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Phosphomannose isomerase (PMI) catalyzes the reversible interconversion of mannose 6-phosphate and fructose 6-phosphate. Plant cells lacking this enzyme are incapable of surviving on synthetic medium containing mannose as a carbon source.... more
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      Plant BiologyEscherichia coliMaizePlant Transformation
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      MultidisciplinaryProtein EngineeringBrainHumans
The mannose 6-phosphate (Man-6-P) lysosomal targeting signal on acid hydrolases is synthesized by the sequential action of uridine 5'-diphosphate-N-acetylglucosamine: lysosomal enzyme N-acetylglucosamine-1-phosphotransferase... more
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      Biological SciencesBrainLivercathepsin D
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      Molecular MedicineMedicineMolecularRNA interference
The formation of scar tissue following nerve injury has been shown to adversely affect nerve regeneration and evidence suggests that mannose-6-phosphate (M6P), a potential scar reducing agent that affects transforming growth factor... more
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      Peripheral Nerve RepairNerve RegenerationScarringMannose-6-Phosphate
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      GeneticsCell lineHumansMice
A mannose selection system was adapted for use in the Agrobacterium-mediated transformation of Liquidambar formosana L. This system makes use of the pmi gene, which encodes phosphomannose isomerase. This protein converts... more
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      TransformationPlant BiologyBacteriaRecovery
Enzymatic Basis of Mannose Toxicity in Honey Bees Abstract. Honey bees have a negligible amount of phosphomannoseisoml-erase, to-gether with a high content of a hexo-kinase which phosphorylates mannose more efficiently than fruLCtose or... more
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      ScienceMultidisciplinaryHoney beeMannose-6-Phosphate
Acid alpha-glucosidase (GAA) is a lysosomal glycogen-catabolizing enzyme, the deficiency of which leads to Pompe disease. Pompe disease can be treated with systemic recombinant human GAA (rhGAA) enzyme replacement therapy (ERT), but the... more
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      Mannose-6-PhosphateLysosomal storage disordersGlycogen Storage Diseases
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      TechnologyProductionPlant biotechnologyGene Silencing
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      Molecular GeneticsHumansFemaleEnzyme
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      Plant BiologyTomatoMannose-6-PhosphateEnzyme activity
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      Protein FoldingProtein Structure and FunctionCell lineHumans
Aspartylglucosaminuria (AGU) is a neurodegenerative lysosomal storage disease that is caused by mutations in the gene encoding for a soluble hydrolase, aspartylglucosaminidase (AGA). In this study, we have used our recently developed... more
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      Cell lineMutagenesisMiceEndocytosis
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      GeneticsMedical GeneticsBiological SciencesHumans
PCR-analysis, multilocus enzyme electrophoresis and molecular karyotyping were used to characterize 52 strains belonging to the genus Galactomyces. The resultant data revealed that a PCR method employing the universal primer N21 and... more
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      GeneticsMicrobiologyPolymorphismMedical Microbiology
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      Molecular GeneticsHumansMiceAnimals
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      KineticsMultidisciplinaryPhylogenySequence alignment
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      KineticsMultidisciplinaryPhylogenySequence alignment
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      Enzyme InhibitorsMolecular GeneticsMolecular chaperonesAnimals
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      Molecular GeneticsHumansFemaleEnzyme
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      Organic ChemistryHumansGlycoproteinsNeoplasms
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      Plant BiologyEscherichia coliMaizePlant Transformation
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      Plant BiologyEcologyPotatoEnzyme
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      Drug metabolismImmunohistochemistryMacrophagesWestern blotting
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      Hepatitis CHumansFemaleMale
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      MultidisciplinaryHumansPhosphorylationGlycoproteins
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      Gene TherapyBiological SciencesCell lineHumans
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      MigrationCell BiologyImmunocytochemistryBiological Sciences
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      Stem CellsHuman Embryonic Stem CellsCell lineCell Differentiation
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      ParasitologyScanning Electron MicroscopyCell lineHumans
Herpes simplex virus (HSV) glycoprotein D (gD) is modified with mannose 6-phosphate (M6P) and binds to M6P receptors (MPRs). MPRs are involved in the well-characterized pathway by which lysosomal enzymes are directed to lysosomes via a... more
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      VirologyBiological SciencesCercopithecus aethiopsCell line
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      GeneticsDevelopmental BiologyReproductionBreeding
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      KineticsGene TherapyHumansKidney
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      Salt StressGene expressionArabidopsis thalianaBiological Sciences
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      Cognitive ScienceBrain developmentWestern blottingBrain
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      GeneticsDevelopmental BiologyReproductionBreeding
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      KineticsBiological SciencesX RaysHumans
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      Electron MicroscopyBiological SciencesLiverEndocytosis
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      Biomedical EngineeringGene regulationDNAHumans
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      GeneticsHuman GeneticsElectron MicroscopyHumans
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      GeneticsCapillary electrophoresisPolysaccharidesBiological Sciences
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      PhytochemistryMetabolismBiological SciencesToxicity
Mucopolysaccharidosis I (MPS I) due to deficient α-L-iduronidase (IDUA) activity results in accumulation of glycosaminoglycans in many cells. Gene therapy could program liver to secrete enzyme with mannose 6-phosphate (M6P), and enzyme in... more
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      TechnologyGene TherapyTreatment OutcomeBiological Sciences
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      ApoptosisVascular biologyExtracellular MatrixSpleen
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      Mass SpectrometryEnzyme InhibitorsMultidisciplinaryHumans
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      Human GeneticsMass SpectrometryBiological SciencesHumans
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      GeneticsFunctional AnalysisCommon PropertyDanio rerio
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      ImmunohistochemistryLiverAnimalsPlant tissue Culture Techniques
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      Drug metabolismImmunohistochemistryMacrophagesWestern blotting