EC Number   |
Disease |
PubMed ID |
Title of Publication  |
Category |
Confidence Level |
|---|
   3.1.3.56 | Carcinoma |
25759212 |
A distinct and replicable variant of the squamous cell carcinoma gene inositol polyphosphate-5-phosphatase modifies the susceptibility of arsenic-associated skin lesions in Bangladesh. |
ongoing research |
1 |
| 3.1.3.56 | Carcinoma |
25759212 |
A distinct and replicable variant of the squamous cell carcinoma gene inositol polyphosphate-5-phosphatase modifies the susceptibility of arsenic-associated skin lesions in Bangladesh. |
unassigned |
0 |
| 3.1.3.56 | Carcinoma, Squamous Cell |
25759212 |
A distinct and replicable variant of the squamous cell carcinoma gene inositol polyphosphate-5-phosphatase modifies the susceptibility of arsenic-associated skin lesions in Bangladesh. |
ongoing research |
1 |
| 3.1.3.56 | Carcinoma, Squamous Cell |
25759212 |
A distinct and replicable variant of the squamous cell carcinoma gene inositol polyphosphate-5-phosphatase modifies the susceptibility of arsenic-associated skin lesions in Bangladesh. |
unassigned |
0 |
| 3.1.3.56 | Neoplasm Metastasis |
33798953 |
A new gene panel as a marker for ESCC poor prognosis; INPP5A, TWIST1, MMP2, and EGFR. |
causal interaction |
4 |
| 3.1.3.56 | Neoplasm Metastasis |
33798953 |
A new gene panel as a marker for ESCC poor prognosis; INPP5A, TWIST1, MMP2, and EGFR. |
unassigned |
0 |
| 3.1.3.56 | Neoplasms |
33798953 |
A new gene panel as a marker for ESCC poor prognosis; INPP5A, TWIST1, MMP2, and EGFR. |
causal interaction |
4 |
| 3.1.3.56 | Neoplasms |
33798953 |
A new gene panel as a marker for ESCC poor prognosis; INPP5A, TWIST1, MMP2, and EGFR. |
unassigned |
0 |
| 3.1.3.56 | Oculocerebrorenal Syndrome |
23692838 |
A novel OCRL1 gene mutation in a Turkish child with Lowe syndrome. |
causal interaction |
3 |
| 3.1.3.56 | Oculocerebrorenal Syndrome |
23692838 |
A novel OCRL1 gene mutation in a Turkish child with Lowe syndrome. |
therapeutic application |
1 |
