Na+ transport in cystic fibrosis respiratory epithelia. Abnormal basal rate and response to adenylate cyclase activation. - Test2 - elhamkhani - TriplyDB

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

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

http://www.wikidata.org/entity/Q30449378

about

Cystic Fibrosis: Lessons from the Sweat Gland Human kidney amiloride-binding protein: cDNA structure and functional expression Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients Airway surface liquid volume regulation determines different airway phenotypes in liddle compared with betaENaC-overexpressing mice Modulation of epithelial sodium channel (ENaC) expression in mouse lung infected with Pseudomonas aeruginosa Inhaled hypertonic saline for cystic fibrosis: Reviewing the potential evidence for modulation of neutrophil signalling and function Gene therapy: light is finally in the tunnel Characterization of defects in ion transport and tissue development in cystic fibrosis transmembrane conductance regulator (CFTR)-knockout rats Molecular basis for pH-dependent mucosal dehydration in cystic fibrosis airways Airway hydration and COPD Hormonal regulation and genomic organization of the human amiloride-sensitive epithelial sodium channel alpha subunit gene Modulation of Ca2+-activated Cl- secretion by basolateral K+ channels in human normal and cystic fibrosis airway epithelia Pathophysiology of gene-targeted mouse models for cystic fibrosis Phylogenetic characterization of the epithelial Na+ channel (ENaC) family Cloning and expression of the beta- and gamma-subunits of the human epithelial sodium channel Activation of the epithelial sodium channel (ENaC) by the alkaline protease from Pseudomonas aeruginosa Cl- interference with the epithelial Na+ channel ENaC Nedd4-2 induces endocytosis and degradation of proteolytically cleaved epithelial Na+ channels Lung infections associated with cystic fibrosis.Binding of the proline-rich region of the epithelial Na+ channel to SH3 domains and its association with specific cellular proteins.Terminal sialylation is altered in airway cells with impaired CFTR-mediated chloride transport.New models of the tracheal airway define the glandular contribution to airway surface fluid and electrolyte composition.Abnormal secretagogue-induced intracellular free Ca2+ regulation in cystic fibrosis nasal epithelial cells Bioelectric properties of cystic fibrosis airways obtained at heart-lung transplantation.Gene therapy for cystic fibrosis.Adult stem cells from bone marrow stroma differentiate into airway epithelial cells: potential therapy for cystic fibrosis.Inter-α-inhibitor blocks epithelial sodium channel activation and decreases nasal potential differences in ΔF508 mice.Impaired cell volume regulation in intestinal crypt epithelia of cystic fibrosis mice Fluid and electrolyte transport by cultured human airway epithelia Current status of gene therapy for cystic fibrosis pulmonary disease.Basolateral potassium channels and epithelial ion transport.Regulation of airway tight junctions by proinflammatory cytokines.Defective fluid transport by cystic fibrosis airway epithelia.Hrs controls sorting of the epithelial Na+ channel between endosomal degradation and recycling pathways The cystic fibrosis transmembrane conductance regulator impedes proteolytic stimulation of the epithelial Na+ channel.CFTR and calcium-activated chloride channels in primary cultures of human airway gland cells of serous or mucous phenotype Human alveolar type II cells secrete and absorb liquid in response to local nucleotide signaling.Intersubunit conformational changes mediate epithelial sodium channel gating.Monoclonal antibodies to the apical chloride channel in Necturus gallbladder inhibit the chloride conductance CFTR chloride channel in the apical compartments: spatiotemporal coupling to its interacting partners.

P2860

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P2860

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

http://www.wikidata.org/entity/Q30449378

description

1986 nî lūn-bûn

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1986 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

1986 թվականի նոյեմբերին հրատարակված գիտական հոդված

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1986年の論文

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1986年論文

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1986年論文

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1986年論文

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1986年論文

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1986年論文

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1986年论文

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name

Na+ transport in cystic fibros ...... adenylate cyclase activation.

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Na+ transport in cystic fibros ...... adenylate cyclase activation.

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type

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Na+ transport in cystic fibros ...... adenylate cyclase activation.

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Na+ transport in cystic fibros ...... adenylate cyclase activation.

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prefLabel

Na+ transport in cystic fibros ...... adenylate cyclase activation.

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Na+ transport in cystic fibros ...... adenylate cyclase activation.

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P1433

Journal of Clinical Investigation

P1476

Na+ transport in cystic fibros ...... adenylate cyclase activation.

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P2093

J T Gatzy

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L Cantley

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M J Stutts

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M R Knowles

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R C Boucher

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P2860

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

Defective beta adrenergic response of cystic fibrosis sweat glands in vivo and in vitro

Chloride impermeability in cystic fibrosis.

Intracellular chloride activities in canine tracheal epithelium. Direct evidence for sodium-coupled intracellular chloride accumulation in a chloride-secreting epithelium.

Relative ion permeability of normal and cystic fibrosis nasal epithelium.

Forskolin: unique diterpene activator of adenylate cyclase in membranes and in intact cells

Beta adrenergic receptors in lymphocytes and granulocytes from patients with cystic fibrosis.

Impaired beta adrenergic receptor binding and function in cystic fibrosis neutrophils

Decreased adenosine 3':5'-monophosphate response to isoproterenol in cystic fibrosis leukocytes.

Neurohormonal receptors and cyclic AMP-binding proteins in rabbit tracheal mucosa-submucosa.

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1245-1252

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10.1172/JCI112708

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5

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78

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19389732

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3771796

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cystic fibrosis

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423810

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