EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
2.6.1.42 | Acute Coronary Syndrome |
32132739 |
THE BRANCHED-CHAIN AMINO ACID TRANSAMINASE 1 -23C/G POLYMORPHISM CONFERS PROTECTION AGAINST ACUTE CORONARY SYNDROME. |
causal interaction diagnostic usage therapeutic application unassigned |
4 1 1 0 |
2.6.1.42 | Adenocarcinoma |
30378334 |
[The Expression and Significance of c-myc and bcat1 in Cervical Cancer]. |
causal interaction diagnostic usage ongoing research unassigned |
4 4 3 0 |
2.6.1.42 | Adenoma |
33478584 |
Evaluation of a panel of tumor-specific differentially-methylated DNA regions in IRF4, IKZF1 and BCAT1 for blood-based detection of colorectal cancer. |
diagnostic usage therapeutic application unassigned |
3 1 0 |
2.6.1.42 | Alzheimer Disease |
24094038 |
THE BRANCHED-CHAIN AMINOTRANSFERASE PROTEINS: NOVEL REDOX CHAPERONES FOR PROTEIN DISULFIDE ISOMERASE- IMPLICATIONS IN ALZHEIMER'S DISEASE. |
causal interaction therapeutic application unassigned |
4 3 0 |
2.6.1.42 | Alzheimer Disease |
25633671 |
Regional Increase in the Expression of the BCAT Proteins in Alzheimer's Disease Brain: Implications in Glutamate Toxicity. |
causal interaction unassigned |
3 0 |
2.6.1.42 | Alzheimer Disease |
26980008 |
Altered Expression of Human Mitochondrial Branched Chain Aminotransferase in Dementia with Lewy Bodies and Vascular Dementia. |
causal interaction diagnostic usage ongoing research therapeutic application |
2 3 3 1 |
2.6.1.42 | Alzheimer Disease |
31982508 |
BCAT-induced autophagy regulates A? load through an interdependence of redox state and PKC phosphorylation-implications in Alzheimer's disease. |
causal interaction unassigned |
3 0 |
2.6.1.42 | Astrocytoma |
30113684 |
Loss of BCAT1 Expression is a Sensitive Marker for IDH-Mutant Diffuse Glioma. |
causal interaction diagnostic usage therapeutic application unassigned |
1 1 1 0 |
2.6.1.42 | Blast Crisis |
28514443 |
Cancer progression by reprogrammed BCAA metabolism in myeloid leukaemia. |
causal interaction diagnostic usage ongoing research therapeutic application |
1 3 2 1 |
2.6.1.42 | Brain Diseases |
31177572 |
Expanding the genetic and phenotypic spectrum of branched-chain amino acid transferase 2 deficiency. |
causal interaction therapeutic application unassigned |
4 3 0 |