Mucin Production and Hydration Responses to Mucopurulent Materials in Normal versus Cystic Fibrosis Airway Epithelia.

about

Mucin Production and Hydration Responses to Mucopurulent Materials in Normal versus Cystic Fibrosis Airway Epithelia.

Item

http://www.wikidata.org/entity/Q54323211

description

2018 nî lūn-bûn

@nan

2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

@yue

2018年學術文章

@zh-hant

name

Mucin Production and Hydration ...... tic Fibrosis Airway Epithelia.

@en

Mucin Production and Hydration ...... tic Fibrosis Airway Epithelia.

@nl

type

Item

label

Mucin Production and Hydration ...... tic Fibrosis Airway Epithelia.

@en

Mucin Production and Hydration ...... tic Fibrosis Airway Epithelia.

@nl

prefLabel

Mucin Production and Hydration ...... tic Fibrosis Airway Epithelia.

@en

Mucin Production and Hydration ...... tic Fibrosis Airway Epithelia.

@nl

P1476

Mucin Production and Hydration ...... tic Fibrosis Airway Epithelia.

@en

P2093

C William Davis

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

Carla M P Ribeiro

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

Giorgia Radicioni

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

Lubna H Abdullah

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

Megan J Webster

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

Mehmet Kesimer

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

Raymond Coakley

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

Richard C Boucher

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

Robert Tarran

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

Yunxiang Zhu

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

P2860

Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice

Muc5b is required for airway defence

Cystic fibrosis airway secretions exhibit mucin hyperconcentration and increased osmotic pressure.

Mucus clearance as a primary innate defense mechanism for mammalian airways.

Proteinases of Pseudomonas aeruginosa evoke mucin release by tracheal epithelium.

Chronic bronchitis and current smoking are associated with more goblet cells in moderate to severe COPD and smokers without airflow obstruction.

Serine proteases degrade airway mucins in cystic fibrosis.

Baseline Goblet Cell Mucin Secretion in the Airways Exceeds Stimulated Secretion over Extended Time Periods, and Is Sensitive to Shear Stress and Intracellular Mucin Stores.

The Relationship of Mucus Concentration (Hydration) to Mucus Osmotic Pressure and Transport in Chronic Bronchitis

Soluble mediators, not cilia, determine airway surface liquid volume in normal and cystic fibrosis superficial airway epithelia.

P304

481-491

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

P31

scholarly article

P356

10.1164/RCCM.201706-1139OC

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

P407

English

P433

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

P478

197

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

P577

2018-02-01T00:00:00Z

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

P698

29099608

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

P921

cystic fibrosis

P932

5821906

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