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News Medical on MSNGene therapy breakthrough offers hope for severe Dravet syndrome casesAAV-Navβ1 gene therapy effectively reduces seizures and prolongs life in a mouse model of SCN1B-linked Dravet syndrome, ...
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DeFiance on MSNAAV Innovation Summit 2025 to Explore AI and Vector Design in Gene TherapyThe AAV Innovation Summit 2025, hosted by Form Bio, will bring together top experts in gene therapy to discuss the latest ...
Organoids were cultured from healthy donor iPSC sources and differentiated using the human iPSC-derived Cerebral Organoid ...
Explore a comprehensive guide to standardizing large scale production and clarification of lentiviral vectors.
Alcami Corporation, a contract development and manufacturing organization (CDMO), has appointed pharmaceutical industry ...
Alcami Corporation ("Alcami"), a leading contract development and manufacturing organization (CDMO), today announced the ...
The major applications of AI in gene therapy development include biomarker prediction, viral vector and biomanufacturing optimization, personalized medicine, target identification and validation, ...
Genprex, Inc. ("Genprex" or the "Company") , a clinical-stage gene therapy company focused on developing life-changing therapies for patients with cancer and diabetes, today announced the advancement ...
Vincent Gaynor remembers, almost to the minute, when he realized his part in birthing the breakthrough gene therapy Zolgensma ...
Results show improved functional outcomes for people with Duchenne muscular dystrophy who are ambulatory. Elevidys, which is ...
The Tokyo-based biotech firm expects RV-001 to be able to alter light sensitivity for patients with limited or no vision regardless of genotype.
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