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Researchers from the Department of Pathology, School of Clinical Medicine at the LKS Faculty of Medicine of the University of ...
A major new study has revealed that the genes we inherit at birth play a much larger role in cancer than previously ...
Researchers have uncovered a surprising mechanism by which a single genetic mutation in the BCL11B gene causes both immune dysfunction and brain development issues.
A study led by King’s College London identified new candidate genes linked to congenital deafness. By analyzing genes ...
For chromosomes to form the iconic X-shape that ensures the accurate passing of genetic information during cell division, a ...
GenomeIndia project publishes preliminary findings from sequencing 10,000 Indian genomes, highlighting unique genetic ...
Researchers have identified key candidate genes linked to congenital deafness, paving the way for better diagnosis and ...
Comprehensive reference genomes have now been assembled for six ape species: siamang (a Southeast Asian gibbon), Sumatran ...
Congenital deafness affects roughly one in 1,000 babies and is often linked to genetic mutations, many of which remain ...
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Qfitlia (fitusiran) is the first therapy for both hemophilia A or B, with or without inhibitors, available in the United ...