Actions of isoprenaline on amylase and total protein content of whole saliva in control, cystic fibrosis and cystic fibrosis heterozygote individuals-Reference-Cited by-同舟云学术

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Actions of isoprenaline on amylase and total protein content of whole saliva in control, cystic fibrosis and cystic fibrosis heterozygote individuals

Published:2008-01-21 Issue:6 Volume:83 Page:664-665
ISSN:0803-5253
Container-title:Acta Paediatrica
language:en
Short-container-title:

Author:

Davies H,Lewis MJ,Goodchild MC,McPherson MA

Publisher

Wiley

Subject

General Medicine,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.1994.tb13106.x/fullpdf

Reference8 articles.

1. Molecular and cellular biology of cystic fibrosis;McPherson;Mol Aspects Med,1991

2. Abnormalities in intracellular regulation in cystic fibrosis;McPherson;Br Med Bull,1992

3. Defective B-adrenergic secretory responses in submandi-bular acinar cells from cystic fibrosis patients;McPherson;Lancet,1986

4. An antibody against a CFTR-derived synthetic peptide, incorporated into living submandibular cells, inhibits beta-adrenergic stimulation of mucin secretion;Lloyd Mills;Biochem Biophys Res Commun,1992

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Intracellular free Ca2+dynamic changes to histamine are reduced in cystic fibrosis human tracheal gland cells;FEBS Letters;1996-05-20

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