EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   2.7.11.19 | Cardiomyopathy, Hypertrophic |
8236826 |
Fatal infantile hypertrophic cardiomyopathy secondary to deficiency of heart specific phosphorylase b kinase. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 2.7.11.19 | Cardiomyopathy, Hypertrophic |
10368461 |
Infantile hypertrophic cardiomyopathy of glycogenosis type IX: isolated cardiac phosphorylase kinase deficiency. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 2.7.11.19 | Colorectal Neoplasms |
28275865 |
Phosphorylase kinase ? affects colorectal cancer cell growth and represents a novel prognostic biomarker. |
diagnostic usage
ongoing research
unassigned |
3
4
0 |
| 2.7.11.19 | Cystic Fibrosis |
16887929 |
Peptide microarray analysis of substrate specificity of the transmembrane Ser/Thr kinase KPI-2 reveals reactivity with cystic fibrosis transmembrane conductance regulator and phosphorylase. |
therapeutic application
unassigned |
1
0 |
| 2.7.11.19 | Diabetes Mellitus, Type 2 |
21132776 |
Kinetics, in silico docking, molecular dynamics, and MM-GBSA binding studies on prototype indirubins, KT5720, and staurosporine as phosphorylase kinase ATP-binding site inhibitors: The role of water molecules examined. |
therapeutic application
unassigned |
3
0 |
| 2.7.11.19 | Diabetes Mellitus, Type 2 |
21287607 |
Kinetics, in silico docking, molecular dynamics, and MM-GBSA binding studies on prototype indirubins, KT5720, and staurosporine as phosphorylase kinase ATP-binding site inhibitors: the role of water molecules examined. |
therapeutic application
unassigned |
3
0 |
| 2.7.11.19 | Diabetes Mellitus, Type 2 |
26364215 |
An evaluation of indirubin analogues as phosphorylase kinase inhibitors. |
causal interaction
therapeutic application
unassigned |
1
2
0 |
| 2.7.11.19 | Fanconi Syndrome |
10987651 |
A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity. |
causal interaction
unassigned |
1
0 |
| 2.7.11.19 | glycogen phosphorylase deficiency |
8655128 |
Genetic deficiencies of the glycogen phosphorylase system. |
causal interaction
unassigned |
4
0 |
| 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 |
