EC Number   |
Disease |
PubMed ID |
Title of Publication  |
Category |
Confidence Level |
|---|
    2.3.1.12 | Liver Cirrhosis, Biliary |
1729364 |
A lipoyl synthetic octadecapeptide of dihydrolipoamide acetyltransferase specifically recognized by anti-M2 autoantibodies in primary biliary cirrhosis. |
causal interaction
diagnostic usage
unassigned |
1
3
0 |
| 2.3.1.12 | Alzheimer Disease |
4004169 |
An immunochemical study of the pyruvate dehydrogenase deficit in Alzheimer's disease brain. |
causal interaction
diagnostic usage
ongoing research
unassigned |
1
2
2
0 |
| 2.3.1.12 | Liver Cirrhosis, Biliary |
8336525 |
Antibody to two forms of dihydrolipoamide acetyltransferase (PDC-E2) in primary biliary cirrhosis. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
1
3
2
1 |
| 2.3.1.12 | Liver Cirrhosis, Biliary |
2473022 |
Antimitochondrial autoantibodies in primary biliary cirrhosis recognize cross-reactive epitope(s) on protein X and dihydrolipoamide acetyltransferase of pyruvate dehydrogenase complex. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
1
1
0 |
| 2.3.1.12 | Autoimmune Diseases |
3049806 |
Autoantibodies of primary biliary cirrhosis recognize dihydrolipoamide acetyltransferase and inhibit enzyme function. |
diagnostic usage
ongoing research
unassigned |
3
4
0 |
| 2.3.1.12 | Liver Cirrhosis, Biliary |
3049806 |
Autoantibodies of primary biliary cirrhosis recognize dihydrolipoamide acetyltransferase and inhibit enzyme function. |
diagnostic usage
ongoing research
unassigned |
3
4
0 |
| 2.3.1.12 | Liver Cirrhosis, Biliary |
8102256 |
Chromosome localization and RFLP analysis of PDC-E2: the major autoantigen of primary biliary cirrhosis. |
diagnostic usage
ongoing research
unassigned |
3
3
0 |
| 2.3.1.12 | pyruvate dehydrogenase (nadp+) deficiency |
16049940 |
Clinical and genetic spectrum of pyruvate dehydrogenase deficiency: dihydrolipoamide acetyltransferase (E2) deficiency. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
3
3
1
1 |
| 2.3.1.12 | Pyruvate Dehydrogenase Complex Deficiency Disease |
16049940 |
Clinical and genetic spectrum of pyruvate dehydrogenase deficiency: dihydrolipoamide acetyltransferase (E2) deficiency. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
3
3
1
1 |
| 2.3.1.12 | Liver Cirrhosis, Biliary |
8460168 |
Combinatorial autoantibodies to dihydrolipoamide acetyltransferase, the major autoantigen of primary biliary cirrhosis. |
diagnostic usage
ongoing research
unassigned |
3
1
0 |
