Expression of the cystic fibrosis phenotype in a renal amphibian epithelial cell line (Q41135250)

27 September 2017

title

Expression of the cystic fibrosis phenotype in a renal amphibian epithelial cell line (English)

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27 September 2017

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9

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Ling BN

1

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Zuckerman JB

2

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Lin C

3

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Harte BJ

4

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McNulty KA

5

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Smith PR

6

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Gomez LM

7

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Worrell RT

8

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Kleyman TR

10

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27 September 2017

language of work or name

English

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publication date

1 January 1997

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Journal of Biological Chemistry

27 September 2017

published in

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volume

272

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27 September 2017

issue

1

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27 September 2017

page(s)

594-600

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

27 September 2017

cites work

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Demonstration That CFTR Is a Chloride Channel by Alteration of Its Anion Selectivity

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Identification and regulation of the cystic fibrosis transmembrane conductance regulator-generated chloride channel

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The Cystic Fibrosis Transmembrane Conductance Regulator

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

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Interaction between cystic fibrosis transmembrane conductance regulator and outwardly rectified chloride channels

21 January 2018

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CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP

21 January 2018

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Na+ transport in cystic fibrosis respiratory epithelia. Abnormal basal rate and response to adenylate cyclase activation

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Evidence for reduced Cl- and increased Na+ permeability in cystic fibrosis human primary cell cultures.

21 January 2018

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Defective fluid transport by cystic fibrosis airway epithelia

21 January 2018

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Normalization of raised sodium absorption and raised calcium-mediated chloride secretion by adenovirus-mediated expression of cystic fibrosis transmembrane conductance regulator in primary human cystic fibrosis airway epithelial cells

21 January 2018

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CFTR as a cAMP-dependent regulator of sodium channels

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Regulation of plasma membrane recycling by CFTR.

21 January 2018

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Renal sodium channels: regulation and single channel properties

21 January 2018

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K(+)-sparing diuretic actions of trimethoprim: inhibition of Na+ channels in A6 distal nephron cells

21 January 2018

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Prostaglandin E2 activates clusters of apical Cl- channels in principal cells via a cyclic adenosine monophosphate-dependent pathway.

21 January 2018

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Identification and developmental expression of the Xenopus laevis cystic fibrosis transmembrane conductance regulator gene.

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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Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

21 January 2018

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DNA sequencing with chain-terminating inhibitors

21 January 2018

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Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

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Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

21 January 2018

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Antisense oligodeoxynucleotide to the cystic fibrosis gene inhibits anion transport in normal cultured sweat duct cells

21 January 2018

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Antisense oligodeoxynucleotide to the cystic fibrosis transmembrane conductance regulator inhibits cyclic AMP-activated but not calcium-activated cell volume reduction in a human pancreatic duct cell line

21 January 2018

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Antisense oligodeoxynucleotides to the cystic fibrosis transmembrane conductance regulator inhibit cAMP-activated but not calcium-activated chloride currents

21 January 2018

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Structure and function of amiloride-sensitive Na+ channels

21 January 2018

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Inhibition of apical Na+ channels in rabbit cortical collecting tubules by basolateral prostaglandin E2 is modulated by protein kinase C.

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.272.1.594

21 January 2018

Identifiers

DOI

10.1074/JBC.272.1.594

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27 September 2017

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