EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category  |
Confidence Level |
|---|
   3.3.2.9 | abc-type xenobiotic transporter deficiency |
21451505 |
Effect of ABCC2 (MRP2) Transport Function on Erythromycin Metabolism. |
causal interaction
unassigned |
3
0 |
| 3.3.2.9 | Aberrant Crypt Foci |
20650809 |
[Effects of astragalosides on induction of colorectal aberrant crypt foci by dimethylhydrazine and metabolizing enzymes in liver microsomes in rats] |
causal interaction
ongoing research
unassigned |
1
4
0 |
| 3.3.2.9 | Abetalipoproteinemia |
8527219 |
The hypobetalipoproteinemias. |
causal interaction
unassigned |
1
0 |
| 3.3.2.9 | Abetalipoproteinemia |
8939939 |
A novel abetalipoproteinemia genotype. Identification of a missense mutation in the 97-kDa subunit of the microsomal triglyceride transfer protein that prevents complex formation with protein disulfide isomerase. |
causal interaction
therapeutic application
unassigned |
1
1
0 |
| 3.3.2.9 | Abetalipoproteinemia |
9824535 |
Using genetically engineered mice to understand apolipoprotein-B deficiency syndromes in humans. |
causal interaction
unassigned |
3
0 |
| 3.3.2.9 | Abetalipoproteinemia |
10225972 |
Analysis of the role of microsomal triglyceride transfer protein in the liver of tissue-specific knockout mice. |
causal interaction
unassigned |
4
0 |
| 3.3.2.9 | Abetalipoproteinemia |
10446076 |
Abetalipoproteinemia caused by maternal isodisomy of chromosome 4q containing an intron 9 splice acceptor mutation in the microsomal triglyceride transfer protein gene. |
causal interaction
unassigned |
4
0 |
| 3.3.2.9 | Abetalipoproteinemia |
14732481 |
Hypobetalipoproteinemia with an apparently recessive inheritance due to a "de novo" mutation of apolipoprotein B. |
causal interaction
unassigned |
3
0 |
| 3.3.2.9 | Abetalipoproteinemia |
20592474 |
Primary deficiency of microsomal triglyceride transfer protein in human abetalipoproteinemia is associated with loss of CD1 function. |
causal interaction
unassigned |
3
0 |
| 3.3.2.9 | Abetalipoproteinemia |
21394827 |
A severe form of abetalipoproteinemia caused by new splicing mutations of microsomal triglyceride transfer protein. |
causal interaction
unassigned |
3
0 |
