EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   3.3.1.1 | Acidosis, Lactic |
34121999 |
Inborn Errors of Metabolism Associated With Autism Spectrum Disorders: Approaches to Intervention. |
causal interaction
unassigned |
4
0 |
| 3.3.1.1 | adenosine deaminase deficiency |
312296 |
In vivo inactivation of erythrocyte S-adenosylhomocysteine hydrolase by 2'-deoxyadenosine in adenosine deaminase-deficient patients. |
causal interaction
unassigned |
3
0 |
| 3.3.1.1 | adenosine deaminase deficiency |
7079734 |
The human genes for S-adenosylhomocysteine hydrolase and adenosine deaminase are syntenic on chromosome 20. |
unassigned |
0 |
| 3.3.1.1 | adenosine deaminase deficiency |
7391654 |
Decreased S-adenosylhomocysteine hydrolase in inborn errors of purine metabolism. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
1
3
0 |
| 3.3.1.1 | adenosine kinase deficiency |
6330251 |
S-adenosylhomocysteine hydrolase inactivation and purine toxicity in cultured human T- and B-lymphoblasts. |
therapeutic application
unassigned |
1
0 |
| 3.3.1.1 | adenosine kinase deficiency |
27671891 |
Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 3.3.1.1 | adenosine kinase deficiency |
34347214 |
S-adenosylmethionine induces mitochondrial dysfunction, permeability transition pore opening and redox imbalance in subcellular preparations of rat liver. |
causal interaction
therapeutic application
unassigned |
3
1
0 |
| 3.3.1.1 | adenosylhomocysteinase deficiency |
2380820 |
Familial hypermethioninemia partially responsive to dietary restriction. |
diagnostic usage
unassigned |
3
0 |
| 3.3.1.1 | adenosylhomocysteinase deficiency |
3989751 |
S-Adenosylhomocysteine hydrolase deficiency in cysteine auxotrophs of Tetrahymena thermophila. |
causal interaction
unassigned |
2
0 |
| 3.3.1.1 | adenosylhomocysteinase deficiency |
6782120 |
Proposed explanation for S-adenosylhomocysteine hydrolase deficiency in purine nucleoside phosphorylase and hypoxanthine-guanine phosphoribosyltransferase-deficient patients. |
causal interaction
unassigned |
3
0 |
