Researchers are exploring fetal gene editing to treat rare genetic disorders before they cause lasting damage.
An expert told Newsweek that carrying an inherited genetic change linked to cancer does not equal developing cancer.
A new review maps how prime editing, a CRISPR-derived tool capable in principle of correcting 89 percent of human pathogenic ...
Gallstone disease is common, but its genetic basis remains incompletely understood. Here, the authors conduct a trans‑ancestry GWAS identifying 116 risk loci, linking gallstone susceptibility to lipid ...
A study reactivated silenced genes in Prader-Willi patient-derived cells and improved some functions in mice, pointing toward a possible treatment strategy.
Using next-generation sequencing (NGS) to profile tumor cells from patients with solid tumors, researchers at Fondazione ...
Setara Biosciences, Inc. (Setara), a clinical-stage biotechnology company leveraging genetics to develop precision medicines ...
An observational study in Calgary found that a small subset of patients in an early psychosis intervention program carried ...
Brugada syndrome genetic testing identified six SCN5A variants in Malaysian patients, highlighting potential screening ...
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Creating a 'Place' Where Children with Genetic Disorders and Their Families Can Walk Their Own Paths
Seisen University, Faculty of Nursing Chiaki KitamuraIntroduction In the late 1980s, through my activities with the 'National ...
IgA vasculitis is a pediatric disease with skin and systemic manifestations. Here, the authors use multiomic data to examine the genetic mechanisms of IgA vasculitis and find therapeutically relevant ...
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