New approach to delivering gene therapy for cystic fibrosis
A lipid nanoparticle-based gene therapy for cystic fibrosis restores biological function in a preclinical model...
A lipid nanoparticle-based gene therapy for cystic fibrosis restores biological function in a preclinical model...
by BioNews
New genetic causes of inherited blindness have been discovered that may offer answers to families with unexplained vision loss...
Over 31,000 new transcripts found in blood cells from non-European populations are absent from current human gene reference maps...
by Dr Teja Rus
A new multipurpose genome editing approach could address around a third of rare genetic diseases...
The largest gene-expression study in African Americans with Alzheimer's disease reveals overexpression of a gene also implicated in those with white European ancestry...
Recovery was observed in mice receiving a stem cell transplant post-stroke, according to new research...
An artificial intelligence tool for helping to create CRISPR workflows can enable beginners to design successful experiments in a single attempt...
Base editing has been used to correct the mutation causing late-onset Tay-Sachs disease in mice and human cells...
by BioNews
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