Dr Alexandra Mc Carron
Grant-Funded Researcher (B)
Adelaide Medical School
Faculty of Health and Medical Sciences
Eligible to supervise Masters and PhD (as Co-Supervisor) - email supervisor to discuss availability.
I am a postdoctoral researcher with the Cystic Fibrosis Airway Research Group (CFARG), based in the Department of Respiratory Medicine at the Women's and Children's Hospital.
My research
My research is in the area of airway gene therapy, a therapeutic approach that has potential to treat or prevent cystic fibrosis lung disease by correcting the underlying genetic defect. My work includes the production of lentiviral gene vectors, characterising and employing cystic fibrosis animal models for trialing of airway gene therapy, and investigating novel methods for enhancing the efficacy of airway gene transfer.
Student projects
I have projects available for Summer Research Scholarship students, Bachelor of Health and Medical Sciences (BHMS) Third Year Research Placement students, and Honours students. The skills developed during these projects can include: rodent handling, airway gene delivery techniques, tissue collection, histology, immunohistochemistry, cell culture, gene vector production, data collection, analysis and interpretation.
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Education
Date Institution name Country Title 2021 The University of Adelaide Australia PhD in Medicine 2015 The University of Adelaide Australia Bachelor of Health Science (Honours) 2014 The University of Adelaide Australia Bachelor of Science (Animal Science)
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Journals
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Conference Papers
Year Citation 2019 Morgan, K. S., Gradl, R., Dierolf, M., Jud, C., Günther, B., Werdiger, F., . . . Donnelley, M. W. (2019). In vivo x-ray imaging of the respiratory system using synchrotron sources and a compact light source. In B. Müller, & G. Wang (Eds.), Developments in X-Ray Tomography XII Vol. 11113 (pp. 111130G-1-111130G-12). online: Society of Photo-optical Instrumentation Engineers.
DOI Scopus12019 Li, J., Quirk, B. C., Delhove, J., Kirk, R., Mc Carron, A., Cmielewski, P., . . . McLaughlin, R. A. (2019). Imaging genetically-modified cells with a miniaturised multimodal optical coherence tomography + fluorescence probem. In Proceedings of the 2019 IEEE Photonics Conference (IPC) (pp. 1-2). Piscataway, NJ: IEEE.
DOI2019 McCarron, A., Donnelley, M., Cmielewski, P., McIntyre, C., & Parsons, D. (2019). Transient Lentiviral Vector Production Using a Packed-Bed Bioreactor System. In MOLECULAR THERAPY Vol. 27 (pp. 209). Washington, DC: CELL PRESS. -
Conference Items
Year Citation 2023 Rout-Pitt, N., Mc Carron, A., Boog, B., Parsons, D., & Donnelley, M. (2023). A twist in the cystic fibrosis story—TGF-β1 treatment affects epithelialmesenchymal transition differentially in two cystic fibrosis rat airway cell models. Poster session presented at the meeting of North American Cystic Fibrosis Conference.
2024 N. Rout-Pitt, A. McCarron, N. Reyne, D. Parsons. M. Donnelley. Cystic Fibrosis Foundation, "Unravelling the Role of Epithelial-Mesenchymal Transition (EMT) in Cystic Fibrosis Lung Disease: Insights, Challenges, and Therapeutic Prospects", $175,000.
2024 P. Asare, C. A Foakwah, B. Ahinkorah, A. McCarron, S. Sterling. Medical Research Future Fund, “Effectiveness of Zinc Supplementation in Respiratory Infections in COPD patients: A randomised control trial”, $990,064.
2024 A. McCarron, R. Smith, K. Morgan, D. Parsons, M. Donnelley. Cystic Fibrosis Geelong Genetic Therapies Innovation Grant, “Harnessing the power of magnets: Improved effectiveness of airway gene therapy for the treatment of cystic fibrosis lung disease”, $80,000.
2023 E. Schneider-Futschik, J. Bourke, D. Parsons, H. Chinnery. J. Taylor-Cousar, P. Middleton, A. McCarron and N. Reyne. Cystic Fibrosis Foundation “Delaying the onset of cystic fibrosis pathologies” $282,000
2023 A. McCarron, N. Reyne. P. Cmielewski, M. Donnelley, D. Parsons. Channel 7 Children’s Research Foundation. “Does the presence of lung infection impact the efficacy of cystic fibrosis airway gene therapy?” $40,060.
2022 M. Donnelley, D. Parsons, A. McCarron, C. Christou, T. Goddard. Cystic Fibrosis Foundation. “Effective delivery of genetic therapeutics for cystic fibrosis airway disease”, $307,512 USD (~$462,000 AUD).
2020 A. McCarron, P. Cmielewski, M. Donnelley, D. Parsons. Women’s and Children’s Hospital Foundation. “Airway gene correction in neonatal cystic fibrosis rats”, $100,000.
2017 M. Donnelley, N. Farrow, P Cmielewski, A. McCarron, D. Parsons. Women’s and Children’s Hospital Foundation. “Effective re-dosing protocols for lasting cystic fibrosis lentiviral airway gene therapy”, $75,240.
2017 M. Donnelley, C. McIntyre, N. Rout-Pitt, A. McCarron, D. Parsons. Channel 7 Children’s Research Foundation. “Improving the efficiency of cystic fibrosis airway gene therapy”, $74,213.
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Current Higher Degree by Research Supervision (University of Adelaide)
Date Role Research Topic Program Degree Type Student Load Student Name 2024 Co-Supervisor Developing an effective airway stem cell therapy for the treatment of Cystic Fibrosis lung disease Doctor of Philosophy Doctorate Full Time Ms Stuti Saini 2023 Co-Supervisor Understanding and improving gene vector targeting with lentiviral magnetic nanoparticles Doctor of Philosophy under a Jointly-awarded Degree Agreement with Doctorate Part Time Ms Madison Michelle Davis 2021 Co-Supervisor Improving the effectiveness of airway lentiviral gene therapy for cystic fibrosis Doctor of Philosophy Doctorate Full Time Mrs Nikki Reyne
Connect With Me
External Profiles