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Keywords: cystic fibrosis
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Articles
Biochem Soc Trans (2023) 51 (3): 1297–1306.
Published: 04 May 2023
...Shogo Taniguchi; Ryosuke Fukuda; Tsukasa Okiyoneda The cystic fibrosis transmembrane conductance regulator (CFTR) is a cAMP-regulated anion channel, which is expressed on the apical plasma membrane (PM) of epithelial cells. Mutations in the CFTR gene cause cystic fibrosis (CF), one of the most...
Articles
Biochem Soc Trans (2020) 48 (5): 2347–2357.
Published: 20 October 2020
... ) 12 8 2020 21 9 2020 22 9 2020 © 2020 The Author(s). Published by Portland Press Limited on behalf of the Biochemical Society 2020 asthma chronic obstructive pulmonary disease cilia cystic fibrosis mucus Xenopus As we breathe, we inhale particles, toxins...
Articles
Biochem Soc Trans (2018) 46 (3): 619–630.
Published: 09 May 2018
... based on their size or function. Two of the more well-known and widely studied ncRNA species are microRNAs (miRNAs) and lncRNAs. These are regulatory RNAs and their altered expression has been implicated in the pathogenesis of a variety of human diseases. Failure to express a functional cystic fibrosis...
Articles
Biochem Soc Trans (2015) 43 (5): 975–982.
Published: 09 October 2015
...Samuel J. Bose; Toby S. Scott-Ward; Zhiwei Cai; David N. Sheppard The anion channel cystic fibrosis transmembrane conductance regulator (CFTR) is a unique ATP-binding cassette (ABC) transporter. CFTR plays a pivotal role in transepithelial ion transport as its dysfunction in the genetic disease...
Includes: Supplementary data
Articles
Biochem Soc Trans (2011) 39 (4): 1045–1050.
Published: 20 July 2011
... defence molecules such as BPI, are of exceptional relevance. In the present review, we highlight possible functions of BPI during acute pneumonia and CF (cystic fibrosis)-associated chronic infections in the lung. 1 To whom correspondence should be addressed (email andre.gessner@klinik.uni...
Articles
Biochem Soc Trans (2011) 39 (4): 1023–1027.
Published: 20 July 2011
... salivary levels of the protein. 1 To whom correspondence should be addressed (email l.bingle@sheffield.ac.uk ). 27 4 2011 © The Authors Journal compilation © 2011 Biochemical Society 2011 cystic fibrosis eutherian lineage mucous cell non-small cell lung carcinoma palate...
Articles
Biochem Soc Trans (2010) 38 (2): 695–701.
Published: 22 March 2010
... review, we discuss a plausible use of genistein in treatment of two genetic disorders: CF (cystic fibrosis) and MPS (mucopolysaccharidosis). Although various biological actions of genistein are employed in these two cases, in vitro studies, tests on animal models and pilot clinical trials suggest...
Articles
Articles
Biochem Soc Trans (2003) 31 (4): 770–773.
Published: 01 August 2003
... subjects with MBL deficiency remain healthy. MBL deficiency is also associated with non-infectious diseases including systemic lupus erythematosus, rheumatoid arthritis, cystic fibrosis and common variable immunodeficiency. MBL deficiency may affect susceptibility to (e.g. meningococcal disease), or alter...