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21h
The Brighterside of News on MSNScientists edit mitochondrial DNA to reverse genetic diseases which often have no cureFor decades, the dream of fixing harmful mutations in mitochondrial DNA felt out of reach. Scientists have long known these ...
The research looked specifically at blood stem cells, which live in the bone marrow and make different types of blood cells.
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is a progressive neurological disease with an ...
Unexpected mutations in blood stem cells may help protect against Alzheimer’s disease. A new study published in the journal ...
Researchers in Chicago believe they’ve found a virus that could be a trigger for Parkinson’s disease. Parkinson’s impacts ...
Replacing defective microglia can halt ALSP—a fatal neurodegenerative disease—in mice and humans, offering hope for broader brain therapies.
Rare genetic diseases are challenging for patients and their families—made all the more overwhelming because symptoms tend to ...
A deeper understanding of how DNA changes over generations helps scientists learn why people differ and how diseases develop.
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New Scientist on MSNFatal genetic disorder treated by replacing the brain's immune cellsMicroglia replacement therapy helps treat people with a rare genetic condition called ALSP, suggesting the approach could ...
1d
AZoLifeSciences on MSNReplacing mutated microglia with healthy microglia halts progression of genetic neurological disease in mice and humansA groundbreaking study led by Prof. Bo Peng at Fudan University demonstrates that microglia replacement effectively halts the ...
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The Times of Israel on MSNScientists develop model to understand rare brain disease found in 40 kids worldwideTel Aviv University researchers say their investigation into a GRIN2D gene mutation will advance research into a protein ...
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