Overview
Availability
- Professor Scott Bell is:
- Available for supervision
Fields of research
Works
Search Professor Scott Bell’s works on UQ eSpace
2017
Journal Article
CFTR-dependent defect in alternatively-activated macrophages in cystic fibrosis
Tarique, Abdullah A., Sly, Peter D., Holt, Patrick G., Bosco, Anthony, Ware, Robert S., Logan, Jayden, Bell, Scott C., Wainwright, Claire E. and Fantino, Emmanuelle (2017). CFTR-dependent defect in alternatively-activated macrophages in cystic fibrosis. Journal of Cystic Fibrosis, 16 (4), 475-482. doi: 10.1016/j.jcf.2017.03.011
2017
Journal Article
Within-host evolution of Burkholderia pseudomallei during chronic infection of seven Australasian cystic fibrosis patients
Viberg, Linda T., Sarovich, Derek S., Kidd, Timothy J., Geake, James B., Bell, Scott C., Currie, Bart J. and Price, Erin P. (2017). Within-host evolution of Burkholderia pseudomallei during chronic infection of seven Australasian cystic fibrosis patients. mBio, 8 (2) e00356-17, 1-17. doi: 10.1128/mBio.00356-17
2017
Journal Article
Treatment decisions for MRSA in patients with cystic fibrosis (CF): When is enough, enough?
Bell, Scott C. and Flume, Patrick A. (2017). Treatment decisions for MRSA in patients with cystic fibrosis (CF): When is enough, enough?. Thorax, 72 (4), 297-299. doi: 10.1136/thoraxjnl-2016-209605
2017
Journal Article
Within-host whole genome analysis of an antibiotic resistant Pseudomonas aeruginosa strain sub-type in cystic fibrosis
Sherrard, Laura J., Tai, Anna S., Wee, Bryan A., Ramsay, Kay A., Kidd, Timothy J., Ben Zakour, Nouri L., Whiley, David M., Beatson, Scott A. and Bell, Scott C. (2017). Within-host whole genome analysis of an antibiotic resistant Pseudomonas aeruginosa strain sub-type in cystic fibrosis. PLoS One, 12 (3) e0172179, e0172179.1-e0172179.15. doi: 10.1371/journal.pone.0172179
2017
Journal Article
A rapid pipeline to model rare neurodevelopmental disorders with simultaneous CRISPR/Cas9 gene editing
Bell, Scott, Peng, Huashan, Crapper, Liam, Kolobova, Ilaria, Maussion, Gilles, Vasuta, Cristina, Yerko, Volodymyr, Pan Wong, Tak and Ernst, Carl (2017). A rapid pipeline to model rare neurodevelopmental disorders with simultaneous CRISPR/Cas9 gene editing. Stem Cells Translational Medicine, 6 (3), 886-896. doi: 10.1002/sctm.16-0158
2017
Journal Article
Lumacaftor/ivacaftor treatment of patients with cystic fibrosis heterozygous for F508del-CFTR
Rowe, Steven M., McColley, Susanna A., Rietschel, Ernst, Li, Xiaolei, Bell, Scott C., Konstan, Michael W., Marigowda, Gautham, Waltz, David and Boyle, Michael P. (2017). Lumacaftor/ivacaftor treatment of patients with cystic fibrosis heterozygous for F508del-CFTR. Annals of the American Thoracic Society, 14 (2), 213-219. doi: 10.1513/AnnalsATS.201609-689OC
2017
Journal Article
Implication of LRRC4C and DPP6 in neurodevelopmental disorders
Maussion, Gilles, Cruceanu, Cristiana, Rosenfeld, Jill A., Bell, Scott C., Jollant, Fabrice, Szatkiewicz, Jin, Collins, Ryan L., Hanscom, Carrie, Kolobova, Ilaria, de Champfleur, Nicolas Menjot, Blumenthal, Ian, Chiang, Colby, Ota, Vanessa, Hultman, Christina, O'Dushlaine, Colm, McCarroll, Steve, Alda, Martin, Jacquemont, Sebastien, Ordulu, Zehra, Marshall, Christian R., Carter, Melissa T., Shaffer, Lisa G., Sklar, Pamela, Girirajan, Santhosh, Morton, Cynthia C., Gusella, James F., Turecki, Gustavo, Stavropoulos, Dimitri J., Sullivan, Patrick F. ... Ernst, Carl (2017). Implication of LRRC4C and DPP6 in neurodevelopmental disorders. American Journal of Medical Genetics, Part A, 173 (2), 395-406. doi: 10.1002/ajmg.a.38021
2017
Journal Article
JCF - 2016
Bell, Scott C., Castellani, Carlo and Flume, Patrick A. (2017). JCF - 2016. Journal of Cystic Fibrosis, 16 (1), 6-6. doi: 10.1016/j.jcf.2016.12.014
2017
Journal Article
Clostridium difficile infection in cystic fibrosis: an uncommon but life-threatening complication
Piccolo, Francesco, Tai, Anna Sze, Ee, Hooi, Mulrennan, Siobhain, Bell, Scott and Ryan, Gerard (2017). Clostridium difficile infection in cystic fibrosis: an uncommon but life-threatening complication. Respirology Case Reports, 5 (1) e00204, e00204. doi: 10.1002/rcr2.204
2017
Journal Article
Limitations to providing adult cystic fibrosis care in Europe: results of a care centre survey
Madge, Susan, Bell, Scott C., Burgel, Pierre- Régis, De Rijcke, Karleen, Blasi, Francesco and Elborn, J. Stuart (2017). Limitations to providing adult cystic fibrosis care in Europe: results of a care centre survey. Journal of Cystic Fibrosis, 16 (1), 85-88. doi: 10.1016/j.jcf.2016.07.001
2017
Journal Article
Effect of Nerve Stimulation Use on the Success Rate of Ultrasound-Guided Subsartorial Saphenous Nerve Block A Randomized Controlled Trial
Montgomery, Shaylyn H., Shamji, Colleen M., Yi, Grace S., Yarnold, Cynthia H., Head, Stephen J., Bell, Scott C. and Schwarz, Stephan K. W. (2017). Effect of Nerve Stimulation Use on the Success Rate of Ultrasound-Guided Subsartorial Saphenous Nerve Block A Randomized Controlled Trial. Regional Anesthesia and Pain Medicine, 42 (1), 25-31. doi: 10.1097/AAP.0000000000000522
2016
Journal Article
Emergence and spread of a human-transmissible multidrug-resistant nontuberculous mycobacterium
Bryant, Josephine M., Grogono, Dorothy M., Rodriguez-Rincon, Daniela, Everall, Isobel, Brown, Karen P., Moreno, Pablo, Verma, Deepshikha, Hill, Emily, Drijkoningen, Judith, Gilligan, Peter, Esther, Charles R., Noone, Peadar G., Giddings, Olivia, Bell, Scott C., Thomson, Rachel, Wainwright, Claire E., Coulter, Chris, Pandey, Sushil, Wood, Michelle E., Stockwell, Rebecca E., Ramsay, Kay A., Sherrard, Laura J., Kidd, Timothy J., Jabbour, Nassib, Johnson, Graham R., Knibbs, Luke D., Morawska, Lidia, Sly, Peter D., Jones, Andrew ... Floto, R. Andres (2016). Emergence and spread of a human-transmissible multidrug-resistant nontuberculous mycobacterium. Science, 354 (6313), 751-757. doi: 10.1126/science.aaf8156
2016
Journal Article
Lesch-Nyhan syndrome: Models, theories, and therapies
Bell, Scott, Kolobova, Ilaria, Crapper, Liam and Ernst, Carl (2016). Lesch-Nyhan syndrome: Models, theories, and therapies. Molecular Syndromology, 7 (6), 302-311. doi: 10.1159/000449296
2016
Journal Article
Standardy opieki Europejskiego Towarzystwa Mukowiscydozy: wytyczne i najlepsze praktyki
Smyth, Alan R., Bell, Scott C., Bojcin, Snezana, Bryon, Mandy, Duff, Alistair, Flume, Patrick, Kashirskaya, Nataliya, Munck, Anne, Ratjen, Felix, Schwarzenberg, Sarah Jane, Sermet-Gaudelus, Isabelle, Southern, Kevin W., Taccetti, Giovanni, Ullrich, Gerald and Wolfe, Sue (2016). Standardy opieki Europejskiego Towarzystwa Mukowiscydozy: wytyczne i najlepsze praktyki. Pediatria Polska, 91 (Supp.1), S30-S53. doi: 10.1016/j.pepo.2016.08.014
2016
Journal Article
The changing prevalence of pulmonary infection in adults with cystic fibrosis: a longitudinal analysis
Ramsay, Kay A., Sandhu, Harpreet, Geake, James B., Ballard, Emma, O'Rourke, Peter, Wainwright, Claire E., Reid, David W., Kidd, Timothy J. and Bell, Scott C. (2016). The changing prevalence of pulmonary infection in adults with cystic fibrosis: a longitudinal analysis. Journal of Cystic Fibrosis, 16 (1), 70-77. doi: 10.1016/j.jcf.2016.07.010
2016
Journal Article
Pulmonary artery enlargement and cystic fibrosis pulmonary exacerbations: a cohort study
Wells, J. Michael, Farris, Roopan F., Gosdin, Taylor A., Dransfield, Mark T., Wood, Michelle E., Bell, Scott C. and Rowe, Steven M. (2016). Pulmonary artery enlargement and cystic fibrosis pulmonary exacerbations: a cohort study. Lancet Respiratory Medicine, 4 (8), 636-645. doi: 10.1016/S2213-2600(16)30105-9
2016
Journal Article
The role of anaerobic bacteria in the cystic fibrosis airway
Sherrard, Laura J., Bell, Scott C. and Tunney, Michael M. (2016). The role of anaerobic bacteria in the cystic fibrosis airway. Current Opinion in Pulmonary Medicine, 22 (6), 637-643. doi: 10.1097/MCP.0000000000000299
2016
Journal Article
A novel method and its application to measuring pathogen decay in bioaerosols from patients with respiratory disease
Johnson, Graham R., Knibbs, Luke D., Kidd, Timothy J., Wainwright, Claire E., Wood, Michelle E., Ramsay, Kay A., Bell, Scott C. and Morawska, Lidia (2016). A novel method and its application to measuring pathogen decay in bioaerosols from patients with respiratory disease. PLoS One, 11 (7) e0158763, e0158763. doi: 10.1371/journal.pone.0158763
2016
Journal Article
The cystic fibrosis foundation patient registry: Design and methods of a national observational disease registry
Stephenson, Anne L. and Bell, Scott C. (2016). The cystic fibrosis foundation patient registry: Design and methods of a national observational disease registry. Annals of the American Thoracic Society, 13 (7), 1014-1015. doi: 10.1513/AnnalsATS.201604-250ED
2016
Journal Article
A phase 3, multi-center, multinational, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of levofloxacin inhalation solution (APT-1026) in stable cystic fibrosis patients
Flume, Patrick A., VanDevanter, Donald R., Morgan, Elizabeth E., Dudley, Michael N., Loutit, Jeffery S., Bell, Scott C., Kerem, Eitan, Fischer, Rainald, Smyth, Alan R., Aaron, Shawn D., Conrad, Douglas, Geller, David E. and Elborn, J. Stuart (2016). A phase 3, multi-center, multinational, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of levofloxacin inhalation solution (APT-1026) in stable cystic fibrosis patients. Journal of Cystic Fibrosis, 15 (4), 495-502. doi: 10.1016/j.jcf.2015.12.004
Funding
Current funding
Supervision
Availability
- Professor Scott Bell is:
- Available for supervision
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Supervision history
Current supervision
-
Doctor Philosophy
Risk and mitigation of cough aerosols for people with cystic fibrosis.
Principal Advisor
Other advisors: Professor Rachel Thomson
-
Doctor Philosophy
The Pharmacokinetics & Pharmacodynamics of Antimycobacterial Drugs in People with Cystic Fibrosis and Drug-Resistant Tuberculosis Infection
Associate Advisor
Other advisors: Professor Rachel Thomson, Professor Jason Roberts
Completed supervision
-
2019
Doctor Philosophy
Impact of built environment, personal protective devices and ventilation on the dispersion of respiratory pathogens
Principal Advisor
-
2019
Master Philosophy
Infectious airborne transport in individuals with cystic fibrosis and mitigation strategies to reduce aerosol dispersal
Principal Advisor
-
2018
Doctor Philosophy
Diversity of environmental and clinical Pseudomonas aeruginosa isolates
Principal Advisor
Other advisors: Associate Professor David Whiley
-
2016
Doctor Philosophy
Heterogeneity within Pseudomonas aeruginosa shared strains in cystic fibrosis: the development and spread of antimicrobial resistance
Principal Advisor
Other advisors: Associate Professor David Whiley
-
2012
Doctor Philosophy
Diagnosis, epidemiology and population structure of Pseudomonas aeruginosa in cystic fibrosis.
Principal Advisor
-
2022
Doctor Philosophy
The effectiveness of ultraviolet C light at inactivating airborne Pseudomonas aeruginosa and Mycobacterium abscessus
Associate Advisor
-
2022
Doctor Philosophy
Deep Sequencing of Microbial Communities in Cystic Fibrosis Airways
Associate Advisor
Other advisors: Professor Ian Henderson
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