Search Results - Prabhakar, Shilpa

Long-term therapeutic efficacy of intravenous AAV-mediated hamartin replacement in mouse model of tuberous sclerosis type 1 by Prabhakar, Shilpa, Cheah, Pike See, Zhang, Xuan, Zinter, Max, Gianatasio, Maria, Hudry, Eloise, Bronson, Roderick T, Kwiatkowski, David J, Rachamimov, Anat Stemmer, Maguire, Casey A, Sena-Esteves, Miguel, Tannous, Bakhos A, Breakefield, Xandra O

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Gene replacement therapy in a schwannoma mouse model of neurofibromatosis type 2 by Prabhakar, Shilpa, Beauchamp, Roberta L., Cheah, Pike See, Yoshinaga, Akiko, Haidar, Edwina Abou, Lule, Sevda, Mani, Gayathri, Maalouf, Katia, Stemmer-Rachamimov, Anat, Jung, David H., Welling, D. Bradley, Giovannini, Marco, Plotkin, Scott R., Maguire, Casey A., Ramesh, Vijaya, Breakefield, Xandra O.

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Engineered AAV capsids mediate transduction of murine neurofibroma and sciatic nerve by Abou Haidar, Edwina, Prabhakar, Shilpa, Cheah, Pike See, Hanlon, Killian S., Espinoza, Paula, Crain, Adam V., Patel, Nikita, Radcliff, Greta W., Cheng, Ming, Hernández, Iván Coto, Minderler, Steven, de la Cruz, Demitri, Ng, Carrie, da Hora, Cintia Carla, Charest, Alain, Stemmer-Rachamimov, Anat, Jowett, Nate, Breakefield, Xandra O., Maguire, Casey A.

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