What is really news and what do we know about model embryos?
July 05, 2023
The science behind the headlines.“Breakthrough!” “A major scientific first!” “The world’s first human synthetic embryos!” These are some of the breathless headlines that have appeared in the media since researchers announced they had developed embryo models...
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How Foundation donors are helping scientists attract more funding
May 26, 2023
Thank you to our donors! You're helping emerging science leaders attract more funding from other sources. With your support, we have awarded 18 promising researchers with Metcalf Prizes for Stem Cell Research.Each year, we award two $60,000 prizes...
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Teaspoons of treatment for the tiniest of patients
February 08, 2023
Extremely premature babies’ own stem cells could hold the key to a new treatment for brain injury associated with preterm birth. Monash University researcher Associate Professor Atul Malhotra, backed by the Foundation, is leading a clinical trial...
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Vale Alan Mackay-Sim
January 05, 2023
Nasal stem cell research legend and 2017 Australian of the Year Professor Emeritus Alan Mackay-Sim AM died on 4 January 2023. “Professor Emeritus Alan Mackay-Sim’s work in understanding the human brain and stem cells was game-changing and...
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What do new gene and cell therapies have to offer?
November 24, 2022
What do new gene and cell therapies have to offer conditions like cancer, inherited eye diseases, spinal muscular atrophy and other degenerative diseases? Can we engineer immune cells to treat cancer? Or bring eye sight by...
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Using stem cells to give sight and controlling rogue blood stem cells
November 15, 2022
Researchers working with stem cells to restore sight and fight blood cancers are the two winners of the 2022 Metcalf Prizes for Stem Cell Research, awarded by the National Stem Cell Foundation of Australia. Dr...
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Turning blood cells into muscle cells to test treatments for childhood muscular dystrophy
October 25, 2022
Melbourne researcher Dr Peter Houweling is growing mini-muscles in the lab, in order to study muscular dystrophy in children, without the need for invasive and painful tissue biopsies. “Basically, we take an ordinary blood sample and regress...
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