EC Number   |
Disease  |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   3.4.22.54 | Autosomal Emery-Dreifuss Muscular Dystrophy |
10838245 |
Nuclear proteins and cell death in inherited neuromuscular disease. |
causal interaction
unassigned |
2
0 |
| 3.4.22.54 | Brain Neoplasms |
11807032 |
The Drosophila melanogaster gene brain tumor negatively regulates cell growth and ribosomal RNA synthesis. |
causal interaction
unassigned |
1
0 |
| 3.4.22.54 | Brain Neoplasms |
18528333 |
Mei-P26 regulates microRNAs and cell growth in the Drosophila ovarian stem cell lineage. |
ongoing research
unassigned |
3
0 |
| 3.4.22.54 | Bulbo-Spinal Atrophy, X-Linked |
10838245 |
Nuclear proteins and cell death in inherited neuromuscular disease. |
causal interaction
unassigned |
2
0 |
| 3.4.22.54 | calpain 8 deficiency |
22825607 |
Analysis of calpain-3 protein in muscle biopsies of different muscular dystrophies from India. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
2
3
3
1 |
| 3.4.22.54 | calpain-3 deficiency |
9309711 |
Calpain-3 deficiency causes a mild muscular dystrophy in childhood. |
causal interaction
unassigned |
4
0 |
| 3.4.22.54 | calpain-3 deficiency |
10229226 |
Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IkappaB alpha/NF-kappaB pathway in limb-girdle muscular dystrophy type 2A. |
causal interaction
unassigned |
1
0 |
| 3.4.22.54 | calpain-3 deficiency |
10567047 |
Mutations of calpain 3 gene in patients with sporadic limb-girdle muscular dystrophy in Japan. |
causal interaction
unassigned |
4
0 |
| 3.4.22.54 | calpain-3 deficiency |
11134085 |
Loss of calpain 3 proteolytic activity leads to muscular dystrophy and to apoptosis-associated IkappaBalpha/nuclear factor kappaB pathway perturbation in mice. |
causal interaction
ongoing research
unassigned |
1
1
0 |
| 3.4.22.54 | calpain-3 deficiency |
11245721 |
Calpain-3 and dysferlin protein screening in patients with limb-girdle dystrophy and myopathy. |
causal interaction
diagnostic usage
unassigned |
3
3
0 |
