Live Science's health channel editor makes predictions about the medical breakthroughs and public health shifts to come in ...
A new CRISPR approach can control genes without cutting DNA, opening a safer path for treating genetic diseases. A newly ...
In an exciting scientific first, researchers at the Allen Institute successfully designed a new gene therapy that reversed symptoms related to SYNGAP1-related disorders (SRD) in mice. These are a ...
Abu Dhabi successfully completes its first gene therapy for genetic blood disorders, revolutionizing treatment approaches for ...
The introduction of Jude Samulski’s PhD thesis contained a bold goal: develop a gene therapy vector that could be used to treat the world’s genetic diseases. By 1982, he had first cloned the ...
X-linked retinoschisis gene replacement therapy, aiming to improve retinal architecture and visual function in young male ...
Argininosuccinate lyase deficiency (ASLD), also known as argininosuccinic aciduria, is a disease that has been enriched in the Finnish genetic heritage. In this severe metabolic disease, the body does ...
Three start-ups are aiming to create gene-edited babies. Columnist Michael Le Page has no doubt that editing our offspring ...
New research from Queen Mary University of London (QMUL) has identified a novel syndrome in patients with kidney and adrenal disease. The research, published in the Journal of Clinical Investigation, ...
Researchers have identified a gene that causes heart defects in Down syndrome, a condition that results from an additional copy of chromosome 21. Reducing the overactivity of this gene partially ...
A study qualifies for my ‘Enough Is Enough’ series when bad science crosses the line to total absurdity. Today’s entry is Identification and Replication of a Combined Epigenetic and Genetic Biomarker ...
The Iowa State University Extension and Outreach Dairy Team monthly webinar series continues from noon to 1 p.m. April 2. The program will help Holstein breeders understand the muscle weakness genetic ...