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RNA modifications provide new insights into disease brain states

Recently, researchers have used advanced microscopy to investigate the role that RNA modifications play in ‘synaptic tagging’ within the brain. […]

Genetic overlap between metabolites and migraines

Researchers have conducted a comprehensive genetic analysis to estimate the polygenic genetic overlap between 316 unique blood metabolite levels and […]

AI has been used to rapidly diagnose critically ill patients with rare genetic diseases

Recently, researchers used Fabric GEM, an artificial intelligence algorithm, to detect disease causing variants in newborns and rare disease patients […]

Changes in gut microbiome associated with brain damage in infants

In a new study, published in Cell Host & Microbe, researchers identified changes in the gut microbiome that are associated […]

Positively selected gene inactivation results in changes in brain size

A new study, published in Molecular Biology and Evolution, has revealed that gene inactivation that naturally occurs in some individuals […]

Lab-grown brain organoids develop rudimentary eyes

A new study, published in Cell Stem Cell, has grown brain organoids in the lab that developed basic eye structures, […]

Illumina closes $8bn Grail merger

Illumina has finalised its acquisition of cancer screening company Grail, despite both antitrust concerns from the EU and a pending […]

Patient Perspectives: Vaila Morrison – Architect, Mother and Rare Disease Advocate (KAT6A syndrome)

Vaila Morrison is an architect focused on sustainable and inclusive design as well as a mother to a child with […]

Actionable metastatic cancer genomes remain stable over time

A new study, published in Nature Medicine, has found that driver mutations in metastatic cancer genomes remain stable over time. […]

Patient Perspectives: Nina Knight – Mother, Advocate and Chair of Acrodysostosis Support & Research

Nina Knight is a mother, advocate and Chair of the Acrodysostosis Support & Research Charity. Knight’s daughter, Lily, was diagnosed […]