Published in Cell Reports Medicine, results of a VHIO-led study support the feasibility of using RAD51 testing to complement ...
A recent paper published in Science magazine by researcher Blanca Barquera, Ph.D., professor of biological sciences at ...
A study reveals DNA and RNA epigenetics work together as a complementary system for precise gene regulation, crucial for cell ...
Rutgers Health researchers have discovered that brain immune cells from people with a high genetic risk for alcohol use disorder (AUD) behave differently than cells from low-risk people when exposed ...
Second, although differential expression analysis was performed using the R package limma, these analyses rely on existing biological databases, which may limit the exploration of certain key genes’ ...
The TP53 gene or its proteins are also referred to as tumor protein TP53, cellular tumor antigen TP53, phosphoprotein TP53, antigen NY-CO-13, or transformation-related protein 53. Learn more below ...
Affected patients are otherwise healthy until reaching adolescence, when they experience a rapid decline in kidney function and eventual kidney failure. “Early genetic diagnosis has enabled our ...
Britain’s National Health Service (NHS) announced on Thursday that it has begun offering individuals with Jewish ancestry swabs to check for mutations in their BRCA genes, which are associated ...
The screening programme looks for mutations in the BRCA genes which push up a person’s risk of cancer. Everyone has BRCA1 and BRCA2 genes, but people who have changes in the gene are at higher ...
For 30 years, researchers have known that Huntington’s disease is caused by an inherited mutation in the Huntingtin (HTT) gene in which a three-letter ... many cognitive functions, and motivation.
But Gounder had an idea: Perhaps Wolff's genes could point them in the right direction. Dr. Mrinal Gounder, a sarcoma medical oncologist at Memorial Sloan Kettering Cancer Center (MSK) in New York ...
This mutation alters the production or function of proteins responsible for black fur, resulting in a brown color. When the ARHGAP36 gene functions normally without the mutation, black fur appears.