Glycoengineered Acid α-Glucosidase With Improved Efficacy at Correcting the Metabolic Aberrations and Motor Function Deficits in a Mouse Model of Pompe DiseaseYunxiang Zhu, Seng H. Cheng, Robin J. Ziegler et al.|Molecular Therapy|2009Cited by 169
Mucolipidosis II (I-Cell Disease) and Mucolipidosis IIIA (Classical Pseudo-Hurler Polydystrophy) Are Caused by Mutations in the GlcNAc-Phosphotransferase α/β–Subunits Precursor GeneMariko Kudo, William M. Canfield, Michael S. Brem|The American Journal of Human Genetics|2006Cited by 158
The α- and β-subunits of the Human UDP-N-acetylglucosamine:Lysosomal Enzyme Phosphotransferase Are Encoded by a Single cDNAMariko Kudo, William M. Canfield, Ming Bao et al.|Journal of Biological Chemistry|2005Cited by 117
Functions of the α, β, and γ Subunits of UDP-GlcNAc:Lysosomal Enzyme N-Acetylglucosamine-1-phosphotransferaseYi Qian, Stuart Kornfeld, Intaek Lee et al.|Journal of Biological Chemistry|2009Cited by 80
Cation-independent Mannose 6-Phosphate ReceptorRichard N. Bohnsack, Nancy Dahms, Xuezheng Song et al.|Journal of Biological Chemistry|2009Cited by 74