Norrie Disease is an ultra-rare genetic disorder causing congenital blindness, progressive hearing loss and neurological challenges. One Indian mother's journey reveals how misunderstood the condition ...
The National Assisted Reproduction Authority in our country has issued instructions for informing families who have had a ...
A sperm donor with a dangerous genetic mutation linked to cancer has fathered at least 197 children. Investigation revealed ...
Israel is one of the top-ranked countries in the world in genomic research, he declares. “These are people who lead genomic ...
Researchers at the Department of Cell and Molecular Biology, Karolinska Institutet have captured the first detailed molecular snapshots of human polynucleotide phosphorylase (hPNPase) in action, ...
A groundbreaking study from Virginia Tech researchers reveals that bed bugs in Virginia and beyond are evolving resistance to ...
An international research team involving the German Primate Center—Leibniz Institute for Primate Research (DPZ), Hannover ...
Decades ago, India’s tigers were on the brink of extinction. Slowly, their numbers have rebounded. But that ecological success has prompted a dire problem—and a race to save many of them from genetic ...
Overall response rate (ORR) of 55% and median progression-free survival of 14.5 months in patients without TP53 gene mutationPhase 2 results ...
A sperm donor with a rare genetic mutation linked to an increased risk of developing cancer fathered at least 197 children ...
Scientists have uncovered a surprising genetic workaround that helps cells cope with Friedreich’s ataxia, a rare and devastating disorder.
Scientists discovered a new blood type, but only 3 people on Earth share it. Here's why this discovery matters.
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