Defective regulation of outwardly rectifying Cl- channels by protein kinase A corrected by insertion of CFTR.
about
CLC-2 single nucleotide polymorphisms (SNPs) as potential modifiers of cystic fibrosis disease severityThe relevance of sweat testing for the diagnosis of cystic fibrosis in the genomic era.Defective regulation of gap junctional coupling in cystic fibrosis pancreatic duct cellsMechanisms of lipid malabsorption in Cystic Fibrosis: the impact of essential fatty acids deficiencyOntogeny of CLCN3 chloride channel gene expression in human pulmonary epitheliumHyperacidification of cellubrevin endocytic compartments and defective endosomal recycling in cystic fibrosis respiratory epithelial cellsChloride channels: an emerging molecular picturePseudomonas aeruginosa exploits lipid A and muropeptides modification as a strategy to lower innate immunity during cystic fibrosis lung infectionLung infections associated with cystic fibrosis.De novo biosynthetic profiling of high abundance proteins in cystic fibrosis lung epithelial cells.Molecular insights into the physiology of the 'thin film' of airway surface liquid.Expression of cystic fibrosis transmembrane conductance regulator in paracervical ganglia.Disruption of interleukin-1β autocrine signaling rescues complex I activity and improves ROS levels in immortalized epithelial cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.Repeated delivery of adeno-associated virus vectors to the rabbit airway.Cystic fibrosis transmembrane conductance regulator. Structure and function of an epithelial chloride channel.Intracellular pH regulation of CA1 neurons in Na(+)/H(+) isoform 1 mutant mice.Effect of allergy and inflammation on eicosanoid gene expression in CFTR deficiency.Impaired cell volume regulation in intestinal crypt epithelia of cystic fibrosis miceChloride channels and salivary gland function.Molecular basis for defective glycosylation and Pseudomonas pathogenesis in cystic fibrosis lung.Organic solutes rescue the functional defect in delta F508 cystic fibrosis transmembrane conductance regulator.Slow conversions among subconductance states of cystic fibrosis transmembrane conductance regulator chloride channelRectification of cystic fibrosis transmembrane conductance regulator chloride channel mediated by extracellular divalent cations.Cystic fibrosis transmembrane conductance regulator and the outwardly rectifying chloride channel: a relationship between two chloride channels expressed in epithelial cells.Two cystic fibrosis transmembrane conductance regulator mutations have different effects on both pulmonary phenotype and regulation of outwardly rectified chloride currents.Cysteine residues in the nucleotide binding domains regulate the conductance state of CFTR channels.Cystic fibrosis-niche adaptation of Pseudomonas aeruginosa reduces virulence in multiple infection hostsCFTR mutations and polymorphisms in male infertility.Single gene disorders affecting the gastrointestinal tract.Effects of cystic fibrosis and congenital bilateral absence of the vas deferens-associated mutations on cystic fibrosis transmembrane conductance regulator-mediated regulation of separate channelsThe mitochondrial complex I activity is reduced in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.Endosomal hyperacidification in cystic fibrosis is due to defective nitric oxide-cylic GMP signalling cascadeRetrovirus-mediated gene transfer to cystic fibrosis airway epithelial cells: effect of selectable marker sequences on long-term expressionCell-bound IL-8 increases in bronchial epithelial cells after arylsulfatase B silencing due to sequestration with chondroitin-4-sulfate.Differential sensitivity of normal and cystic fibrosis airway epithelial cells to epinephrine.Nasal airway ion transport is linked to the cystic fibrosis phenotype in adult patients.Normalization of raised sodium absorption and raised calcium-mediated chloride secretion by adenovirus-mediated expression of cystic fibrosis transmembrane conductance regulator in primary human cystic fibrosis airway epithelial cells.The prevalence of common CFTR mutations in Iranian infertile men with non-CAVD obstructive azoospermia by using ARMS PCR techniques.Structure and pharmacology of swelling-sensitive chloride channels, I(Cl,swell).Continuous detection of extracellular ATP on living cells by using atomic force microscopy
P2860
Q21261465-26B7AE25-6B1F-432C-B39F-4B541EB2C8D5Q24535769-CFFCCFB3-0FFB-4E93-ADF7-A0FB18C8347BQ24563188-8C0D972C-82A8-4D03-8D05-04E923DE140CQ24806288-006EE25D-783F-4F7B-8FCB-71A48983A150Q28212863-A43F9C21-A1BA-451A-9FEC-66AF4AB38045Q28216541-EE74B692-E73C-4D51-9AF9-1E56DA8C9772Q28304402-2AC1CA1D-1846-46B7-8512-9A02DD50DC8EQ28472320-A1983D67-2F69-4E1F-A489-55EE0C9AAD24Q30080000-07E74AF2-C896-4D2E-AABF-11A0631844ADQ33249392-EFDF707E-1AA8-47DA-BD81-93AE1193D3EEQ33592224-6AF2D6AB-1865-463A-AC3F-19019156C627Q33638309-C1CE3B94-CABA-4E5C-B771-7591A233D115Q33717303-6772C2DC-96CB-4FB1-AAF7-974AEE9D2EF4Q33823405-34AE1C0B-1D0E-4C31-9E2C-72DAAEFDA210Q33830343-1EB1D6A7-F782-46AF-A9EE-2E19A65C0A04Q33857998-E54AC74E-52B1-4F58-B4BC-95158B663D53Q33863162-57F03629-606A-4AE9-9DE9-6F3F256850DCQ33881778-7A6D2900-CB1E-4DFC-A5E7-D84DA945CA5BQ33888344-E722C5DF-0359-40A4-A708-5ADDA531E074Q33950252-58C316AD-5952-427C-A556-19464F34F90CQ33973031-5F868FF6-C3B3-43FA-A2E7-CE5E7663E2BFQ34017151-9BEEC953-C18D-4987-A5FC-5EAE11FF17C4Q34040994-71DE68C7-A44B-4419-BABE-0F9CDEEC176BQ34079148-037775A0-2667-4AFD-9DF5-21CADB0274BCQ34080254-EDB43117-87D3-4392-8D20-343700AED950Q34177343-98AF7E7F-F9A8-4D7A-8381-C28FA0B6A1FCQ34256578-B1524629-1DE2-4EDB-847B-93F87B197DB8Q34349874-F9C1A4E0-9B37-45B5-B106-40E4483E8D5DQ34377128-32C2A734-1E28-4AF2-8A3B-214200EF68BEQ34390399-B8F0B9B3-09BD-4794-B6D3-B8F4C1768385Q34489613-F99AE02A-1A7E-4471-85BB-084E2CEB8F54Q34683157-B5C07856-CA58-4124-913E-10E789D7B203Q34967934-A0F65E3B-61D2-4CA1-AD37-081533A6096EQ34974247-8DCA8D0E-7966-4C51-9ED0-B1E85724678EQ35041465-5EF4653D-9069-409E-BC04-D0CF7DEC5938Q35536342-64994275-9171-4C02-9EB8-A9DCECEABEBFQ35554260-D852915D-69DE-452D-9D1D-5C625569C3CFQ35573352-9B84B043-951F-48F8-88C5-DA7B2A2700A0Q35619645-B607B3C1-0221-42A1-AF3F-462E5BE053CDQ35736759-7425FB50-0E3B-49C0-AEBD-DCEF8C37E15D
P2860
Defective regulation of outwardly rectifying Cl- channels by protein kinase A corrected by insertion of CFTR.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Defective regulation of outwar ...... orrected by insertion of CFTR.
@en
type
label
Defective regulation of outwar ...... orrected by insertion of CFTR.
@en
prefLabel
Defective regulation of outwar ...... orrected by insertion of CFTR.
@en
P2093
P4510
P356
P1433
P1476
Defective regulation of outwar ...... orrected by insertion of CFTR.
@en
P2093
Guggino WB
Zeitlin PL
P2888
P304
P356
10.1038/358581A0
P407
P577
1992-08-01T00:00:00Z
P6179
1019593294