Literature DB >> 6823316

Chloride impermeability in cystic fibrosis.

P M Quinton.   

Abstract

Cystic fibrosis is the most common fatal genetic disease affecting caucasians and is perhaps best characterized as an exocrinopathy involving a disturbance in fluid and electrolyte transport. A high NaCl concentration in the sweat is characteristic of patients with this disease; the basic physiological reason for this abnormality is unknown. We have microperfused isolated sweat ducts from control subjects and cystic fibrosis patients, and report here results which suggest that abnormally low Cl- permeability in cystic fibrosis leads to poor reabsorption of NaCl in the sweat duct, and hence to a high concentration of NaCl in the sweat.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6823316     DOI: 10.1038/301421a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  153 in total

1.  Vacuolar-type H+ -ATPase distribution in unstimulated and acetylcholine-activated isolated human eccrine sweat glands.

Authors:  D L Bovell; M T Clunes; E Roussa; J Burry; H Y Elder
Journal:  Histochem J       Date:  2000-07

2.  Quantitative analysis of inflammatory cells infiltrating the cystic fibrosis airway mucosa.

Authors:  C Hubeau; M Lorenzato; J P Couetil; D Hubert; D Dusser; E Puchelle; D Gaillard
Journal:  Clin Exp Immunol       Date:  2001-04       Impact factor: 4.330

Review 3.  Role of epithelial HCO3⁻ transport in mucin secretion: lessons from cystic fibrosis.

Authors:  Paul M Quinton
Journal:  Am J Physiol Cell Physiol       Date:  2010-10-06       Impact factor: 4.249

Review 4.  The biochemical defect in cystic fibrosis.

Authors:  A W Cuthbert
Journal:  J R Soc Med       Date:  1992       Impact factor: 5.344

5.  Cystic fibrosis genotypes and views on screening are both heterogeneous and population related.

Authors:  C R Scriver; T M Fujiwara
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

6.  Surface fluid absorption and secretion in small airways.

Authors:  A K M Shamsuddin; P M Quinton
Journal:  J Physiol       Date:  2012-04-30       Impact factor: 5.182

7.  Sparkling water--bicarbonate for cervix and cystic fibrosis.

Authors:  Gunnar C Hansson
Journal:  J Physiol       Date:  2010-08-01       Impact factor: 5.182

Review 8.  New insights into the pathogenesis of cystic fibrosis sinusitis.

Authors:  Eugene H Chang
Journal:  Int Forum Allergy Rhinol       Date:  2013-11-26       Impact factor: 3.858

9.  Properties and regulation of chloride channels in cystic fibrosis and normal airway cells.

Authors:  K Kunzelmann; H Pavenstädt; R Greger
Journal:  Pflugers Arch       Date:  1989-11       Impact factor: 3.657

Review 10.  Outwardly rectifying chloride channels and CF: a divorce and remarriage.

Authors:  W B Guggino
Journal:  J Bioenerg Biomembr       Date:  1993-02       Impact factor: 2.945

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.