(Q40598163)

21 September 2017

title

CFTR localization in native airway cells and cell lines expressing wild-type or F508del-CFTR by a panel of different antibodies (English)

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21 September 2017

author

Margarida Duarte Amaral

7

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21 September 2017

Paulo Nogueira

4

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author name string

Isabel Carvalho-Oliveira

1

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21 September 2017

Alexandra Efthymiadou

2

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21 September 2017

Rui Malhó

3

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21 September 2017

Maria Tzetis

5

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21 September 2017

Emmanuel Kanavakis

6

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21 September 2017

Deborah Penque

8

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21 September 2017

publication date

1 February 2004

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Journal of Histochemistry and Cytochemistry

21 September 2017

published in

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21 September 2017

volume

52

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21 September 2017

issue

2

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21 September 2017

page(s)

193-203

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Modified epithelial cell distribution in chronic airways inflammation.

21 September 2017

cites work

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https://api.crossref.org/works/10.1177%2F002215540405200207

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F002215540405200207

Cystic fibrosis: molecular biology and therapeutic implications

21 January 2018

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https://api.crossref.org/works/10.1177%2F002215540405200207

Immunocytochemical localization of the cystic fibrosis gene product CFTR

21 January 2018

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https://api.crossref.org/works/10.1177%2F002215540405200207

Quantitative assessment of the epithelial and inflammatory cell populations in large airways of normals and individuals with cystic fibrosis

21 January 2018

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Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia

21 January 2018

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https://api.crossref.org/works/10.1177%2F002215540405200207

CFTR and differentiation markers expression in non-CF and delta F 508 homozygous CF nasal epithelium

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F002215540405200207

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F002215540405200207

Molecular cloning, characterization, and dynamics of rat formiminotransferase cyclodeaminase, a Golgi-associated 58-kDa protein

21 January 2018

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Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

21 January 2018

1 reference

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C-terminal truncations destabilize the cystic fibrosis transmembrane conductance regulator without impairing its biogenesis. A novel class of mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F002215540405200207

Multiple proteolytic systems, including the proteasome, contribute to CFTR processing

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F002215540405200207

DeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis

21 January 2018

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https://api.crossref.org/works/10.1177%2F002215540405200207

Biosynthesis and degradation of CFTR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F002215540405200207

Beta-COP localizes mainly to the cis-Golgi side in exocrine pancreas

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F002215540405200207

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F002215540405200207

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

21 January 2018

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In vivo cell-specific expression of the cystic fibrosis transmembrane conductance regulator

21 January 2018

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10.1177/002215540405200207

21 January 2018

Identifiers

DOI

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21 September 2017

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