Disease-causing mutations within the lysosomal integral membrane protein type 2 (LIMP-2) reveal the nature of binding to its ligand β-glucocerebrosidase
Judith Blanz(Northwestern University), Michael Schwake(Bielefeld University)
Cited by 94
Related Papers
Structure of LIMP-2 provides functional insights with implications for SR-BI and CD36
|Nature|2013|287
Lysosomal integral membrane protein-2 (LIMP-2/SCARB2) is involved in lysosomal cholesterol export
|Nature Communications|2019|162
LAMP-2 deficiency leads to hippocampal dysfunction but normal clearance of neuronal substrates of chaperone-mediated autophagy in a mouse model for Danon disease
|Acta Neuropathologica Communications|2015|80