Epithelial cell specific properties and genetic complementation in a delta F508 cystic fibrosis nasal polyp cell line (Q41300710)

29 September 2017

title

Epithelial cell specific properties and genetic complementation in a delta F508 cystic fibrosis nasal polyp cell line (English)

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29 September 2017

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K Kunzelmann

1

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29 September 2017

D C Lei

2

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29 September 2017

K Eng

3

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29 September 2017

L C Escobar

4

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29 September 2017

T Koslowsky

5

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29 September 2017

D C Gruenert

6

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29 September 2017

publication date

1 September 1995

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In Vitro Cellular & Developmental Biology - Animal

29 September 2017

published in

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29 September 2017

volume

31

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29 September 2017

issue

8

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29 September 2017

page(s)

617-624

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https://scigraph.springernature.com/pub.10.1007/bf02634315

29 September 2017

exact match

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cites work

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Gene expression from adeno-associated virus vectors in airway epithelial cells

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An immortalized cystic fibrosis tracheal epithelial cell line homozygous for the delta F508 CFTR mutation

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A Cystic Fibrosis Bronchial Epithelial Cell Line: Immortalization by Adeno-12-SV40 Infection

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Cyclic amphipathic peptide-DNA complexes mediate high-efficiency transfection of adherent mammalian cells

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Soluble 80-kd fragment of cell-CAM 120/80 disrupts cell-cell adhesion

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

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

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

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Defective regulation of outwardly rectifying Cl- channels by protein kinase A corrected by insertion of CFTR

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Characterization of immortal cystic fibrosis tracheobronchial gland epithelial cells

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A transformed human epithelial cell line that retains tight junctions post crisis

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Papilloma virus immortalized tracheal epithelial cells retain a well-differentiated phenotype

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Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosis.

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Cystic fibrosis: a disease in electrolyte transport.

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12 December 2020

The delta F508 mutation decreases the stability of cystic fibrosis transmembrane conductance regulator in the plasma membrane. Determination of functional half-lives on transfected cells

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Ca(2+)- and swelling-induced activation of ion conductances in bronchial epithelial cells

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Monoclonal antibodies directed against human airway secretions. Localization and characterization of antigens

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Persistence of abnormal chloride conductance regulation in transformed cystic fibrosis epithelia.

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Episomal expression of wild-type CFTR corrects cAMP-dependent chloride transport in respiratory epithelial cells

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12 December 2020

Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene

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12 December 2020

In vivo transfer of the human cystic fibrosis transmembrane conductance regulator gene to the airway epithelium

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12 December 2020

Transformed sweat gland and nasal epithelial cell lines from control and cystic fibrosis individuals

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CFTR channels in immortalized human airway cells

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

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Identifiers

DOI

10.1007/BF02634315

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Dimensions Publication ID

29 September 2017

1010477282

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