Merck, a leading science and technology company, today announced that the Japan Patent Office and the Intellectual Property Office of Singapore have each allowed the company's patent application for the use of paired CRISPR nickases, bringing Merck's number of patents to 22 worldwide
Weekly Review #52 – Summary of the latest news in science and technology research across the world, carefully handpicked by team Research Stash
Scientists have developed a new variant of currently popular gene editing tool, CRISPR-Cas9, and have shown that this variant can increase precision in editing genome while avoiding unintended changes in DNA
Weekly Review #40 – Summary of the latest news In science and technology research across the world, carefully handpicked by team Research Stash
Weekly Review #36 – Summary of the latest news In science and technology research across the world, carefully handpicked by team Research Stash
Weekly Review #31 – Summary of the latest news In science and technology research across the world, carefully handpicked by team Research Stash
Weekly Review #24 – Summary of the latest news in science and technology research across the world, carefully handpicked by team Research Stash
Weekly Review #23 – Summary of the latest news in science and technology research across the world, carefully handpicked by team Research Stash
Summary of the latest news in science and technology research across the world, carefully handpicked by team Research Stash
Latest research news in science and technology across the globe, handpicked by Research Stash team
Latest stories in science and technology across the globe handpicked by Research Stash team
Banana is a popular fruit crop and in India is its largest producer globally. It is the fourth most important food crop after wheat, rice, and corn in terms of gross value of production. Now Indian scientists have used latest gene-editing techniques to modify the banana genome, for the first time.
Scientists have demonstrated an effective way of using a gene-editing tool to correct a disease-causing gene mutation in human embryos and stop it from passing to future generations.
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