Sujuan Xu

NPC2, the Protein Deficient in Niemann-Pick C2 Disease, Consists of Multiple Glycoforms That Bind a Variety of Sterols*>

Ann M Stock, P. Lobel, G. Tint, 2006, Journal of Biological Chemistry.

Intrathecal tripeptidyl-peptidase 1 reduces lysosomal storage in a canine model of late infantile neuronal ceroid lipofuscinosis.

S. Bunting, C. O’Neill, L. Tsuruda, 2011, Molecular genetics and metabolism.

Structural Basis of Sterol Binding by NPC2, a Lysosomal Protein Deficient in Niemann-Pick Type C2 Disease*

Ann M Stock, P. Lobel, H. Liou, 2007, Journal of Biological Chemistry.

Large-volume intrathecal enzyme delivery increases survival of a mouse model of late infantile neuronal ceroid lipofuscinosis.

Lingling Wang, D. Sleat, P. Lobel, 2011, Molecular therapy : the journal of the American Society of Gene Therapy.

Glial fibrillary acidic protein is elevated in the lysosomal storage disease classical late-infantile neuronal ceroid lipofuscinosis, but is not a component of the storage material.

M. Jadot, D. Sleat, P. Lobel, 2010, The Biochemical journal.