lysosomal storage disease

释义

溶酶体贮积症；

[Lysosomal storage disease]
A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration
Acid Sphingomyelinase-Deficient Mice Mimic the Neurovisceral Form of Human Lysosomal Storage Disease (Niemann-Pick Disease)
Neonatal gene transfer leads to widespread correction of pathology in a murine model of lysosomal storage disease.
Dysfunction of endocytic and autophagic pathways in a lysosomal storage disease
A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration.
Functional Correction of Established Central Nervous System Deficits in an Animal Model of Lysosomal Storage Disease with Feline Imm...
Loss of the chloride channel ClC-7 leads to lysosomal storage disease and neurodegeneration.
Inhibition of substrate synthesis as a strategy for glycolipid lysosomal storage disease therapy
Lysosomal storage disease upon disruption of the neuronal chloride transport protein ClC-6.