Pages that link to "Q48895251"
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The following pages link to Brain lysosomal hydrolases in neuronal ceroid-lipofuscinoses (Q48895251):
Displaying 10 items.
- Defective lysosomal arginine transport in juvenile Batten disease (Q24292865) (← links)
- A hereditary spastic paraplegia mouse model supports a role of ZFYVE26/SPASTIZIN for the endolysosomal system (Q27318572) (← links)
- A novel interaction of CLN3 with nonmuscle myosin-IIB and defects in cell motility of Cln3(-/-) cells (Q34014206) (← links)
- Palmitoyl-protein thioesterase 1 deficiency in Drosophila melanogaster causes accumulation of abnormal storage material and reduced life span (Q34588532) (← links)
- Cln6 mutants associated with neuronal ceroid lipofuscinosis are degraded in a proteasome-dependent manner (Q37171634) (← links)
- A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration (Q39922868) (← links)
- Specific alterations in levels of mannose 6-phosphorylated glycoproteins in different neuronal ceroid lipofuscinoses (Q41010705) (← links)
- Loss of the chloride channel ClC-7 leads to lysosomal storage disease and neurodegeneration (Q41376427) (← links)
- Ectopic expression of alpha1,6 fucosyltransferase in mice causes steatosis in the liver and kidney accompanied by a modification of lysosomal acid lipase (Q43565280) (← links)
- Sensitive method for the quantification of beta-glucuronidase activity in human urine using capillary electrophoresis with fluorescence detection (Q74756075) (← links)