Human lysosomal alpha-glucosidase: functional characterization of the glycosylation sites.
about
Leaky splicing mutation in the acid maltase gene is associated with delayed onset of glycogenosis type IIRecombinant human acid alpha-glucosidase corrects acid alpha-glucosidase-deficient human fibroblasts, quail fibroblasts, and quail myoblastsFunctional characterization of the N-glycosylation sites of human acid sphingomyelinase by site-directed mutagenesisGlycogenosis type II (acid maltase deficiency)Ultrastructural analysis of development of myocardium in calreticulin-deficient miceN-glycans of recombinant human acid alpha-glucosidase expressed in the milk of transgenic rabbits.Structural determinants of protein folding.High-level production of recombinant human lysosomal acid alpha-glucosidase in Chinese hamster ovary cells which targets to heart muscle and corrects glycogen accumulation in fibroblasts from patients with Pompe diseasePompe disease: from pathophysiology to therapy and back againOral delivery of Acid Alpha Glucosidase epitopes expressed in plant chloroplasts suppresses antibody formation in treatment of Pompe mice.Mistargeting of the lectin ERGIC-53 to the endoplasmic reticulum of HeLa cells impairs the secretion of a lysosomal enzyme.Homozygosity for multiple contiguous single-nucleotide polymorphisms as an indicator of large heterozygous deletions: identification of a novel heterozygous 8-kb intragenic deletion (IVS7-19 to IVS15-17) in a patient with glycogen storage disease tyStructural aspects of therapeutic enzymes to treat metabolic disorders.The genotype-phenotype correlation in Pompe disease.N-glycosylation is crucial for folding, trafficking, and stability of human tripeptidyl-peptidase I.Erythrocyte-mediated delivery of recombinant enzymes.Characterization of iduronate sulphatase mutants affecting N-glycosylation sites and the cysteine-84 residueThe conservative substitution Asp-645-->Glu in lysosomal alpha-glucosidase affects transport and phosphorylation of the enzyme in an adult patient with glycogen-storage disease type II.Human alpha-galactosidase A: glycosylation site 3 is essential for enzyme solubility.Inhibition of some hepatic glycosidases by the diseco nucleoside, 4-amino-3-(D-glucopentitol-1-yl)-5-mercapto-1,2,4-triazole and its 3-methyl analog.Structural modeling of mutant alpha-glucosidases resulting in a processing/transport defect in Pompe disease.
P2860
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P2860
Human lysosomal alpha-glucosidase: functional characterization of the glycosylation sites.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
1993年论文
@zh
1993年论文
@zh-cn
name
Human lysosomal alpha-glucosid ...... on of the glycosylation sites.
@en
type
label
Human lysosomal alpha-glucosid ...... on of the glycosylation sites.
@en
prefLabel
Human lysosomal alpha-glucosid ...... on of the glycosylation sites.
@en
P2093
P2860
P356
P1433
P1476
Human lysosomal alpha-glucosid ...... on of the glycosylation sites.
@en
P2093
P2860
P304
P356
10.1042/BJ2890681
P407
P478
289 ( Pt 3)
P577
1993-02-01T00:00:00Z