Pages that link to "Q78107696"

The following pages link to Intracellular transport of acid beta-glucosidase and lysosome-associated membrane proteins is affected in Gaucher's disease (G202R mutation) (Q78107696):

Displaying 24 items.

• Cathepsin A regulates chaperone-mediated autophagy through cleavage of the lysosomal receptor (Q24337837) (← links)
• The iminosugar isofagomine increases the activity of N370S mutant acid beta-glucosidase in Gaucher fibroblasts by several mechanisms (Q24673451) (← links)
• Immunological cells and functions in Gaucher disease (Q26827675) (← links)
• Structure of acid beta-glucosidase with pharmacological chaperone provides insight into Gaucher disease (Q27643401) (← links)
• Binding of 3,4,5,6-Tetrahydroxyazepanes to the Acid-β-glucosidase Active Site: Implications for Pharmacological Chaperone Design for Gaucher Disease (Q27675348) (← links)
• Optimization and validation of two miniaturized glucocerebrosidase enzyme assays for high throughput screening (Q33392239) (← links)
• Identification and characterization of ambroxol as an enzyme enhancement agent for Gaucher disease (Q33478327) (← links)
• Analysis and classification of 304 mutant alleles in patients with type 1 and type 3 Gaucher disease (Q34390674) (← links)
• Phenotype, diagnosis, and treatment of Gaucher's disease (Q34907714) (← links)
• Immunological cell type characterization and Th1-Th17 cytokine production in a mouse model of Gaucher disease (Q36055464) (← links)
• Isofagomine- and 2,5-anhydro-2,5-imino-D-glucitol-based glucocerebrosidase pharmacological chaperones for Gaucher disease intervention. (Q36892352) (← links)
• Pharmacological chaperone design for reducing risk factor of Parkinson's disease from traditional chinese medicine (Q37556518) (← links)
• Gaucher disease paradigm: from ERAD to comorbidity (Q38012690) (← links)
• New Directions in Gaucher Disease (Q38905996) (← links)
• Secretion of human glucocerebrosidase from stable transformed insect cells using native signal sequences (Q40293563) (← links)
• Endoplasmic reticulum Ca2+ increases enhance mutant glucocerebrosidase proteostasis. (Q41976836) (← links)
• Glucocerebrosidase pseudogene variation and Gaucher disease: Recognizing pseudogene tracts in GBA alleles (Q48376924) (← links)
• Genetics of Gaucher's disease. Genotype-phenotype correlation (Q50518887) (← links)
• Characterization of two alpha-galactosidase mutants (Q279E and R301Q) found in an atypical variant of Fabry disease. (Q52579605) (← links)
• GBA-Associated Parkinson's Disease and Other Synucleinopathies (Q57040370) (← links)
• Distinguishing the differences in beta-glycosylceramidase folds, dynamics, and actions informs therapeutic uses (Q57047286) (← links)
• Fetal gene therapy for neurodegenerative disease of infants (Q59356806) (← links)
• Gaucher's disease: identification of novel mutant alleles and genotype-phenotype relationships (Q73489118) (← links)
• Analysis of glucocerebrosidase activity in dry blood spots using tandem mass spectrometry (Q82427179) (← links)