Trafficking of GFP-tagged DeltaF508-CFTR to the plasma membrane in a polarized epithelial cell line (Q40769992)

23 September 2017

title

Trafficking of GFP-tagged DeltaF508-CFTR to the plasma membrane in a polarized epithelial cell line (English)

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23 September 2017

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Loffing-Cueni D

1

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23 September 2017

Loffing J

2

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23 September 2017

Shaw C

3

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23 September 2017

Taplin AM

4

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23 September 2017

Govindan M

5

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23 September 2017

Stanton CR

6

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23 September 2017

Stanton BA

7

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23 September 2017

publication date

1 December 2001

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American Journal of Physiology - Cell Physiology

23 September 2017

published in

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23 September 2017

volume

281

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23 September 2017

issue

6

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23 September 2017

page(s)

C1889-97

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Activation of deltaF508 CFTR in a cystic fibrosis respiratory epithelial cell line by 4-phenylbutyrate, genistein and CPX.

23 September 2017

cites work

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Chemical chaperones correct the mutant phenotype of the delta F508 cystic fibrosis transmembrane conductance regulator protein

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Strategies for correcting the delta F508 CFTR protein-folding defect

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Protein trafficking and polarity in kidney epithelium: from cell biology to physiology

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Functional activation of the cystic fibrosis trafficking mutant delta F508-CFTR by overexpression

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Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

21 January 2018

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Generation and characterization of a delta F508 cystic fibrosis mouse model.

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Functional cystic fibrosis transmembrane conductance regulator tagged with an epitope of the vesicular stomatis virus glycoprotein can be addressed to the apical domain of polarized cells

21 January 2018

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Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

21 January 2018

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Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia

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Modulation of Cl- secretion by benzimidazolones. II. Coordinate regulation of apical GCl and basolateral GK.

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Differential expression of ORCC and CFTR induced by low temperature in CF airway epithelial cells

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A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo

21 January 2018

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Characterization of two MDCK-cell subtypes as a model system to study principal cell and intercalated cell properties

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Surface expression of the cystic fibrosis transmembrane conductance regulator mutant DeltaF508 is markedly upregulated by combination treatment with sodium butyrate and low temperature

21 January 2018

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Genistein potentiates wild-type and delta F508-CFTR channel activity

21 January 2018

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cAMP-independent activation of CFTR Cl channels by the tyrosine kinase inhibitor genistein

21 January 2018

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Expression of normal and cystic fibrosis phenotypes by continuous airway epithelial cell lines

21 January 2018

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Aggresomes: a cellular response to misfolded proteins

21 January 2018

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The cystic fibrosis mutation (delta F508) does not influence the chloride channel activity of CFTR.

21 January 2018

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Functional expression and apical localization of the cystic fibrosis transmembrane conductance regulator in MDCK I cells

21 January 2018

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Polarization-dependent apical membrane CFTR targeting underlies cAMP-stimulated Cl- secretion in epithelial cells

21 January 2018

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A PDZ-interacting domain in CFTR is an apical membrane polarization signal

21 January 2018

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Membrane trafficking of the cystic fibrosis gene product, cystic fibrosis transmembrane conductance regulator, tagged with green fluorescent protein in madin-darby canine kidney cells

21 January 2018

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Correction of the apical membrane chloride permeability defect in polarized cystic fibrosis airway epithelia following retroviral-mediated gene transfer

21 January 2018

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Mutant (delta F508) cystic fibrosis transmembrane conductance regulator Cl- channel is functional when retained in endoplasmic reticulum of mammalian cells.

21 January 2018

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21 January 2018

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In vitro pharmacologic restoration of CFTR-mediated chloride transport with sodium 4-phenylbutyrate in cystic fibrosis epithelial cells containing delta F508-CFTR.

21 January 2018

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Glycerol reverses the misfolding phenotype of the most common cystic fibrosis mutation.

21 January 2018

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Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.

21 January 2018

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Novel pharmacologic therapies for cystic fibrosis

21 January 2018

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Butyrate increases apical membrane CFTR but reduces chloride secretion in MDCK cells

21 January 2018

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Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation

21 January 2018

1 reference

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10.1152/AJPCELL.2001.281.6.C1889

21 January 2018

Identifiers

DOI

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1 reference