New study maps out the timeline of DNA damage for multiple myeloma
A new study maps out the timeline of DNA damage for multiple myeloma, the second most common blood…
Supporting genetic research with UV microscope objectives
Key takeaways A global leader in agricultural genetics sought durable, economical UV microscope objectives. Issues in meeting these…
Parkview Health offers no-cost DNA insights to Fort Wayne area | News
FORT WAYNE, Ind. (WFFT) — Parkview Health has expanded its DNA Insights program, allowing the public to participate…
South Africa amended its research guidelines to allow for heritable human genome editing
Update: since this article was published, South Africa’s health authorities have withdrawn the section on heritable human genome…
Study uncovers three-way relationships between gut fungi, genetics and disease risk
A new genome-wide study uncovers evidence of the first three-way relationships between human genetic variation, variation in the…
LNPs Powering the Future of Gene Editing & Therapy
Gene therapy has long promised to transform the treatment of genetic and acquired diseases by addressing the underlying…
Reproductive Genetics Market Evolution by 2032
Reproductive Genetics Analysis The worldwide “Reproductive Genetics Market” 2025 Research Report presents a professional and complete analysis of…
NHS plans to DNA test all babies in England to assess disease risk
The government’s 10-year plan for the NHS, which is set to be revealed over the coming few weeks,…
The genetic mystery of why some people develop autism
These gene variants exist throughout the population of both neurotypical and neurodivergent people, and the individual contribution of…
Light Switches Give Scientists Control Over Cells
Imagine being able to flip a light switch to control disease pathways inside a living cell. A team…
Doctors say strokes in young adults congenital, advise early genetic screening
Always confident about his health, this man, who worked as a technician and whose name is not revealed,…
Bilingualism possible in people with rare genetic condition that normally limits speech
Rett syndrome is a rare neurological condition that disrupts physical and linguistic development, affecting around one in 10,000…