Impaired PGE2-stimulated Cl- and HCO3- secretion contributes to cystic fibrosis airway disease.

about

The protective effect of the EP2 receptor on TGF-β1 induced podocyte injury via the PI3K / Akt signaling pathway.

P2860

Q54110960-0015FA49-BA6C-4C5F-97FB-AD3482605D37

P2860

Impaired PGE2-stimulated Cl- and HCO3- secretion contributes to cystic fibrosis airway disease.

Item

http://www.wikidata.org/entity/Q48342278

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Impaired PGE2-stimulated Cl- a ...... ystic fibrosis airway disease.

@en

Impaired PGE2-stimulated Cl- a ...... ystic fibrosis airway disease.

@nl

type

Item

label

Impaired PGE2-stimulated Cl- a ...... ystic fibrosis airway disease.

@en

Impaired PGE2-stimulated Cl- a ...... ystic fibrosis airway disease.

@nl

prefLabel

Impaired PGE2-stimulated Cl- a ...... ystic fibrosis airway disease.

@en

Impaired PGE2-stimulated Cl- a ...... ystic fibrosis airway disease.

@nl

P1476

Impaired PGE2-stimulated Cl- a ...... ystic fibrosis airway disease.

@en

P2093

Beate Illek

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

Eric Sibley

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

Gopika Hari

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

Horst Fischer

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

Jackson Souza-Menezes

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

Jeffrey J Wine

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

Marcelo M Morales

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

Miriam Frankenthal Figueira

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

Nam Soo Joo

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

P2860

Function of the HVCN1 proton channel in airway epithelia and a naturally occurring mutation, M91T

A new phospholipase-C-calcium signalling pathway mediated by cyclic AMP and a Rap GTPase

NADPH oxidase-dependent acid production in airway epithelial cells

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

Marked increases in mucociliary clearance produced by synergistic secretory agonists or inhibition of the epithelial sodium channel.

Native small airways secrete bicarbonate.

Mucus secretion from individual submucosal glands of the ferret trachea.

CFTR-adenylyl cyclase I association responsible for UTP activation of CFTR in well-differentiated primary human bronchial cell cultures.

Molecular structure and physiological function of chloride channels.

Pseudomonas aeruginosa triggers CFTR-mediated airway surface liquid secretion in swine trachea.

P304

e0189894

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

P31

scholarly article

P356

10.1371/JOURNAL.PONE.0189894

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

Zachary M Sellers

P577

2017-12-27T00:00:00Z

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

P698

29281691

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

P921

cystic fibrosis

P932

5744969

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

Impaired PGE2-stimulated Cl- and HCO3- secretion contributes to cystic fibrosis airway disease.

about

P2860

P2860

Impaired PGE2-stimulated Cl- and HCO3- secretion contributes to cystic fibrosis airway disease.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932