EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   7.2.2.14 | Acidosis |
6224783 |
Protonic inhibition of the mitochondrial oligomycin-sensitive adenosine 5'-triphosphatase in ischemic and autolyzing cardiac muscle. Possible mechanism for the mitigation of ATP hydrolysis under nonenergizing conditions. |
ongoing research
therapeutic application
unassigned |
1
1
0 |
| 7.2.2.14 | Adenocarcinoma |
25347473 |
Membrane protein CNNM4-dependent Mg2+ efflux suppresses tumor progression. |
causal interaction
diagnostic usage
ongoing research
unassigned |
1
2
4
0 |
| 7.2.2.14 | Adenocarcinoma |
31076559 |
Magnesium transporter protein solute carrier family 41 member 1 suppresses human pancreatic ductal adenocarcinoma through magnesium-dependent Akt/mTOR inhibition and bax-associated mitochondrial apoptosis. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
4
4
3
4 |
| 7.2.2.14 | Amelogenesis Imperfecta |
19200525 |
Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta. |
unassigned |
0 |
| 7.2.2.14 | Amelogenesis Imperfecta |
19200527 |
Mutations in CNNM4 cause recessive cone-rod dystrophy with amelogenesis imperfecta. |
causal interaction
unassigned |
2
0 |
| 7.2.2.14 | Amelogenesis Imperfecta |
20706282 |
Cone-rod dystrophy and amelogenesis imperfecta (Jalili syndrome): phenotypes and environs. |
causal interaction
unassigned |
1
0 |
| 7.2.2.14 | Amelogenesis Imperfecta |
21393841 |
Purification, crystallization and preliminary crystallographic analysis of the CBS pair of the human metal transporter CNNM4. |
causal interaction
unassigned |
3
0 |
| 7.2.2.14 | Amelogenesis Imperfecta |
24194943 |
Dental phenotype in Jalili syndrome due to a c.1312 dupC homozygous mutation in the CNNM4 gene. |
causal interaction
unassigned |
3
0 |
| 7.2.2.14 | Amelogenesis Imperfecta |
24339795 |
Basolateral Mg2+ extrusion via CNNM4 mediates transcellular Mg2+ transport across epithelia: a mouse model. |
causal interaction
unassigned |
2
0 |
| 7.2.2.14 | Amelogenesis Imperfecta |
29421294 |
Jalili Syndrome: Cross-sectional and Longitudinal Features of Seven Patients With Cone-Rod Dystrophy and Amelogenesis Imperfecta. |
causal interaction
therapeutic application
unassigned |
1
1
0 |
