Acid Sphingomyelinase Inhibitors Normalize Pulmonary Ceramide and Inflammation in Cystic Fibrosis-Reference-Cited by-同舟云学术

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Acid Sphingomyelinase Inhibitors Normalize Pulmonary Ceramide and Inflammation in Cystic Fibrosis

Published:2010-06 Issue:6 Volume:42 Page:716-724
ISSN:1044-1549
Container-title:American Journal of Respiratory Cell and Molecular Biology
language:en
Short-container-title:Am J Respir Cell Mol Biol

Author:

Becker Katrin Anne,Riethmüller Joachim,Lüth Anja,Döring Gerd,Kleuser Burkhard,Gulbins Erich

Publisher

American Thoracic Society

Subject

Cell Biology,Clinical Biochemistry,Pulmonary and Respiratory Medicine,Molecular Biology

Reference27 articles.

1. Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA

2. Sheppard DN, Welsh MJ. Structure and function of the CFTR chloride channel.Physiol Rev1999;79:S23–S45.

3. Ceramide accumulation mediates inflammation, cell death and infection susceptibility in cystic fibrosis

4. Cystic fibrosis and innate immunity: how chloride channel mutations provoke lung disease

5. Schultz MJ, Rijneveld AW, Florquin S, Edwards CK, Dinarello CA, van der Poll T. Role of interleukin-1 in the pulmonary immune response duringPseudomonas aeruginosapneumonia.Am J Physiol Lung Cell Mol Physiol2002;282:L285–L290.

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