EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   3.1.3.32 | Adenoma |
18414202 |
Polynucleotide kinase 3' phosphatase variant, dietary variables and risk of adenoma recurrence in the Polyp Prevention Trial. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
1
1
2
2 |
| 3.1.3.32 | Apraxias |
15367657 |
A new XRCC1-containing complex and its role in cellular survival of methyl methanesulfonate treatment. |
unassigned |
0 |
| 3.1.3.32 | Apraxias |
28821613 |
The RIR motif in the scaffold protein XRCC1 mediates a low-affinity interaction with polynucleotide kinase/phosphatase (PNKP) during DNA single-strand break repair. |
causal interaction
therapeutic application
unassigned |
3
1
0 |
| 3.1.3.32 | Apraxias |
31436889 |
From congenital microcephaly to adult onset cerebellar ataxia: Distinct and overlapping phenotypes in patients with PNKP gene mutations. |
causal interaction
therapeutic application
unassigned |
1
1
0 |
| 3.1.3.32 | Apraxias |
32010037 |
A Novel Homozygous Variant in the Fork-Head-Associated Domain of Polynucleotide Kinase Phosphatase in a Patient Affected by Late-Onset Ataxia With Oculomotor Apraxia Type 4. |
causal interaction
unassigned |
3
0 |
| 3.1.3.32 | Ataxia |
15367657 |
A new XRCC1-containing complex and its role in cellular survival of methyl methanesulfonate treatment. |
unassigned |
0 |
| 3.1.3.32 | Ataxia |
28821613 |
The RIR motif in the scaffold protein XRCC1 mediates a low-affinity interaction with polynucleotide kinase/phosphatase (PNKP) during DNA single-strand break repair. |
causal interaction
therapeutic application
unassigned |
3
1
0 |
| 3.1.3.32 | Ataxia |
31436889 |
From congenital microcephaly to adult onset cerebellar ataxia: Distinct and overlapping phenotypes in patients with PNKP gene mutations. |
causal interaction
therapeutic application
unassigned |
1
1
0 |
| 3.1.3.32 | Ataxia |
32010037 |
A Novel Homozygous Variant in the Fork-Head-Associated Domain of Polynucleotide Kinase Phosphatase in a Patient Affected by Late-Onset Ataxia With Oculomotor Apraxia Type 4. |
causal interaction
unassigned |
3
0 |
| 3.1.3.32 | Ataxia |
32504494 |
Pathological mutations in PNKP trigger defects in DNA single-strand break repair but not DNA double-strand break repair. |
causal interaction
unassigned |
2
0 |
