(Q24528082)

English

Human aspartylglucosaminidase. A biochemical and immunocytochemical characterization of the enzyme in normal and aspartylglucosaminuria fibroblasts

scientific article

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scholarly article

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Human aspartylglucosaminidase. A biochemical and immunocytochemical characterization of the enzyme in normal and aspartylglucosaminuria fibroblasts (English)

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aspartylglucosaminuria

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based on heuristic

inferred from title

author name string

N Enomaa

1

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T Heiskanen

2

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R Halila

3

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R Sormunen

4

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R Seppälä

5

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M Vihinen

6

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L Peltonen

7

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language of work or name

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publication date

1 September 1992

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Biochemical Journal

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286 ( Pt 2)

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613-8

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Association of alpha- and beta-subunits during the biosynthesis of beta-hexosaminidase in cultured human fibroblasts

1 reference

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24 March 2017

Purification and characterization of rat liver glycosylasparaginase

1 reference

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24 March 2017

Human leucocyte aspartylglucosaminidase. Evidence for two different subunits in a more complex native structure

1 reference

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24 March 2017

Aspartylglucosaminuria: cDNA encoding human aspartylglucosaminidase and the missense mutation causing the disease

1 reference

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A general method applicable to the search for similarities in the amino acid sequence of two proteins

1 reference

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Rapid and sensitive protein similarity searches

1 reference

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Prediction of the Secondary Structure of Proteins from their Amino Acid Sequence

1 reference

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Some factors in the interpretation of protein denaturation

1 reference

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β-Aspartylglucosylamine Amido Hydrolase of Rat Liver and Kidney

1 reference

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Human placental neuraminidase. Activation, stabilization and association with beta-galactosidase and its protective protein

1 reference

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Cloning and sequence analysis of a cDNA for human glycosylasparaginase. A single gene encodes the subunits of this lysosomal amidase

1 reference

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In vitro mutagenesis helps to unravel the biological consequences of aspartylglucosaminuria mutation

1 reference

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1 reference

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1 reference

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Synthesis of beta-hexosaminidase in cell-free translation and in intact fibroblasts: an insoluble precursor alpha chain in a rare form of Tay-Sachs disease

1 reference

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Genetic analysis of protein stability and function

1 reference

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Control of protein exit from the endoplasmic reticulum

1 reference

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Isolation and characterization of low and high affinity goat antibodies directed to single antigenic sites on human hemoglobin

1 reference

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A new method of preparing gold probes for multiple-labeling cytochemistry.

1 reference

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Isolation of a human hepatic 60 kDa aspartylglucosaminidase consisting of three non-identical polypeptides

1 reference

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The antigenic index: a novel algorithm for predicting antigenic determinants.

1 reference

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Intracellular degradation of the transport-impaired human PiZ alpha 1-antitrypsin variant. Biochemical mapping of the degradative event among compartments of the secretory pathway

1 reference

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Glycosaparaginase from human leukocytes. Inactivation and covalent modification with diazo-oxonorvaline.

1 reference

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1 reference

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Convenient and quantitative determination of the frequency of a mutant allele using solid-phase minisequencing: application to aspartylglucosaminuria in Finland

1 reference

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An algorithm for simultaneous comparison of several sequences

1 reference

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Enzymatic cleavage of glycopeptides

1 reference

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An absolute method for protein determination based on difference in absorbance at 235 and 280 nm

1 reference

https://pubmed.ncbi.nlm.nih.gov/1530592

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purification and properties of human hepatic aspartylglucosaminidase

1 reference

https://pubmed.ncbi.nlm.nih.gov/1530592

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based on heuristic

inferred from PubMed ID database lookup

Accumulation of glycoprotein-derived metabolites in neural and visceral tissue in aspartylglycosaminuria

1 reference

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inferred from PubMed ID database lookup

A modified colorimetric method for the estimation of N-acetylamino sugars

1 reference

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inferred from PubMed ID database lookup

Identifiers

10.1042/BJ2860613

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