GGenetics Read More Yale researchers uncover new RNA editing tools for safer genetic surgeryAugust 21, 2025 The ability to correct disease-causing genetic mistakes using genome editors holds great promise in medicine, but it is…
GGenetics Read More Genetic evidence confirms early puberty accelerates ageing, disease: StudyAugust 21, 2025 Washington, DC [US], August 22 (ANI): Researchers discovered that early puberty or childbirth doubles women’s risk for major…
GGenetics Read More Genetic variants influencing vitamin D synthesis, metabolism, and transportAugust 21, 2025 From skin tone to rare mutations, scientists uncover how your genes influence vitamin D levels, and why standard…
GGenetics Read More AI model detects genetic changes in colorectal cancer from tissue imagesAugust 20, 2025 An international, interdisciplinary research team led by Prof. Jakob N. Kather from the Else Kröner Fresenius Center (EKFZ) for…
SScience Read More Somatic mutations drive vascular aging and muscle weakness over timeAugust 20, 2025 Two new studies from Karolinska Institutet in Sweden have investigated how mutations that occur in muscles and blood…
GGenetics Read More ChronODE method offers precision in timing gene therapy treatmentsAugust 20, 2025 A Yale research team has created a new computer tool that can pinpoint when exactly genes turn on…
HHealth Read More Alzheimer’s gene risks differ by ancestry, major study reveals 133 new variantsAugust 18, 2025 New genome study uncovers 133 previously unknown dementia-linked variants and shows how genetic risks vary across global populations,…
GGenetics Read More New generation of CRISPR shows safer path to treating genetic diseasesAugust 17, 2025 A new generation of CRISPR technology developed at UNSW Sydney offers a safer path to treating genetic diseases…
GGenetics Read More Gene editing restores hearing and balance in adult mice with DFNA41 deafnessAugust 15, 2025 Zheng-Yi Chen, DPhil, associate scientist at the Eaton-Peabody Laboratories, and Ines and Fredrick Yeatts Chair in Otolaryngology, at…
HHealth Read More Early use of risdiplam in newborns with SMA shows improvements in motor developmentAugust 14, 2025 Spinal muscular atrophy (SMA) is a rare genetic condition that causes progressive muscle weakness, which, when untreated, prevents…
GGenetics Read More Researchers find CFI deficiency alarmingly high in old order AmishAugust 13, 2025 Researchers from the Children’s Hospital of Philadelphia (CHOP) and the Clinic for Special Children found that complement factor…
GGenetics Read More New research highlights combined impact of genes and lifestyle on dilated cardiomyopathyAugust 12, 2025 An international team, led by scientists from the Victor Chang Cardiac Research Institute has studied around 3000 people…