Empowerment Through DNA Knowledge – Saucon Source
Jessica Burke of Allentown remembered she previously signed up to participate in the St. Luke’s DNA Answers research…
New genetic test redefines diagnosis and management of hereditary pancreatitis
A new genetic test developed at Mayo Clinic is redefining how clinicians diagnose and manage hereditary pancreatitis. Pancreatitis, inflammation…
Rare ABCA7 gene variants linked to Alzheimer’s risk
A new study from MIT neuroscientists reveals how rare variants of a gene called ABCA7 may contribute to…
Microbial piracy offers clues to fighting antimicrobial resistance
Researchers have discovered how ‘pirate phages’ hijack other viruses to break into bacteria, sharing new genetic material for…
BlueGenesLab Expands Genetic Panel to Include Three New GLP-1-Related Genes
SCOTTSDALE, Ariz., Sept. 08, 2025 (GLOBE NEWSWIRE) — BlueGenesLab, a precision genomics company headquartered in Scottsdale, Arizona, today…
Preclinical Data Spotlights Gene with Therapeutic Potential for Barth Syndrome
Barth Syndrome is a rare X-linked genetic condition caused by a mutation in the Tafazzin gene, which is…
Understanding how mRNA stability influences immune diseases
A pizza shop with 30 delivery people ought to be able to deliver a lot of pizzas –…
Gene expression maps explain why diseases often occur together
By grouping patients based on gene activity, scientists show that shared molecular pathways, especially immune-related ones, help explain…
Smell loss emerges as the early behavioural sign of Alzheimer’s
New research reveals that immune cells attack brainstem nerve fibers linked to smell, making loss of smell the…
Nanostructures boost CRISPR delivery for genetic medicine
With the power to rewrite the genetic code underlying countless diseases, CRISPR holds immense promise to revolutionize medicine.…
Male and female bovine embryos show distinct development paths
Cornell researchers have uncovered the genetic triggers that cause male and female bovine embryos to develop differently, as…
Insights into clinical features and genetic variants of Cornelia de Lange syndrome in China
Cornelia de Lange syndrome (CdLS) is a rare genetic disorder with symptoms, including facial anomalies (such as fused…