Chuah, Marinee K.

Identification of a myotropic AAV by massively parallel in vivo evaluation of barcoded capsid variants

Weinmann, J., Weis, S., Sippel, J., Tulalamba, W., Remes, A., El Andari, J., Herrmann, A.-K., Pham, Q. H., Borowski, C., Hille, S., et al. (2020) · Nature Communications

Virus-based gene therapy researchRNA Interference and Gene Delivery

Cited by 259

Liver-directed lentiviral gene therapy in a dog model of hemophilia B

Cantore, A., Ranzani, M., Bartholomae, C. C., Volpin, M., Valle, P. D., Sanvito, F., Sergi, L. S., Gallina, P., Benedicenti, F., Bellinger, D., et al. (2015) · Science Translational Medicine

Virus-based gene therapy researchHemophilia Treatment and Research

Cited by 158

Hyperfunctional coagulation factor IX improves the efficacy of gene therapy in hemophilic mice

Cantore, A., Nair, N., Della Valle, P., Di Matteo, M., Màtrai, J., Sanvito, F., Brombin, C., Di Serio, C., D'Angelo, A., Chuah, M., et al. (2012) · Blood

Hemophilia Treatment and ResearchVirus-based gene therapy research

Cited by 101

Universal allogeneic CAR T cells engineered with Sleeping Beauty transposons and CRISPR-CAS9 for cancer immunotherapy

Tipanee, J., Samara-Kuko, E., Gevaert, T., Chuah, M. K., & VandenDriessche, T. (2022) · Molecular Therapy

CAR-T cell therapy researchCRISPR and Genetic Engineering

Cited by 76

Biosafety of Adenoviral Vectors

Chuah, M. K. L., Collen, D., & VandenDriessche, T. (2003) · Current Gene Therapy

Virus-based gene therapy researchRNA Interference and Gene Delivery

Cited by 71