With an aim to normalise social and economic activities, Japan government will simultaneously start a new genomic surveillance program, under which entrants with symptoms such as fever are tested voluntarily to detect new infectious diseases, as per Kyodo News.
New Delhi [India], March 29 (ANI/NewsReach): World-leading healthcare specialists Bravo Pharma have officially entered a strategic partnership with the region's pioneering AI-powered healthcare company G42 Healthcare. In addition to this partnership, Bravo Pharma has also organized and parti
A team of scientists led by Dr Kei-ichi TAKATA from the Institute for Basic Science's Center for Genomic Integrity (CGI) discovered a new type of DNA repair mechanism that cancer cells use to recover from next-generation cancer radiation therapy.
Two to three metres of DNA can fit inside a single cell, thus it can only be stored by being wound tightly into coils. The answer is chromatin, a compound of DNA encased in histone-like proteins. This complex gradually folds into the multi-layered arrangement of loops, domains, and compartme
Bengaluru (Karnataka) [India], March 10 (ANI/NewsVoir): Health and wellness knowledge platform, Happiest Health, hosted the 'Future of Medicine 2023', the first annual summit that shared insights from leading minds in medicine, research, and technology, to foster innovation in the healthcare
Computer modelling was used by National Institutes of Health (NIH) researchers to find mutations in the human genome that are likely to have changed how human intelligence evolved. This groundbreaking human genomics study may advance our understanding of human health and pave the way for the
Researchers from the National Institutes of Health (NIH) employed computer modelling to identify mutations in the human genome that are likely to have altered the evolution of human intellect. This pioneering human genomics study might lead to a greater knowledge of human health and the deve
Migraines are a pain in the head and in the hip pocket, but newly discovered genetic causes by QUT researchers could lead the way to new preventative drugs and therapies. Genetic analysis findings were published in The American Journal of Human Genetics by Professor Dale Nyholt and his PhD c
A team of researchers from the Agency for Science, Technology, and Research and the National University of Singapore created software that accurately predicts chemical alterations of RNA molecules based on genomic data.
Understanding the many different genetic causes of childhood-onset hearing loss suggests that genomic testing could aid in treatment planning, including optimal treatment timing.