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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 ...
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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 ...
Replacing defective microglia can halt ALSP—a fatal neurodegenerative disease—in mice and humans, offering hope for broader brain therapies.
In a paper published last month, researchers at UT Southwestern Medical Center introduced lipid nanoparticles — hollow, fatty ...
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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 ...
DNA makes RNA, RNA makes protein, protein makes phenotype—was the guiding framework for understanding inheritance and disease ...
The FDA has approved Zegfrovy (sunvozertinib) for locally advanced or metastatic NSCLC with EGFR exon 20 insertion mutations.
Researchers believe a usually harmless virus could trigger Parkinson’s disease. Researchers in Chicago believe they’ve found ...
Scientists have uncovered DNA from 214 ancient pathogens in prehistoric humans, including the oldest known evidence of plague ...
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News-Medical.Net on MSNNew gene editing approach targets mutation behind common genetic heart diseaseFourteen million people worldwide suffer from enlarged hearts, or hypertrophic cardiomyopathy (HCM), a genetic disease that ...
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