GGenetics Read More Empowerment Through DNA Knowledge – Saucon SourceSeptember 16, 2025 Jessica Burke of Allentown remembered she previously signed up to participate in the St. Luke’s DNA Answers research…
GGenetics Read More New genetic test redefines diagnosis and management of hereditary pancreatitisSeptember 11, 2025 A new genetic test developed at Mayo Clinic is redefining how clinicians diagnose and manage hereditary pancreatitis. Pancreatitis, inflammation…
GGenetics Read More Rare ABCA7 gene variants linked to Alzheimer’s riskSeptember 11, 2025 A new study from MIT neuroscientists reveals how rare variants of a gene called ABCA7 may contribute to…
SScience Read More Rapid neuronal evolution linked to high prevalence of autism in humansSeptember 10, 2025 A new paper in Molecular Biology and Evolution, published by Oxford University Press, finds that the relatively high…
GGenetics Read More BlueGenesLab Expands Genetic Panel to Include Three New GLP-1-Related GenesSeptember 8, 2025 SCOTTSDALE, Ariz., Sept. 08, 2025 (GLOBE NEWSWIRE) — BlueGenesLab, a precision genomics company headquartered in Scottsdale, Arizona, today…
GGenetics Read More Preclinical Data Spotlights Gene with Therapeutic Potential for Barth SyndromeSeptember 6, 2025 Barth Syndrome is a rare X-linked genetic condition caused by a mutation in the Tafazzin gene, which is…
HHealth Read More Gene expression maps explain why diseases often occur togetherSeptember 5, 2025 By grouping patients based on gene activity, scientists show that shared molecular pathways, especially immune-related ones, help explain…
HHealth Read More Smell loss emerges as the early behavioural sign of Alzheimer’sSeptember 4, 2025 New research reveals that immune cells attack brainstem nerve fibers linked to smell, making loss of smell the…
GGenetics Read More Nanostructures boost CRISPR delivery for genetic medicineSeptember 3, 2025 With the power to rewrite the genetic code underlying countless diseases, CRISPR holds immense promise to revolutionize medicine.…
GGenetics Read More Insights into clinical features and genetic variants of Cornelia de Lange syndrome in ChinaAugust 30, 2025 Cornelia de Lange syndrome (CdLS) is a rare genetic disorder with symptoms, including facial anomalies (such as fused…
HHealth Read More New mouse models reveal mechanisms of RP59 retinal degenerationAugust 30, 2025 Retinitis pigmentosa retinal degeneration is caused by a family of hereditary mutations in nearly 100 genes that slowly…
TTechnology Read More Male and female bovine embryos show distinct development pathsAugust 29, 2025 Cornell researchers have uncovered the genetic triggers that cause male and female bovine embryos to develop differently, as…