(Q44546807)

4 December 2017

title

Activation of CFTR by genistein in human airway epithelial cell lines (English)

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4 December 2017

Charlotte Andersson

1

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4 December 2017

Zhanna Servetnyk

series ordinal

2

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4 December 2017

Godfried M Roomans

series ordinal

3

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4 December 2017

language of work or name

English

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publication date

1 August 2003

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Biochemical and Biophysical Research Communications

4 December 2017

published in

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4 December 2017

volume

308

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4 December 2017

issue

3

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4 December 2017

page(s)

518-522

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Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

4 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

Degradation of CFTR by the ubiquitin-proteasome pathway

7 January 2021

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Conformational maturation of CFTR but not its mutant counterpart (delta F508) occurs in the endoplasmic reticulum and requires ATP

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

DeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis

7 January 2021

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Cystic fibrosis F508del patients have apically localized CFTR in a reduced number of airway cells.

7 January 2021

1 reference

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The human DnaJ homologue (Hdj)-1/heat-shock protein (Hsp) 40 co-chaperone is required for the in vivo stabilization of the cystic fibrosis transmembrane conductance regulator by Hsp70

7 January 2021

1 reference

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The Hdj-2/Hsc70 chaperone pair facilitates early steps in CFTR biogenesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

The common variant of cystic fibrosis transmembrane conductance regulator is recognized by hsp70 and degraded in a pre-Golgi nonlysosomal compartment

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

The molecular chaperone Hsc70 assists the in vitro folding of the N-terminal nucleotide-binding domain of the cystic fibrosis transmembrane conductance regulator

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

The Hsc70 co-chaperone CHIP targets immature CFTR for proteasomal degradation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

Ubiquitin-dependent degradation of certain protein substrates in vitro requires the molecular chaperone Hsc70

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

Sodium 4-phenylbutyrate downregulates Hsc70: implications for intracellular trafficking of DeltaF508-CFTR

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

Sodium 4-phenylbutyrate downregulates HSC70 expression by facilitating mRNA degradation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

Induction of HSP70 promotes DeltaF508 CFTR trafficking

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

Inhibition of ATPase, GTPase and adenylate kinase activities of the second nucleotide-binding fold of the cystic fibrosis transmembrane conductance regulator by genistein.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

Actions of genistein on cystic fibrosis transmembrane conductance regulator channel gating. Evidence for two binding sites with opposite effects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

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

7 January 2021

1 reference

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Development and biological applications of chloride-sensitive fluorescent indicators

7 January 2021

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Chloride conductive and cotransport mechanisms in cultures of canine tracheal epithelial cells measured by an entrapped fluorescent indicator.

7 January 2021

1 reference

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Pharmacological modulation of ion transport across wild-type and DeltaF508 CFTR-expressing human bronchial epithelia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

Effect of genistein on native epithelial tissue from normal individuals and CF patients and on ion channels expressed in Xenopus oocytes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

Alternate stimulation of apical CFTR by genistein in epithelia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

Daidzein is a more bioavailable soymilk isoflavone than is genistein in adult women

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

Modulation of CFTR chloride channels by calyculin A and genistein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

Submucosal glands are the predominant site of CFTR expression in the human bronchus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

Activation of wild-type and deltaF508-CFTR by phosphodiesterase inhibitors through cAMP-dependent and -independent mechanisms

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2901436-0

10.1016/S0006-291X(03)01436-0

7 January 2021

Identifiers

DOI

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4 December 2017

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