Revolutionising CRISPR-Cas
Researchers have refined the famous CRISPR-Cas method. Now, for the very first time, it is possible to modify dozens, if not hundreds, of genes in a cell simultaneously.
genetics
AI helps determine human biological age
Scientists participating in the project “DrugTarget” have now developed a method that can quickly check the condition of the genome. This will help develop points of intervention for new medicines
AI detects rare diseases
With artificial intelligence to a diagnosis of rare hereditary diseases: The neural network combines data from portrait images with gene and patient data.
Machine learning makes proteomics research more effective
Using AI, researchers have succeeded in making the mass analysis of proteins from any organism significantly faster than before and almost error-free.
AI detects a new class of mutations behind autism
Using artificial intelligence, researchers have decoded the functional impact of genome mutations in people with autism spectrum disorder.
CRISPR-powered device detects genetic mutations in minutes
Engineers have combined CRISPR with electronic transistors made from graphene to create a new hand-held device that can detect specific genetic mutations in a matter of minutes.
CasX, the smaller CRISPR gene editor
Scientists find new and smaller gene editor: the new gene-editing protein, CasX, may give CRISPR-Cas9 a run for its money.
CRISPR repurposed to develop better antibiotics
Researchers have repurposed the gene-editing tool CRISPR to study which genes are targeted by particular antibiotics, providing clues on how to improve existing antibiotics or develop new ones.
CRISPR: Giving Cas9 an ‘on’ switch
Researchers have given CRISPR-Cas9 an “on” switch, allowing users to keep the #Cas9 gene editor turned off in all cells except its designated target.
Could an AI predict a healthy old age?
Researchers analyze skin cells from mre than 100 people of different ages to find molecular signatures that change as people get older.
Big datasets help identify causes for pediatric diseases
Researchers use the analogy of raindrops on the sidewalk to explain their new method to identify genetic variations that cause severe pediatric diseases.
CRISPR opens door to new therapy options- ‘genome surgery’
Scientists plan to edit their genomes to correct rare genetic mutations and slow or halt progression of their diseases.
Liver-on-a-chip, the ideal test environment for CRISPR
Research project is aimed at improving therapeutic options for both rare and common diseases, including supporting methods to improve editing the human genome.
“Brain-on-a-Chip” reveals how the brain folds
Researchers describe a method they developed for growing tiny “brains on chips” from human cells that enabled them to track the physical and biological mechanisms underlying the wrinkling process.