A new mechanism for accessing damaged DNA
UV light damages the DNA of skin cells, which can lead to skin cancer. But this process is counteracted by […]
When the Human Genome Project was completed, in 2003, it opened the door to a radical new idea of health […] St. Jude Children’s Research Hospital scientists have identified genetic variations in a fourth gene that are associated with an increased […] The people who hold the most extreme views opposing genetically modified (GM) foods think they know most about GM food […] Scientists led by Dr. Daniel De Carvalho at Princess Margaret Cancer Centre have discovered a gene signature biomarker that may […] Scientists may be on the road to solving the mystery of a group of mostly incurable blood diseases called myelodysplastic […] Almost one year after the U.S. Food and Drug Administration (FDA) approval of chimeric antigen receptor (CAR) T-cell therapy for […] A biological switch that reliably turns protein expression on at will has been invented by University of Bath and Cardiff […] Scientists conducting one of the largest full DNA analyses of a rare disease have identified a gene mutation associated with […] In what researchers are calling a game changer for future ataxia treatments, a new study showed the ability to turn […]Gene Therapy
Understanding gene interactions holds key to personalized medicine: Gene interaction networks hold clues to disease susceptibility and treatment response
Genetic variations in a fourth gene linked to elevated leukemia risk in Hispanic children
Genetically modified food opponents know less than they think, research finds
Gene signature discovery may predict response to immune therapy
Scientists close in on mystery surrounding dangerous blood syndromes: Genetically driven MDS enabled by gene linked to metabolism and oxygen in cells
Acute lymphoblastic leukemia: Comprehensive pediatric CAR T guidelines developed
Biological switch reliably turns protein expression on at will
Scientists unravel DNA code behind rare neurologic disease
Using gene silencing to alleviate common ataxia