EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
7.6.2.15 | Adenocarcinoma |
27803021 |
Interaction of 2,4-Diaminopyrimidine-Containing Drugs Including Fedratinib and Trimethoprim with Thiamine Transporters. |
diagnostic usage ongoing research therapeutic application unassigned |
3 4 4 0 |
7.6.2.15 | Anemia |
10391222 |
The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter. |
ongoing research unassigned |
1 0 |
7.6.2.15 | Anemia |
16373304 |
Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families. |
causal interaction unassigned |
2 0 |
7.6.2.15 | Anemia |
16642288 |
Deletion of SLC19A2, the high affinity thiamine transporter, causes selective inner hair cell loss and an auditory neuropathy phenotype. |
diagnostic usage unassigned |
1 0 |
7.6.2.15 | Anemia |
17132746 |
Thiamine transporter mutation: an example of monogenic diabetes mellitus. |
causal interaction unassigned |
3 0 |
7.6.2.15 | Anemia |
18556972 |
Thiamine withdrawal can lead to diabetic ketoacidosis in thiamine responsive megaloblastic anemia: report of two siblings. |
causal interaction unassigned |
4 0 |
7.6.2.15 | Anemia |
20835854 |
Thiamine-responsive megaloblastic anemia syndrome. |
causal interaction unassigned |
3 0 |
7.6.2.15 | Anemia |
22837935 |
Thiamine responsive megaloblastic anemia syndrome associated with patent ductus arteriosus: First case report from Kashmir Valley of the Indian subcontinent. |
causal interaction unassigned |
1 0 |
7.6.2.15 | Anemia, Megaloblastic |
10074490 |
Defective high-affinity thiamine transporter leads to cell death in thiamine-responsive megaloblastic anemia syndrome fibroblasts. |
unassigned |
0 |
7.6.2.15 | Anemia, Megaloblastic |
10391223 |
Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndrome. |
unassigned |
0 |