A new study has demonstrated how a gene called HAND2 can play a role in the timing of labour. The […]
For my undergraduate research project, I studied a rare neurological disease known as Landau-Kleffner Syndrome. It was then that I […]
Researchers have found that uninherited mutations that occur randomly during the earliest stages of embryonic development can cause spina bifida. […]
The ease of new gene editing technologies has opened opportunities to explore in more detail the genetic underpinnings of disease, […]
Researchers from Max Planck and their collaborators have revealed the transformation of colon organoids in vitro. Colorectal cancer Colorectal cancer […]
Another round-up of the latest genomics news and research from the past week – enjoy! Top stories from the past […]
Researchers find that cell-free circulating tumour DNA (ctDNA) analyses before and during treatment could help guide selection of therapy for […]
Using whole-exome sequencing (WES), researchers have identified underlying variants in children with rare genetic paediatric diseases. Rare genetic paediatric diseases […]
A recent study published in Nature reports that metformin and dextromethorphan, two drugs already in use to treat other diseases, […]
Written by Anja Brunner (Marketing Manager at Samplix) Genome editing Undoubtedly, advances in gene editing have allowed us to imagine a […]
