Pages that link to "Q24310793"
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The following pages link to Characterization of human lysosomal neuraminidase defines the molecular basis of the metabolic storage disorder sialidosis (Q24310793):
Displaying 50 items.
- glycoproteinosis (Q2019832) (← links)
- Neuraminidase 1 (Q21116879) (← links)
- Cloning, expression, and chromosomal mapping of a human ganglioside sialidase (Q22010257) (← links)
- Identification and expression of NEU3, a novel human sialidase associated to the plasma membrane (Q22254346) (← links)
- Neu4, a novel human lysosomal lumen sialidase, confers normal phenotype to sialidosis and galactosialidosis cells (Q24297476) (← links)
- Molecular cloning and characterization of NEU4, the fourth member of the human sialidase gene family (Q24307924) (← links)
- Molecular mechanism of lysosomal sialidase deficiency in galactosialidosis involves its rapid degradation (Q24530675) (← links)
- Transport of human lysosomal neuraminidase to mature lysosomes requires protective protein/cathepsin A (Q24533181) (← links)
- Up-regulation of plasma membrane-associated ganglioside sialidase (Neu3) in human colon cancer and its involvement in apoptosis suppression (Q24533672) (← links)
- Loss of Cellular Sialidases Does Not Affect the Sialylation Status of the Prion Protein but Increases the Amounts of Its Proteolytic Fragment C1 (Q27341885) (← links)
- Molecular basis of GM1 gangliosidosis and Morquio disease, type B. Structure-function studies of lysosomal beta-galactosidase and the non-lysosomal beta-galactosidase-like protein (Q28138408) (← links)
- Lysosomal sialidase (neuraminidase-1) is targeted to the cell surface in a multiprotein complex that facilitates elastic fiber assembly (Q28284064) (← links)
- Degradation of G(M1) and G(M2) by mammalian sialidases (Q28363347) (← links)
- Ozz-E3, a muscle-specific ubiquitin ligase, regulates beta-catenin degradation during myogenesis (Q28509160) (← links)
- Progressive ataxia, myoclonic epilepsy and cerebellar apoptosis in cystatin B-deficient mice (Q28511355) (← links)
- In silico identification of new putative pathogenic variants in the NEU1 sialidase gene affecting enzyme function and subcellular localization (Q28542527) (← links)
- NEU1 Sialidase Expressed in Human Airway Epithelia Regulates Epidermal Growth Factor Receptor (EGFR) and MUC1 Protein Signaling (Q30421980) (← links)
- The atomic model of the human protective protein/cathepsin A suggests a structural basis for galactosialidosis (Q30429249) (← links)
- Neuraminidase 1 is a negative regulator of lysosomal exocytosis (Q30486788) (← links)
- Stable expression of protective protein/cathepsin A-green fluorescent protein fusion genes in a fibroblastic cell line from a galactosialidosis patient. Model system for revealing the intracellular transport of normal and mutated lysosomal enzymes (Q30631709) (← links)
- High-throughput substrate specificity studies of sialidases by using chemoenzymatically synthesized sialoside libraries (Q33267875) (← links)
- CD8( ) T cells induce platelet clearance in the liver via platelet desialylation in immune thrombocytopenia (Q33433254) (← links)
- Regulation of intracellular signaling by extracellular glycan remodeling. (Q33675552) (← links)
- Molecular cloning, characterization and expression analysis of cathepsin A gene in Chinese mitten crab, Eriocheir sinensis (Q33684386) (← links)
- Expression of a novel human sialidase encoded by the NEU2 gene (Q33880257) (← links)
- Mutations in sialidosis impair sialidase binding to the lysosomal multienzyme complex (Q33940580) (← links)
- Muscle degeneration in neuraminidase 1-deficient mice results from infiltration of the muscle fibers by expanded connective tissue (Q34004164) (← links)
- Dysregulation of the neural cell adhesion molecule and neuropsychiatric disorders (Q34061096) (← links)
- Splice donor site mutation in the lysosomal neuraminidase gene causing exon skipping and complete loss of enzyme activity in a sialidosis patient (Q34084901) (← links)
- Identification of a CTL4/Neu1 fusion transcript in a sialidosis patient. (Q34133659) (← links)
- Three novel beta-galactosidase gene mutations in Han Chinese patients with GM1 gangliosidosis are correlated with disease severity (Q34221523) (← links)
- Comparative enzymology, biochemistry and pathophysiology of human exo-alpha-sialidases (neuraminidases). (Q34241483) (← links)
- Molecular pathology of NEU1 gene in sialidosis (Q34266127) (← links)
- Lysosomal multienzyme complex: biochemistry, genetics, and molecular pathophysiology (Q34364491) (← links)
- New insights on the sialidase protein family revealed by a phylogenetic analysis in metazoa (Q34406409) (← links)
- A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy (Q34448160) (← links)
- Genetics of epilepsy: current status and perspectives. (Q34804508) (← links)
- Recent development in mammalian sialidase molecular biology (Q34955783) (← links)
- Molecular mechanisms of pathogenesis in a glycosphingolipid and a glycoprotein storage disease (Q35086239) (← links)
- Molecular background of progressive myoclonus epilepsy (Q35174621) (← links)
- Structural basis for substrate specificity of mammalian neuraminidases (Q35252939) (← links)
- Sialidase and malignancy: a minireview (Q35748328) (← links)
- Neuraminidase-Dependent Degradation of Polysialic Acid Is Required for the Lamination of Newly Generated Neurons (Q35885507) (← links)
- NEU1 and NEU3 sialidase activity expressed in human lung microvascular endothelia: NEU1 restrains endothelial cell migration, whereas NEU3 does not (Q35939859) (← links)
- An intrinsic mechanism of secreted protein aging and turnover (Q36268471) (← links)
- Sialic acid metabolism and sialyltransferases: natural functions and applications (Q36501918) (← links)
- Pathogenesis, Emerging therapeutic targets and Treatment in Sialidosis (Q36649026) (← links)
- Chaperone-mediated gene therapy with recombinant AAV-PPCA in a new mouse model of type I sialidosis (Q37224436) (← links)
- Aberrant expression of sialidase and cancer progression (Q37347015) (← links)
- Heterodimerization of the sialidase NEU1 with the chaperone protective protein/cathepsin A prevents its premature oligomerization (Q37460020) (← links)