Research of Galactosialidosis has been linked to Lysosomal Storage Diseases, Type I Mucolipidosis, Gangliosidoses, Storage Disease, Mucolipidoses. The study of Galactosialidosis has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Galactosialidosis include Transport, Excretion, Proteolysis, Localization, Pathogenesis. These pathways complement our catalog of research reagents for the study of Galactosialidosis including antibodies and ELISA kits against CTSA, GLB1, NEU1, EGFL7, APC.
Galactosialidosis Bioinformatics Tool
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Galactosialidosis below!
For more information on how to use Laverne, please read the How to Guide.
We have 1824 products for the study of Galactosialidosis that can be applied to Flow Cytometry, Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Galactosialidosis is also known as galactosialidosis, neuraminidase deficiency with beta-galactosidase deficiency, goldberg syndrome, ppca deficiency, neuraminidase/beta-galactosidase expression, lysosomal protective protein deficiency of, protective protein/cathepsin a deficiency, lysosomal protective protein deficiency, neuraminidase 1 deficiency, cathepsin a deficiency of, deficiency of cathepsin a, malnutrition, gsl.