Amy Frederick

AAVS1-Targeted Plasmid Integration in AAV Producer Cell Lines.

Seng H. Cheng, S. Wadsworth, Yuxia Luo, 2017, Human gene therapy methods.

Generation and characterization of adeno-associated virus producer cell lines for research and preclinical vector production.

S. Wadsworth, F. Poulin, Yuxia Luo, 2013, Human gene therapy methods.

Long Circulating Nanoparticles as Potential Antigen Carriers in Angiogenic Blood Vessels: Towards Tolerogenesis

J. Buriak, D. Cramb, L. West, 2014 .

Universal Method for the Purification of Recombinant AAV Vectors of Differing Serotypes

Seng H. Cheng, C. O’Riordan, Amy Frederick, 2017, Molecular therapy. Methods & clinical development.

In vivo potency testing of subretinal rAAV5.hCNGB1 gene therapy in the Cngb1 knockout mouse model of retinitis pigmentosa.

M. Biel, S. Michalakis, S. Petersen-Jones, 2021, Human Gene Therapy.

Engineered Capsids for Efficient Gene Delivery to the Retina and Cornea.

N. Kollu, M. Lukason, Xiaoying Jin, 2020, Human gene therapy.

The human UNP locus at 3p21.31 encodes two tissue-selective, cytoplasmic isoforms with deubiquitinating activity that have reduced expression in small cell lung carcinoma cell lines

M. Rolfe, Amy Frederick, M. I. Chiu, 1998, Oncogene.