Modulation of Ca2+-activated Cl- secretion by basolateral K+ channels in human normal and cystic fibrosis airway epithelia - Wikidata - thesis-toulmin - TriplyDB

Modulation of Ca2+-activated Cl- secretion by basolateral K+ channels in human normal and cystic fibrosis airway epithelia

Modulation of Ca2+-activated Cl- secretion by basolateral K+ channels in human normal and cystic fibrosis airway epithelia

http://www.wikidata.org/entity/Q28213143

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CLC-2 single nucleotide polymorphisms (SNPs) as potential modifiers of cystic fibrosis disease severity CFTR and TMEM16A are separate but functionally related Cl- channels Bestrophin-1 enables Ca2+-activated Cl- conductance in epithelia Enhancement of P2Y6-induced Cl- secretion by IL-13 and modulation of SK4 channels activity in human bronchial cells The role of CLCA proteins in inflammatory airway disease Inflammatory Responses Regulating Alveolar Ion Transport during Pulmonary Infections.A biophysical model for integration of electrical, osmotic, and pH regulation in the human bronchial epithelium.The K+ channel opener 1-EBIO potentiates residual function of mutant CFTR in rectal biopsies from cystic fibrosis patients.Potentiator ivacaftor abrogates pharmacological correction of ΔF508 CFTR in cystic fibrosis.Functional apical large conductance, Ca2+-activated, and voltage-dependent K+ channels are required for maintenance of airway surface liquid volume.Vasotocin and vasopressin stimulation of the chloride secretion in the human bronchial epithelial cell line, 16HBE14o-.Genetic variation in genes encoding airway epithelial potassium channels is associated with chronic rhinosinusitis in a pediatric population.The porcine chloride channel calcium-activated family member pCLCA4a mirrors lung expression of the human hCLCA4.Complementary roles of KCa3.1 channels and β1-integrin during alveolar epithelial repair Molecular and functional expression of anion exchangers in cultured normal human nasal epithelial cells Luminal cholinergic signalling in airway lining fluid: a novel mechanism for activating chloride secretion via Ca²⁺-dependent Cl⁻ and K⁺ channels.Moderate intensity exercise mediates comparable increases in exhaled chloride as albuterol in individuals with cystic fibrosis.In situ measurement of airway surface liquid [K+] using a ratioable K+-sensitive fluorescent dye UTP regulation of ion transport in alveolar epithelial cells involves distinct mechanisms.Role of CFTR in epithelial physiology.Evidence of K+ channel function in epithelial cell migration, proliferation, and repair.Ion transport by pulmonary epithelia.Why Do We have to Move Fluid to be Able to Breathe?Role of the potassium channel KCa3.1 in diabetic nephropathy.Emerging roles of calcium-activated K channels and TRPV4 channels in lung oedema and pulmonary circulatory collapse.POU2AF1 Functions in the Human Airway Epithelium To Regulate Expression of Host Defense Genes.EGF and K+ channel activity control normal and cystic fibrosis bronchial epithelia repair.A Ba2+-resistant, acid-sensitive K+ conductance in Na+-absorbing H441 human airway epithelial cells.Pattern of Ca2+ increase determines the type of secretory mechanism activated in dog pancreatic duct epithelial cells.Mathematical model reveals role of nucleotide signaling in airway surface liquid homeostasis and its dysregulation in cystic fibrosis.Effects of dietary lectins on ion transport in epithelia.Differentiation of human bronchial epithelial cells: role of hydrocortisone in development of ion transport pathways involved in mucociliary clearance.Regulation of ENaC and CFTR expression with K+ channel modulators and effect on fluid absorption across alveolar epithelial cells.Involvement of KATP and KvLQT1 K+ channels in EGF-stimulated alveolar epithelial cell repair processes.Primary bronchial epithelial cell culture from explanted cystic fibrosis lungs.Flagellin/TLR5 signaling potentiates airway serous secretion from swine tracheal submucosal glands.Purinergic P2Y6 receptors induce Ca2+ and CFTR dependent Cl- secretion in mouse trachea.Oxidant stress stimulates Ca2+-activated chloride channels in the apical activated membrane of cultured nonciliated human nasal epithelial cells.Ion channels of the lung and their role in disease pathogenesis.CFTR induces extracellular acid sensing in Xenopus oocytes which activates endogenous Ca²⁺-activated Cl⁻ conductance.

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Modulation of Ca2+-activated Cl- secretion by basolateral K+ channels in human normal and cystic fibrosis airway epithelia

http://www.wikidata.org/entity/Q28213143

description

2003 nî lūn-bûn

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2003 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2003年の論文

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2003年論文

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2003年论文

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Modulation of Ca2+-activated C ...... stic fibrosis airway epithelia

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Modulation of Ca2+-activated C ...... stic fibrosis airway epithelia

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Modulation of Ca2+-activated C ...... stic fibrosis airway epithelia

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Modulation of Ca2+-activated C ...... stic fibrosis airway epithelia

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Modulation of Ca2+-activated C ...... stic fibrosis airway epithelia

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Modulation of Ca2+-activated C ...... stic fibrosis airway epithelia

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01.PDR.0000057204.51420.DC

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Pediatric Research

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Modulation of Ca2+-activated C ...... stic fibrosis airway epithelia

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Hans H Seydewitz

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Joachim Kuehr

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Jörg Thomas

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Karl Kunzelmann

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Marcus Mall

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Matthias Brandis

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Rainer Schreiber

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Tanja Gonska

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P2860

Identification of three novel members of the calcium-dependent chloride channel (CaCC) family predominantly expressed in the digestive tract and trachea

A constitutively open potassium channel formed by KCNQ1 and KCNE3

hSK4, a member of a novel subfamily of calcium-activated potassium channels

The small conductance K+ channel, KCNQ1: expression, function, and subunit composition in murine trachea

Na+ transport in cystic fibrosis respiratory epithelia. Abnormal basal rate and response to adenylate cyclase activation.

Chloride secretory response of cystic fibrosis human airway epithelia. Preservation of calcium but not protein kinase C- and A-dependent mechanisms.

Relationship of a non-cystic fibrosis transmembrane conductance regulator-mediated chloride conductance to organ-level disease in Cftr(-/-) mice

Regulation of transepithelial ion transport and intracellular calcium by extracellular ATP in human normal and cystic fibrosis airway epithelium.

Bicarbonate and chloride secretion in Calu-3 human airway epithelial cells.

Polarized signaling via purinoceptors in normal and cystic fibrosis airway epithelia.

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cystic fibrosis