EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   7.6.2.1 | abc-type xenobiotic transporter deficiency |
24914347 |
ABCB4 mutations underlie hormonal cholestasis but not pediatric idiopathic gallstones. |
therapeutic application
unassigned |
1
0 |
| 7.6.2.1 | Acute Lung Injury |
30636723 |
Oxidative stress induces club cell proliferation and pulmonary fibrosis in Atp8b1 mutant mice. |
causal interaction
ongoing research
unassigned |
3
4
0 |
| 7.6.2.1 | Adenocarcinoma |
2836053 |
Photosensitizing effects of hematoporphyrin derivative and photofrin II on the plasma membrane enzymes 5'-nucleotidase, Na+K+-ATPase, and Mg2+-ATPase in R3230AC mammary adenocarcinomas. |
diagnostic usage
ongoing research
therapeutic application
unassigned |
3
4
1
0 |
| 7.6.2.1 | Adenocarcinoma |
16631473 |
Genomic array and expression analysis of frequent high-level amplifications in adenocarcinomas of the gastro-esophageal junction. |
diagnostic usage
unassigned |
3
0 |
| 7.6.2.1 | Adenocarcinoma |
20927484 |
Identification of Phospholipid Scramblase 1 as a biomarker and it's prognostic value for Colorectal Cancer. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
4
4
0 |
| 7.6.2.1 | Adenocarcinoma of Lung |
28178989 |
Individualized analysis reveals CpG sites with methylation aberrations in almost all lung adenocarcinoma tissues. |
unassigned |
0 |
| 7.6.2.1 | Adenocarcinoma of Lung |
33029490 |
Aberrant Methylation and Differential Expression of SLC2A1, TNS4, GAPDH, ATP8A2, and CASZ1 Are Associated with the Prognosis of Lung Adenocarcinoma. |
causal interaction
diagnostic usage
unassigned |
3
2
0 |
| 7.6.2.1 | Adenoma |
15564289 |
The PPAR{gamma} Pro12Ala polymorphism and risk for incident sporadic colorectal adenomas. |
diagnostic usage
unassigned |
2
0 |
| 7.6.2.1 | Agranulocytosis |
15328404 |
Adiposity, dyslipidemia, and insulin resistance in mice with targeted deletion of phospholipid scramblase 3 (PLSCR3). |
causal interaction
ongoing research
therapeutic application
unassigned |
1
3
1
0 |
| 7.6.2.1 | Alagille Syndrome |
25737299 |
Exome sequencing reveals compound heterozygous mutations in ATP8B1 in a JAG1/NOTCH2 mutation-negative patient with clinically diagnosed Alagille syndrome. |
causal interaction
unassigned |
2
0 |
