Bypassing broken genes
New approach to gene therapy can correct any disease-causing mutation within a gene.
Apr 21st, 2021
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New approach to gene therapy can correct any disease-causing mutation within a gene.
Apr 21st, 2021
Read moreScientists have developed a new biomaterial that regrows blood vessels and bone, potentially providing a single-stage approach when repairing large bone defects.
Apr 20th, 2021
Read moreResearchers present a study that proves stem cells ability to cure glaucoma. It is the world's first successful attempt to grow and transplant retinal ganglion cells in laboratory settings. It establishes a path for further cell therapy development, growing and transplanting other organs and parts of them.
Apr 19th, 2021
Read moreScientists have figured out how to modify CRISPR's basic architecture to extend its reach beyond the genome and into what's known as the epigenome -- proteins and small molecules that latch onto DNA and control when and where genes are switched on or off.
Apr 16th, 2021
Read moreBy combining the 'chassis' of an oil-producing microalgae with genes from a Cuphea plant, scientists can turn the algae into a microbial cell factory that can produce various oils with different properties.
Apr 15th, 2021
Read moreResearchers have shown in cells in culture that an ion pump can deliver drugs more accurately, which gives less severe adverse effects in chemotherapy.
Apr 15th, 2021
Read moreResearchers have found a way to fine-tune the molecular assembly line that creates antibiotics via engineered biosynthesis. The work could allow scientists to improve existing antibiotics as well as design new drug candidates quickly and efficiently.
Apr 13th, 2021
Read moreResearchers have genetically engineered a probiotic yeast to produce beta-carotene in the guts of laboratory mice. The advance demonstrates the utility of work the researchers have done to detail how a suite of genetic engineering tools can be used to modify the yeast.
Apr 12th, 2021
Read moreScientists have developed a technique that makes it possible to examine how different versions of histones bind to the genome in tens of thousands of individual cells at the same time. The technique was applied to the mouse brain and can be used to study epigenetics at a single-cell level in other complex tissues.
Apr 12th, 2021
Read moreSynthetic biologists explored ways to fold artificial proteins into diverse shapes like origamis. They constructed diamond-shaped protein cages, and managed to transform them to different shapes.
Apr 12th, 2021
Read moreScientists develop signals that could bring color vision and improved clarity to prosthesis for the blind.
Apr 9th, 2021
Read moreNew, reversible CRISPR method can control gene expression while leaving underlying DNA sequence unchanged.
Apr 9th, 2021
Read moremRNA, the messenger molecule that's been in every living cell for billions of years is the key ingredient in some COVID-19 vaccines.
Apr 9th, 2021
Read moreScientists are digging into the bizarre bacteria-produced nanomachines that could fast-track microbiome science.
Apr 7th, 2021
Read moreThe veiny skeleton of a spinach leaf shows for the first time it can support the growth of artificial meat.
Mar 31st, 2021
Read moreResearchers reprogram host liver with genetic circuits to direct the synthesis and self-assembly of siRNAs into secretory exosomes. In vivo assembled siRNAs are systematically distributed to multiple tissues or targeted to specific tissues, inducing potent target gene silencing in these tissues.
Mar 30th, 2021
Read moreA hydrogel successfully reverted cancer cells back to cancer stem cells within 24 hours, in six different human cancer types. This could lead to the development of anti-cancer stem cell drugs and personalized medicines.
Mar 29th, 2021
Read moreResearchers developed a new method to synthesize and screen libraries of peptoid nanostructures.
Mar 26th, 2021
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