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Disease Info Card
Sialuria
Information about Sialuria: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Sialuria
Most recent studies have shown that Sialuria shares some biological mechanisms with ataxia, developmental-delay-(disorder), fetal-diseases, inborn-errors-of-metabolism, infantile-sialic-acid-storage-disease, lysosomal-storage-diseases, metabolic-diseases, mucolipidoses, muscle-hypotonia, myopathy, neurodegenerative-disorders, sialic-acid-storage-disease-finnish-type-(disorder), storage-disease, type-i-mucolipidosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Sialuria, and have been seen in publications frequently: Amino Acid Transport, Aspartate Transport, Cell Adhesion, Cell Cycle, Cell Recognition, Endosomal Transport, Excretion, Gene Silencing, Glycosylation, Intracellular Transport, Localization, Lysosomal Transport, Monosaccharide Transport, Myelination, Oligodendrocyte Development, Pathogenesis, Regeneration, Secretion, Sialic Acid Transport, Transport
Quite a number of genes have been found to play important roles in Sialuria, such as APOC3, ASAH1, ATP7A, CMAS, CSF2, CTNS, EPO, EPX, ERCC8, GNE, HSPA9, LAMC2, LYZ, MUC1, PRDX2, RANGAP1, RENBP, SCARB2, SLC17A5, TIMP1. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.