Other signs of potential FH include yellowish fatty collections called xanthomas seen under the skin; around the eyes; or at the back of the hands, palms, or soles or a gray ring called a corneal ...
New Scientist on MSN
Genetic trick to make mosquitoes malaria resistant passes key test
The rollout of a type of genetic technology called a gene drive for tackling malaria could be edging closer after a lab study ...
Science Unbound on MSN
What will we be eating in 2050?
Explore the Future of Food in 2050! From lab-grown meat to edible water, witness the culinary revolution. Discover ...
Karthik and her team aimed to use CRISPR as a way to identify and isolate a protein generated by the bacteria that cause Lyme ...
The donation from Don and Anne Edwards aims to speed research, treatment and diagnosis for children with rare and genetic ...
ABC 7 Los Angeles on MSN
Experimental gene therapy treatment created at UCLA gives 'bubble girl' a new life
An experimental gene therapy treatment created at UCLA gave a "bubble girl" born with a rare genetic disorder a new life.
Backed by Italy-based Fondazione Telethon ETS, Waskyra, for Wiskott-Aldrich syndrome, is the first gene therapy from a ...
18hon MSN
At least 197 children were fathered by sperm donor with cancer-causing gene. Some have already died
A sperm donor with a rare genetic mutation linked to an increased risk of developing cancer fathered at least 197 children across Europe, some of whom have already died from the disease, according to ...
A single sperm donor who carries a rare cancer-causing genetic mutation has fathered at least 197 children across 14 ...
A new University of California San Diego School of Medicine study offers a unified biological model to explain how genetic predispositions and environmental exposures converge to cause autism spectrum ...
22hon MSN
Sperm donor with cancer-causing gene fathered nearly 200 children across Europe, investigation finds
A genetic mutation that carries a 90% cancer risk has been passed on by an unwitting sperm donor to dozens of children, a Europe-wide investigation has revealed.
The US Food and Drug Administration said on Tuesday it had approved the first gene therapy for a rare and life-threatening immune disorder. The therapy, Waskyra, was approved for Wiskott-Aldrich ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results