin 6 is an essential component of the outwardly rectifying chloride channel (Q24293563) (← links)
- 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) (← links)
- Defective regulation of gap junctional coupling in cystic fibrosis pancreatic duct cells (Q24563188) (← links)
- Inhibition of cystic fibrosis transmembrane conductance regulator by novel interaction with the metabolic sensor AMP-activated protein kinase (Q24617464) (← links)
- International Union of Pharmacology LVIII: update on the P2Y G protein-coupled nucleotide receptors: from molecular mechanisms and pathophysiology to therapy (Q24629255) (← links)
- Diversity of Cl(-) channels (Q24642246) (← links)
- Pheromone-regulated genes required for yeast mating differentiation (Q24678064) (← links)
- Ileal mucosal bile acid absorption is increased in Cftr knockout mice (Q24793377) (← links)
- Emerging role of cystic fibrosis transmembrane conductance regulator - an epithelial chloride channel in gastrointestinal cancers (Q26753851) (← links)
- Structure and function of TMEM16 proteins (anoctamins) (Q26851981) (← links)
- Astrocytic adenosine: from synapses to psychiatric disorders (Q26995121) (← links)
- Nonsynaptic Communication Through ATP Release from Volume-Activated Anion Channels in Axons (Q27329978) (← links)
- Similarities between UDP-glucose and adenine nucleotide release in yeast: involvement of the secretory pathway (Q27940175) (← links)
- Anion transport in heart (Q28141703) (← links)
- Extracellular nucleotide signaling: a mechanism for integrating local and systemic responses in the activation of bone remodeling (Q28188125) (← links)
- Ontogeny of CLCN3 chloride channel gene expression in human pulmonary epithelium (Q28212863) (← links)
- Hyperacidification of cellubrevin endocytic compartments and defective endosomal recycling in cystic fibrosis respiratory epithelial cells (Q28216541) (← links)
- Membrane insertion, processing, and topology of cystic fibrosis transmembrane conductance regulator (CFTR) in microsomal membranes (Q28237929) (← links)
- Pathophysiology of gene-targeted mouse models for cystic fibrosis (Q28295602) (← links)
- The ABC of channel regulation (Q28297235) (← links)
- Stimulation of ATP secretion in the liver by therapeutic bile acids (Q28345188) (← links)
- Homologues of the human multidrug resistance genes MRP and MDR contribute to heavy metal resistance in the soil nematode Caenorhabditis elegans (Q28379341) (← links)
- Lung infections associated with cystic fibrosis (Q30080000) (← links)
- Mechanisms of ATP release and signalling in the blood vessel wall (Q30417856) (← links)
- Cystic fibrosis transmembrane conductance regulator facilitates ATP release by stimulating a separate ATP release channel for autocrine control of cell volume regulation (Q31663553) (← links)
- A primitive ATP receptor from the little skate Raja erinacea (Q31790822) (← links)
- Terminal sialylation is altered in airway cells with impaired CFTR-mediated chloride transport (Q31834361) (← links)
- Frontiers in research on cystic fibrosis: understanding its molecular and chemical basis and relationship to the pathogenesis of the disease (Q32086395) (← links)
- Immunolocalization and regulation of cystic fibrosis transmembrane conductance regulator in the adult rat epididymis (Q33197380) (← links)
- Role of purinergic signaling pathways in V-ATPase recruitment to apical membrane of acidifying epididymal clear cells (Q33523672) (← links)
- Novel pharmacologic therapies for cystic fibrosis (Q33533857) (← links)
- Emerging roles of purinergic signaling in gastrointestinal epithelial secretion and hepatobiliary function. (Q33545025) (← links)
- X-linked adrenoleukodystrophy: genes, mutations, and phenotypes (Q33607735) (← links)
- Connexins regulate calcium signaling by controlling ATP release (Q33610043) (← links)
- Structure and function of the cystic fibrosis transmembrane conductance regulator (Q33716379) (← links)
- Release of ATP and UTP from astrocytoma cells (Q33768392) (← links)
- Connexins and the kidney. (Q33841038) (← links)
- ATP and purinergic receptor-dependent membrane traffic in bladder umbrella cells (Q33919968) (← links)
- ATP transduces signals from ASGM1, a glycolipid that functions as a bacterial receptor (Q33929758) (← links)
- Molecular basis for defective glycosylation and Pseudomonas pathogenesis in cystic fibrosis lung (Q33950252) (← links)
- Genotype-phenotype relationships in cystic fibrosis (Q33953461) (← links)
- Advances in signalling by extracellular nucleotides. the role and transduction mechanisms of P2Y receptors (Q33964294) (← links)
- Salivary histatin 5 and human neutrophil defensin 1 kill Candida albicans via shared pathways. (Q33980976) (← links)
- Released ATP is an extracellular cytotoxic mediator in salivary histatin 5-induced killing of Candida albicans (Q34005242) (← links)
- Identification of cystic fibrosis transmembrane conductance regulator channel-lining residues in and flanking the M6 membrane-spanning segment. (Q34017913) (← links)
- Basal release of ATP: an autocrine-paracrine mechanism for cell regulation (Q34020834) (← links)
- Rectification of cystic fibrosis transmembrane conductance regulator chloride channel mediated by extracellular divalent cations (Q34040994) (← links)