(Q35203677)

7 August 2017

title

An isozyme of acid alpha-glucosidase with reduced catalytic activity for glycogen (English)

1 reference

7 August 2017

Beratis NG

1

1 reference

7 August 2017

LaBadie GU

series ordinal

2

1 reference

7 August 2017

Hirschhorn K

series ordinal

3

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 March 1980

1 reference

American Journal of Human Genetics

7 August 2017

published in

1 reference

7 August 2017

volume

32

1 reference

7 August 2017

issue

2

1 reference

7 August 2017

page(s)

137-149

1 reference

Protein measurement with the Folin phenol reagent

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686008

alpha-Glucosidase deficiency in generalized glycogenstorage disease (Pompe's disease).

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686008

Further purification and characterization of the acid α-glucosidase

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686008

Further kinetic and structural characterization of the lysosomal α-d-glucoside glucohydrolase from cattle liver

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686008

Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686008

Adult myopathy from glycogen storage disease due to acid maltase deficiency

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686008

Acid maltase deficiency in adults: studies in four cases of a syndrome which may mimic muscular dystrophy or other myopathies

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686008

Biochemical, immunological, and cell genetic studies in glycogenosis type II

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686008

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686008

Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686008

Late-onset acid maltase deficiency. Detection of patients and heterozygotes by urinary enzyme assay

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686008

Antibodies to papain. A selective fractionation according to inhibitory capacity

13 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6770674

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Discontinuous buffer systems for analytical and preparative electrophoresis of enzymes on polyacrylamide gel

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6770674

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Adult acid maltase deficiency. Abnormalities in fibroblasts cultured from patients

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6770674

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMC publication ID

1686008

1 reference

7 August 2017

1 reference