Characterization of novel airway submucosal gland cell models for cystic fibrosis studies (Q40394646)

20 September 2017

title

Characterization of novel airway submucosal gland cell models for cystic fibrosis studies (English)

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8

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Margarida Duarte Amaral

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Anabela S Ramalho

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Carlos M Farinha

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Carlos M Farinha

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Jiraporn Ousingsawat

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Jiraporn Ousingsawat

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Ana Carina da Paula

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Judy Cheung

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Rosalie Maurisse

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Dieter C Gruenert

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publication date

1 January 2005

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Cellular Physiology and Biochemistry

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published in

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volume

15

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issue

6

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page(s)

251-262

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The spectrum of cystic fibrosis mutations

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cites work

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Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epithelia

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Applicability of different antibodies for the immunohistochemical localization of CFTR in respiratory and intestinal tissues of human and murine origin.

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Liquid secretion properties of airway submucosal glands

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Fluid transport across cultures of human tracheal glands is altered in cystic fibrosis

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Established cell lines used in cystic fibrosis research

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CFTR expression and chloride secretion in polarized immortal human bronchial epithelial cells

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An Immortalized Cystic Fibrosis Tracheal Epithelial Cell Line Homozygous for the ΔF508 CFTR Mutation

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Turnover of the cystic fibrosis transmembrane conductance regulator (CFTR): slow degradation of wild-type and delta F508 CFTR in surface membrane preparations of immortalized airway epithelial cells

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

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Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance

21 January 2018

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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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A comparison of 14 antibodies for the biochemical detection of the cystic fibrosis transmembrane conductance regulator protein.

21 January 2018

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Decreased expression of the cystic fibrosis transmembrane conductance regulator protein in remodeled airway epithelium from lung transplanted patients

21 January 2018

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Efficient intracellular processing of the endogenous cystic fibrosis transmembrane conductance regulator in epithelial cell lines

21 January 2018

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Human tracheobronchial submucosal gland cells in culture.

21 January 2018

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SV40-transformed simian cells support the replication of early SV40 mutants

21 January 2018

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Enhanced transformation of human fibroblasts by origin-defective simian virus 40.

21 January 2018

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Methods for RNA extraction, cDNA preparation and analysis of CFTR transcripts.

21 January 2018

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Quantitative methods for the analysis of CFTR transcripts/splicing variants.

21 January 2018

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Targeted replacement of normal and mutant CFTR sequences in human airway epithelial cells using DNA fragments

21 January 2018

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Five Percent of Normal Cystic Fibrosis Transmembrane Conductance Regulator mRNA Ameliorates the Severity of Pulmonary Disease in Cystic Fibrosis

21 January 2018

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Antibodies for CFTR studies.

21 January 2018

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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

21 January 2018

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

21 January 2018

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Transcript analysis of the cystic fibrosis splicing mutation 1525-1G>A shows use of multiple alternative splicing sites and suggests a putative role of exonic splicing enhancers.

21 January 2018

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An mRNA surveillance mechanism that eliminates transcripts lacking termination codons

21 January 2018

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Ionomycin, thapsigargin, ryanodine, and sperm induced Ca2+ release increase during meiotic maturation of mouse oocytes

21 January 2018

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Bicarbonate and chloride secretion in Calu-3 human airway epithelial cells

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Absent secretion to vasoactive intestinal peptide in cystic fibrosis airway glands

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Biochemical methods to assess CFTR expression and membrane localization

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

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21 January 2018

Identifiers

DOI

10.1159/000087235

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20 September 2017

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