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UnknownGlycoprotein hyposialylation gives rise to a nephrotic-like syndrome that is prevented by sialic acid administration in GNE V572L point-mutant mice.
Not available
S-EPMC3258264 | biostudies-literature
UnknownDynamic Glycoprotein Hyposialylation Promotes Chemotherapy Evasion and Metastatic Seeding of Quiescent Circulating Tumor Cell Clusters in Breast Cancer.
Not available
S-EPMC10481132 | biostudies-literature
UnknownIncreased amyloid β-peptide uptake in skeletal muscle is induced by hyposialylation and may account for apoptosis in GNE myopathy.
Not available
S-EPMC4924647 | biostudies-literature
UnknownThe Gne M712T mouse as a model for human glomerulopathy.
Not available
S-EPMC3349896 | biostudies-literature
UnknownKrebs von den Lungen 6 decreased in the serum and muscle of GNE myopathy patients.
Not available
S-EPMC7983952 | biostudies-literature
UnknownRationale and Design for a Phase 1 Study of N-Acetylmannosamine for Primary Glomerular Diseases.
Not available
S-EPMC6829193 | biostudies-literature
UnknownPhase 1 Study of Oral N-Acetylmannosamine in Primary Podocytopathies.
Not available
S-EPMC12861195 | biostudies-literature
UnknownPeracetylated N-acetylmannosamine, a synthetic sugar molecule, efficiently rescues muscle phenotype and biochemical defects in mouse model of sialic acid-deficient myopathy.
Not available
S-EPMC3268427 | biostudies-literature
UnknownSialic acid deficiency is associated with oxidative stress leading to muscle atrophy and weakness in GNE myopathy.
Not available
S-EPMC6075185 | biostudies-literature
UnknownSialylation of Thomsen-Friedenreich antigen is a noninvasive blood-based biomarker for GNE myopathy.
Not available
S-EPMC4160177 | biostudies-literature
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