EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    1.14.18.1 | Acquired Immunodeficiency Syndrome |
15161941 |
Carbohydrates act as sorting determinants in ER-associated degradation of tyrosinase. |
therapeutic application
unassigned |
1
0 |
| 1.14.18.1 | Adenocarcinoma |
10085416 |
The role of the detection of hematogenous micrometastasis in prostate adenocarcinoma and malignant melanoma by RT-PCR. |
diagnostic usage
ongoing research
therapeutic application
unassigned |
4
4
2
0 |
| 1.14.18.1 | Adrenal Hyperplasia, Congenital |
1496017 |
Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutations. |
causal interaction
unassigned |
4
0 |
| 1.14.18.1 | Albinism |
28370 |
Characterization of human hairbulb tyrosinase: properties of normal and albino enzyme. |
unassigned |
0 |
| 1.14.18.1 | Albinism |
1476926 |
Do pigmented naevi in albinism provide evidence of tyrosinase positivity? |
unassigned |
0 |
| 1.14.18.1 | Albinism |
1693779 |
Murine and human b locus pigmentation genes encode a glycoprotein (gp75) with catalase activity. |
unassigned |
0 |
| 1.14.18.1 | Albinism |
1910093 |
Tyrosinase positive albinism with familial 46,XY,t(2;4) (q31.2;q31.22) balanced translocation. |
unassigned |
0 |
| 1.14.18.1 | Albinism |
2110899 |
A point mutation in the tyrosinase gene of BALB/c albino mouse causing the cysteine----serine substitution at position 85. |
ongoing research
unassigned |
4
0 |
| 1.14.18.1 | Albinism |
2126367 |
Comparative genetics of albinism. |
causal interaction
unassigned |
3
0 |
| 1.14.18.1 | Albinism |
2663665 |
Free radical reduction in the human epidermis. |
diagnostic usage
ongoing research
unassigned |
2
4
0 |
