EC Number   |
Disease |
PubMed ID  |
Title of Publication |
Category |
Confidence Level |
|---|
   2.7.11.19 | Glycogen Storage Disease |
168880 |
Glycogen phosphorylase and its converter enzymes in haemolysates of normal human subjects and of patients with type VI glycogen-storage disease. A study of phosphorylase kinase deficiency. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
1
4
0 |
| 2.7.11.19 | phosphorylase kinase deficiency |
168880 |
Glycogen phosphorylase and its converter enzymes in haemolysates of normal human subjects and of patients with type VI glycogen-storage disease. A study of phosphorylase kinase deficiency. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
1
4
0 |
| 2.7.11.19 | phosphorylase kinase deficiency |
207857 |
Comparison of the mechanism of isoproterenol-stimulated glycogenolysis in skeletal muscle of normal and phosphorylase kinase-deficient mice (I strain). |
causal interaction
ongoing research
unassigned |
4
2
0 |
| 2.7.11.19 | phosphorylase kinase deficiency |
228813 |
[Regulation of glycogen metabolism in the liver and hepatic glycogenosis due to phosphorylase system deficiency] |
causal interaction
diagnostic usage
unassigned |
1
3
0 |
| 2.7.11.19 | phosphorylase kinase deficiency |
739734 |
Hepatic phosphorylase kinase deficiency: a survey of phosphorylase kinase activity in erythrocytes. |
causal interaction
unassigned |
4
0 |
| 2.7.11.19 | phosphorylase kinase deficiency |
820556 |
The molecular basis of skeletal muscle phosphorylase kinase deficiency. |
causal interaction
diagnostic usage
unassigned |
1
1
0 |
| 2.7.11.19 | phosphorylase kinase deficiency |
978457 |
Stimulation of glycogenolysis by beta adrenergic agonists in skeletal muscle of mice with the phosphorylase kinase deficiency mutation (I strain). |
causal interaction
ongoing research
unassigned |
1
2
0 |
| 2.7.11.19 | phosphorylase kinase deficiency |
1203056 |
The phosphorylase kinase deficiency (Phk) locus in the mouse: evidence that the mutant allele codes for an enzyme with an abnormal structure. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 2.7.11.19 | Glycogen Storage Disease |
1372435 |
cDNA cloning of a liver isoform of the phosphorylase kinase alpha subunit and mapping of the gene to Xp22.2-p22.1, the region of human X-linked liver glycogenosis. |
causal interaction
ongoing research
unassigned |
1
2
0 |
| 2.7.11.19 | phosphorylase kinase deficiency |
1372435 |
cDNA cloning of a liver isoform of the phosphorylase kinase alpha subunit and mapping of the gene to Xp22.2-p22.1, the region of human X-linked liver glycogenosis. |
causal interaction
ongoing research
unassigned |
1
2
0 |
