A new study in the journal Human Gene Therapy indicates that DNA impurities derived from plasmid and host cell DNA are ...
Previous efforts to circumvent the problem of the size limitation imposed by the AAV vector have focused mainly on altering the candidate genes into ‘mini-expression cassettes’ suitable for ...
For central nervous system (CNS) applications, attempts are being made to deliver AAV gene therapy directly to the brain parenchyma or the cerebrospinal fluid (CSF) space by intra-cisterna magna ...
The Adeno Associated Virus Vector Manufacturing market, valued at USD 1,148.4 million in 2024, is expected to register robust revenue CAGR of 19.6%.Request free copy of this report: March 14, 2025 - ...
"Protein design is a hard problem because the mapping from DNA sequence to protein structure and function ... for the viral ...
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