Although cystic fibrosis is a single gene mutation, there are more than 1,000 different ways the CFTR gene can mutate in ...
The Hospital for Sick Children. "Newly uncovered mechanism could drive next-gen cystic fibrosis treatments." ScienceDaily. ScienceDaily, 13 March 2025. <www.sciencedaily.com / releases / 2025 / 03 / ...
From today, the updated indication for TRIKAFTA is as follows: TRIKAFTA is indicated for the treatment of cystic fibrosis in patients aged 2 years and older who have at least one F508del mutation in ...
A new study from The Hospital for Sick Children (SickKids) reveals the process underlying protein organization on cell ...
Learning from examples like congenital heart disease and cystic fibrosis can help health systems and clinicians prepare to care for an influx of patients with neuromuscular diseases as they reach ...
Studying how proteins cluster and organize themselves at the cell membrane could pave the way for innovative cystic fibrosis ...
A new research project focusing on rare genetic mutations that are linked to cystic fibrosis just received $600,000 in ...
The genetic condition cystic fibrosis had no treatments on the NHS before 2019 and a Daily Express campaign - now a miracle ...
A new study from The Hospital for Sick Children (SickKids) reveals the process underlying protein organization on cell membranes, a finding which ...
The Cystic Fibrosis Foundation estimates that close to 40,000 children and adults are currently living with CF in the United States, which expands to roughly 105,000 people across the world.
Rebecca Richards, a Montana parent of a child with disabilities, is among those worried about the implications of the cuts.
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