Alison McVie‐Wylie

Recombinant human acid α-glucosidase enzyme therapy for infantile glycogen storage disease type II: Results of a phase I/II clinical trial

Andrea Amalfitano, A. Resai Bengur, Richard P. Morse et al. · Genetics in Medicine · 2001 · 346 citations · Full text

Translational Medicine, Biochemistry, Inherited Metabolic Disease +5

Development of a simple and rapid method for producing non‐fucosylated oligomannose containing antibodies with increased effector function

Qun Zhou, Srinivas Shankara, André Roy et al. · Biotechnology and Bioengineering · 2007 · 183 citations

Engineering, Glycobiology, Immunology +19

Molecular Cloning of a Novel Member of the GLUT Family of Transporters, SLC2A10 (GLUT10), Localized on Chromosome 20q13.1: A Candidate Gene for NIDDM Susceptibility

Alison McVie‐Wylie, David R. Lamson, Y.T. Chen · Genomics · 2001 · 155 citations

Glut Family, Natural Sciences, Genetics +11

Systemic correction of the muscle disorder glycogen storage disease type II after hepatic targeting of a modified adenovirus vector encoding human acid-α-glucosidase

Andrea Amalfitano, Alison McVie‐Wylie, Hao Hu et al. · Proceedings of the National Academy of Sciences · 1999 · 139 citations

Carbohydrate-remodelled acid α-glucosidase with higher affinity for the cation-independent mannose 6-phosphate receptor demonstrates improved delivery to muscles of Pompe mice

Yunxiang Zhu, Xuemei Li, Alison McVie‐Wylie et al. · Biochemical Journal · 2005 · 109 citations · Full text