Genetic test for early detection of high cardiovascular risk
(Vienna, 30-04-2024) Clonal haematopoiesis is a phenomenon caused by mutations in haematopoietic stem cells and can lead to blood cancer....
Researchers identify over 2,000 genetic signals linked to blood pressure in study of over one million people
The Queen Mary-led study reveals the most detailed picture yet of genetic contributors to blood pressure. The findings lead to...
Scientists discover over 100 new genomic regions linked to blood pressure
National Institutes of Health researchers and collaborators have discovered over 100 new regions of the human genome, also known as...
Genetic adaptations have impacted the blood compositions of two populations from Papua New Guinea
Papua New Guinea (PNG) has a wide range of environments, each presenting unique challenges to human survival. Highlanders and lowlanders...
Healthy lifestyle may offset effects of life-shortening genes by 60%+
A healthy lifestyle may offset the effects of life-shortening genes by more than 60%, suggests an analysis of the findings...
Gene seekers discover atypical two genes that control multiple valuable soybean traits
Ateam led by Purdue University soybean geneticist Jianxin Ma has developed a new biotechnological tool for the domestication of desirable traits from...
After 25 years, researchers uncover genetic cause of rare neurological disease
**EMBARGOED BY NATURE GENETICS UNTIL 10AM BST/ 5AM ET/ 3AM MT, APRIL 29**Credit: Mandi Gandelman, Ph.D. **EMBARGOED BY NATURE GENETICS...
Experts developing way to harness Nobel Prize winning CRISPR technology to deal with antimicrobial resistance (AMR)
**ECCMID has now changed its name to ESCMID Global, please credit ESCMID Global Congress (formerly ECCMID, Barcelona, Spain, 27-30 April)...
CRISPR is promising to tackle antimicrobial resistance, but remember bacteria can fight back
In the second new research review on this subject, Assistant Prof. Ibrahim Bitar, Department of Microbiology, Faculty of Medicine and...
Gene linked to epilepsy, autism decoded in new study
CHICAGO --- A genetic change or variant in a gene called SCN2A is a known cause of infantile seizures, autism spectrum...
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Mothers who receive childcare support from maternal grandparents show more parental warmth, finds NTU Singapore study
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University of Seville Breaks 120-Year-Old Mystery, Revises a Key Einstein Concept
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Bee body mass, pathogens and local climate influence heat tolerance
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Researchers record first-ever images and data of a shark experiencing a boat strike
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Groundbreaking Clinical Trial Reveals Lubiprostone Enhances Kidney Function
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