Ivacaftor-induced sweat chloride reductions correlate with increases in airway surface liquid pH in cystic fibrosis

about

Ivacaftor-induced sweat chloride reductions correlate with increases in airway surface liquid pH in cystic fibrosis

Item

http://www.wikidata.org/entity/Q58792352

description

scientific article published on 09 August 2018

@en

wetenschappelijk artikel

@nl

наукова стаття, опублікована в серпні 2018

@uk

name

Ivacaftor-induced sweat chlori ...... e liquid pH in cystic fibrosis

@en

Ivacaftor-induced sweat chlori ...... e liquid pH in cystic fibrosis

@nl

type

Item

label

Ivacaftor-induced sweat chlori ...... e liquid pH in cystic fibrosis

@en

Ivacaftor-induced sweat chlori ...... e liquid pH in cystic fibrosis

@nl

prefLabel

Ivacaftor-induced sweat chlori ...... e liquid pH in cystic fibrosis

@en

Ivacaftor-induced sweat chlori ...... e liquid pH in cystic fibrosis

@nl

P1476

Ivacaftor-induced sweat chlori ...... e liquid pH in cystic fibrosis

@en

P2093

Brenda Grogan

http://www.w3.org/2001/XMLSchema#string

David A Stoltz

http://www.w3.org/2001/XMLSchema#string

Edward F McKone

http://www.w3.org/2001/XMLSchema#string

Jan L Launspach

http://www.w3.org/2001/XMLSchema#string

Michael J Welsh

http://www.w3.org/2001/XMLSchema#string

Pradeep K Singh

http://www.w3.org/2001/XMLSchema#string

Suzanne Carter

http://www.w3.org/2001/XMLSchema#string

P2860

Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation

Rescue of CF airway epithelial cell function in vitro by a CFTR potentiator, VX-770

Molecular basis for pH-dependent mucosal dehydration in cystic fibrosis airways

Origins of cystic fibrosis lung disease

Endogenous airway acidification. Implications for asthma pathophysiology.

Bicarbonate and functional CFTR channel are required for proper mucin secretion and link cystic fibrosis with its mucus phenotype.

Impact of CFTR Modulation on Intestinal pH, Motility, and Clinical Outcomes in Patients With Cystic Fibrosis and the G551D Mutation.

Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.

Cystic fibrosis pigs develop lung disease and exhibit defective bacterial eradication at birth.

Regulation of airway tight junctions by proinflammatory cytokines.

P31

scholarly article

P356

10.1172/JCI.INSIGHT.121468

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Mahmoud H Abou Alaiwa

Joseph Zabner

P577

2018-08-09T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

30089726

http://www.w3.org/2001/XMLSchema#string

P932

6129116

http://www.w3.org/2001/XMLSchema#string