Cell and Gene therapies Related News
Regenerative therapies for heart disease
Lorna Rothery spoke to cardiovascular regenerative medicine expert, Professor Paolo Madeddu, who co-led a groundbreaking study that identified a mutant anti-ageing gene that could...
How AI can improve genome editing
Researchers have developed an Artificial Intelligence (AI) tool that can predict the efficacy of genome editing repair options, reducing errors in the correction of...
OmniSpirant Limited launch new gene therapy treatment project
INSPIRE is an EU Project funded under the Horizon Europe research and innovation programme to develop a ground-breaking inhaled gene therapy treatment for lung...
Transforming cancer care through genomics
Lorna Rothery spoke to Parker Moss, Chief Partnership Officer at Genomics England about how the organisation’s Cancer 2.0 initiative is harnessing the potential of...
Gene therapy reduces neuropathic pain from spinal injuries
A new Gene therapy investigation may offer hope for spinal cord injury patients who experience neuropathic pain, discovering that the treatment effectively reduces the...
Gene therapy breakthrough could cure rare and fatal brain disease
A new gene therapy could offer a cure for a rare degenerative disease in children called Dopamine Transporter Deficiency Syndrome (DTDS).
A team of scientists...
New therapy could revolutionise treatment for fatal Sanfilippo Syndrome
A new combination therapy could revolutionise treatment for children living with a rare and fatal lysosomal storage disorder called Sanfilippo Syndrome.
GlycoNet researchers are using...
Is CRISPR gene therapy for rare Angelman Syndrome on the horizon?
For the first time, scientists have shown how gene editing techniques could be used as therapy for the rare neurodevelopmental disorder – Angelman syndrome.
Babies...
Successful treatment of patients with the autoimmune disease Lupus
A team of researchers have successfully treated two patients with the autoimmune disease systemic lupus erythematosus for the first time.
The team from Charité -...
Understanding MPS and other similar Lysosomal diseases
MPS Austria wants to make everyday life easier for children with Mucopolysaccharidosis and other similar Lysosomal diseases, and their families, by supporting them with...
Groundbreaking gene therapy could cure haemophilia
A ‘cure’ for haemophilia is one step closer, following results published in the New England Journal of Medicine of a groundbreaking gene therapy trial...
