Scientists Just Made CRISPR 3x More Effective at Treating Genetic Diseases
Scientists developed a new nanostructure that triples CRISPR’s ability to enter cells, unlocking even more power to treat genetic diseases.| Good News Network
Driven by CASGEVY's success, the CRISPR field is experiencing substantial growth with a new wave of companies. The post CRISPR technology’s next wave: Ten companies to watch in 2025 appeared first on Labiotech.eu. © Labiotech UG and Labiotech.eu. Unauthorized use and/or duplication of this material without express and written permission from this site’s author and/or owner is strictly prohibited. Excerpts and links may be used, provided that full and clear credit is given to Labiotech ...| Labiotech.eu
Colossal Biosciences has just had a major breakthrough in its attempt to revive the dodo bird. What are the ethical concerns? The post Resurrecting the dodo: an ethical dilemma or chance at restoring biodiversity? appeared first on Labiotech.eu. © Labiotech UG and Labiotech.eu. Unauthorized use and/or duplication of this material without express and written permission from this site’s author and/or owner is strictly prohibited. Excerpts and links may be used, provided that full and clear...| Labiotech.eu
There is no cure for Huntington’s disease, a devastating brain disorder that causes severe motor loss, dementia, and eventual death. But, a clinical trial delivered positive results this week, finding that patients receiving a new treatment for 36 months experienced 75% less progression of the disease overall (compared to patients who did not receive the […] The post Always Fatal Huntington’s Disease is Successfully Treated for First Time With Gene Therapy appeared first on Good News Ne...| Good News Network
Scientists have created a new version of CRISPR gene editing that makes 60 times fewer errors than before.| Warp News
Scientists developed a new nanostructure that triples CRISPR’s ability to enter cells, unlocking even more power to treat genetic diseases.| Good News Network
Abbie (Roth) Miller, MS, MWC, is a passionate communicator of science. As the manager of medical and science content at Nationwide Children’s Hospital, she shares stories about innovative research and discovery with audiences ranging from parents to preeminent researchers and leaders. She is a Medical Writer Certified®, credentialed by the American Medical Writers Association, and received her masters of science in Health Communication from Boston University.| Pediatrics Nationwide
CRISPR-Cas9 gene editing revolutionized biological and biomedical research virtually overnight. The versatile tool has been used to improve crop yields and cure previously uncurable conditions like sickle cell anemia. In May 2025, the Nobel Prize-winning technology brought about another major biomedical breakthrough, as Kiran Musunuru and Rebecca Ahrens-Nicklas introduced the first personalized CRISPR gene editing... The post The CRISPR revolution continues appeared first on Cold Spring Harbo...| Cold Spring Harbor Laboratory
In May, patient Michael Kalberer wrote about why he joined a revolutionary clinical trial where he was only the second person in the world to receive CRISPR gene editing inside the body. Michael recently provided an update on how he’s been doing since, and in what ways his vision has changed. In September 2020, Michael… Read More »CRISPR Gene Therapy Update: Seeing a Sunset The post CRISPR Gene Therapy Update: Seeing a Sunset appeared first on FOCUS.| FOCUS
CRISPR-based gene editing technology Casgevy has been approved for treatment of sickle cell disease and beta-thalassaemia in the NHS| Genomics Education Programme
AI-enabled drug discovery approach identified potentially game-changing treatment, which has been advanced from the lab bench to an FDA Orphan Drug Designation in record time| Wyss InstituteWyss Institute
CRISPR gene editing of T cells can be performed using CRISPR as cancer therapy to bypass the inactivation of T cells by cancerous cells.| Bitesize Bio
The following is an excerpt from an article by the NEXT LEVEL: Wem gehört das Leben? – Warum wir Gentechnik stoppen müssen / Who Owns Life? – Why We Must Stop Genetic Engineering. Genetic engineeri…| Critical Check
How a new approach to correcting heterozygous mutations and other novel techniques for gene editing are transforming the potential to combat disease| Pediatrics Nationwide
Investigators from Nationwide Children’s Hospital created fratricide-resistant and metabolically-enhanced chimeric antigen receptor (CAR) natural killer (NK) and T cells that have cytotoxic effects on many hematologic tumors.| Pediatrics Nationwide
Scientists discover new gene editing tools in bacterial "jumping genes" that can be modified to cut, paste, and flip any sequence of DNA.| Singularity Hub
Overriding natural evolution, gene drives could add genes that make weeds more vulnerable to herbicides or reduce their pollination and numbers.| SingularityHub
Explore 10 gene therapy companies operating within the biotech industry, as each one hopes to develop their own novel candidates.| Labiotech.eu
Using the safe and sensible CRISPR technology that has the power to help the 300,000 babies born with sickle cell disease each year and the nearly 10 million people estimated to suffer from this genetic disorder globally.| science.thewire.in
de Bailey Kirkpatrick, 28 de fevereiro de 2017 *| IERFH
