Polarized distribution of HCO3- transport in human normal and cystic fibrosis nasal epithelia.
about
SLC26A9 is a constitutively active, CFTR-regulated anion conductance in human bronchial epitheliaFunction of the HVCN1 proton channel in airway epithelia and a naturally occurring mutation, M91TMolecular mechanism of pancreatic and salivary gland fluid and HCO3 secretionDynamic control of cystic fibrosis transmembrane conductance regulator Cl(-)/HCO3(-) selectivity by external Cl(-)Mimicking the host and its microenvironment in vitro for studying mucosal infections by Pseudomonas aeruginosa.Decreased soluble adenylyl cyclase activity in cystic fibrosis is related to defective apical bicarbonate exchange and affects ciliary beat frequency regulation.Abnormal surface liquid pH regulation by cultured cystic fibrosis bronchial epithelium.Cystic fibrosis transmembrane conductance regulator is vital to sperm fertilizing capacity and male fertility.Function of Proton Channels in Lung Epithelia.Molecular and functional expression of anion exchangers in cultured normal human nasal epithelial cellsBiophysical model of ion transport across human respiratory epithelia allows quantification of ion permeabilities.Mechanisms of acid and base secretion by the airway epitheliumAnion secretion by a model epithelium: more lessons from Calu-3.The CF-modifying gene EHF promotes p.Phe508del-CFTR residual function by altering protein glycosylation and trafficking in epithelial cells.Basolateral chloride loading by the anion exchanger type 2: role in fluid secretion by the human airway epithelial cell line Calu-3.Bicarbonate-dependent chloride transport drives fluid secretion by the human airway epithelial cell line Calu-3.Initial interrogation, confirmation and fine mapping of modifying genes: STAT3, IL1B and IFNGR1 determine cystic fibrosis disease manifestationRegulation of CFTR channels by HCO(3)--sensitive soluble adenylyl cyclase in human airway epithelial cells.CK2 is a key regulator of SLC4A2-mediated Cl-/HCO3- exchange in human airway epithelia.The role of the basolateral outwardly rectifying chloride channel in human airway epithelial anion secretion.Expression and distribution of ion transport mRNAs in human nasal mucosa and nasal polyps.
P2860
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P2860
Polarized distribution of HCO3- transport in human normal and cystic fibrosis nasal epithelia.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
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2003年學術文章
@zh-hant
name
Polarized distribution of HCO3 ...... stic fibrosis nasal epithelia.
@en
Polarized distribution of HCO3 ...... stic fibrosis nasal epithelia.
@nl
type
label
Polarized distribution of HCO3 ...... stic fibrosis nasal epithelia.
@en
Polarized distribution of HCO3 ...... stic fibrosis nasal epithelia.
@nl
prefLabel
Polarized distribution of HCO3 ...... stic fibrosis nasal epithelia.
@en
Polarized distribution of HCO3 ...... stic fibrosis nasal epithelia.
@nl
P2093
P2860
P1476
Polarized distribution of HCO3 ...... stic fibrosis nasal epithelia.
@en
P2093
Anthony M Paradiso
Raymond D Coakley
Richard C Boucher
P2860
P304
P356
10.1113/JPHYSIOL.2002.034447
P407
P577
2003-01-31T00:00:00Z