Researchers uncover mechanism for how common gene therapy vectors enter cells
Identification of GPR108 as 'lock' for adeno-associated virus vector (AAV) is crucial to this emerging novel class of genetic medicine ...
Identification of GPR108 as 'lock' for adeno-associated virus vector (AAV) is crucial to this emerging novel class of genetic medicine ...
Scientists find unexpected connection between 2 main forms of AMDCredit: Dan Addison | UVA Communications Researchers have successfully treated age-related ...
Research identifies mechanism of synaptic damage in certain neurodegenerative disordersCredit: UMass Medical School New research by Dorothy P. Schafer, PhD, ...
UNIGE researchers have discovered a new gene that causes blindness and cardiomyopathy; they have also managed to halt the progression ...
New open access journal to launch in 2020Credit: Courtesy Dr. Bamshad Rockville, MD - The American Society of Human Genetics ...
Credit: UNH DURHAM, N.H. - Researchers at the University of New Hampshire have reported the first structural model for a ...
Credit: Jess Brassard/Michigan Tech Viruses are not easy to characterize. But we need to because being able to quickly predict ...
Credit: Hua Bai AMES, Iowa - Researchers may have discovered a way to turn back the clock on aging heart ...
Credit: Mary Ann Liebert, Inc., publishers New Rochelle, NY, January 7, 2020--In a radical new approach to treat cocaine addition, ...
Credit: Mary Ann Liebert, Inc., publishers New Rochelle, NY, January 3, 2020--A new study shows the feasibility of using gene ...
Credit: Mary Ann Liebert, Inc., publishers New Rochelle, NY, December 31, 2019--Before gene therapy can be used to treat renal ...
Novel spinal therapy/delivery approach prevented disease onset in neurodegenerative ALS disease model in adult mice and blocked progression in animals ...
New subtype of muscle stem cells that can be used in the development of gene therapiesCredit: Spuler lab, MDC Anyone ...
Technique developed at Human Genome and Stem Cell Research Center, funded by FAPESP and hosted by the University of São ...
Credit: Maria Litovchenko & Roel Bevers (EPFL) Many of the characteristics that make people so different from each other, are ...
Invented at Carnegie Mellon, the bivalent nucleic acid recognition platform is being used to develop treatments for rare genetic diseasesCredit: ...
Dyno Therapeutics founders and collaborators demonstrate machine-guided AAV capsid engineering with the potential to transform gene therapy Credit: Eric Kelsic, ...
High-throughput synthetic biology approach reveals hidden AAV features and could help fast-track future gene therapiesCredit: Wyss Institute at Harvard University ...
Credit: Mary Ann Liebert, Inc., publishers New Rochelle, NY, November 12, 2019--A new study has shown that a commonly used ...
New technique to help explore genetic diseases, benefit drug developmentCredit: Dan Addison | UVA Communications Scientists at the University of ...
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