EC Number   |
Disease |
PubMed ID |
Title of Publication  |
Category |
Confidence Level |
|---|
   7.2.2.3 | Hemiplegia |
18811707 |
'Absence of T378N mutation of ATP1A2 gene in five patients with alternating hemiplegia of childhood'. |
unassigned |
0 |
| 7.2.2.3 | Neoplasms |
3034663 |
(3H)ouabain binding to leukaemic cells and intralymphocytic sodium content in chronic lymphocytic leukaemia; no evidence for alterations of the Na+/K+-pump. |
causal interaction
therapeutic application
unassigned |
2
2
0 |
| 7.2.2.3 | Menkes Kinky Hair Syndrome |
28451781 |
13 novel putative mutations in ATP7A found in a cohort of 25 Italian families. |
causal interaction
unassigned |
2
0 |
| 7.2.2.3 | Neoplasms |
26822609 |
2.3 Å resolution cryo-EM structure of human p97 and mechanism of allosteric inhibition. |
therapeutic application
unassigned |
2
0 |
| 7.2.2.3 | Apnea |
26102761 |
2B.03: URIC ACID LEVELS RELATED TO OBSTRUCTIVE SLEEP APNEA SYNDROME IN PATIENTS WITH HYPERTENSION FROM XINJIANG OF CHINA. |
unassigned |
0 |
| 7.2.2.3 | Sleep Apnea, Obstructive |
26102761 |
2B.03: URIC ACID LEVELS RELATED TO OBSTRUCTIVE SLEEP APNEA SYNDROME IN PATIENTS WITH HYPERTENSION FROM XINJIANG OF CHINA. |
unassigned |
0 |
| 7.2.2.3 | Migraine Disorders |
22759692 |
A case of familial hemiplegic migraine associated with a novel ATP1A2 gene mutation. |
causal interaction
unassigned |
4
0 |
| 7.2.2.3 | Migraine with Aura |
22759692 |
A case of familial hemiplegic migraine associated with a novel ATP1A2 gene mutation. |
causal interaction
unassigned |
4
0 |
| 7.2.2.3 | Starvation |
12115059 |
A chimeric Anabaena/ Escherichia coli KdpD protein (Anacoli KdpD) functionally interacts with E. coli KdpE and activates kdp expression in E. coli. |
therapeutic application
unassigned |
1
0 |
| 7.2.2.3 | Migraine Disorders |
31053037 |
A Chinese family with familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2. |
causal interaction
unassigned |
4
0 |
