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Claire E Wainwright

Showing results (21-30 of 96) with videos related to

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Gene|October 7, 2018
Mutations in the HFE gene can be associated with increased lung disease severity in cystic fibrosisDaniel J Smith, Kerenaftali Klein, Gunter Hartel, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 8, 2015
Pseudomonas aeruginosa genotypes acquired by children with cystic fibrosis by age 5-yearsTimothy J Kidd, Kay A Ramsay, Suzanna Vidmar, et al.
Thorax|October 5, 2010
Value of serology in predicting Pseudomonas aeruginosa infection in young children with cystic fibrosisTonia A Douglas, Siobhain Brennan, Luke Berry, et al.
Scientific Reports|July 25, 2020
Author Correction: Increased susceptibility of airway epithelial cells from ataxia-telangiectasia to S. pneumoniae infection due to oxidative damage and impaired innate immunityAbrey J Yeo, Anna Henningham, Emmanuelle Fantino, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 23, 2020
Total bacterial load, inflammation, and structural lung disease in paediatric cystic fibrosisSteven L Taylor, Lex E X Leong, Kerry L Ivey, et al.
Journal of Clinical Microbiology|September 20, 2013
Factors influencing acquisition of Burkholderia cepacia complex organisms in patients with cystic fibrosisKay A Ramsay, Claire A Butler, Stuart Paynter, et al.
Journal of Medical Microbiology|October 22, 2004
Rapid genotyping of Pseudomonas aeruginosa isolates harboured by adult and paediatric patients with cystic fibrosis using repetitive-element-based PCR assaysMelanie W Syrmis, Mark R O'Carroll, Theo P Sloots, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 7, 2022
Neutrophil respiratory burst activity is not exaggerated in cystic fibrosisDean Kelk, Jayden Logan, Isabella Andersen, et al.
Scientific Reports|February 24, 2019
Increased susceptibility of airway epithelial cells from ataxia-telangiectasia to S. pneumoniae infection due to oxidative damage and impaired innate immunityAbrey J Yeo, Anna Henningham, Emmanuelle Fantino, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 28, 2017
Recovery of lung function following a pulmonary exacerbation in patients with cystic fibrosis and the G551D-CFTR mutation treated with ivacaftorPatrick A Flume, Claire E Wainwright, D Elizabeth Tullis, et al.
Pageof 10

Showing results (21-30 of 96) with videos related to

Sort By:
Pageof 10
Gene|October 7, 2018
Mutations in the HFE gene can be associated with increased lung disease severity in cystic fibrosisDaniel J Smith, Kerenaftali Klein, Gunter Hartel, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 8, 2015
Pseudomonas aeruginosa genotypes acquired by children with cystic fibrosis by age 5-yearsTimothy J Kidd, Kay A Ramsay, Suzanna Vidmar, et al.
Thorax|October 5, 2010
Value of serology in predicting Pseudomonas aeruginosa infection in young children with cystic fibrosisTonia A Douglas, Siobhain Brennan, Luke Berry, et al.
Scientific Reports|July 25, 2020
Author Correction: Increased susceptibility of airway epithelial cells from ataxia-telangiectasia to S. pneumoniae infection due to oxidative damage and impaired innate immunityAbrey J Yeo, Anna Henningham, Emmanuelle Fantino, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 23, 2020
Total bacterial load, inflammation, and structural lung disease in paediatric cystic fibrosisSteven L Taylor, Lex E X Leong, Kerry L Ivey, et al.
Journal of Clinical Microbiology|September 20, 2013
Factors influencing acquisition of Burkholderia cepacia complex organisms in patients with cystic fibrosisKay A Ramsay, Claire A Butler, Stuart Paynter, et al.
Journal of Medical Microbiology|October 22, 2004
Rapid genotyping of Pseudomonas aeruginosa isolates harboured by adult and paediatric patients with cystic fibrosis using repetitive-element-based PCR assaysMelanie W Syrmis, Mark R O'Carroll, Theo P Sloots, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 7, 2022
Neutrophil respiratory burst activity is not exaggerated in cystic fibrosisDean Kelk, Jayden Logan, Isabella Andersen, et al.
Scientific Reports|February 24, 2019
Increased susceptibility of airway epithelial cells from ataxia-telangiectasia to S. pneumoniae infection due to oxidative damage and impaired innate immunityAbrey J Yeo, Anna Henningham, Emmanuelle Fantino, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 28, 2017
Recovery of lung function following a pulmonary exacerbation in patients with cystic fibrosis and the G551D-CFTR mutation treated with ivacaftorPatrick A Flume, Claire E Wainwright, D Elizabeth Tullis, et al.
Pageof 10