Understanding how cells transform into specialized types during human development is a central challenge in biology. This ...

New research has investigated the mechanism by which bivalency functions to poise genes for expression during cell differentiation, providing insight into a long-standing paradigm in the regulation of ...

A new, comprehensive map of all the genes essential for blood infections in Plasmodium knowlesi (P. knowlesi), a parasite ...

This app uses Apple Intelligence to generate custom images on your device. You can choose from a list of suggested prompts, or you can enter your own description of an image and your iPhone will ...

New research suggests that brain ageing might be influenced by genetic factors passed down from your mother, raising intriguing questions about the role of maternal DNA in cognitive health.

Female mammals typically carry two X chromosomes — one from each parent ... but were very active on the paternal X. Using the gene-editing tool CRISPR, they investigated what would happen ...

eLife is a non-profit organisation inspired by research funders and led by scientists. Our mission is to help scientists accelerate discovery by operating a platform for research communication that ...

Anonymous image hosting can be important when wanting to upload content that might be sensitive or controversial, especially if you're a journalist or a whistleblower looking to expose something ...

Add articles to your saved list and come back to them any time. Now that Carlton president Luke Sayers, the club and the AFL integrity unit made it clear in a series of statements they are working ...

Learn More Black Forest Labs has quickly made a name for itself as the premiere, high-quality open-source AI image generation startup — even surpassing the quality of models offered by ...

Mutations in a gene called OTP cause obesity by controlling the output of another gene already targeted by an anti-obesity drug, a study led by UT Southwestern Medical Center researchers shows.

is caused when a small portion of chromosome 22 is missing. The condition can occur in individuals born from a parent with the dominant contiguous gene or parents without the gene. Variants in ...