EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    6.1.1.21 | Arthritis, Rheumatoid |
16192292 |
The potential role of human endogenous retrovirus K10 in the pathogenesis of rheumatoid arthritis: a preliminary study. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
4
2
1
0 |
| 6.1.1.21 | Ataxia |
23748049 |
Severe manifestation of Leber's hereditary optic neuropathy due to 11778G>A mtDNA mutation in a female with hypoestrogenism due to Perrault syndrome. |
causal interaction
ongoing research
unassigned |
2
2
0 |
| 6.1.1.21 | Autoimmune Diseases |
6866113 |
Myositis autoantibody inhibits histidyl-tRNA synthetase: a model for autoimmunity. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
1
3
2
1 |
| 6.1.1.21 | Autoimmune Diseases |
10430027 |
Histidyl-tRNA synthetase. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
4
2
4
0 |
| 6.1.1.21 | Autoimmune Diseases |
15966441 |
[The Jo-1 Syndrome--immunological findings and clinical manifestations] |
unassigned |
0 |
| 6.1.1.21 | Autoimmune Diseases |
17522890 |
Hodgkin's lymphoma in a patient with Jo-1 syndrome. |
causal interaction
unassigned |
1
0 |
| 6.1.1.21 | Autoimmune Diseases |
33131414 |
Isolation of monoclonal antibodies from anti-synthetase syndrome patients and affinity maturation by recombination of independent somatic variants. |
unassigned |
0 |
| 6.1.1.21 | Carcinoma |
8929351 |
Localization of histidyl-tRNA synthetase (Jo-1) in human laryngeal epithelial carcinoma cell line (HEp-2 cells). |
diagnostic usage
ongoing research
unassigned |
3
4
0 |
| 6.1.1.21 | Carcinoma, Hepatocellular |
1549469 |
Human histidyl-tRNA synthetase: recognition of amino acid signature regions in class 2a aminoacyl-tRNA synthetases. |
diagnostic usage
ongoing research
unassigned |
3
4
0 |
| 6.1.1.21 | Charcot-Marie-Tooth Disease |
32333447 |
Bi-allelic mutations in HARS1 severely impair histidyl-tRNA synthetase expression and enzymatic activity causing a novel multisystem ataxic syndrome. |
causal interaction
unassigned |
1
0 |
