Longevity gene from supercentenarians offers hope for disease that causes rapid aging in children
Credit: Pixabay/CC0 Public Domain A new breakthrough in a rare genetic disease which causes children to age rapidly…
Expanding PRRT2 Syndrome: A Case Study
A recent case study has delved into a Chinese family grappling with the complexities of infantile convulsion and…
Zennetix Forms Breeders’ Council to Deliver Award-Winning Genetics Through Tissue Culture Technology
[PRESS RELEASE] – HOUSTON, Oct. 14, 2025 – Zennetix, a tissue culture lab based in Conroe, Texas, announced…
Gene-activity map of developing brain reveals new clues about autism’s sex bias
Male and female human fetuses show distinct patterns of gene activity and DNA regulation in the cerebral cortex,…
Baylor Genetics Presents New Data on Clinical and
HOUSTON, Oct. 15, 2025 (GLOBE NEWSWIRE) — Baylor Genetics, a clinical diagnostic laboratory at the forefront of genetic…
Bacterial Transporter Hijacked for Genetic Expansion
In a groundbreaking study poised to revolutionize the field of synthetic biology and genetic code expansion, researchers have…
Nabsys Highlights OhmX™ Platform’s Ability to Accurately Verify Structural Variants in Undiagnosed Disorders and Workflow Optimizations at American Society of Human Genetics (ASHG) 2025 Annual Meeting
Newswise — PROVIDENCE, R.I., Oct. 15, 2025 — Nabsys 2.0, LLC (Nabsys), a pioneer in electronic genome mapping technology,…
Researchers Show Benefit Of Ultra-deep RNA Sequencing In Mendelian Disorder Diagnostics
RNA sequencing (RNA-seq) is a powerful tool in diagnosing Mendelian disorders, but the optimized sequencing depth for this…
Reporter’s Notebook: The Overdue Breakout for Gene Therapy and Gene Editing
As gene editing enters a new era, leaders discuss Baby KJ’s implications for families, science, and industry. (Left…
ACSS1’s Crucial Role in Mammary Development Explored
In an era where genetics and molecular biology converge to illuminate the intricacies of mammalian physiology, the emerging…