Female-specific mechanism enhances heat production in brown fat
Higher activity of PGC-1α enables brown fat cells in females to thermogenic activity and energy expenditure compared to…
Study identifies C1orf122 as prognostic marker in liver cancer
Primary liver cancer is the third leading cause of cancer-related deaths, of which hepatocellular carcinoma (HCC) accounts for…
AI toolset reveals links between lung fibrosis and aging
A new research paper was published in Volume 17, Issue 8 of Aging-US on August 8, 2025, titled “AI-driven toolset for…
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…
Rapid neuronal evolution linked to high prevalence of autism in humans
A new paper in Molecular Biology and Evolution, published by Oxford University Press, finds that the relatively high…
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…
‘Rogue’ DNA rings identified as drivers of aggressive brain cancer
An international team of scientists has revealed how rogue rings of DNA that float outside of our chromosomes…
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…
Targeting metabolic reprogramming to overcome immune suppression in head and neck cancer
Head and neck cancer remains a major global health challenge, ranking among the six most common cancers worldwide…
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…
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…