(Q34548079)

2 August 2017

title

Excess purine degradation in exercising muscles of patients with glycogen storage disease types V and VII. (English)

1 reference

2 August 2017

main subject

glycogen storage disease

1 reference

I Mineo

1

1 reference

2 August 2017

N Kono

2

1 reference

2 August 2017

T Shimizu

3

1 reference

2 August 2017

N Hara

4

1 reference

2 August 2017

Y Yamada

5

1 reference

2 August 2017

S Sumi

6

1 reference

2 August 2017

K Nonaka

7

1 reference

2 August 2017

S Tarui

8

1 reference

2 August 2017

language of work or name

English

0 references

publication date

1 August 1985

1 reference

Journal of Clinical Investigation

2 August 2017

published in

1 reference

2 August 2017

volume

76

1 reference

2 August 2017

issue

2

1 reference

2 August 2017

page(s)

556-560

1 reference

PHOSPHOFRUCTOKINASE DEFICIENCY IN SKELETAL MUSCLE. A NEW TYPE OF GLYCOGENOSIS.

2 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=423860

Phosphoglycerate kinase deficiency: another cause of recurrent myoglobinuria.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423860

Myoadenylate deaminase deficiency. Functional and metabolic abnormalities associated with disruption of the purine nucleotide cycle

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423860

Disruption of the purine nucleotide cycle by inhibition of adenylosuccinate lyase produces skeletal muscle dysfunction

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423860

7 July 2018

Protons and anaerobiosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423860

Human Muscle Phosphoglycerate Mutase Deficiency: Newly Discovered Metabolic Myopathy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423860

Heterogeneity of the molecular lesions in inherited phosphofructokinase deficiency

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423860

The purine nucleotide cycle. 3. Oscillations in metabolite concentrations during the operation of the cycle in muscle extracts.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423860

A kinetic determination of ammonia in plasma.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423860

Exercise-induced changes in blood ammonia levels in humans

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423860

Metabolic adaptation in phosphorylase kinase deficiency. Changes in metabolite concentrations during tetanic stimulation of mouse leg muscles

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423860

Muscle phosphofructokinase deficiency: two cases with unusual polysaccharide accumulation and immunologically active enzyme protein.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423860

Exercising muscle does not produce hypoxanthine in adenylate deaminase deficiency

27 October 2018

1 reference

12 December 2020

Hereditary deficiency of lactate dehydrogenase M-subunit

1 reference

12 December 2020

Increased ammonia production during forearm ischemic work test in McArdle's disease

1 reference

12 December 2020

Adenylate deaminase from rat muscle. Regulation by purine nucleotides and orthophosphate in the presence of 150 mM KCl

1 reference

12 December 2020

HPLC analysis of aromatic amino acids, nucleosides, and bases in plasma of acute lymphocytic leukemia on chemotherapy

1 reference

12 December 2020

Phosphofructokinase (PFK) deficiency due to a catalytically inactive mutant M-type subunit

1 reference

12 December 2020

Examination of a case of suspected McArdle's syndrome by 31P nuclear magnetic resonance

1 reference

12 December 2020

Hypoxanthine and Mcardle disease: a clue to metabolic stress in the working forearm

1 reference

12 December 2020

Replenishment of citric acid cycle intermediates by the purine nucleotide cycle in rat skeletal muscle

1 reference

12 December 2020

Contracture in McArdle's disease. Stability of adenosine triphosphate during contracture in phosphorylase-deficient human muscle

1 reference

12 December 2020

Metabolic basis of improved exercise tolerance: muscle phosphorylase deficiency after glucagon administration

1 reference

12 December 2020

On a possible role of IMP in the regulation of phosphorylase activity in skeletal muscle

1 reference

12 December 2020

Ammonia and IMP in different skeletal muscle fibers after exercise in rats

1 reference

12 December 2020

High energy phosphate depletion in a model of defective muscle glycolysis

1 reference

12 December 2020

Possible correlation between binding of muscle type AMP deaminase to myofibrils and ammoniagenesis in rat skeletal muscle on electrical stimulation

1 reference

12 December 2020

Purine metabolism during strenuous muscular exercise in man

1 reference

12 December 2020

A comparative study on glucagon effect between mcardle disease and tarui disease

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI112006

1 reference

2 August 2017

1 reference

2 August 2017

1 reference