EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
3.1.14.1 | Arthritis, Infectious |
10024541 |
Alpha-toxin and gamma-toxin jointly promote Staphylococcus aureus virulence in murine septic arthritis. |
causal interaction ongoing research therapeutic application unassigned |
2 4 1 0 |
3.1.14.1 | Carcinoma |
17200614 |
Induction of the interferon-inducible RNA-degrading enzyme, RNase L, by stress-inducing agents in the human cervical carcinoma cells. |
causal interaction ongoing research therapeutic application unassigned |
4 3 2 0 |
3.1.14.1 | Corneal Dystrophies, Hereditary |
26204393 |
Polymorphism of the APEX nuclease 1 gene in keratoconus and Fuchs endothelial corneal dystrophy. |
ongoing research unassigned |
2 0 |
3.1.14.1 | Endophthalmitis |
9533895 |
Assessment of the role of gamma-toxin in experimental endophthalmitis using a hlg-deficient mutant of Staphylococcus aureus. |
diagnostic usage ongoing research therapeutic application unassigned |
3 4 2 0 |
3.1.14.1 | Fanconi Anemia |
32220227 |
Case report: a 58 -year -old man with small kidneys and elevated liver enzymes. |
causal interaction unassigned |
3 0 |
3.1.14.1 | Fanconi Anemia |
32450113 |
Common variants in FAN1, located in 15q13.3, confer risk for schizophrenia and bipolar disorder in Han Chinese. |
causal interaction unassigned |
3 0 |
3.1.14.1 | Fuchs' Endothelial Dystrophy |
26204393 |
Polymorphism of the APEX nuclease 1 gene in keratoconus and Fuchs endothelial corneal dystrophy. |
ongoing research unassigned |
2 0 |
3.1.14.1 | Huntington Disease |
32589923 |
Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier Effects. |
unassigned |
0 |
3.1.14.1 | Hypersensitivity |
11994165 |
KTI11 and KTI13, Saccharomyces cerevisiae genes controlling sensitivity to G1 arrest induced by Kluyveromyces lactis zymocin. |
causal interaction therapeutic application unassigned |
3 3 0 |
3.1.14.1 | Infections |
9533895 |
Assessment of the role of gamma-toxin in experimental endophthalmitis using a hlg-deficient mutant of Staphylococcus aureus. |
diagnostic usage ongoing research therapeutic application unassigned |
3 4 2 0 |