EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   1.16.1.8 | Abortion, Spontaneous |
23302731 |
[Association of methionine synthase reductase gene polymorphism with unexplained recurrent spontaneous abortion]. |
diagnostic usage
unassigned |
3
0 |
| 1.16.1.8 | Abortion, Spontaneous |
26345779 |
Polymorphisms in the methylene tetrahydrofolate reductase and methionine synthase reductase genes and their correlation with unexplained recurrent spontaneous abortion susceptibility. |
causal interaction
ongoing research
unassigned |
4
2
0 |
| 1.16.1.8 | Abruptio Placentae |
17376725 |
Polymorphisms in methionine synthase reductase and betaine-homocysteine S-methyltransferase genes: risk of placental abruption. |
causal interaction
diagnostic usage
unassigned |
2
3
0 |
| 1.16.1.8 | Adenocarcinoma |
21603981 |
Gene polymorphisms involved in folate and methionine metabolism and increased risk of sporadic colorectal adenocarcinoma. |
diagnostic usage
ongoing research
therapeutic application
unassigned |
2
1
1
0 |
| 1.16.1.8 | Adenoma |
17389618 |
Twenty-four non-synonymous polymorphisms in the one-carbon metabolic pathway and risk of colorectal adenoma in the Nurses' Health Study. |
causal interaction
diagnostic usage
unassigned |
3
1
0 |
| 1.16.1.8 | Adenoma |
31740010 |
Low folate status, and MTHFR 677C?>?T and MTR 2756A?>?G polymorphisms associated with colorectal cancer risk in Thais: a case-control study. |
diagnostic usage
ongoing research
therapeutic application
unassigned |
3
3
1
0 |
| 1.16.1.8 | Anemia, Megaloblastic |
10484769 |
Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism. |
causal interaction
diagnostic usage
unassigned |
2
1
0 |
| 1.16.1.8 | Anemia, Megaloblastic |
17554763 |
Polymorphic background of methionine synthase reductase modulates the phenotype of a disease-causing mutation. |
unassigned |
0 |
| 1.16.1.8 | Arthritis, Rheumatoid |
17611986 |
2756GG genotype of methionine synthase reductase gene is more prevalent in rheumatoid arthritis patients treated with methotrexate and is associated with methotrexate-induced nodulosis. |
causal interaction
diagnostic usage
ongoing research
unassigned |
3
4
4
0 |
| 1.16.1.8 | Atherosclerosis |
20209990 |
[Features of allele polymorphism of genes involved in homocysteine and folate metabolism in patients with atherosclerosis of the lower extremity arteries] |
diagnostic usage
ongoing research
unassigned |
2
1
0 |
