Literature DB >> 16469862

Acid in the airways. Focus on "Hyperacidity of secreted fluid from submucosal glands in early cystic fibrosis".

Jeffrey J Wine.   

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Year:  2006        PMID： 16469862     DOI： 10.1152/ajpcell.00525.2005

Source DB:  PubMed          Journal:  Am J Physiol Cell Physiol        ISSN： 0363-6143            Impact factor:   4.249


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  5 in total

1.  Repurposing tromethamine as inhaled therapy to treat CF airway disease.

Authors:  Mahmoud H Abou Alaiwa; Janice L Launspach; Kelsey A Sheets; Jade A Rivera; Nicholas D Gansemer; Peter J Taft; Peter S Thorne; Michael J Welsh; David A Stoltz; Joseph Zabner
Journal:  JCI Insight       Date:  2016-06-02

2.  SLC26A9 is a Cl(-) channel regulated by the WNK kinases.

Authors:  Michael R Dorwart; Nikolay Shcheynikov; Youxue Wang; Steve Stippec; Shmuel Muallem
Journal:  J Physiol       Date:  2007-08-02       Impact factor: 5.182

Review 3.  The ABC protein turned chloride channel whose failure causes cystic fibrosis.

Authors:  David C Gadsby; Paola Vergani; László Csanády
Journal:  Nature       Date:  2006-03-23       Impact factor: 49.962

Review 4.  The porcine lung as a potential model for cystic fibrosis.

Authors:  Christopher S Rogers; William M Abraham; Kim A Brogden; John F Engelhardt; John T Fisher; Paul B McCray; Geoffrey McLennan; David K Meyerholz; Eman Namati; Lynda S Ostedgaard; Randall S Prather; Juan R Sabater; David Anthony Stoltz; Joseph Zabner; Michael J Welsh
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2008-05-16       Impact factor: 5.464

5.  SLC26A9 is a constitutively active, CFTR-regulated anion conductance in human bronchial epithelia.

Authors:  Carol A Bertrand; Ruilin Zhang; Joseph M Pilewski; Raymond A Frizzell
Journal:  J Gen Physiol       Date:  2009-03-16       Impact factor: 4.086
  5 in total

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