EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    6.3.1.1 | Adenocarcinoma |
26355551 |
Asparagine Synthetase Expression and Phase I Study With L-Asparaginase Encapsulated in Red Blood Cells in Patients With Pancreatic Adenocarcinoma. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
4
3
4
1 |
| 6.3.1.1 | arylsulfatase (type i) deficiency |
27106218 |
Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder. |
causal interaction
unassigned |
4
0 |
| 6.3.1.1 | aspartate-ammonia ligase deficiency |
25227173 |
Asparagine synthetase deficiency detected by whole exome sequencing causes congenital microcephaly, epileptic encephalopathy and psychomotor delay. |
causal interaction
unassigned |
4
0 |
| 6.3.1.1 | aspartate-ammonia ligase deficiency |
25663424 |
Asparagine Synthetase Deficiency: New Inborn Errors of Metabolism. |
causal interaction
therapeutic application
unassigned |
4
3
0 |
| 6.3.1.1 | aspartate-ammonia ligase deficiency |
26318253 |
Asparagine Synthetase Deficiency causes reduced proliferation of cells under conditions of limited asparagine. |
causal interaction
unassigned |
4
0 |
| 6.3.1.1 | aspartate-ammonia ligase deficiency |
27106218 |
Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder. |
causal interaction
unassigned |
4
0 |
| 6.3.1.1 | aspartate-ammonia ligase deficiency |
27268761 |
Worsening of Seizures After Asparagine Supplementation in a Child with Asparagine Synthetase Deficiency. |
causal interaction
therapeutic application
unassigned |
4
2
0 |
| 6.3.1.1 | aspartate-ammonia ligase deficiency |
27422383 |
Hyperekplexia, microcephaly and simplified gyral pattern caused by novel ASNS mutations, case report. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
4
1
1
0 |
| 6.3.1.1 | aspartate-ammonia ligase deficiency |
27469131 |
Diaphragmatic Eventration in Sisters with Asparagine Synthetase Deficiency: A Novel Homozygous ASNS Mutation and Expanded Phenotype. |
causal interaction
unassigned |
4
0 |
| 6.3.1.1 | aspartate-ammonia ligase deficiency |
27743885 |
The first report of Japanese patients with asparagine synthetase deficiency. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
4
2
2
0 |
