Projects per year
Projects
- 5 Finished
Search results
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Finished
Accelerating the identification and treatment of splice-altering mutations underlying inherited retinal diseases
Chen, F. (Investigator 01), Fletcher, S. (Investigator 02), McLenachan, S. (Investigator 03) & Cunningham, P. (Investigator 04)
NHMRC National Health and Medical Research Council
1/01/20 → 31/12/24
Project: Research
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2020 - Topcon OCT System with OCTA and Anterior Segment Options
Yu, D.-Y. (Investigator 01), Morgan, W. (Investigator 02), Mackey, D. (Investigator 03), Mian, A. (Investigator 04), Cringle, S. (Investigator 05), McAllister, I. (Investigator 06), Balaratnasingam, C. (Investigator 07), Chen, F. (Investigator 08), McLenachan, S. (Investigator 09), Yu, P. (Investigator 10), Mehnert, A. (Investigator 11), Jones, T. (Investigator 12), Davis, E. (Investigator 13) & Clark, A. (Investigator 14)
NHMRC National Health and Medical Research Council
1/01/20 → 31/12/20
Project: Research
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Utilising patient-specific retinal organoids in vitro to investigate the effects of an SNRNP200 mutation causing early onset retinitis pigmentosa
Mellough, C. (Investigator 01), McLenachan, S. (Investigator 02) & Chen, F. (Investigator 03)
1/01/18 → 31/12/18
Project: Research
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Xenotec OcuScience ERG System (Electroretinogram)
Degli-Esposti, M. (Investigator 01), Hunt, D. (Investigator 02), Forrester, J. (Investigator 03), Andoniou, C. (Investigator 04), dos Santos Carvalho, L. (Investigator 05), Hemmi, J. (Investigator 06), McLenachan, S. (Investigator 07) & Chen, F. (Investigator 08)
NHMRC National Health and Medical Research Council
1/01/16 → 31/12/17
Project: Research
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Developing personalized disease modelling for testing novel treatment in inherited retinal disease due to RP1 mutation
McLenachan, S. (Investigator 01) & Chen, F. (Investigator 02)
Ophthalmic Research Institute of Australia
1/01/16 → 31/12/16
Project: Research