(Q45133882)

9 December 2017

Lysosomal acid alpha-glucosidase consists of four different peptides processed from a single chain precursor (English)

1 reference

9 December 2017

Rodney J Moreland

1

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9 December 2017

Xiaoying Jin

2

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9 December 2017

X Kate Zhang

3

1 reference

9 December 2017

Roger W Decker

4

1 reference

9 December 2017

Karen L Albee

5

1 reference

9 December 2017

Karen L Lee

6

1 reference

9 December 2017

Robert D Cauthron

7

1 reference

9 December 2017

Kevin Brewer

8

1 reference

9 December 2017

Tim Edmunds

9

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9 December 2017

William M Canfield

10

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9 December 2017

language of work or name

English

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publication date

1 November 2004

1 reference

Journal of Biological Chemistry

9 December 2017

12

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based on heuristic

inferred from page(s)

published in

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9 December 2017

280

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9 December 2017

8

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9 December 2017

6780-6791

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Purification and characterization of two components of acid alpha-glucosidase from pig liver

9 December 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M404008200

The molecular heterogeneity of purified human liver lysosomal α-Glucosidase (acid α-Glucosidase)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M404008200

Heat-stable protein that stimulates acid alpha-glucosidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M404008200

Targeted disruption of the acid alpha-glucosidase gene in mice causes an illness with critical features of both infantile and adult human glycogen storage disease type II

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M404008200

Correction of glycogen storage disease type II by enzyme replacement with a recombinant human acid maltase produced by over-expression in a CHO-DHFR(neg) cell line

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M404008200

Computer assisted cloning of human neutral alpha-glucosidase C (GANC): a new paralog in the glycosyl hydrolase gene family 31.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M404008200

Measurement of protein using bicinchoninic acid

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M404008200

Activation of human acid sphingomyelinase through modification or deletion of C-terminal cysteine

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M404008200

Local alignment statistics

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M404008200

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 disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M404008200

Characterization of glycoproteins and their associated oligosaccharides through the use of endoglycosidases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M404008200

alpha-Mannosidosis: functional cloning of the lysosomal alpha-mannosidase cDNA and identification of a mutation in two affected siblings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M404008200

Acid ?-glucosidase: A new polymorphism in man demonstrable by ?affinity? electrophoresis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M404008200

The 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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M404008200

Generalized glycogen storage and cardiomegaly in a knockout mouse model of Pompe disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M404008200

21 January 2018

Identifiers

DOI

10.1074/JBC.M404008200

1 reference

9 December 2017

1 reference