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Maximillian Woodall
Also known as: Max Woodall
University College London Institute of Child Health, St George's, University of London, University of Leeds, The King's School, Gloucester, Cystic Fibrosis Trust
Research areas: Medicine · Infectious Diseases · COVID-19 Clinical Research Studies · SARS-CoV-2 and COVID-19 Research · Cystic Fibrosis Research Advances
0000-0003-4511-9171
Employment
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University College London Institute of Child Health Research Fellow2020 - Present
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St George's, University of London Resident advisor/Student Counselor2018 - 2020
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Cystic Fibrosis Trust Research Scientist2016 - 2020
Education
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University of Leeds Biological Sciences (1st Class)2013 - 2016
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The King's School, Gloucester A Level2009 - 2011
Projects & Funding
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Personalised Engineered Cell Therapies for Cystic Fibrosis Cystic Fibrosis Trust2016 - 2020
Publications (14)
- Antiviral drug synergy and mutational signatures in different epithelial cell models of RSV and hPIV infection Save
- Efficient in vitro assay for evaluating drug efficacy and synergy against emerging SARS-CoV-2 strains Save
- Salivary IgA and vimentin differentiate in vitro SARS-CoV-2 infection: A study of 290 convalescent COVID-19 patients Save
- Lung viral infection modelling in a bioengineered whole-organ Save
- The emergence of goblet inflammatory or ITGB6hinasal progenitor cells determines age-associated SARS-CoV-2 pathogenesis Save
- K978C CFTR restores essential epithelial function with greater efficiency than wildtype CFTR when expressed in CF airway cells Save
- Human models for COVID‐19 research Save
- E-cigarette constituents propylene glycol and vegetable glycerin decrease glucose uptake and its metabolism in airway epithelial cells in vitro Save
- Investigating different Cystic Fibrosis Transmembrane Regulator gene sequences for use in gene therapy Save
- The effect of cystic fibrosis sputum on cystic fibrosis transmembrane regulator mediated Cl- transport and airway-surface-liquid height. Is gene editing sufficient to restore function in the cystic fibrosis environment? Save
- Can enhancing the expression and activity of the Cystic Fibrosis Transmembrane Regulator improve efficacy of gene therapy for Cystic Fibrosis? Save
- The effect of CF sputum on CFTR mediated Cl- transport and ASL height. Is gene editing sufficient to restore function in the CF environment? Save
- Development of an enhanced Cystic Fibrosis transmembrane regulator gene construct for homology-independent targeted integration in Cystic Fibrosis cell lines Save
- Effect of hyperglycaemia on CFTR function in Calu3 airway epithelial cells Save